Professional Documents
Culture Documents
CMNA0115
CMNA0115
Editor
IRL B. HIRSCH
MEDICAL CLINICS
OF NORTH AMERICA
www.medical.theclinics.com
Consulting Editors
DOUGLAS S. PAAUW
EDWARD R. BOLLARD
KEYWORDS
Classification of diabetes mellitus Gestational diabetes mellitus
Latent autoimmune diabetes of adults Monogenic diabetes
Maturity-onset diabetes of the young Neonatal diabetes Secondary diabetes
Type 1 and Type 2 diabetes mellitus
KEY POINTS
The classification of diabetes mellitus is evolving as we work to fully understand the path-
ogenesis of the major forms.
The goal of classification is to say something meaningful about the cause, natural history,
genetics, heritability, clinical phenotype and optimum treatments of a disease. In the case
of diabetes, this is getting harder to do rather than easier.
Monogenic diabetes mellitus remains undiagnosed in more than 90% of the individuals
who have this form of diabetes caused by one of the known gene mutations.
The first step in wisdom is to know the things themselves; this notion consists in
having a true idea of the objects; objects are distinguished and known by classi-
fying them methodically and giving them appropriate names. Therefore, classifi-
cation and name-giving will be the foundation of our science.
Carolus Linnaeus, 1735
INTRODUCTION
This work was partially supported by the Chicago Diabetes Research and Training Center P30
DK020595.
a
Department of Medicine, Section of Endocrinology, Diabetes and Metabolism, The University
of Chicago, 5841 South Maryland Avenue, MC 1027, Chicago, IL 60637, USA; b Department of
Pediatrics, Section of Endocrinology, Diabetes and Metabolism, The University of Chicago, 900
East 57th Street, Chicago, IL 60637, USA
* Corresponding author. Department of Medicine, The University of Chicago, 900 East 57th
Street, Chicago, IL 60637.
E-mail address: [email protected]
organs, especially the eyes, kidneys, nerves, heart, and blood vessels.1,2 The goal in
diagnosing diabetes mellitus is to identify those with significantly increased premature
mortality and increased risk of microvascular and cardiovascular complications.
Although there are several existing useful classifications (see American Diabetes
Association 2014 guidelines for example), one can envision three schema to classify
the disease: (1) based on the pathophysiology, (2) based on a specific gene defect it-
self, or (3) based on another common phenotype. Some classifications are more
appropriate for research, others for patient care. The goal of classification is to say
something meaningful about the cause, natural history, genetics, heritability, clinical
phenotype, and optimum therapies. In the case of diabetes, this is getting harder to
do rather than easier. No classification scheme is ideal, and all have some inconsis-
tences and overlap. Diabetes mellitus classification will continue to evolve as we
work to fully understand the pathogenesis of the major forms.
The World Health Organization (WHO) diagnostic criteria for diabetes mellitus include
fasting plasma glucose level 126 mg/dL (7.0 mmol/L) or 2-hour plasma glucose level
200 mg/dL (11.1 mmol/L) after a 75-g oral glucose load.1 More recently, a glycated
hemoglobin level of 6.5% is recommended by WHO as the cut point for diagnosing
diabetes.3 Impaired glucose tolerance, a condition of intermediate hyperglycemia with
increased risk of progression to frank diabetes, is defined as a 2-hour plasma glucose
level 140 mg/dL (7.8 mmol/L) and less than 200 mg/dL (11.1 mmol/L) after a 75-g oral
glucose load. Impaired fasting glucose is defined as fasting glucose level between
110 mg/dL and 125 mg/dL (6.16.9 mmol/L).
These categories, impaired glucose tolerance and impaired fasting glucose,
as well as a glycated hemoglobin value between 5.7% and 6.4% are collectively
associated with increased risk of diabetes development and are often known as
prediabetes.4
EXISTING CLASSIFICATIONS
Until recently, the prevailing conceptual classification was that there were two primary
types of diabetes mellitus: autoimmune (type 1) and nonautoimmune (type 2). Every
other metabolic disorder of glucose regulation was classified into a special category
of (mostly type 2 related, nonautoimmune) diabetes, such as, monogenic, gestational,
steroid induced, cystic fibrosis related, postpancreatectomy, acromegaly associated,
human immunodeficiency virus (HIV) associated, hepatitis C virus associated, polycy-
stic ovary syndrome related, and ketosis prone diabetes.
Classification of diabetes mellitus has suffered from a lack of clear etiology of either
type 1 or type 2. Advances in classification terminology have included the evolution of
autoimmune diabetes from juvenile to insulin dependent to type 1 diabetes mellitus
(T1DM). However T1DM has been further divided into antibody positive (type 1a)
and antibody negative (type 1b).5 Others have shown that the slower adult-onset
forms (latent autoimmune diabetes of adults [LADA]) can also be further subdivided
and may include more subtle forms of immune involvement, which furthermore may
include a subset of individuals otherwise thought to have type 2 (Fig. 1).6
Type 1 Diabetes Mellitus
T1DM is generally autoimmune in etiology with, 1 of 4 autoantibodies to b-cell antigens
are being positive, including islet cell antibodies, glutamic acid decarboxylase-65 anti-
body, insulinoma antigen-2 antibody, or insulin autoantibodies.6,7 Autoantibodies that
Diabetes Classification 3
Diabetes Mellitus
bind to specific proteins found in the pancreatic islet cells were first described more
than 30 years ago.8 Although there is some debate as to the definition of autoimmune
disease, the frequent presence of autoantibodies, reproduction of autoimmune dis-
ease in experimental animals, and experimental disease with immunopathologic le-
sions that parallel those in the natural disease all suggest autoimmunity.9 However,
autoimmunity is a mechanism for the manifestation of T1DM but may not be its primary
cause.10,11 The disease presents in genetically susceptible individuals, likely as a
result of an environmental trigger. The immune system attacks the b-cells in the islets
of Langerhans of the pancreas, destroying or damaging them sufficiently to reduce
and eventually eliminate insulin production. Despite extensive research on the autoim-
mune nature of T1DM, questions remain regarding the timeframe and nature of b-cell
destruction and dysfunction. Type 1 could almost be considered monogenic with its
high linkage to human leukocyte antigen (HLA) region, but this is not the case for
some nonwhite populations.12,13 Concordance rates between monozygotic twins
are approximately 50%, whereas between dizygotic twins it is approximately
10%.14,15 Although with longer follow-up, disease may ultimately develop in discor-
dant twins.16 Clinical onset of T1DM is thought to result from a combination of overt
b-cell loss and b-cell dysfunction. However, our understanding of how b-cell meta-
bolic abnormalities arise during the pathogenesis of the disease remains incomplete.
(UKPDS), approximately 10% of adults with presumed type 2 diabetes mellitus (T2DM)
at diagnosis had evidence of islet autoimmunity in the form of circulating islet cell an-
tibodies or glutamic acid decarboxylase-65 antibodies.17 Most of these adults pro-
gressed to insulin dependence within 6 years. Controversy exists as to whether
LADA and adult-onset T1DM are the same clinical entity. There is epidemiologic evi-
dence suggesting that T1DM peaks around the time of puberty and again with a lesser
peak at age 40 years.18 The Immunology of Diabetes Society19 proposed that patients
classified as having LADA be 30 years of age, positive for at least 1 of the 4 anti-
bodies commonly found in T1DM, and not treated with insulin within the first 6 months
after diagnosis. This final criterion of a period of insulin independence after diagnosis is
intended to distinguish LADA from T1DM. One group found that the level of insulin
secretion in LADA was intermediate between type 1 diabetes and type 2 diabetes.20
This study found that fasting and stimulated C-peptide were reduced in patients
with LADA compared with type 2 diabetes patients and healthy control subjects
and that a rapid decline in stimulated C-peptide secretion occurred within a few years
of diagnosis in LADA patients treated with oral hypoglycemic agents. In UKPDS and
another European study on LADA, the highest-risk HLA phenotypes for T1DM (DR3/
4 and DQ2/8) were more prevalent in LADA patients than in healthy control subjects,
consistent with the known genetic predisposition to islet autoimmunity.21,22 Epidemi-
ologic studies suggest that LADA may account for 2% to 12% of all cases of dia-
betes.6 Clinicians should maintain vigilance in identifying this entity amongst the
many cases of T2DM.
Monogenic Diabetes
Monogenic diabetes is potentially the most important class for clinicians to consider
as a possible etiology, as most causes can be determined down to a single base
change in DNA or a deletion/insertion of a methylation defect. Although many of these
highly penetrant causes were first discovered in the 1990s, more than 94% of MODY
cases remain undiagnosed in the United States.39 There are 2 basic subtypes:
neonatal and MODY-like. Classification is increasingly complicated by the realization
that the full expression of phenotypes owing to highly penetrant genes is not yet
known. For example, although mutations in FOXP3 cause IPEX (immune dysregula-
tion, polyendocrinopathy, enteropathy, X-linked) syndrome, an early-onset, anti-
body-positive form of monogenic T1DM without other syndromic findings may
appear first and obscure the existence of syndromic diabetes.
Neonatal diabetes mellitus (NDM) is defined as diabetes mellitus with onset before
approximately 6 months of age. Some forms might better be termed congenital
diabetes (Greeley SA, personal communication, 2009). The term encompasses dia-
betes of any etiology, but it is recognized that diabetes diagnosed before age 6 months
is almost always monogenic in nature, although it can be (rarely) autoimmune.40 NDM
subtypes include transient NDM (TNDM) and permanent NDM (PNDM). TNDM often
develops within the first few weeks of life and resolves by a few months of age. How-
ever, relapse occurs in adolescence or adulthood in approximately 50% of cases.
TNDM is most frequently caused by abnormalities in the imprinted region of chromo-
some 6q24, leading to overexpression of paternally derived genes. Mutations in the
genes KCNJ11 and ABCC8, which encode the 2 subunits of the adenosine triphos-
phatesensitive potassium channel on the b-cell membrane, can cause TNDM or
PNDM. Importantly, diabetes secondary to mutations in KCNJ11 and ABCC8 often
responds to sulfonylureas. Mutations in other genes critical to b-cell function and
regulation, and in the insulin gene itself, also cause NDM. In approximately 40% of
NDM cases, the genetic cause remains unknown.40 The population prevalence of
PNDM was recently studied and estimated to be 1 in 250,000 in youth less than
20 years of age.41
MODY describes a heterogeneous group of disorders caused by mutations in genes
important for b-cell development, function and regulation, glucose sensing, and in the
insulin gene itself.27,42 MODY should be suspected and recognized if a type 2
diabeteslike condition occurs in 2 to 3 or more generations in an autosomal dominant
pattern of inheritance. However, de novo cases certainly occur. Mutations in at least 8
different genes can cause MODY.43 The natural history varies based on the underlying
genetic defect.
Mutations in HNF1A (MODY 3) are the most common cause of MODY, responsible
for 52% of monogenic diabetes in a large UK series, and in a US cohort, 27 of 49
MODY mutations identified (55%) were in the HNF1A gene.39,44 HNF1A encodes a
transcription factor important for pancreatic development and b-cell differentiation
and function. The mutation is highly penetrant, and diabetes develops by age
25 years in more than 60% of mutation carriers.45 Sulfonylureas are the treatment
of choice in HNF1A diabetes. In one study, 70% of individuals with a genetic diag-
nosis of HNF1A diabetes successfully switched from insulin to sulfonylurea treatment
Diabetes Classification 7
and remained off insulin for a median of 39 months with relatively good glycemic
control.46
HNF4A (MODY 1) also encodes a transcription factor important for pancreatic
development and b-cell differentiation and function. HNF4A mutations account for
approximately 10% of MODY.44 HNF4A mutations cause a similar clinical phenotype
as HNF1A mutations characterized by progressive insulin deficiency, diabetes onset
before age 25 years, and a response to relatively low-dose sulfonylurea therapy.
HNF1A mutations were identified in 8 of 49 (16%) MODY mutations found in a study
of 586 American youth with diabetes mellitus.39
Glucokinase catalyzes the first step in glycogen storage and glycolysis, phosphor-
ylation of glucose to glucose-6-phosphate. Glucokinase acts as the glucose sensor in
b-cells and liver linking insulin secretion to increases in serum glucose. Heterozygous
inactivating mutations in GCK (MODY 2) increase the set point for insulin secretion in
response to increased blood sugar, causing a stable, mild fasting hyperglycemia.
Complications are extremely rare, and generally glucokinase-related diabetes does
not require any therapy. Importantly, treatment with insulin or oral hypoglycemic
agents does not change overall glycemia.47 Family history often reveals borderline
diabetes or gestational diabetes in parents and grandparents. Women with GCK mu-
tations are commonly treated with insulin during pregnancy to avoid fetal macrosomia.
However, the optimal treatment of GCK hyperglycemia during pregnancy is uncer-
tain.48 With weight gain or obesity and aging, the average blood sugars may increase,
but recent work continues to suggest that individuals with GCK hyperglycemia do not
progress to diabetes complications development.47
Mutations in HNF1B (MODY 5) most often cause developmental renal disease,
particularly renal cysts. HNF1B mutations can also cause isolated diabetes or dia-
betes associated with kidney disease (renal cysts and diabetes syndrome). Urogenital
tract anomalies and atrophy of the pancreas may also occur.
MODY caused by mutations in PDX, NEUROD1, CEL, and INS (also a rare cause of
type 1b diabetes) is very rare. Overall, 10% to 20% of patients with a classic MODY
phenotype do not have a mutation in any of the known MODY genes.48
Mitochondrial diabetes is also monogenic in etiology and can be discriminated from
MODY based on maternal transmission and, in those with maternally inherited dia-
betes and deafness syndrome, bilateral hearing impairment in most carriers. The
disease associates with a range of mutations in mitochondrial DNA, with the most
common (maternally inherited diabetes and deafness) an A3434G mutation.49 This
mutation is estimated to account for 0.2% to 2% of diabetes cases with high pene-
trance, as greater than 85% of carriers will have diabetes during their lifetime.50
Diabetes associated with Wolfram syndrome (WFS1 and WFS2) is also monogenic
in etiology. Cystic fibrosisrelated diabetes (CFRD) could also be considered a
monogenic form of the disease (see later discussion).
normal or only slightly decreased, except in the settings of acute illness or glucocor-
ticoid treatment when insulin resistance can be severe.52
Initially, the disorder was thought to be caused by damage to the endocrine
pancreas after scarring and fibrosis of the exocrine pancreas. However, histopathol-
ogy studies have found that patients with cystic fibrosis with CFRD do not necessarily
have more pancreatic fibrosis at autopsy than patients with cystic fibrosis without
CFRD. More recent evidence suggests that the cystic fibrosis transmembrane
conductance regulator (CFTR) defect itself might be involved in impaired insulin
secretion.52
Chronic pancreatitis
Chronic pancreatitis is a disease characterized by pancreatic inflammatory and fibrotic
injury, resulting in irreversible parenchymal damage. The condition is associated with
many genetic mutations and polymorphisms that predispose to disease along with
environmental triggers.53 Development of diabetes mellitus in chronic pancreatitis
mainly occurs from the destruction of islet cells by pancreatic inflammation. In some
tropical countries there is an idiopathic variety of early-onset, chronic, calcific, nonal-
coholic pancreatitis that is associated with malnutrition that has been termed tropical
chronic pancreatitis.54 A WHO study group termed the associated diabetes fibrocalcu-
lous pancreatic diabetes.55 Persons with secondary diabetes from chronic pancreatitis
are often misclassified as having T2DM and, if treated with sulfonylureas, are at
increased risk of hypoglycemia given the diminished action of glucagon.
Hereditary hemochromatosis
Hereditary hemochromatosis was originally described as a triad of diabetes, cirrhosis,
and skin pigmentation. Recent studies show the prevalence of diabetes to be 13% to
22% and impaired glucose tolerance 18% to 30%.56,57 The pathophysiology of dia-
betes associated with hereditary hemochromatosis is controversial, with evidence
suggesting that both insulin deficiency and insulin resistance are contributing factors.
Similar disease processes are seen in patients with transfusion iron overload, espe-
cially beta thalassemia major.
Pancreatic neoplasia
Most diabetes associated with pancreatic cancer is diagnosed either concomitantly
with the cancer or during the 2 years before the cancer is found.58 Glucose intolerance
is present in 80% of cases of pancreatic neoplasia and diabetes in approximately
50%.59 This and other data suggest that recently developed glucose intolerance or
diabetes may be a consequence of pancreatic cancer, and for some patients, recent
onset of glucose intolerance or diabetes may be an early sign of pancreatic cancer.
Several studies have found that diabetes in pancreatic cancer patients is character-
ized by peripheral insulin resistance.60 Insulin resistance is also found in nondiabetic
or glucose-intolerant pancreatic cancer patients, although to a lesser degree.61
Result of Surgery/Trauma
Postpancreatectomy
Pancreatectomy for chronic pancreatitis results in secondary diabetes. Islet auto-
transplantation after the pancreatectomy offers some patients a chance for insulin
independence.62
Drug Associated
Many medications are associated with derangements in glucose metabolism via
different mechanisms. Some drugs impair insulin secretion and may not cause
Diabetes Classification 9
diabetes by themselves but may precipitate diabetes in individuals with preexisting in-
sulin resistance. Certain toxins such as Vacor (a rat poison), streptozotocin, and intra-
venous pentamidine can permanently destroy pancreatic b-cells. Also many drugs
and hormones impair insulin action. The following medications are some of the
more commonly used drugs associated with the development of diabetes.
Glucocorticoids
One of the most distressing side effects for patients treated long term with glucocor-
ticoids is weight gain, often with abnormal fat deposition. In humans treated with glu-
cocorticoids, the accumulation of adipocytes occurs primarily in the visceral fat and
interscapular depots, leading to characteristic truncal obesity and dorsocervical fat
pad or buffalo hump. This occurs through effects of glucocorticoids on differentia-
tion of preadipocytes into mature adipocytes. Glucocorticoids also induce insulin
resistance, hyperglycemia, and hyperlipidemia. Although increases in visceral fat
contribute to the insulin resistance that occurs with glucocorticoid therapy, direct
actions of glucocorticoids on muscle, liver, and other tissues also play a role. Gluco-
corticoids have been found to inhibit several steps in the insulin-signaling network
through several different mechanisms. In skeletal muscle, glucocorticoids cause insu-
lin resistance by decreasing transcription of IRS-1, while increasing transcription of 2
proteins that counter insulin action, protein tyrosine phosphatase type 1B (PTP1B) and
p38MAPK. A similar increase in transcription of p38MAPK is observed in the liver.63
Atypical antipsychotics
Although clozapine, olanzapine, and other atypical antipsychotic drugs (APDs) have
fewer extrapyramidal side effects, they have serious metabolic side effects such as
substantial weight gain, intra-abdominal obesity, and hyperglycemia64 with a predom-
inant type 2 phenotype when overt diabetes develops. Accumulated data from both
clinical and animal studies suggest that increasing appetite and food intake as well
as delayed satiety signaling are key behavioral changes related to APD-induced
weight gain. Less well understood is the extent to which changes of resting metabolic
rate, decreased activity and sedation affect weight gain associated with this class of
medications. Analysis of the US Food and Drug Administration Adverse Event data-
base also showed that adjusted report ratios for type 2 diabetes were the following:
olanzapine, 9.6 (95% confidence interval [CI], 9.210.0); risperidone, 3.8 (95% CI,
3.54.1); quetiapine, 3.5 (95% CI, 3.23.9); clozapine, 3.1 (95% CI, 2.93.3); ziprasi-
done, 2.4 (95% CI, 2.02.9); aripiprazole, 2.4 (95% CI, 1.92.9); and haloperidol, 2.0
(95% CI, 1.72.3), which suggests differential risks of diabetes across various APDs
but also a class effect.65
Box 1
Drug-associated diabetes mellitus
Glucocorticoids
Diazoxide
Calcineurin/mammalian targets of rapamycin inhibitors
Atypical antipsychotics
Antiretroviral agents
Thiazide diuretics
Nicotinic acid
Statins
b-adrenergic agonists
Others
Diabetes Classification 11
diabetes risk include an increase in viral burden of 0.5 log over a 6-month period, a
lower CD4 count, and longer duration of HIV infection.73 The increased accumula-
tion of visceral fat, with wasting of subcutaneous fat, noted in these patients, cre-
ates higher levels of inflammatory cytokines such as tumor necrosis factor a. This
leads to diabetes or impaired glucose tolerance by increasing insulin resistance
(Box 2).
Box 2
Other genetic syndromes (that may be associated with diabetes mellitus)
SUMMARY
REFERENCES
14. Redondo MJ, Fain PR, Krischer JP, et al. Expression of beta-cell autoimmunity
does not differ between potential dizygotic twins and siblings of patients with
type 1 diabetes. J Autoimmun 2004;23(3):2759. http://dx.doi.org/10.1016/j.
jaut.2004.07.001.
15. Melanitou E, Fain P, Eisenbarth GS. Genetics of type 1A (immune mediated) dia-
betes. J Autoimmun 2003. http://dx.doi.org/10.1016/S0896-8411(03)00097-0.
16. Kyvik KO. Concordance rates of insulin dependent diabetes mellitus: a popula-
tion based study of young Danish twins. BMJ 1995;311:9137.
17. UK prospective diabetes study 16: overview of 6 years therapy of type II dia-
betes: a progressive disease. U.K. Prospective Diabetes Study Group. Diabetes
1995;44(11):124958.
18. Karjalainen J, Salmela P, Ilonen J. A comparison of childhood and adult type I
diabetes mellitus. N Engl J Med 1989;320(14):8816.
19. Fourlanos S, Dotta F, Greenbaum CJ, et al. Latent autoimmune diabetes in
adults (LADA) should be less latent. Diabetologia 2005. http://dx.doi.org/10.
1007/s00125-005-1960-7.
20. Gottsater A, Landin-Olsson M, Fernlund P, et al. b-cell function in relation to islet
cell antibodies during the first 3 Yr after clinical diagnosis of diabetes in type ii
diabetic patients. Diabetes Care 1993;16(6):90210. http://dx.doi.org/10.2337/
diacare.16.6.902.
21. Turner R, Stratton I, Horton V, et al. UKPDS 25: autoantibodies to islet-cell
cytoplasm and glutamic acid decarboxylase for prediction of insulin require-
ment in type 2 diabetes. Lancet 1997;350(9087):128893. http://dx.doi.org/10.
1016/S0140-6736(97)03062-6.
22. Tuomi T, Carlsson A, Li H, et al. Clinical and genetic characteristics of type 2 dia-
betes with and without GAD antibodies. Diabetes 1999;48(1):1507. http://dx.
doi.org/10.2337/diabetes.48.1.150.
23. Gale E. Is type 2 diabetes a category error? Lancet 2013;381(9881):19567.
24. Mohan V, Amutha A, Ranjani H, et al. Associations of b-cell function and insulin
resistance with youth-onset type 2 diabetes and prediabetes among Asian
Indians. Diabetes Technol Ther 2013;15(4):31522. http://dx.doi.org/10.1089/
dia.2012.0259.
25. Mitsui R, Fukushima M, Nishi Y, et al. Factors responsible for deteriorating
glucose tolerance in newly diagnosed type 2 diabetes in Japanese men. Meta-
bolism 2006;55(1):538. http://dx.doi.org/10.1016/j.metabol.2005.07.006.
26. Butler AE, Janson J, Bonner-Weir S, et al. b-cell deficit and increased b-Cell
apoptosis in humans with type 2 diabetes. Diabetes 2003;52(1):10210. http://
dx.doi.org/10.2337/diabetes.52.1.102.
27. Bell GI, Polonsky KS. Diabetes mellitus and genetically programmed defects in
b-cell function. Nature 2001;414(6865):78891. http://dx.doi.org/10.1038/
414788a.
28. Del Prato S. Role of glucotoxicity and lipotoxicity in the pathophysiology of Type
2 diabetes mellitus and emerging treatment strategies. Diabet Med 2009;
26(12):118592.
29. Epstein FH, Hoppener J, Ahren B. Islet amyloid and type 2 diabetes mellitus.
N Engl J Med 2000. http://dx.doi.org/10.1056/NEJM200008103430607.
30. Meigs JB, Muller DC, Nathan DM, et al. The natural history of progression from
normal glucose tolerance to type 2 diabetes in the Baltimore Longitudinal Study
of Aging. Diabetes 2003;52(6):147584.
31. Winter WE, Maclaren NK, Riley WJ. Maturity-onset diabetes of youth in black
Americans. N Engl J Med 1987;316(6):28591.
14 Thomas & Philipson
47. Steele AM, Shields BM, Wensley KJ, et al. Prevalence of vascular complications
among patients with glucokinase mutations and prolonged, mild hyperglycemia.
JAMA 2014. http://dx.doi.org/10.1001/jama.2013.283980.
48. Naylor RN, Philipson LH. Who should have genetic testing for maturity-onset
diabetes of the young? Clin Endocrinol (Oxf) 2011;75:4226.
49. Maassen JA, Hart LM, van Essen E, et al. Mitochondrial Diabetes Molecular
Mechanisms and Clinical Presentation. Diabetes 2004;53(suppl 1):S1039.
http://dx.doi.org/10.2337/diabetes.53.2007.S103.
50. Maassen JA, t Hart LM, Janssen GM, et al. Mitochondrial diabetes and its
lessons for common Type 2 diabetes. Biochem Soc Trans 2006;34(5):819.
http://dx.doi.org/10.1042/BST0340819.
51. Battezzati A, Mari A, Zazzeron L, et al. Identification of insulin secretory defects
and insulin resistance during oral glucose tolerance test in a cohort of cystic
fibrosis patients. Eur J Endocrinol 2011;165(1):6976.
52. Ode KL, Moran A. New insights into cystic fibrosis-related diabetes in children.
Lancet Diabetes Endocrinol 2013;1(1):528.
53. Gupte AR, Forsmark CE. Chronic pancreatitis. Curr Opin Gastroenterol 2014;
30(5):5005. http://dx.doi.org/10.1097/MOG.0000000000000094.
54. Papita R, Nazir A, Anbalagan VP, et al. Secular trends of fibrocalculous pancre-
atic diabetes and diabetes secondary to alcoholic chronic pancreatitis at a
Tertiary Care Diabetes Centre in South India. JOP 2012;13(2):2059. http://dx.
doi.org/10.6092/1590-8577/608.
55. Khatib OM. Guidelines for the prevention, management and care of diabetes
mellitus. World Health Organization: WHO Press; 2006.
56. Hatunic M, Finucane FM, Brennan AM, et al. Effect of iron overload on glucose
metabolism in patients with hereditary hemochromatosis. Metabolism 2010.
http://dx.doi.org/10.1016/j.metabol.2009.08.006.
57. McClain DA, Abraham D, Rogers J, et al. High prevalence of abnormal glucose
homeostasis secondary to decreased insulin secretion in individuals with hered-
itary haemochromatosis. Diabetologia 2006. http://dx.doi.org/10.1007/s00125-
006-0200-0.
58. Gullo L, Pezzilli R. Diabetes and the risk of pancreatic cancer. N Engl J Med
1994;331(2):814.
59. Pannala R, Basu A, Petersen GM, et al. New-onset diabetes: a potential clue to
the early diagnosis of pancreatic cancer. Lancet Oncol 2009;10(1):8895. http://
dx.doi.org/10.1016/S1470-2045(08)70337-1.
60. Permert J, Ihse I, Jorfeldt L, et al. Pancreatic cancer is associated with impaired
glucose metabolism. Eur J Surg 1993;159(2):1017.
61. Muniraj T, Chari ST. Diabetes and pancreatic cancer. Minerva Gastroenterolog-
ica e Dietologica 2014;122.
62. Bramis K, Gordon-Weeks AN, Friend PJ, et al. Systematic review of total pancre-
atectomy and islet autotransplantation for chronic pancreatitis. Br J Surg 2012;
99(6):7616. http://dx.doi.org/10.1002/bjs.8713.
63. Ferris HA, Kahn CR. New mechanisms of glucocorticoid-induced insulin resis-
tance: make no bones about it. J Clin Invest 2012;122(11):38547.
64. Deng C. Effects of antipsychotic medications on appetite, weight, and insulin
resistance. Endocrinol Metab Clin North Am 2013. http://dx.doi.org/10.1016/j.
ecl.2013.05.006.
65. Baker RA, Pikalov A, Tran QV, et al. Atypical antipsychotic drugs and diabetes
mellitus in the US Food and Drug Administration Adverse Event database: a
16 Thomas & Philipson
KEYWORDS
Diabetes Glycemic control Hypoglycemia Self-monitoring of blood glucose
Internet medicine Internet blood glucose monitoring system
KEY POINTS
Internet blood glucose monitoring systems (IBGMS) result in glycemic improvement in
patients with type 1 or 2 diabetes, including those with poorly controlled glycemia at
baseline.
IBGMS help decrease glycemic levels without increasing the risk of hypoglycemia.
Other benefits, seen in some studies of IBGMS, include improvements in cardiovascular
risk markers and quality of life outcomes.
Glycemic improvements with IBGMS are not limited to patients on insulin or to those who
increase their frequency of glucose self-monitoring as a result of the intervention.
Glycemic improvements likely result from a combination of factors, including increased pa-
tient motivation and increased communication between patient and health care provider.
INTRODUCTION
Disclosures: H.D. Tildesley uses Internet blood glucose monitoring routinely in managing
patients with diabetes. M.D. Po and S.A. Ross declare that they have no financial or other
competing interest in the topics discussed here.
a
Department of Endocrinology and Metabolism, St Pauls Hospital, University of British
Columbia, Room 410, 1033 Davie Street, Vancouver, British Columbia V6E 1M7, Canada;
b
SCRIPT, 2010 Yonge St, Toronto, ON M4N 2K4, Canada; c University of Calgary, 2500 Univer-
sity Dr NW, Calgary, AB T2N 1N4, Canada
* Corresponding author.
E-mail address: [email protected]
the early glycemic control is lost at a later point, patients who establish and maintain
good control early in the course of their disease may enjoy reduced risk of macrovas-
cular and microvascular complications of diabetes over a period of years to de-
cades.35 For this reason, current treatment guidelines emphasize the need for
timely introduction of lifestyle and, if necessary, pharmacologic interventions, to bring
patients to appropriate glycemic targets within months of diagnosis.6 Despite this
guidance, and despite clear evidence that effective glycemic control can prevent dia-
betic complications, only half of North American patients achieve the standard glyce-
mic target of hemoglobin A1c (HbA1c) level less than 7%.79
For patients with T1D and insulin-using patients with T2D, American Diabetes Asso-
ciation (ADA) and Canadian Diabetes Association (CDA) treatment guidelines support
regular self-monitoring of blood glucose (SMBG), which allows the patient to titrate in-
sulin doses, evaluate their success in reaching glycemic targets, and gauge their risk
of hypoglycemia.6,10 However, the clinical usefulness and cost-effectiveness of SMBG
in controlling glycemic levels in noninsulin-using patient with T2D is less clear. A
recent meta-analysis showed that regular SMBG in this patient population was asso-
ciated with a statistically significant but quantitatively minor glycemic benefit.11 Uncer-
tainty about the role of SMBG outside the context of insulin dose adjustment is
reflected in the 2014 ADA guidelines; these guidelines recommend SMBG as a part
of a broader educational context, and to help guide treatment decisions for non
insulin-using, as well as insulin-using, patients.10
We have proposed elsewhere1214 that increased patient-physician communica-
tion, in the form of ongoing Internet-based contact, could increase the effectiveness
of SMBG as a means to improve diabetes management in combination with regular
care. In this article, a systematic review of Internet blood glucose monitoring systems
(IBGMS) is provided, which facilitate regular health care provider review and feedback
regarding a patients SMBG results. In such systems (Fig. 1), patients carry out regular
glucose monitoring and upload the resulting data to a secure Web site. From there, the
data are reviewed by a health care professional, who provides feedback on the results,
offers encouragement, and, as appropriate, recommends changes to the patients
monitoring practices, insulin titration, or diet.
In this article, the efficacy, safety and other outcomes are evaluated from numerous
small studies comparing patients using IBGMS with other patients with more
Fig. 1. IBGMs. All Internet-based interventions considered in this review include the
following: (1) patients SMBG, (2) uploading and transmitting the SMBG data to a health
care professional (HCP), (3) the HCP reviewing and submitting feedback to the patient.
Internet Blood Glucose Monitoring Systems 19
METHODS
We performed PubMed searches in March, 2014, using the following terms to find
research articles reporting IBGMS trials: Internet 1 diabetes, Web-based 1 diabetes,
telemedicine 1 diabetes, and telehealth 1 diabetes. Additional articles were chosen
by examining the reference lists of relevant reviews. Forward searching using Web
of Science identified works in which key articles were cited.
Publications on T1D or T2D were included in this analysis if they reported random-
ized controlled trials of standard practice versus IBGMS, which were defined as sys-
tems with 3 components: Web-based uploading of patients SMBG data, regular
review of the data by a health care professional, and digital or telephonic feedback.
Studies were excluded if they included only adolescent patients or if they did not
report HbA1c as an outcome. No formal evaluation of levels of evidence was
conducted.
It was anticipated that patients using IBGMS might monitor their glucose more
frequently than other patients.
We identified 6 randomized controlled trials that reported SMBG frequency in both
the IBGMS and control groups. In the 3 T1D studies identified,1517 there were no sig-
nificant differences in SMBG frequency between patients in IBGMS and control
groups. In the 3 T2D studies identified, patients on IBGMS self-monitored significantly
more often than patients on conventional care: 55.7 times/mo versus 14.9 times/mo,
P<.001,18 23.8 times/mo versus 12.7 times/mo, significance not reported19 and
34 times/mo versus 22 times/mo, P 5 .024.20
We identified 9 randomized controlled IBGMS trials that enrolled type 2 patients and 4
studies that enrolled patients with either T1D or T2D (Table 1). All but 1 of these
studies21 showed significantly improved HbA1c level in the IBGMS group compared
with the control group, as seen either in a significant difference in glycosylated hemo-
globin change (DHbA1c) between groups or in a significant decrease in HbA1c level in
the IBGMS group but not the control group.
Of the 12 T2D studies, 718,20,2226 enrolled 50% or more noninsulin-using patients,
suggesting that IBGMS is effective in non-insulin-using patients. In the 1 study that
failed to find a significant improvement in HbA1c level with IBGMS in the total patient
population, a subanalysis of noninsulin-using patients nevertheless showed a signif-
icant decline in HbA1c level in the IBGMS group relative to controls: mean HbA1c level
decreased from 6.95% to 6.66% in the IBGMS group compared with 7.21% to 7.2% in
the control group (P 5 .02). In 3 studies, some patients were treated with diet and ex-
ercise alone, with no pharmacotherapy for diabetes.18,25,27 However, because these
20
Table 1
Randomized controlled studies of IBGMS versus conventional care: glycemic, cardiovascular risk, and quality of life outcomes
Mean HbA1c
Levels in P Value, QOL at
Participants Mean HbA1c Control D HbA1c CVD Outcomes at Follow-Up in
(Intervention Description of IBGMS Levels in IBGMS, Group, from Levels Follow-Up in IBGMS IBGMS Compared
vs Usual Treatments in Duration (Method of Upload; from Baseline to Baseline to Between Compared with with Control
Study Care) Use (mo) Review; Feedback) Follow-Up (%) Follow-Up (%) Groups Control Group Group
T2D
Shea et al,25 55, 352 vs 65% OHA alone, 60 Home telemedicine 7.437.09, NR 7.457.38, NR <.001 Significant No significant
2009; Trief 353 14% insulin unit; nurse improvement in difference in
et al,46 2007 alone, 15% managers SBP, DBP depression or
insulin + OHA, (diabetologists diabetes
5% diet alone consulted when distress
needed); Web-
based
Stone et al,28 64 vs 73 76% OHA, 6 Wireless glucometer; 9.67.9 9.48.6 <.001 Significant
2010 79% insulin nurse under improvement in
(breakdown supervision of an LDL
of OHA alone endocrinologist;
and insulin phone
alone not
reported)
Ralston 30 vs 35 Diet, OHAs or 12 Web-based; diabetes 8.27.3, P 5 .01 7.98.1, NR <.01 No significant
et al,24 2009 insulin (38% case manager; CVD benefits
used insulin) e-mail identified
Kim et al,20 25 vs 26 67% OHA, 31% 12 Web-based; diabetic 8.097.04, P<.05 7.597.70, NS .011 No significant
2007 insulin educator or CVD benefits
professor; text identified
message
Cho et al,18 40 vs 40 69% OHA, 12% 30 Web-based; clinical 7.76.7, P<.05 7.57.4, NS .022 Significant
2006 insulin only, investigator, daily; improvement in
10% OHA + Web-based triglycerides
insulin, 9%
exercise/diet
Kwon et al,19 51 vs 50 NR 3 Web-based; 7.596.94, P<.001 7.197.62, NR <.05
2004 endocrinology
fellow; Web-based
Tildesley 24 vs 23 Insulin 6 Web-based; 8.87.6, P<.001 8.58.4, <.05 Significant
et al,14 2010; endocrinologist; P 5 .51 improvement in
Tildesley Web-based total cholesterol
et al,13 2011 and LDL
Kim et al,22 Obese 18 vs16 68% OHA, 32% 12 Web-based; diabetic 8.166.67, P<.05 7.668.19, NS NR
2008 insulin educator or
professor; both by
phone and Web-
based
Yoon and 25 vs 26 69% on OHA 12 Web-based; 8.096.77, P<.05 7.598.4, P<.05 NR No significant
Kim,26 2008 only, 31% endocrinologist/ CVD benefits
insulin professor; text identified
message
Bujnowska- 50 vs 50 50% insulin, 6 Wireless glucometer; 7.67.4, NR 7.67.4, NR NS No significant No significant
Fedak et 50% physician; phone CVD benefits QOL differences
al,21 2011 noninsulin identified
T1D and T2D
Bond et al,27 60 y old 36 49% insulin, 6 Web-based; nurse; 7.06.4, NR 7.17.0, NR .01 Significant Significant
2007; Bond vs 31 45% insulin + e-mail or instant improvements in improvements
et al,41 2010 OHA, 6% diet messaging total cholesterol, in depression
and exercise HDL, SBP (CES-D), QOL
(PAID)
Harno et al,40 101 vs 74 NR 12 Glucometer; diabetes 7.87.3, NR 8.27.8, NR <.05 Significant
2006 team; text message improvements in
total cholesterol,
LDL, TG, DBP
21
22
Table 1
(continued )
Mean HbA1c
Levels in P Value, QOL at
Participants Mean HbA1c Control D HbA1c CVD Outcomes at Follow-Up in
(Intervention Description of IBGMS Levels in IBGMS, Group, from Levels Follow-Up in IBGMS IBGMS Compared
vs Usual Treatments in Duration (Method of Upload; from Baseline to Baseline to Between Compared with with Control
Study Care) Use (mo) Review; Feedback) Follow-Up (%) Follow-Up (%) Groups Control Group Group
McMahon HbA1c 9% 51% on OHA, 12 Web-based; nurse, 1.6 reduction 1.2 reduction <.05 Significant
et al,23 2005 52 vs 52 49% on physician; Web- from baseline, from improvements in
insulin based P<.001 baseline, HDL, TG, SBP
P<.001
Tjam et al,29 34 vs 19 NR 12 Web-based; nurse; 6.76.5, P 5 .045 6.86.8, NR
2006 Web-based P 5 .88
T1D only
Charpentier 61 vs 59 Insulin 6 cell-phone; physician; 9.118.41, NR 8.919.1, NR <.001 No significant
et al,15 2011 phone; Additional: differences by
Diabeo Decision- DQOL and
support software Diabetes Health
Profile
Kirwan et al,30 36 vs 36 Insulin 6 Smartphone app; 9.087.8, P<.001 8.478.58, NS <.001 No significant
2013 diabetes educator; differences by
text message DQOL
Montori 16 vs 16 Insulin 6 Direct upload from 9.17.8, NR 8.88.2, NR .03
et al,16 2004 glucometer; nurse
(supervised by
endocrinologist;
phone call)
Jansa et al,36 16 vs 14 Insulin 12 Glucometer 8.47.6, P 5 .008 8.97.6, NS No significant
2006 through phone P 5 .001 differences by
line; nurse; phone DQOL
(teleconsultations
took the place of
in-person visits)
Gomez et al,47 10 (crossover Insulin 14 PDA; physicians and 8.47.9, NR 8.18.15, NR .053
2002 design) nurses; PDA-based
Benhamou 15 vs 15 Continuous 6 PDA/cell; 8.318.18, 8.228.34, .097 Significant
et al,32 2007 subcutaneous investigator; text P 5 .17 P 5 .33 improvements
insulin message in DQOL global
infusion score and DQOL
satisfaction
with life
subscale
Rossi et al,17 63 vs 64 Insulin 6 Cell phone; physician; 8.47.9, <.0001 8.47.9, <.0001 .73 No significant Significant
2013 text message; CVD benefits improvements
Additional: identified in perceived
automatic dosage frequency of
calculation based hyperglycemic
on carb intake episodes on
DTSQ and social
relations on
DQOL
McCarrier 25 vs 16 Insulin 12 Web-based; nurse; 7.997.62, NS 8.058.16, NS .16
et al,48 2009 e-mail
Biermann 27 vs 16 Insulin 8 Web-based; 8.37.1, NR 8.06.8, NR NS
et al,35 2002 physician; phone
(teleconsultations
took the place of
in-person visits)
Abbreviations: CES-D, Centre for Epidemiological Studies Depression scale; CVD, cardiovascular disease; DBP, diastolic blood pressure; DQOL, diabetes-specific quality of life
questionnaire; DTSQ, diabetes treatment satisfaction questionnaire; HDL, high-density lipoprotein; LDL, low-density lipoprotein; NR, not reported; NS, nonsignificant; OHA,
oral hypoglycemic agent; PAID, problem areas in diabetes; PDA, personal digital assistant (a small handheld computer); QOL, quality of life; SBP, systolic blood pressure; TG,
triglycerides.
23
24 Tildesley et al
Studies focusing on patients with higher HbA1c level at baseline have shown some of
the most remarkable improvements in glycemic control with IBGMS. Of 6 T2D studies
featuring mean baseline HbA1c level 8% or greater (1 with insulin only14; 5 with oral
agents with or without insulin20,2224,28), the mean decrease in HbA1c level ranged
from 1.05% to 1.7%, with the largest decrease seen in the study with the highest base-
line HbA1c level.28
In addition, patients with T2D who are at or near their glycemic target seem to main-
tain or improve their degree of glycemic control with IBGMS. Thus, in a study of both
T1D and T2D, with patients on a variety of therapies, mean HbA1c level declined from
7.0% to 6.4% in the Internet intervention group, whereas the control group HbA1c level
declined nonsignificantly from 7.1% to 7.0%.27 Two studies that carried out a subanal-
ysis of patients with baseline HbA1c level less than 7.0% both showed a significant dif-
ference between intervention and control groups with regard to follow-up HbA1c
level.18,19 Moreover, in the IBGMS study with the best glycemic control at baseline,
HbA1c level decreased significantly from a mean of 6.7% to 6.5% (P 5 .045) in the
IBGMS group, versus 6.8% to 6.8% (not significant) in the control group.29 Hence,
baseline glycemic control does not seem to be a limitation in patient selection for
IBGMS.
Although Internet interventions in T1D do not result in the same widespread im-
provement as seen in T2D studies, IBGMS result in a consistent trend toward greater
Internet Blood Glucose Monitoring Systems 25
HbA1c level reduction. This improvement reached statistical significance in some T1D
trials, namely those in which patients experienced poor glycemic control at baseline.
Of the 9 identified trials of T1D, 3 showed a glycemic benefit for IBGMS compared
with conventional care.15,16,30 All of the studies that showed a significant glycemic
benefit in the intervention arm had a mean baseline HbA1c level of 8.4% or greater,
whereas all the studies that failed to show a significant benefit of IBGMS use had a
mean baseline HbA1c level of 8.4% or less. As in comparable studies in T2D, greater
change in HbA1c level with IBGMS occurs in patients with poorly controlled disease.
Insulin and some oral agents decrease glycemic exposure at the cost of heightening
patients risk of overall and serious hypoglycemia.1,2 This dose-limiting toxicity is
important clinically, because of the intrinsic adverse effects of hypoglycemia, and
also because of its psychological effect, whereby fear of hypoglycemia delays treat-
ment implementation and reduces treatment adherence.31
Several studies reporting overall and severe hypoglycemic episodes rates showed
no significant change in either outcome with IBGMS use.15,16,20,23,32 This finding is
interesting in itself, given that frequency of SMBG commonly increases with the intro-
duction of IBGMS (see earlier discussion). Because biochemically defined hypoglyce-
mia commonly goes unnoticed by patients,33,34 it might have been expected that mild
hypoglycemia would be detected in IBGMS patients at an increased rate. However, no
study has reported such an effect. Rather, studies have reported nonsignificant trends
toward a lower hypoglycemia rate or, in 2 cases, a significant decrease in the fre-
quency of moderately severe17 and severe hypoglycemia.21 Crucially, this apparent
increase in treatment safety with IBGMS was seen in insulin-using16,17,32,35,36 as
well as noninsulin-using patients,20,21,23 and in studies of patients with poor baseline
glycemic control, in which changes in HbA1c level with treatment were particularly
striking.
Because use of IBGMS increases monitoring by a health care professional, this
intervention is expected to address these psychological barriers to effective pharma-
cotherapy. In 1 T1D study, patients with IBGMS reported an improved fear of hypogly-
cemia dimension of the Diabetes-Specific Quality of Life Scale Questionnaire
compared with control patients, but this difference did not reach statistical signifi-
cance (P 5 .06).17 Given the apparent decline in hypoglycemia incidence in patients
using IBGMS, we speculate that broader implementation will help to alleviate fear of
hypoglycemia in both health professionals and patients.
encouragement being the most frequent type of feedback.18 Therefore, support and
encouragement to increase frequency of SMBG and improve diet and exercise may
be more important factors to explain the benefits of IBGMS, compared with any effect
on insulin doses.
The beneficial effect of SMBG as an explanation of IBGMS outcomes is more diffi-
cult to rule out. SMBG frequency is expected to increase with IBGMS; as noted earlier,
several studies have documented this effect.18,19 However, other studies confirming
the efficacy of IBGMS have found no increase in SMBG frequency.15,16 Moreover,
even in studies in which SMBG frequency increased, no correlation has been found
between patients SMBG frequency and improvement in HbA1c level. These studies
suggest that although SMBG may contribute to better glycemic control, increased
SMBG alone does not explain the glycemic benefits of IBGMS.
In addition to a possible effect of increased SMBG frequency, patients using IBGMS
often report increased self-motivation, because of being followed more closely by their
health care provider. The number of data uploads from a given patient may offer a
quantitative measure of this self-motivation, and this measurement seems to correlate
well with IBGMS efficacy. Thus, McMahon and colleagues23 identified a significant as-
sociation between data upload frequency and improvement in HbA1c level (decreases
of 2.1% and 1.0% in the highest and lowest tertiles, respectively; P<.02). Another
study, not reaching statistical significance, reported a similar trend.24
We propose that glycemic improvements seen in patients on IBGMS result from a
combination of factors that stem from increased self-motivation and increased
patient-physician communication. Such factors may include improved diet, increased
exercise, and, in some cases, increased frequency of SMBG or more effective use of
medications.
Three studies reported significantly improved quality of life (QOL) in the Internet inter-
vention group, compared with control groups,17,32,41 and 5 reported no significant
difference.15,21,30
Of the 3 showing QOL benefits, 141 reported a significant improvement in HbA1c
levels compared with controls, 1 showed a trend to improvement in HbA1c levels
compared with controls,32 and 1 showed significant improvement in both intervention
and control arms, but there was no significance between the groups.17 This finding
suggests that patients may experience benefits from IBGMS beyond those detected
by clinical measures. In a study in which HbA1c level change was not significantly
different between the IBGMS and control arms, 85% of patients in the intervention
Internet Blood Glucose Monitoring Systems 27
arm believed that the Internet intervention was better than conventional care. Reasons
cited included better surveillance of SMBG data by the physician and faster interven-
tion in the case of problems.35
IBGMS is emerging as the standard of care for patients with diabetes in the Canadian
province of British Columbia. In this jurisdiction, family physicians, general internists,
and endocrinologists are now remunerated for reviewing patient glucose reports.
Patients are asked to upload their SMBG data every 2 weeks through a choice of plat-
forms. The patients physician then reviews the readings and sends feedback via
e-mail.
A total of 1200 patients have been enrolled, and outcome data on the first 409 pa-
tients showed significant improvement of HbA1c levels after 3 to 9 months of follow-up
(Fig. 2). Glycemic control improved significantly after introduction of IBGMS in pa-
tients with T1D and baseline HbA1c level 6.9% or greater. Similarly, patients with
T2D, treated with insulin or oral agents, showed significant improvement in HbA1c
level.44 As was previously reported in a clinical trial, individuals who used the IBGMS
frequently (frequent uploaders) experienced greater improvement in glycemic control,
relative to infrequent uploaders.23
These real-world findings generally agree with results from randomized controlled
trials, in that IBGMS seems effective in T2D, irrespective of baseline glycemia
or mode of treatment, as well as in T1D for patients with poor glycemic control.
Moreover, more frequent use of the system to upload of SMBG data (presumably
reflecting greater patient self-motivation) was associated with improved HbA1c
levels.
8.8
8.6 Baseline HbA1c
8.2
8
HbA1c, %
7.8
7.6
7.4
7.2
7
115 44 71 256 116 35 81 140 41 99
6.8
Totala Freq Infreq Total Total Freq Infreq Total Freq Infreq
Repb Repb Rep Rep Rep Rep
OHA Insulin +/- OHA
Type 1 Type 2
Fig. 2. Mean HbA1c level at baseline and follow-up in patients with IBGMS who upload their
blood glucose data frequently (Freq Rep) versus infrequently (Infreq Rep). When patients
with HbA1c level less than 6.9% were excluded, patients with T1D showed a significant
improvement in HbA1c level at follow-up (P<.01). Total T2D, T2D on OHA only, and T2D
patients on insulin OHA all showed significant decreases in HbA1c level at follow-up (all
P<.001). P 5 .05 for frequent reporters compared with infrequent reporters for each type
of diabetes. a Excluding patient HbA1c level less than 6.9%; b excluding patient HbA1c level
less than 7.4%. OHA, oral hypoglycemic agent. (Data from Tildesley HD, Conway ME, Ross
SA, et al. Review of the effect of internet therapeutic intervention in patients with type 1
and type 2 diabetes. Diabetes Care 2014;37(2):e312.)
Internet Blood Glucose Monitoring Systems 29
Box 1
Sample messages to patients
High in the AM; please increase evening metformin to 750 mg at supper. Lets see if there is any
shift in 2 weeks.
Your lunch value is excellent, but supper is showing variability. Please work on having supper at
the same time each day, which should improve consistency, and report again in 2 weeks.
Thanks.
Your sugar levels are a little high at lunch and supper. Try a carb ratio of 10:1 at breakfast and
lunch. Please report again in 2 weeks. Thanks
One key to efficient implementation of IBGMS is the use of clear and standardized re-
ports of patient glucose levels. Reports should clearly indicate time of day, average
glucose levels, range and standard deviation (SD) of glucose values. They should
be organized so that raw data, as well as summary data, can be accessed easily.
As a general rule, testing frequency should be such that there are at least 10 values
for a given time of day across the reporting period, for instance 10 before breakfast
measurements within 2 weeks, or else the statistics may be less accurate to their
true values. Most glucose meters and some insulin pumps and sensors are designed
to facilitate the uploading and transmission of stored data.
One rule of thumb is to first check the SD of glucose levels by time of day. In general,
if the SD is less than 50 mg/dL (<2.8 mmol/L for measurements in SI units), the data
can be used for determining appropriate therapeutic changes. If the SD is increased,
therapeutic changes should be delayed until the patient is able to provide more
consistent values. Larger SD values are related to meal timing, meal content, timing
of medications, or possibly, major stresses, which result in less focus on diabetes
self-management. Possible causes could include major life events such as the death
of a family member, recent unemployment, or development of a mental health disor-
der; for such situations, the cause of stress should be addressed directly, often with
the aid of a mental health professional. The next step is to decide if average values
are at target by time of day; if not, medications are adjusted according to their onset
and duration of action and effect.
With practice, reports can be reviewed efficiently, allowing a health professional to
offer clear guidance in a concise text or e-mail message to the patient. Typically, such
a message suggests changes in diet (eg, carbohydrate ratio for specific meals) or in
the timing or dose of insulin or an oral agent. The patient should always be asked to
follow up at a specified time (eg, 2 weeks later) to discuss the outcomes of these
changes (Box 1).
We have argued here that IBGMS is broadly useful in patients with T1D and T2D, in
large part because it improves communication between patients and their health care
providers. Widespread rollout of IBGMS is ongoing in some locations, and experience
from these nascent programs should answer lingering questions about the benefits
and cost-effectiveness of the approach. The findings are encouraging. Since 2011,
the Canadian province of British Columbia has reimbursed endocrinologists for the re-
view of IBGMS data.
Although a cost analysis of this IBGMS implementation is not available, a health pro-
fessional is typically able to review patient data and send feedback to the patient via
e-mail in just a few minutes per case, performed every 2 to 4 weeks. Most recently,
the United Kingdom has undertaken a 30-month study called HeLP-Diabetes (Healthy
Living for People with type 2 Diabetes). The study will be conducted in 2 inner city Lon-
don boroughs, in which there are w14,000 potential users of HeLP-Diabetes,45 making
this the largest IBGMS program yet designed. Data from this study are eagerly awaited.
Available study data on IBGMS support the clinical usefulness of this approach to
diabetes management, with improved glycemic control in all types of diabetes
patients and no increase in hypoglycemia risk. IBGMS seems to be well accepted
by patients and to involve minimal time commitment from the health professional,
with some evidence of health care cost savings and reduced burden on clinical re-
sources. IBGMS thus warrants consideration, both for widespread implementation
and for insurance coverage.
ACKNOWLEDGMENTS
The authors wish to thank John Ashkenas, PhD (SCRIPT, Toronto, Canada) for
editorial assistance. H.D. Tildesley gratefully acknowledges the Endocrine Research
Society for financial support for this project.
REFERENCES
8. Hoerger TJ, Segel JE, Gregg EW, et al. Is glycemic control improving in US
adults? Diabetes Care 2008;31(1):816.
9. Ali MK, Bullard KM, Saaddine JB, et al. Achievement of goals in US diabetes
care, 1999-2010. N Engl J Med 2013;368(17):161324.
10. American Diabetes Association. Standards of medical care in diabetes2014.
Diabetes Care 2014;37(Suppl 1):S1480.
11. Malanda UL, Welschen LM, Riphagen II, et al. Self-monitoring of blood glucose
in patients with type 2 diabetes mellitus who are not using insulin. Cochrane Data-
base Syst Rev 2012;(1):CD005060.
12. Ross SA, Tildesley HD, Ashkenas J. Barriers to effective insulin treatment: the
persistence of poor glycemic control in type 2 diabetes. Curr Med Res Opin
2011;27(Suppl 3):1320.
13. Tildesley HD, Mazanderani AB, Chan JH, et al. Efficacy of A1c reduction using
internet intervention in patients with type 2 diabetes treated with insulin. Can J
Diabetes 2011;35(3):2503.
14. Tildesley HD, Mazanderani AB, Ross SA. Effect of Internet therapeutic interven-
tion on A1C levels in patients with type 2 diabetes treated with insulin. Diabetes
Care 2010;33(8):173840.
15. Charpentier G, Benhamou PY, Dardari D, et al. The Diabeo software enabling
individualized insulin dose adjustments combined with telemedicine support im-
proves HbA1c in poorly controlled type 1 diabetic patients: a 6-month, random-
ized, open-label, parallel-group, multicenter trial (TeleDiab 1 Study). Diabetes
Care 2011;34(3):5339.
16. Montori VM, Helgemoe PK, Guyatt GH, et al. Telecare for patients with type 1 dia-
betes and inadequate glycemic control: a randomized controlled trial and meta-
analysis. Diabetes Care 2004;27(5):108894.
17. Rossi MC, Nicolucci A, Lucisano G, et al. Impact of the diabetes interactive di-
ary telemedicine system on metabolic control, risk of hypoglycemia, and quality
of life: a randomized clinical trial in type 1 diabetes. Diabetes Technol Ther 2013;
15(8):6709.
18. Cho JH, Chang SA, Kwon HS, et al. Long-term effect of the Internet-based
glucose monitoring system on HbA1c reduction and glucose stability: a 30-month
follow-up study for diabetes management with a ubiquitous medical care system.
Diabetes Care 2006;29(12):262531.
19. Kwon HS, Cho JH, Kim HS, et al. Establishment of blood glucose monitoring sys-
tem using the internet. Diabetes Care 2004;27(2):47883.
20. Kim C, Kim H, Nam J, et al. Internet diabetic patient management using a short
messaging service automatically produced by a knowledge matrix system. Dia-
betes Care 2007;30(11):28578.
21. Bujnowska-Fedak MM, Puchala E, Steciwko A. The impact of telehome care on
health status and quality of life among patients with diabetes in a primary care
setting in Poland. Telemed J E Health 2011;17(3):15363.
22. Kim SI, Kim HS. Effectiveness of mobile and internet intervention in patients with
obese type 2 diabetes. Int J Med Inform 2008;77(6):399404.
23. McMahon GT, Gomes HE, Hickson Hohne S, et al. Web-based care manage-
ment in patients with poorly controlled diabetes. Diabetes Care 2005;28(7):
16249.
24. Ralston JD, Hirsch IB, Hoath J, et al. Web-based collaborative care for type 2 dia-
betes: a pilot randomized trial. Diabetes Care 2009;32(2):2349.
25. Shea S, Weinstock RS, Teresi JA, et al. A randomized trial comparing telemedi-
cine case management with usual care in older, ethnically diverse, medically
32 Tildesley et al
underserved patients with diabetes mellitus: 5 year results of the IDEATel study.
J Am Med Inform Assoc 2009;16(4):44656.
26. Yoon KH, Kim HS. A short message service by cellular phone in type 2 diabetic
patients for 12 months. Diabetes Res Clin Pract 2008;79(2):25661.
27. Bond GE, Burr R, Wolf FM, et al. The effects of a web-based intervention on the
physical outcomes associated with diabetes among adults age 60 and older: a
randomized trial. Diabetes Technol Ther 2007;9(1):529.
28. Stone RA, Rao RH, Sevick MA, et al. Active care management supported by
home telemonitoring in veterans with type 2 diabetes: the DiaTel randomized
controlled trial. Diabetes Care 2010;33(3):47884.
29. Tjam EY, Sherifali D, Steinacher N, et al. Physiological outcomes of an internet
disease management program vs. in-person counselling: a randomized,
controlled trial. Can J Diabetes 2006;30(4):397405.
30. Kirwan M, Vandelanotte C, Fenning A, et al. Diabetes self-management smart-
phone application for adults with type 1 diabetes: randomized controlled trial.
J Med Internet Res 2013;15(11):e235.
31. Cryer PE. Hypoglycaemia: the limiting factor in the glycaemic management of
type I and type II diabetes. Diabetologia 2002;45(7):93748.
32. Benhamou PY, Melki V, Boizel R, et al. One-year efficacy and safety of Web-
based follow-up using cellular phone in type 1 diabetic patients under insulin
pump therapy: the PumpNet study. Diabetes Metab 2007;33(3):2206.
33. Chico A, Vidal-Rios P, Subira M, et al. The continuous glucose monitoring system
is useful for detecting unrecognized hypoglycemias in patients with type 1 and
type 2 diabetes but is not better than frequent capillary glucose measurements
for improving metabolic control. Diabetes Care 2003;26(4):11537.
34. Weber KK, Lohmann T, Busch K, et al. High frequency of unrecognized hypogly-
caemias in patients with type 2 diabetes is discovered by continuous glucose
monitoring. Exp Clin Endocrinol Diabetes 2007;115(8):4914.
35. Biermann E, Dietrich W, Rihl J, et al. Are there time and cost savings by using tel-
emanagement for patients on intensified insulin therapy? A randomised,
controlled trial. Comput Methods Programs Biomed 2002;69(2):13746.
36. Jansa M, Vidal M, Viaplana J, et al. Telecare in a structured therapeutic education
programme addressed to patients with type 1 diabetes and poor metabolic con-
trol. Diabetes Res Clin Pract 2006;74(1):2632.
37. Hirsch IB, Bode BW, Childs BP, et al. Self-monitoring of blood glucose (SMBG) in
insulin- and non-insulin-using adults with diabetes: consensus recommendations
for improving SMBG accuracy, utilization, and research. Diabetes Technol Ther
2008;10:41939.
38. Karter AJ, Parker MM, Moffet HH, et al. Longitudinal study of new and prevalent
use of self-monitoring of blood glucose. Diabetes Care 2006;29(8):175763.
39. Strowig SM, Raskin P. Improved glycemic control in intensively treated type 1 dia-
betic patients using blood glucose meters with storage capability and computer-
assisted analyses. Diabetes Care 1998;21(10):16948.
40. Harno K, Kauppinen-Makelin R, Syrjalainen J. Managing diabetes care using an
integrated regional e-health approach. J Telemed Telecare 2006;12(Suppl 1):135.
41. Bond GE, Burr RL, Wolf FM, et al. The effects of a web-based intervention on psy-
chosocial well-being among adults aged 60 and older with diabetes: a random-
ized trial. Diabetes Educ 2010;36(3):44656.
42. Moreno L, Dale SB, Chen AY, et al. Costs to medicare of the informatics for dia-
betes education and telemedicine (IDEATel) home telemedicine demonstration:
findings from an independent evaluation. Diabetes Care 2009;32(7):12024.
Internet Blood Glucose Monitoring Systems 33
43. Malanda UL, Bot SD, Nijpels G. Self-monitoring of blood glucose in noninsulin-
using type 2 diabetic patients: it is time to face the evidence. Diabetes Care
2013;36(1):1768.
44. Tildesley HD, Conway ME, Ross SA, et al. Review of the effect of internet thera-
peutic intervention in patients with type 1 and type 2 diabetes. Diabetes Care
2014;37(2):e312.
45. Ross J, Stevenson F, Dack C, et al. Evaluating the implementation of HeLP-
Diabetes within NHS services: study protocol. BMC Health Serv Res 2014;14:51.
46. Trief PM, Teresi JA, Izquierdo R, et al. Psychosocial outcomes of telemedicine
case management for elderly patients with diabetes: the randomized IDEATel
trial. Diabetes Care 2007;30(5):12668.
47. Gomez EJ, Hernando ME, Garcia A, et al. Telemedicine as a tool for intensive
management of diabetes: the DIABTel experience. Comput Methods Programs
Biomed 2002;69(2):16377.
48. McCarrier KP, Ralston JD, Hirsch IB, et al. Web-Based Collaborative Care for
Type 1 Diabetes: A Pilot Randomized Trial. Diabetes Technol Ther 2009;11(4):
2117.
Monitoring Glycemia in
Diabetes
Sara J. Healy, MD, Kathleen M. Dungan, MD, MPH*
KEYWORDS
Glucose monitor Self-monitored blood glucose Continuous glucose monitoring
HbA1c
KEY POINTS
Hemoglobin A1C (HbA1c) is the most important global measure of glucose control but
must be interpreted with caution in some circumstances.
Capillary glucose self-monitoring should be performed in patients requiring complex insu-
lin regimens and in patients who are properly trained to interpret and use the results for
adjusting therapy.
Professional continuous glucose monitoring requires little training and may be useful for
patients with type 1 or type 2 diabetes who are not meeting glucose targets.
Personal continuous glucose monitoring may be beneficial for adults and children with
type 1 diabetes who can demonstrate near-daily use. As technology advances, however,
its use will likely expand.
INTRODUCTION
Monitoring of glycemia has evolved substantially since the first home glucose monitor
became available in the late 1970s. Since then, monitoring of glycemic control has
become an indispensable component of any diabetes therapeutic regimen, whether
it consists of periodic hemoglobin A1C (HbA1c) measurement or continuous interstitial
glucose monitoring. This article highlights the advantages, disadvantages, indications,
and implementation of approaches for monitoring glycemia.
Disclosures: K.M. Dungan reports research support from Novo Nordisk, Merck, AstraZeneca,
and advisory board for Eli Lilly. S.J. Healy has nothing to disclose.
Division of Endocrinology, Diabetes and Metabolism, The Ohio State University Wexner Medi-
cal Center, 5th Floor McCampbell Hall, 1581 Dodd Drive, Columbus, OH 43210, USA
* Corresponding author.
E-mail address: [email protected]
3 months. Although the average lifespan of an erythrocyte is 120 days, more recent
glycemic levels contribute more to the HbA1c level.1 The Diabetes Control and Com-
plications Trial (DCCT) and the United Kingdom Prospective Diabetes Study demon-
strated that HbA1c has strong predictive value for diabetes complications. HbA1c
may be used to diagnose diabetes (cutoff point 6.5% for diagnosis) and monitor
overall control 2 to 4 times per year. Point-of care testing for HbA1c is recommended
to facilitate timely treatment changes.
Table 1
Correlation of hemoglobin A1c and estimated average glucose
Box 1
Factors affecting hemoglobin A1c
as for HbA1c.4,7,8 Each marker has advantages and disadvantages that may be lever-
aged in individual situations. Early data suggest that a combination of markers may
provide a more complete picture of glucose control and complication risk but this re-
quires confirmation before routine use can be recommended.79
SMBG was introduced in the 1980s and its benefit has been reasonably established in
insulin-treated patients. SMBG allows the patient to identify hypoglycemia and hyper-
glycemia; get immediate feedback about the effect of food choices, stress, activity,
and insulin dosing on glucose levels; and determine whether medication adjustment
is needed. Self-monitoring of glucose can identify recurrent hypoglycemia or hyper-
glycemia even in the setting of an acceptable HbA1c.10 The frequency and timing of
SMBG depends on several factors, particularly on whether a patient is meeting treat-
ment goals or a requiring complex insulin regimen. The routine measurement of post-
prandial glucose levels or glycemic variability remains controversial but may be useful
for patients who fail to meet HbA1c targets. Glycemic variability is a strong predictor of
severe hypoglycemia and thus may be used to target the intensity of treatment
interventions.11
Self-Monitored Blood Glucose in Patients Requiring Insulin
Previous studies in type 1 diabetes have associated increased frequency of SMBG
with lower HbA1c and fewer complications.12,13 American Diabetes Association
(ADA) guidelines recommend frequent SMBG in most patients with type 1 diabetes
or on intensive insulin regimens such as multiple-dose insulin or insulin pump therapy.
SMBG should be performed before meals and snacks, occasionally postprandial, at
bedtime, before exercise, when low glucose is suspected, after treating low glucose,
and before critical tasks such as driving.4 Although needs vary by individual, testing
may be required 6 to 8 times per day.
38 Healy & Dungan
diabetes care plan in order to attain agreed treatment goals.14 Performing periodic
focused SMBG over short periods of time may help identify glucose patterns that
reflect daily glycemic control (Fig. 1).14,24 A structured SMBG program improves gly-
cemic control and facilitates more timely and aggressive treatment changes.19
SMBG may miss important fluctuations in glucose that are easily identifiable using
CGM. CGM data may be used to help patients manage glucose trends in real time
or retrospectively. A system is categorized according to whether it is owned by a
health care provider and features only retrospective data (professional CGM) or it pro-
vides real-time (RT) data (personal CGM or RT-CGM).
Fig. 1. Two possible schemes for focused SMBG. (A) Periodic 7-point glucose profile ob-
tained once or twice per week. (B) Paired readings before meals and after meals sampled
throughout the week. (Data from International Diabetes Federation Clinical Practice Guide-
lines: Self-monitoring of blood glucose in noninsulin-treated type 2 diabetes. 2009; and
Schnell O, Alawi H, Battelino T, et al. Addressing schemes of self-monitoring of blood
glucose in type 2 diabetes: a European perspective and expert recommendation. Diabetes
Technol Ther 2011;13:95965.)
40 Healy & Dungan
Table 2
Professional society recommendations for use of continuous glucose monitoring
Fig. 2. Retrospective download of Personal CGM. This daily glucose overlay during the
period of monitoring shows a pattern of hypoglycemia that is most pronounced in the
late morning and afternoon, and overnight hypoglycemia.
real-time may improve quality of life and HbA1c reduction50 as well as facilitate
patient self-adjustment.51
Toward Closed-Loop Insulin Delivery
It should be emphasized that most prospective randomized controlled trials enroll
highly motivated subjects. It is less clear whether RT-CGM can be useful for patients
in the real-world setting, in which there are fewer resources for training, and less moti-
vated patients may be overwhelmed with the additional data.52,53 Closed-loop insulin
delivery (the artificial pancreas) holds promise for automating insulin delivery in
response to CGM data and potentially will allow more patients to take advantage of
CGM. Recently, low-glucose threshold-suspend technology has been implemented
as the first step toward an artificial pancreas. In a study of 247 subjects with type 1 dia-
betes and documented nocturnal hypoglycemia who were randomized to sensor-
augmented pump with or without a low-glucose threshold-suspend feature, there
was a lower frequency of nocturnal hypoglycemia in the low-glucose threshold-sus-
pend group and no difference in frequency of diabetic ketoacidosis.54 Progress toward
a fully automated closed loop system is likely to progress incrementally, with overnight
closed loop and hyperglycemia minimizer features as future steps.
REFERENCES
1. Goldstein DE, Little RR, Lorenz RA, et al. Tests of glycemia in diabetes. Diabetes
Care 2004;27:176173.
2. Little RR, Rohlfing CL, Sacks DB. Status of hemoglobin A1c measurement and
goals for improvement: from chaos to order for improving diabetes care. Clin
Chem 2011;57:20514.
3. Nathan DM, Kuenen J, Borg R, et al. Translating the A1C assay into estimated
average glucose values. Diabetes Care 2008;31:14738.
4. American Diabetes Association. Standards of medical care in diabetes2014.
Diabetes Care 2014;37(Suppl 1):S1480.
5. Gallagher EJ, Le Roith D, Bloomgarden Z. Review of hemoglobin A(1c) in the
management of diabetes. J Diabetes 2009;1:917.
6. Little RR, Roberts WL. A review of variant hemoglobins interfering with hemoglo-
bin A1c measurement. J Diabetes Sci Technol 2009;3:44651.
7. Selvin E, Rawlings AM, Grams M, et al. Fructosamine and glycated albumin for
risk stratification and prediction of incident diabetes and microvascular compli-
cations: a prospective cohort analysis of the Atherosclerosis Risk in Commu-
nities (ARIC) study. Lancet Diabetes Endocrinol 2014;2:27988.
8. Nathan DM, McGee P, Steffes MW, et al. Relationship of glycated albumin to
blood glucose and HbA1c values and to retinopathy, nephropathy, and cardio-
vascular outcomes in the DCCT/EDIC study. Diabetes 2014;63:28290.
9. Dungan KM. Predicting outcomes and assessing control with alternate glycemic
markers. Diabetes Technol Ther 2012;14:74952.
Monitoring Glycemia in Diabetes 43
10. Dailey G. Assessing glycemic control with self-monitoring of blood glucose and
hemoglobin A(1c) measurements. Mayo Clin Proc 2007;82:22935 [quiz: 236].
11. Kilpatrick ES, Rigby AS, Goode K, et al. Relating mean blood glucose and
glucose variability to the risk of multiple episodes of hypoglycaemia in type 1
diabetes. Diabetologia 2007;50:255361.
12. Miller KM, Beck RW, Bergenstal RM, et al. Evidence of a strong association be-
tween frequency of self-monitoring of blood glucose and hemoglobin A1c
levels in T1D exchange clinic registry participants. Diabetes Care 2013;36:
200914.
13. Ziegler R, Heidtmann B, Hilgard D, et al. Frequency of SMBG correlates with
HbA1c and acute complications in children and adolescents with type 1 dia-
betes. Pediatr Diabetes 2011;12:117.
14. International Diabetes Federation Clinical Practice Guidelines: self-monitoring of
blood glucose in non-insulin treated type 2 diabetes. Brussels: International Dia-
betes Federation; 2009.
15. Farmer AJ, Perera R, Ward A, et al. Meta-analysis of individual patient data in
randomised trials of self monitoring of blood glucose in people with non-
insulin treated type 2 diabetes. BMJ 2012;344:e486.
16. Malanda UL, Welschen LM, Riphagen II, et al. Self-monitoring of blood glucose
in patients with type 2 diabetes mellitus who are not using insulin. Cochrane
Database Syst Rev 2012;(1):CD005060.
17. Schnell O, Alawi H, Battelino T, et al. Self-monitoring of blood glucose in type 2
diabetes: recent studies. J Diabetes Sci Technol 2013;7:47888.
18. Weinger K, Beverly EA, Lee Y, et al. The effect of a structured behavioral inter-
vention on poorly controlled diabetes: a randomized controlled trial. Arch Intern
Med 2011;171:19909.
19. Polonsky WH, Fisher L, Schikman CH, et al. Structured self-monitoring of blood
glucose significantly reduces A1C levels in poorly controlled, noninsulin-treated
type 2 diabetes: results from the structured testing program study. Diabetes
Care 2011;34:2627.
20. Klonoff DC, Blonde L, Cembrowski G, et al. Consensus report: the current role of
self-monitoring of blood glucose in non-insulin-treated type 2 diabetes.
J Diabetes Sci Technol 2011;5:152948.
21. In vitro diagnostic test systemsrequirements for blood-glucose monitoring
systems for self-testing in managing diabetes mellitus. ISO 15197:2013.
Geneva: International Organization for Standardization; 2013.
22. Freckmann G, Schmid C, Baumstark A, et al. System accuracy evaluation of 43
blood glucose monitoring systems for self-monitoring of blood glucose accord-
ing to DIN EN ISO 15197. J Diabetes Sci Technol 2012;6:106075.
23. Freckmann G, Baumstark A, Schmid C, et al. Evaluation of 12 blood glucose
monitoring systems for self-testing: system accuracy and measurement repro-
ducibility. Diabetes Technol Ther 2014;16:11322.
24. Schnell O, Alawi H, Battelino T, et al. Addressing schemes of self-monitoring of
blood glucose in type 2 diabetes: a European perspective and expert recom-
mendation. Diabetes Technol Ther 2011;13:95965.
25. Given JE, OKane MJ, Coates VE, et al. Comparing patient generated blood
glucose diary records with meter memory in type 2 diabetes. Diabetes Res
Clin Pract 2014;104(3):35862.
26. Katz LB, Dirani RG, Li G, et al. Automated glycemic pattern analysis can
improve health care professional efficiency and accuracy. J Diabetes Sci Tech-
nol 2013;7:1636.
44 Healy & Dungan
27. Parkin CG, Davidson JA. Value of self-monitoring blood glucose pattern
analysis in improving diabetes outcomes. J Diabetes Sci Technol 2009;3:
5008.
28. Shashaj B, Busetto E, Sulli N. Benefits of a bolus calculator in pre- and post-
prandial glycaemic control and meal flexibility of paediatric patients using
continuous subcutaneous insulin infusion (CSII). Diabet Med 2008;25:
103642.
29. Maurizi AR, Lauria A, Maggi D, et al. A novel insulin unit calculator for the man-
agement of type 1 diabetes. Diabetes Technol Ther 2011;13:4258.
30. Ziegler R, Cavan DA, Cranston I, et al. Use of an insulin bolus advisor improves
glycemic control in multiple daily insulin injection (MDI) therapy patients with
suboptimal glycemic control: first results from the ABACUS trial. Diabetes
Care 2013;36:36139.
31. Charpentier G, Benhamou PY, Dardari D, et al. The Diabeo software enabling
individualized insulin dose adjustments combined with telemedicine support im-
proves HbA1c in poorly controlled type 1 diabetic patients: a 6-month, random-
ized, open-label, parallel-group, multicenter trial (TeleDiab 1 study). Diabetes
Care 2011;34:5339.
32. Del Prato S, Nicolucci A, Lovagnini-Scher AC, et al. Telecare provides compa-
rable efficacy to conventional self-monitored blood glucose in patients with
type 2 diabetes titrating one injection of insulin glulisine-the ELEONOR study.
Diabetes Technol Ther 2012;14:17582.
33. Demidowich AP, Lu K, Tamler R, et al. An evaluation of diabetes self-
management applications for Android smartphones. J Telemed Telecare 2012;
18:2358.
34. Welsh JB, Kaufman FR, Lee SW. Accuracy of the Sof-sensor glucose sensor
with the iPro calibration algorithm. J Diabetes Sci Technol 2012;6:4756.
35. Tamborlane WV, Beck RW, Bode BW, et al. Continuous glucose monitoring and
intensive treatment of type 1 diabetes. N Engl J Med 2008;359:146476.
36. Bergenstal RM, Tamborlane WV, Ahmann A, et al. Effectiveness of sensor-
augmented insulin-pump therapy in type 1 diabetes. N Engl J Med 2010;363:
31120.
37. Langendam M, Luijf YM, Hooft L, et al. Continuous glucose monitoring systems
for type 1 diabetes mellitus. Cochrane Database Syst Rev 2012;(1):CD008101.
38. Yeh HC, Brown TT, Maruthur N, et al. Comparative effectiveness and safety of
methods of insulin delivery and glucose monitoring for diabetes mellitus: a sys-
tematic review and meta-analysis. Ann Intern Med 2012;157:33647.
39. Pickup JC. The evidence base for diabetes technology: appropriate and inap-
propriate meta-analysis. J Diabetes Sci Technol 2013;7:156774.
40. Pickup JC, Freeman SC, Sutton AJ. Glycaemic control in type 1 diabetes during
real time continuous glucose monitoring compared with self monitoring of blood
glucose: meta-analysis of randomised controlled trials using individual patient
data. BMJ 2011;343:d3805.
41. Battelino T, Phillip M, Bratina N, et al. Effect of continuous glucose monitoring on
hypoglycemia in type 1 diabetes. Diabetes Care 2011;34:795800.
42. Rubin RR, Peyrot M. Health-related quality of life and treatment satisfaction in
the sensor-augmented pump therapy for A1C Reduction 3 (STAR 3) trial. Dia-
betes Technol Ther 2012;14:14351.
43. Beck RW, Buckingham B, Miller K, et al. Factors predictive of use and of benefit
from continuous glucose monitoring in type 1 diabetes. Diabetes Care 2009;32:
194753.
Monitoring Glycemia in Diabetes 45
44. Buse JB, Dailey G, Ahmann AA, et al. Baseline predictors of A1C reduction in
adults using sensor-augmented pump therapy or multiple daily injection ther-
apy: the STAR 3 experience. Diabetes Technol Ther 2011;13:6016.
45. Klonoff DC, Buckingham B, Christiansen JS, et al. Continuous glucose moni-
toring: an Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab
2011;96:296879.
46. Blevins TC, Bode BW, Garg SK, et al. Statement by the American Association of
Clinical Endocrinologists Consensus Panel on continuous glucose monitoring.
Endocr Pract 2010;16:73045.
47. Keenan DB, Mastrototaro JJ, Zisser H, et al. Accuracy of the Enlite 6-day
glucose sensor with guardian and Veo calibration algorithms. Diabetes Technol
Ther 2012;14:22531.
48. Christiansen M, Bailey T, Watkins E, et al. A new-generation continuous glucose
monitoring system: improved accuracy and reliability compared with a previous-
generation system. Diabetes Technol Ther 2013;15:8818.
49. Luijf YM, Mader JK, Doll W, et al. Accuracy and reliability of continuous glucose
monitoring systems: a head-to-head comparison. Diabetes Technol Ther 2013;
15:7227.
50. Jenkins AJ, Krishnamurthy B, Best JD, et al. An algorithm guiding patient re-
sponses to real-time-continuous glucose monitoring improves quality of life. Dia-
betes Technol Ther 2011;13:1059.
51. Buckingham B, Xing D, Weinzimer S, et al. Use of the DirecNet applied treat-
ment algorithm (DATA) for diabetes management with a real-time continuous
glucose monitor (the FreeStyle Navigator). Pediatr Diabetes 2008;9:1427.
52. Norgaard K, Scaramuzza A, Bratina N, et al. Routine sensor-augmented pump
therapy in type 1 diabetes: the INTERPRET study. Diabetes Technol Ther 2013;
15:27380.
53. Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study
Group. Effectiveness of continuous glucose monitoring in a clinical care environ-
ment: evidence from the Juvenile Diabetes Research Foundation continuous
glucose monitoring (JDRF-CGM) trial. Diabetes Care 2010;33:1722.
54. Bergenstal RM, Klonoff DC, Garg SK, et al. Threshold-based insulin-pump inter-
ruption for reduction of hypoglycemia. N Engl J Med 2013;369:22432.
55. Roberts K, Jaffe A, Verge C, et al. Noninvasive monitoring of glucose levels: is
exhaled breath the answer? J Diabetes Sci Technol 2012;6:65964.
56. Zhang J, Hodge W, Hutnick C, et al. Noninvasive diagnostic devices for dia-
betes through measuring tear glucose. J Diabetes Sci Technol 2011;5:16672.
57. Estimated average glucose, eAG. Available at: http://professional.diabetes.org/
GlucoseCalculator.aspx. Accessed May 19, 2014.
G l y c e m i c Tar g e t s
What is the Evidence?
a,b, a,c
Silvio Inzucchi, MD *, Sachin Majumdar, MD
KEYWORDS
Glycemic targets Diabetes Microvascular Macrovascular Glycemic control
KEY POINTS
The available evidence supports targeting near-normal glucose levels for the prevention
and reduction of the microvascular complications of diabetes.
Although there is a strong relationship between glucose levels and macrovascular disease
in diabetes, the evidence for preventing and reducing the macrovascular complications of
diabetes by glucose lowering is limited.
Glycemic targets must be individualized and based on patient specific factors that bal-
ance the benefits of therapy with its harms.
Ants, bees, and ancient physicians recognized a sweet taste in the urine of individuals
afflicted by a condition of polyuria and wasting. With the attachment of the Latin term,
mellitus, diabetes was forever linked to a disorder of glucose metabolism. Although
many other metabolic abnormalities exist in diabetes, its diagnosis and, to a large
degree, its management are unified through the presence of hyperglycemia. In
1943, Dr Eliot Joslin1 observed that life expectancy after the onset of diabetes had
increased from less than 5 years to greater than 14 years with the introduction of
insulin therapy, and more patients were living long enough to suffer from its complica-
tions. These complications have been divided into 2 general categories: (1) microvas-
cular: retinopathy, nephropathy, and neuropathy; and (2) macrovascular, affecting the
coronary, cerebral, and peripheral vascular systems. The central question is whether
the obvious abnormality of diabetes (ie, hyperglycemia) is responsible for these com-
plications. This is the basis of the glucose hypothesis: that hyperglycemia is their
direct cause and that, by normalizing systemic glucose levels, these morbidities can
be prevented.
a
Department of Endocrinology, Yale University School of Medicine, New Haven, CT; b Medical
Director, Yale Diabetes Center, Yale-New Haven Hospital, New Haven, CT; c Section of Endocri-
nology, Bridgeport Hospital, Yale New Haven Health System, Bridgeport, CT
* Corresponding author. Department of Endocrinology, Yale University School of Medicine,
New Haven, CT
E-mail address: [email protected]
Diabetes is the leading cause of retinopathy, end-stage renal disease, and peripheral
neuropathy in the United States.24 These conditions also occur in nondiabetic individ-
uals but their excess occurrence in diabetes and relationship to hyperglycemia are
specific enough to be considered disease defining.57
In a 15-year cohort study of nondiabetic individuals, the cumulative incidence of
retinopathy was 14% and was linked to baseline age, blood pressure, and the pres-
ence of chronic kidney disease.8 In comparison, in a cohort of type 1 and 2 diabetics,
the incidence of retinopathy over a 10-year period ranged from 67% to 89%.9 The
Wisconsin Epidemiologic Study of Diabetic Retinopathy reported a 97% cumulative
incidence of any degree of retinopathy over a period of 25 years in type 1 diabetic pa-
tients.10 Although this was not an intervention study, the most powerful predictor of
retinopathy progression was glycemic control (Fig. 1). Findings are similar for micro-
albuminuria, with prevalence rates of 2.6% to 6.6% in nondiabetic populations
compared with 13.8% to 16.4% for those with diabetes, with progression to overt pro-
teinuria at rates of 36% to 44% over 10 years.9,11 Neuropathy is similarly associated
with both diabetes and glycemic control (Fig. 2).12,13
But at what levels of glycemia do microvascular complications occur and is there
a threshold? Several studies show that the prevalence of retinopathy increases
from less than 5% to greater than 10% as fasting glucose levels exceed 120 to
126 mg/dL and the 2-hour glucose level during an oral glucose tolerance test
(OGTT) exceeds 195 to 207 mg/dL.6,14,15 For example, a Finnish study showed a
transition point around a fasting glucose of approximately120 mg/dL (Fig. 3).16
The prevalence of retinopathy has also been reported in individuals ranging from
normal to diabetic, and a threshold hemoglobin A1c (HbA1c) of approximately
6.2% was able to identify those at higher risk for retinopathy in one analysis
(Fig. 4).14,17 Several large population studies suggest a more continuous relationship
6
Hazard Rao
0
<9.5 9.5 - 10.5 10.6 - 12.0 12.1 - 19.5
HbA1c (%)
Fig. 1. Hazard ratios for the progression of proliferative retinopathy according to HbA1c
category in the Wisconsin Epidemiologic Study of Diabetic Retinopathy. (Data from
Klein R, Knudston MD, Lee KE, et al. The Wisconsin epidemiologic study of diabetic retinop-
athy XXII: the twenty-five-year progression of retinopathy in persons with type 1 diabetes.
Ophthalmology 2008;115:185968.)
Glycemic Targets 49
50
40
30
Percent
20
10
0
<5.4 5.4-6.4 6.5-7.7 7
HbA1c (%)
Fig. 2. Prevalence of neuropathy according to HbA1c category in the EURODIAB study. (Data
from Tesfaye S, Stevens LK, Stephenson JM, et al, EURODIAB IDDM Study Group. Prevalence
of diabetic peripheral neuropathy and its relation to glycaemic control and potential risk
factors: the EURODIAB IDDM Complications Study. Diabetologia 1996;39:137784.)
without a clear threshold although rates of moderate retinopathy rose with fasting
glucose concentrations greater than 112 mg/dL, with greater increases above con-
centrations of 128 to 140 mg/dL.18
Epidemiologic associations between glycemia and microvascular disease are
strong but cannot determine whether the relationship is causal. Basic investigations
have been helpful in identifying the effects of elevated glucose in tissues where micro-
vascular disease occurs, primarily involving protein glycation, basement membrane
20
15
Percent
10
0
< 109.8 109.8 - 118.8 120.6
Fasng Glucose (mg/dL)
Fig. 3. Prevalence of retinopathy according to fasting glucose values in a Finnish popula-
tion. (Data from Rajala U, Laakso M, Qiao Q, et al. Prevalence of retinopathy in people
with diabetes, impaired glucose tolerance, and normal glucose tolerance. Diabetes Care
1998;21:16649.)
50 Inzucchi & Majumdar
40
30
Percent
20
10
0
5.3 6 8.2 10.6
HbA1c (%)
Fig. 4. Prevalence of retinopathy according to diabetes status. HbA1c categories represent-
ing nondiabetic (5.3%) impaired glucose metabolism (6%), newly diagnosed diabetes
(8.2%), and established diabetes (10.6%). (Data from Van Leiden HA, Dekker JM, Moll,
AC, et al. Blood pressure, lipids, and obesity are associated with retinopathy: the Hoorn
Study. Diabetes Care 2002;25:13205.)
expansion, and endothelial injury, but are beyond the scope of this review.19 If the
glucose hypothesis is correct, however, these complications should be preventable
or perhaps even reversible by normalizing glucose levels.
60
40
20
0
No DM, No CHD DM, No CHD No DM, CHD DM + CHD
DM and CHD Status
Fig. 5. CV mortality according to presence or absence of diabetes mellitus (DM), coronary
heart disease (CHD) or both, at baseline. (Data from Juutilainen A, Lehto S, Ronnemaa T,
et al. Type 2 diabetes as a coronary heart disease equivalent. Diabetes Care 2005;28:29017.)
lower CV risk with HbA1c levels of 7.2% versus 9.0%.29 Still, it is not clear from these
studies whether glucose is directly responsible for the higher risk or whether it is more
of a marker.
Fasting glucose, the response to an OGTT, and HbA1c can predict risk of CVD.3034
This risk increases with degrees of glycemia that are either within or slightly above the
normal range, for example, fasting glucose greater than 101 mg/dL or HbA1c greater
than 5% (Fig. 6).3032 Twenty-year follow-up of several large studies has even
40
CV Events (per 100 persons)
30
20
10
0
<5 5.0 - 5.4 5.5 - 5.9 6.0 - 6.4 6.5 - 6.9 >7
HbA1c (%)
Fig. 6. CV events according to HbA1c in the European Prospective Investigation of Cancer
(EPIC)-Norfolk study. (Data from Khaw KT, Wareham N, Luben R, et al. Glycated hemoglobin,
diabetes, and mortality in men in Norfolk cohort of European Prospective Investigation of
Cancer and Nutrition (EPIC-Norfolk). BMJ 2001;322:16.)
52 Inzucchi & Majumdar
shown elevated CVD and mortality in nondiabetic individuals with glucose levels
ranging from 100 to 169 mg/dL after 2-hour OGTT compared with levels less than
100 mg/dL.35 Glucose tolerance also corresponds to a significant increase in the
prevalence of peripheral vascular disease, particularly with 2-hour levels greater
than 200 mg/dL.6,36,37 The bulk of the data suggest no specific threshold as exists
with microvascular disease and, although basic science supports a role for hypergly-
cemia in promoting atherosclerosis, its origins and progression are influenced by an
interplay of factors, including dyslipidemia, hypertension, inflammation, insulin resis-
tance, and genetics. These factors make the independent effect of glucose on
atherogenesis more difficult to discern, contrasting with microvascular disease,
which predominantly involves injury to a single endothelial layer and seems primarily
driven by hyperglycemia.19,38
Given all the uncertainty regarding the precise effects of hyperglycemia on vascular
diseases, particularly as it relates to treatment targets, clinical trials of glucose-
lowering therapies have constituted the necessary test of the glucose hypothesis
for both microvascular and macrovascular complications. Herein lies the bulk of the
knowledge on this fundamentally important clinical question in diabetes care.
2158; P 5 .01) in the primary and secondary intervention cohorts, and those for neu-
ropathy were 69% (95% CI, 2487; P 5 .006) and 57% (95% CI, 2973; P.001).
When the entire study population was analyzed according to HbA1c, retinopathy rates
were dependent on glycemic control and independent of treatment assignment, with
all individuals maintaining HbA1c levels of 6.5% to 7.49% having low rates of retinop-
athy and those with HbA1c levels of 8.5% to 9.49% having higher ratessupporting
the hypothesis that glucose was the determining factor.41 CV events were insignifi-
cant. The major side effects of intensive therapy were weight gain and hypoglycemic
events, with 62 versus 19 severe episodes of hypoglycemia (per 100 patient years) in
the intensive versus conventional group.
After the trial, conventionally treated subjects were trained in intensive therapy and
both groups returned to the care of their individual providers. They were also asked to
participate in an observational study, the Epidemiology of Diabetes Interventions and
Complications (EDIC) study, with follow-up now available to 18 years post-trial.40 Dur-
ing the EDIC study, the mean HbA1c levels for the original conventional and intensive
groups were similar at approximately 8%, and, despite loss of the initial differences in
HbA1c, there were significant reductions in all clinically meaningful endpoints, such as
advanced retinopathy, nephropathy, and CV events, for those originally assigned to
intensive therapy.40,4244 CV benefits became significant after a mean follow-up of
17 years, when the average age of participants was 45 years in EDIC study year 11,
and significant reductions in microvascular events persisted at 18 and 24 years
(Figs. 79).40,42,44 It was estimated from the EDIC experience that a 10% relative
decrease in HbA1c was associated with a 20% risk reduction in CV events.42 The
EDIC study also reported on a musculoskeletal condition associated with diabetes,
cheiroarthropathy, or periarticular thickening of the skin of the hands, resulting in sig-
nificant disability.43 At EDIC years 18 and 19, it was present in 64% and 68% of inten-
sive and conventional subjects, respectively, and was proportional to diabetes
duration and glycemic control and associated with the presence of microvascular
complications.
The DCCT showed that achieving near-normal glucose levels in young adults with
type 1 diabetes mellitus can prevent microvascular complications, supporting the
glucose hypothesis and establishing intensive therapy as the standard of care for
this form of the disease. EDIC suggested that initial intensive therapy has long-term
health benefits despite later deterioration in glucose control, giving rise to the some-
what theoretic terms, metabolic memory and legacy effect.
40
Primary Intensive
Secondary Intensive
20
Secondary Convenonal
10
0
End DCCT EDIC 12
Study Groups
Fig. 7. Prevalence of proliferative retinopathy at the end of DCCT and at EDIC year 12
according to cohort, primary prevention and secondary prevention, and treatment interven-
tion, intensive versus conventional. (Data from Diabetes Control and Complications Trial/
Epidemiology of Diabetes Interventions and Complications Research Group. Prolonged
effect of intensive therapy on the risk of retinopathy complications in patients with type
1 diabetes mellitus: 10 years after the diabetes control and complications trial. Arch Oph-
thalmol 2008;126(12):170715.)
40
Intensive
30 Convenonal
Percent (%)
20
10
0
PR End DCCT PR EDIC 18 SN End DCCT SN EDIC 18
Study Groups
Fig. 8. Proliferative retinopathy (PR) and severe nephropathy (SN) at the end of the DCCT
and at EDIC year 18 in combined primary and secondary intervention cohorts, by intensive
versus conventional therapy. Severe nephropathy defined as albumin excretion ratio (AER)
greater than 300 mg/d or end-stage renal disease. (Data from Nathan DM. The diabetes con-
trol and complications trial/epidemiology of diabetes interventions and complications study
at 30 years: overview. Diabetes Care 2014;37:916.)
Glycemic Targets 55
10
Intensive
7.5 Convenonal
Percent (%)
2.5
0
Any Event Select Events
Cardiovascular Events
Fig. 9. CV events at EDIC year 11 according to original treatment assignment. Any event:
death from CVD, nonfatal acute MI, silent MI, revascularization, angina, or nonfatal cere-
brovascular event. Select events: nonfatal MI, stroke, and death from CV disease. (Data
from The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions
and Complications (DCCT/EDIC) Study Research Group. Intensive diabetes treatment and
cardiovascular disease in patients with type 1 diabetes. N Engl J Med 2005;353:264353.)
glucose less than 270 mg/dL and the absence of hyperglycemic symptoms. For inten-
sive therapy, the sulfonylureas used were chlorpropamide, glibenclamide, and glipi-
zide, with dosing adjusted to achieve glycemic targets. Insulin-treated patients
began with once-daily basal insulin, such as ultralente or isophane (ie, NPH) insulin.
If daily doses were more than 14 units per day or premeal or bedtime glucose values
were greater than 126 mg/dL, regular human insulin was added for meals and home
glucose monitoring was encouraged. In a small substudy within the UKPDS, over-
weight subjects (>120% ideal body weight) were additionally randomized to intensive
therapy with metformin (instead of sulfonylurea or insulin). Study protocols were later
modified in an effort to maintain glucose control by adding insulin or metformin to sul-
fonylurea therapy.47,49 Conventional group participants were randomized to insulin,
sulfonylurea, or metformin if they became symptomatic or if fasting glucose levels
exceeded 270 mg/dL.
Intensive therapy with sulfonylureas or insulin resulted in a difference in HbA1c of
approximately 0.9% over 10 years with median HbA1c values of 7% and 7.9%,
respectively, compared with conventional therapy.46 Microvascular outcomes were
reduced by 25% (RRR) (95% CI, 0%40%; P 5 .009), and there was a trend toward
reduced risk of MI by 16% (RRR) (95% CI, 0%29%; P 5.052). In obese subjects
randomized to metformin, a difference in HbA1c of 0.6% was maintained between
intensive and conventional groups (7.4% vs 8.0%) over a median of 10.7 years,
and there were RRRs of 36% in the aggregate endpoint of all-cause mortality
(95% CI, 955; P 5 .011), 32% in any diabetes-related endpoint (95% CI, 1347;
P 5 .002), 42% in diabetes-related death (95% CI, 963; P 5 .017), and 39% in
MI (95% CI, 1159; P 5 .01). There were no significant reductions in microvascular
endpoints,47 likely a reflection of the higher mean HbA1c in this group (7.4%) or
reduced power to detect differences, based on the small study sample, with only
342 patients randomized to metformin.
56 Inzucchi & Majumdar
When all subjects were stratified according to glycemic control, similar to the type 1
diabetes mellitus patients in DCCT, there was a clear relationship between glycemic
control and microvascular complications. When HbA1c was compared across tertiles
from less than 6.2%, to 6.2% to 7.4%, to greater than or equal to 7.5%, the relative
risks (RRs) of developing new retinopathy were 1.4 (95% CI, 1.11.8) and 2.5 (95%
CI, 2.03.2) for the second and third tertiles, and for those with preexisting retinopathy,
RRs of progression were 4.1 (95% CI, 3.15.6) and 8.1 (95% CI, 6.310.5) for the sec-
ond and third tertiles.50 An analysis of complications according to HbA1c estimated
that for every 1% reduction in HbA1c the risk reductions in microvascular endpoints,
MI, and diabetes-related death were 37%, 14%, and 21%, respectively.51
As with DCCT, nonrandomized follow-up study of the original UKPDS cohort was
arranged. Shortly after the trial ended in 1997, differences in HbA1c were lost between
the 2 groups and over the next 10 years HbA1c was maintained at approximately 8%,
and despite this, there were persistent reductions in complications, including overall
mortality and diabetes-related death in groups originally assigned to intensive ther-
apy.48 At a median follow-up of 16.8 years, those initially treated more intensively
with insulin or sulfonylureas had RRRs of 24% (95% CI, 1136; P 5 .001) in microvas-
cular disease. Also, because the accumulation of more events over time, a statistically
significant, although still modest, 15% relative reduction in MI was observed (95% CI,
326; P 5 .01). For those originally randomized to metformin, there were significant re-
ductions in MI (RRR 33%; 95% CI, 1149; P 5 .005) but, again, no benefit in microvas-
cular endpoints, at a median follow-up of 17.7 years.
The UKPDS had several major findings regarding glucose lowering: (1) achieving
near-normal glucose levels in newly diagnosed type 2 diabetics can reduce the micro-
vascular complications of diabetes; (2) for those able to maintain tighter glycemic con-
trol, complication rates were lower; (3) in obese subjects, metformin reduced
macrovascular events and mortality, suggesting a glucose-independent benefit of
metformin on macrovascular disease; (4) monotherapies failed to maintain glycemic
control over time, largely due to declining b-cell function, yet (5) the impact of initial
intensive therapy had long-term benefits on micro- and macrovascular disease that
were apparent 15 to 20 years laterdespite deterioration in glucose control.
Kumamoto Study
The Kumamoto study was a randomized clinical trial with a similar design to DCCT and
sought to answer 2 main questions in adults with previously diagnosed type 2 diabetes
mellitus: (1) Will intensive insulin therapy prevent microvascular complications in those
without preexisting complications (primary prevention) and (2) Will intensive insulin
therapy prevent the progression of early microvascular complications (secondary
prevention)?
The small study was done in Japan at a single university center and consisted of just
110 adult diabetic patients with an average age of 49 and diabetes duration of 6 to
10 years.52 Initial HbA1c levels were approximately 9% and patients were divided
into 2 groups of 55 each: those with no retinopathy or nephropathy (UAE <30 mg/
24 h) and those with early retinopathy and microalbuminuria (UAE <300 mg/24 h).
Each group of 55 subjects was then randomly assigned to intensive versus conven-
tional insulin therapy. Intensive therapy consisted of 3 or more injections of insulin
daily with rapid-acting insulin for meals and intermediate insulin at bedtime and aimed
for fasting glucose concentrations of less than 140 mg/dL, 2-hour postprandial
glucose less than 200 mg/dL, HbA1c less than 7%, and mean amplitude of glycemic
excursions of less than 100 mg/dL. Visits to clinics were made biweekly to achieve
and maintain goals. Conventional therapy consisted of 1 to 2 injections of
Glycemic Targets 57
Abbreviations: ARE, absolute risk increase; ARR, absolute risk reduction; DM, diabetes mellitus; FU, follow up; Int, intensive; std, standard therapy HbA1c goals.
a
These are the primary prevention group data.
b
UKPDS-I-SU is the insulin-sulfonylurea study and UKPDS-MET is the metformin study.
Glycemic Targets 59
assignment. There was a trend toward benefit with intensive control for those without
prior CV events whose baseline HbA1c levels were less than 8%, suggesting that
aggressive glycemic reductions may be safer (and more effective) in patients without
preexisting CV disease but riskier (and ineffective) once atherosclerosis is overt.
ADVANCE randomized 11,140 patients to compare CV outcomes between inten-
sive therapy aiming to achieve HbA1c levels of less than 6.5% versus 7% (see
Table 1).55 At baseline, 32% of the participants had experienced a prior CV event,
and others had at least one CV risk factor or had microvascular disease. The primary
outcomes were composites of macro- and microvascular outcomes (CV death,
nonfatal MI and stroke, new or worsening nephropathy or retinopathy). After a median
follow-up of 5 years when HbA1c levels were 6.5% versus 7.3%, there were no signif-
icant differences in macrovascular events or mortality. A significant reduction in
nephropathy was found, however, mainly in the form of macroalbuminuria, progress-
ing in 2.9% of the intensive versus 4.1% of the standard control group (P.001). Over-
all, new or worsening nephropathy occurred in 4.1% of intensive versus 5.2% in the
standard group (P 5 .006). There were no differences in retinopathy, but this was
defined by its more advanced forms, such as proliferative retinopathy and diabetes-
related blindness. The frequency of severe hypoglycemia was low but significantly
different, occurring in 2.7% of the intensive and 1.5% of the standard groups
(P.0001).
Post-trial follow-up at a median of 5.4 years was recently reported for ADVANCE.56
Similar to DCCT and UKPDS differences in glycemic control between treatment
groups were lost after the study ended, but unlike the earlier studies there was no
evidence of emerging CV benefits and there was only a suggestion of persisting
benefits on nephropathy reduction, which may reflect benefits carried forward from
the original trial.
The VADT randomized 1791 patients to intensive therapy aiming for an absolute
reduction in HbA1c of 1.5% between the intensive and standard groups (see
Table 1).57 More than 95% of participants were men, and they were at high CV risk,
with approximately 40% having experienced a previous macrovascular event. The
VADT participants had a longer duration of disease (11.5 years) and a higher HbA1c
(9.4%) that the other trials. The primary outcome was time to first occurrence of any
one of a composite of CV endpoints (MI; stoke; CV death; CHF; the need for interven-
tion on cardio-, cerebral-, or peripheral vascular disease; or amputation for ischemic
gangrene). After a median follow-up of 5.6 years during which mean HbA1c levels were
6.9% versus 8.4%, no differences were found in CV events or mortality. The only sig-
nificant differences were in reductions of albuminuria, and, when reported as any in-
crease in albuminuria, there was progression in 9.1% of the intensive versus 13.8%
in the standard group (P 5 .01). There were no differences in clinically significant or
proliferative retinopathy. Serious adverse events were more common in the intensive
group, occurring in 24.1% versus 17.6% (P 5 .05), with many of these due to hypogly-
cemia, of which severe episodes were the strongest predictors of death at 90 days.
Subgroup analysis suggested CV benefits for tighter control in individuals with lower
coronary artery calcification scores at baseline and shorter diabetes duration.60,61
ADVANCE, ACCORD, and VADT did not show a benefit of tight glycemic control for
reducing composite macrovascular events in type 2 diabetes mellitus, although there
was evidence for reduced progression of nephropathy and perhaps nonfatal MI. The
results of ACCORD, however, have specifically raised concerns for harm associated
with tight glycemic control, particularly in those with pre-established CVD.
Compared with DCCT, UKPDS, and their respective observational studies, these
trials differed in ways that may have obscured benefits in the intensive groups while
60 Inzucchi & Majumdar
increasing risk for adverse events because of tighter control. (1) Glycemic targets were
substantially lower in all treatment groups with intensively managed patients
approaching the euglycemic range and standard therapy groups having HbA1c levels
closer to those achieved in the tight control groups from older studies which could (see
Table 1) have minimized differences between groups. However, allowing for looser
control (eg, HbA1c approximately 9% vs lower) was not possible due to ethical con-
cerns, given the known benefits of tighter control on microvascular events. Reduced
targets also meant more hypoglycemia, and, despite the data indicating that hypogly-
cemia was not the direct cause of events in these studies, it still may have attenuated
any benefit from improved glycemia. (2) Study durations, including the post-trial
follow-up for ADVANCE, were also shorter, whereas major differences in macrovascu-
lar events were seen after only 10 years or more in UKPDS and DCCTand mainly in
their follow-up studies (see Table 1). Moreover, certain differences in microvascular
endpoints may have gone undetected, because study durations may have been too
short to observe differential effects, in, for example, retinopathy. (3) Patients were
older, had longer durations of poorly controlled diabetes, were at higher CV risk,
and were on more-intensive blood pressure and lipid-lowering regimens, all factors
that could have minimize changes in CV outcomes. (4) Finally, direct harm from certain
pharmacologic agents used in these later trials may have masked the benefits from
glucose control, a discussion beyond the scope of this review.
Several meta-analyses have examined the relationship between tight glycemic control
and macrovascular outcomes.6264 One that included ADVANCE, ACCORD, VADT,
UKPDS, and Prospective Pioglitazone Clinical Trial in Macrovascular Events sug-
gested a 17% reduction in nonfatal MI (odds ratio [OR] 0.83; 95% CI, 0.750.93)
and a 15% reduction in events related to CHD (OR 0.85; 95% CI, 0.770.93) but no
significant reductions in stroke or all-cause mortality.62 Another meta-analysis of
only ADVANCE, ACCORD, VADT, and UKPDS was directionally consistent with these
findings, suggesting pooled RRRs of 10% (95% CI, 2%17%) for CVD and 11% (95%
CI, 419) for CHD but not in CV death or all-cause mortality. Severe hypoglycemia was
increased 2-fold: RR 2.03 (95% CI, 1.462.81) in the pooled analysis.63 Other analyses
support the conclusions that tighter glycemic control can result in some, albeit small,
reductions in CV events but not in overall mortality, and that for some individuals
tighter control may results in more harm, whether due to hypoglycemia or other
patient-specific factors.64 The overall data at this point support individualization of
glycemic targets to patient characteristics so the risks and benefits of treatment goals
can be considered.
The extensive evidence for glucose lowering, reviewed previously, helps guide the treat-
ment of patients with diabetes and specifically in the determination of glycemic treat-
ment targets. The evidence is reasonably clear for microvascular diseaseachieving
near-normal glucose levels can prevent its development and progression. Even though
data on major life-altering complications, such as visual or limb loss, or the need for dial-
ysis are more limited, it is logical to presume that preventing the progression of more
subtle endpoints will translate into long-term benefits for these outcomes. The DCCT,
UKPDS, and Kumamoto study all provide rationale for glycemic targets associated
with minimal risk of microvascular complications and form the basis for current treat-
ment guidelines (Tables 2 and 3). Complications were essentially avoided in individuals
Glycemic Targets 61
Table 2
Glycemic targets in tight control groups of various trials and the time after the trials began
when significant complication reductions were reported
with HbA1c less than 7% in DCCT, less than 6.2% in UKPDS, and less than 6.5% in the
Kumamoto study. In ADVANCE and VADT, nephropathy progression was reduced, with
HbA1c less than 7% despite shorter time frames than other trials.
The evidence for macrovascular disease is extremely limited, with the suggestion of
a benefit on nonfatal MI but not on other outcomes or overall mortality. There may,
however, be benefits in select patient groupsyounger, newly diagnosed patients,
and those with minimal CVD at baseline. In ADVANCE, ACCORD, and VADT, there
was evidence for benefit in those with shorter diabetes durations (<5 years), age
less than 65, and absence of micro- or macrovascular disease at baseline.60,61 More-
over, the follow-up studies of DCCT (in type 1) and UKPDS (in type 2) do suggest that
any benefits of tight glycemic control on atherosclerosis-related endpoints are only
observed over many years of treatment (see Table 1).
The costs of tight glycemic control are clear and consistent across studies and age
groups: increased hypoglycemic events and weight gain, particularly with insulin. The
increased mortality in ACCORD and lack of overall CV benefit in ACCORD, ADVANCE,
and VADT coupled with adverse events make it difficult to recommend tight glycemic
control for all patients.
What are the considerations for individualized diabetes treatment? Each patient
presents a unique set of circumstances and for each a rational HbA1c target should
be determined. This approach has been discussed extensively by Ismail-Beigi and
Table 3
Current diagnostic criteria for diabetes in nonpregnant adults and treatment targets set by
various organizations
Abbreviations: ADA, American Diabetes Association; AACE, American Association of Clinical Endo-
crinologists; DM, diabetes mellitus; IDF, International Diabetes Federation.
a
After OGTT or random glucose 1 symptoms of diabetes.
Data from Refs.6770
62 Inzucchi & Majumdar
Fig. 10. Individualized approach to glycemic targets, ADA-EASD. Depiction of the elements of
decision making used to determine appropriate efforts to achieve glycaemic targets. Greater
concerns about a particular domain are represented by increasing height of the ramp. Thus,
characteristics/predicaments toward the left justify more stringent efforts to lower HbA1c,
whereas those toward the right are compatible with less stringent efforts. Where possible,
such decisions should be made in conjunction with the patient, reflecting his or her prefer-
ences, needs, and values. This scale is designed not to be applied rigidly but to be used as a
broad construct to help guide clinical decisions. (From Inzucchi SE, Bergenstal RM, Buse JB,
Diamant M, Ferrannini E, Nauck M, Peters AL, Tsapas A, Wender R, Matthews DR. Manage-
ment of hyperglycemia in type 2 diabetes: A patient-centered approach. Diabetes Care
2012;35:1366; with permission.)
Glycemic Targets 63
control may be reasonable in older patients on medications with minimal risk for hypo-
glycemia, little comorbidity, no CVD, and a good life expectancy with a high functional
status. Alternatively, it may be harmful or impractical in younger patients with a history
of severe hypoglycemia or advanced diabetes duration and complications; the frail;
and those with limited life expectancy, limited social resources, and poor self-care
ability or functional status.6567 These are some of several considerations that must
be made in the context of shared decision making between physician and patient in
developing a comprehensive treatment plan.
Finally, although glucose remains a central feature of diabetes mellitus and glucose
lowering has been confirmed as a way to reduce the complications of diabetes, it has
become clear that this alone is not the only factor that must be addressed in the treat-
ment of diabetes.67 Age, blood pressure, lipid levels, other risk factors, and the side
effects of glucose-lowering therapies must be incorporated into individualized treat-
ment strategies that aim to achieve maximal benefits in both complication reduction
and quality of life, while minimizing harm.
REFERENCES
14. Engelgau MM, Thompson TJ, Herman WH, et al. Comparison of fasting and
2-hour glucose and HbA1c levels for diagnosing diabetes: diagnostic criteria
and performance revisited. Diabetes Care 1997;20:78591.
15. McCance DR, Hanson RL, Charles MA, et al. Comparison of tests for glycated
hemoglobin and fasting and two hour plasma glucose concentrations as diag-
nostic methods for diabetes. BMJ 1994;308:13238.
16. Rajala U, Laakso M, Qiao Q, et al. Prevalence of retinopathy in people with
diabetes, impaired glucose tolerance, and normal glucose tolerance. Diabetes
Care 1998;21:16649.
17. Van Leiden HA, Dekker JM, Moll AC, et al. Blood pressure, lipids, and obesity are
associated with retinopathy: the hoorn study. Diabetes Care 2002;25:13205.
18. Wong TY, Liew G, Tapp RJ, et al. Relationship between fasting glucose and
retinopathy for diagnosis of diabetes: three population-based cross-sectional
studies. Lancet 2008;371:73643.
19. Brownlee M. Biochemistry and molecular cell biology of diabetic complications.
Nature 2001;414:81320.
20. Kannel WB, McGee DL. Diabetes and cardiovascular disease. JAMA 1979;241:
20358.
21. Stamler J, Vaccaro O, Neaton JD, et al, For The Multiple Risk Factor Intervention
Trial Research Group. Diabetes, other risk factors, and 12-yr cardiovascular
mortality for men screened in the multiple risk factor intervention trial. Diabetes
Care 1993;16:43444.
22. Gregg EW, Li Y, Wang J, et al. Changes in diabetes-related complications in the
United States, 1990-2010. N Engl J Med 2014;370:151423.
23. Haffner SM, Lehto S, Ronnemaa T, et al. Mortality from coronary heart disease in
subjects with type 2 diabetes and in nondiabetic subjects with and without prior
myocardial infarction. N Engl J Med 1998;339:22939.
24. Juutilainen A, Lehto S, Ronnemaa T, et al. Type 2 diabetes as a coronary heart
disease equivalent. Diabetes Care 2005;28:29017.
25. Saely CH, Drexel H. Is type 2 diabetes really a coronary heart disease risk
equivalent? Vascul Pharmacol 2013;59:118.
26. Bulugahapitiya U, Siyambalapitiya S, Sithole J, et al. Is diabetes a coronary risk
equivalent? Systematic review and meta-analysis. Diabet Med 2009;26:1428.
27. Andersson DK, Svardsudd K. Long-term glycemic control relates to mortality in
type II diabetes. Diabetes Care 1995;18(12):153443.
28. Eeg-Olofsson K, Cederholm J, Nilsson PM, et al. New Aspects of HbA1c as a risk
factor for cardiovascular disease in type 2 diabetes: an observational study from
the Swedish National Diabetes Register (NDR). J Intern Med 2010;268:47182.
29. Eeg-Olofsson K, Cederholm J, Nilsson PM, et al. Glycemic control and cardio-
vascular disease in 7,454 patients with type 1 diabetes: an observational study
from the Swedish National Diabetes Register (NDR). Diabetes Care 2010;33:
16406.
30. The Emerging Risk Factors Collaboration. Diabetes mellitus, fasting glucose
concentration, and risk of vascular disease: a collaborative meta-analysis of
102 prospective studies. Lancet 2010;375:221522.
31. Khaw KT, Wareham N, Luben R, et al. Glycated hemoglobin, diabetes, and mor-
tality in men in Norfolk cohort of European Prospective Investigation of Cancer
and Nutrition (EPIC-Norfolk). BMJ 2001;322:16.
32. Khaw KT, Wareham N, Bingham S, et al. Association of hemoglobin A1c with
cardiovascular disease and mortality in adults: the European Prospective Inves-
tigation into Cancer in Norfolk. Ann Intern Med 2004;141:41320.
Glycemic Targets 65
33. Rodriguez BL, Lau N, Burchfiel CM, et al. Glucose intolerance and 23-year risk
of coronary heart disease and total mortality. the Honolulu Hear Program.
Diabetes Care 1999;22:12625.
34. The DECODE Study Group, on behalf of the European Diabetes Epidemiology
Group. Prediction of the risk of cardiovascular mortality using a score that in-
cludes glucose as a risk factor. The DECODE study. Diabetologia 2004;47:
211828.
35. Balkau B, Shipley M, Jarrett RJ, et al. High blood glucose concentration is a risk
factor for mortality in middle-aged nondiabetic men. 20-year follow-up in the
Whitehall Study, the Paris prospective study, and the Helsinki policemen study.
Diabetes Care 1998;21:3607.
36. Jackson CA, Yudkin JS, Forrest RD. A comparison of the relationships of the
glucose tolerance test and the glycated hemoglobin assay with diabetic
vascular disease in the community. The Islington diabetes survey. Diabetes
Res Clin Pract 1992;17:11123.
37. Beks PJ, Mackaay AJ, de Neeling JN, et al. Peripheral arterial disease in relation
to glycaemic level in an elderly Caucasian population: the Hoorn study. Diabe-
tologia 1995;38:8696.
38. Brownlee M. The pathobiology of diabetic complications: a unifying mechanism.
Diabetes 2005;54:161525.
39. The Diabetes Control and Complications Trial Research Group. The effect of
intensive treatment of diabetes on the development and progression of long-
term complications in insulin-dependent diabetes mellitus. N Engl J Med
1993;329:97786.
40. Nathan DM. The diabetes control and complications trial/epidemiology of
diabetes interventions and complications study at 30 years: overview. Diabetes
Care 2014;37:916.
41. Lachin JM, Genuth S, Nathan DM, et al, for The DCCT/EDIC Research Group. Ef-
fect of glycemic exposure on the risk of microvascular complications in the dia-
betes control and complications trialrevisited. Diabetes 2008;57:9951001.
42. The Diabetes Control and Complications Trial/Epidemiology of Diabetes Inter-
ventions and Complications (DCCT/EDIC) Study Research Group. Intensive
diabetes treatment and cardiovascular disease in patients with type 1 diabetes.
N Engl J Med 2005;353:264353.
43. Larkin ME, Barnie A, Braffett BH, et al, The Diabetes Control and Complications
Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC)
Study Research Group. Musculoskeletal complications in type 1 diabetes.
Diabetes Care 2014;37:18639.
44. De Boer IH, for the DCCT/EDIC Research Group. Kidney disease and related
findings in the diabetes control and complications trial/epidemiology of diabetes
interventions and complications study. Diabetes Care 2014;37:2430.
45. UK Prospective Diabetes Study (UKPDS) VIII. Study design, progress and
performance. Diabetologia 1991;34:87790.
46. UK Prospective Diabetes Study Group. Intensive blood-glucose control with
sulphonylureas or insulin compared with conventional treatment and risk of com-
plications in patients with type 2 diabetes (UKPDS 33). Lancet 1998;352:83753.
47. UK Prospective Diabetes Study Group. Effect of intensive blood-glucose control
with metformin on complications in overweight patients with type 2 diabetes
(UKPDS 34). Lancet 1998;352:85465.
48. Holman RR, Sanjoy PK, Bethel A, et al. 10-year follow up of intensive glucose
control in type 2 diabetes. N Engl J Med 2008;359:157789.
66 Inzucchi & Majumdar
49. Wright A, Burden AC, Paisey RB, et al, for The U.K. Prospective Diabetes Study
Group. Sulfonylurea inadequacy: effect of addition of insulin over 6 years in
patients with type 2 diabetes in the U. K. Prospective Diabetes Study
(UKPDS 57). Diabetes Care 2002;25(2):3306.
50. Stratton IM, Kohner EM, Aldington SJ, et al, for The UKPDS Group. UKPDS 50:
risk factors for incidence and progression of retinopathy in type II diabetes over
6 years from diagnosis. Diabetologia 2001;44:15663.
51. Stratton IM, Adler AI, Neil AW, et al, on behalf of the UK Prospective Diabetes
Study Group. Association of glycemia with macrovascular and microvascular
complications of type 2 diabetes (UKPDS 35): prospective observational study.
BMJ 2000;321:40512.
52. Ohkubo Y, Kishikawa H, Araki E, et al. Intensive insulin therapy prevents the
progression of diabetic microvascular complications in Japanese patients with
non-insulin-dependent diabetes mellitus: a randomized prospective 6-year
study. Diabetes Res Clin Pract 1995;28:10317.
53. Shichiri M, Kishikawa H, Ohkubo Y, et al. Long-term results from the Kumamoto
study on optimal diabetes control in type 2 diabetic patients. Diabetes Care
2000;23(S2):B219.
54. The Action to Control Cardiovascular Risk in Diabetes Study Group. Effects of
intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:
254559.
55. The ADVANCE Collaborative Group. Intensive blood glucose control and
vasculat outcomes in patients with type 2 diabetes. N Engl J Med 2008;
358:256072.
56. Zoungas S, Chalmers J, Neal L, et al. Follow-up of blood pressure lowering and
glucose control in type 2 diabetes. NEJM 2014;371:1392406.
57. Duckworth W, Abriara C, Moritz T, et al, for the VADT Investigators. Glucose
control and vascular complications in veterans with type 2 diabetes. N Engl J
Med 2009;360:12939.
58. Riddle MC, Ambrosius WT, Brillon DJ, et al, for the Action to Control Cardio-
vascular Risk in Diabetes (ACCORD) Investigators. Epidemiologic relation-
ships between A1C and all-cause mortality during a median 3.4 year
follow-up of glycemic treatment in the ACCORD trial. Diabetes Care 2010;
33(5):98390.
59. Bonds DE, Miller ME, Bergenstall RM, et al. The association between symptom-
atic, severe hypoglycaemia and mortality in type 2 diabetes: retrospective
epidemiological analysis of the ACCORD study. BMJ 2010;340:b4909.
60. Reaven PD, Moritz TE, Schwenke DC, et al, for the Veterans Affairs Diabetes
Trial. Intensive glucose-lowering therapy reduces cardiovascular disease
events in veterans affairs diabetes trial participants with lower calcified coronary
atherosclerosis. Diabetes 2009;58:26428.
61. Duckworth WC, Abraira C, Moritz TE, et al, for the Investigators of the VADT. The
duration of diabetes affects the response to intensive glucose control in type 2
diabetes subjects: the VA Diabetes Trial. J Diabetes Complications 2001;25:
35561.
62. Ray KK, Seshasai RK, Wijesuriya S, et al. Effect of intensive control of glucose
on cardiovascular outcomes and death in patients with diabetes mellitus: a
meta-analysis of randomized controlled trials. Lancet 2009;373:176572.
63. Kelly TN, Bazzano LA, Fonseca VA, et al. Systematic review: glucose control
and cardiovascular disease in type 2 diabetes. Ann Intern Med 2009;151:
394403.
Glycemic Targets 67
64. Turnbull FM, Abraira C, Anderson RJ, et al. Intensive glucose control and macro-
vascular outcomes in type 2 diabetes. Diabetologia 2009;52:228898.
65. Ismail-Beigi F, Moghissi E, Tiktin M, et al. Individualizing glycemic targets in type
2 diabetes mellitus: implications of recent clinical trials. Ann Intern Med 2011;
154:5549.
66. Inzucchi SI, Bergenstal RM, Buse JB, et al. Management of hyperglycemia in
type-2 diabetes: a patient-centered approach. Diabetes Care 2012;35:136479.
67. American Diabetes Association. Standards of medical care in diabetes2014.
Diabetes Care 2014;37(S1):S1480.
68. American Association of Clinical Endocrinologists. American College of Endo-
crinology Consensus Statement on Guidelines for Glycemic Control. Endocr
Pract 2002;8(S1):511.
69. Available at: http://www.staff.ncl.ac.uk/philip.home/t1dgch3b.htm#AssessLevels.
Accessed May 15, 2014.
70. Available at: http://www.idf.org/sites/default/files/IDF-Guideline-for-Type-2-
Diabetes.pdf. Accessed May 15, 2014.
Life s tyle I n t er ven t i o n
Nutrition Therapy and Physical Activity
a, b
Alison B. Evert, MS, RD, CDE *, Michael C. Riddell, PhD
KEYWORDS
Medical nutrition therapy Weight loss Carbohydrate Lifestyle intervention
Physical activity Exercise
KEY POINTS
An individualized nutrition plan should be discussed with patients in a series of encounters
with a registered dietitian starting at the time of diabetes diagnosis.
Diabetes meal planning approaches should include instruction on a variety of topics
including carbohydrate counting, healthy food choices, glycemic index, Mediterranean-
style diet, low and high sodium foods, low-fat and low-carbohydrate diets.
Early engagement in physical activity halts or slows the progression of type 2 diabetes
development. Activities should include aerobic activities (at least 150 minutes per week)
and resistance training 2-3 days per week.
Accommodation to permit physical activity engagement for all patients with obesity and or
diabetes should be performed.
For patients attempting to lose weight, a mild to moderate daily energy deficit is needed
(10-25% relative caloric restriction).
INTRODUCTION
Diabetes and obesity are major health concerns in the United States.15 It is estimated
that more than 3 out of every 4 adults with diabetes are overweight.6 In a nationally
representative sample of US adults, the prevalence of diabetes was found to increase
with increasing weight classes.7 The survey revealed that nearly one-fourth of adults
with diabetes in this sample had poor glycemic control (defined as hemoglobin A1c
[HbA1c] level >8.0%) and nearly half were considered obese.7 Being obese with dia-
betes increases insulin resistance and negatively affects glucose tolerance, thereby
making glycemic targets more difficult to achieve pharmacologically.
a
Diabetes Education Programs, Diabetes Care Center, University of Washington Medical Cen-
ter, 4245 Roosevelt Way Northeast, 3rd Floor, Seattle, WA 98105, USA; b Muscle Health
Research Center, School of Kinesiology and Health Science, Bethune College, York University,
4700 Keele Street, 3rd Floor, Toronto, Ontario M3J1P3, Canada
* Corresponding author.
E-mail address: [email protected]
Public health authorities and medical professionals have recommended weight loss
as a therapeutic strategy for patients who are obese or who are overweight with co-
morbid conditions such as diabetes for several years.8 The 1998 Clinical Guidelines
on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults
state that, the initial goal of weight loss therapy should be to reduce body weight
by approximately 10% from baseline.9 Recommended weight-loss strategies
included a low-calorie diet to create a deficit of 500 to 1000 kcal/d, behavior therapy,
and increased physical activity. More recently, lifestyle intervention strategies have
been incorporated into clinically effective diabetes prevention trials around the
world.5,10,11 These strategies have also been found to be integral components of
the treatment and management of type 2 diabetes, with documented improvements
in weight, depression scores, quality of life, and various biochemical markers of health
status.12,13 Lifestyle intervention seems to be particularly beneficial early in the natural
history of type 2 diabetes, before loss of beta cell function and mass becomes so
extensive that multidrug pharmacotherapy is required to achieve optimal glycemic
control.14,15
As type 2 diabetes progresses over the years with the continued loss of beta cell
function and enduring insulin resistance, medications are often added to the treatment
plan to achieve optimal glycemic control. From a lifestyle perspective, a reduced en-
ergy intake with an emphasis on nutrient-dense, fiber-rich foods (Box 1) along with
regular physical activity should be priorities for all individuals living with type 2 dia-
betes.2 However, people with diabetes, as well as their health care providers, are
reluctant to initiate the use of medication for fear of weight gain. Referral to a regis-
tered dietitian (RD) for nutrition therapy has been shown to help mitigate this unwanted
side effect of treatment.1620 In addition, successful lifestyle intervention typically re-
duces the reliance on pharmacologic agents to achieve glycemic targets.12 Therefore,
regardless of duration of diabetes in years, nutrition therapy remains a key treatment
strategy.
Because of the importance of physical activity in enhancing weight loss and sup-
porting weight maintenance, and the increasingly strong evidence that increased
physical activity and fitness level can affect health independently of body mass in-
dex,21 it is important to have interventions available that can lead to sustained
changes in physical activity. The role of physical activity in treatment of type 2 diabetes
is elaborated later in this article.
Box 1
Nutrient-dense foods
Nutrient density is a measure of the amount of nutrients a food contains compared with the
number of calories. A food is more nutrient dense when the level of nutrients is high in relation
to the number of calories the food contains.
Nutrient-dense food choices include the following:
Grains, especially whole grains
Fruits and vegetables: fresh, frozen, or canned with so-called lite sodium
Fat-free or low-fat milk or dairylike products
Lean protein sources or meat alternatives such as beans, lentils, and unsalted nuts
Substitute unsaturated (liquid fats such as olive, canola, corn, safflower oil) for foods higher
in saturated (solid fats) or trans fats as much as possible.
Lifestyle Intervention 71
Regular physical activity can help people with type 2 diabetes achieve a variety of
goals,27,28 including:
Increased cardiorespiratory fitness and vigor
Improved glycemic control
Decreased insulin resistance
An improved lipid profile
Reduced blood pressure
Maintenance of a healthy body mass after weight loss
Less depression and anxiety
Less sleep apnea
Less medication use
An overall improved quality of life
However, it is doubtful whether increased physical activity provides significant pro-
tection against premature mortality from heart disease and stroke in patients already
diagnosed with type 2 diabetes.12 Nonetheless, a healthful eating plan and regular ex-
ercise when implemented soon after diagnosis in a real-world health care setting im-
proves markers of inflammation and the cardiovascular risk profile in patients with type
2 diabetes.29 In adolescents with type 2 diabetes, regular physical activity is associ-
ated with lower HbA1c levels, lower body mass index, and higher HDL-cholesterol
levels but not lower medication use.30
Lifestyle Intervention 73
Table 1
American College of Sports Medicine and the ADA recommendations for aerobic and
resistance-type exercise for people with prediabetes or type 2 diabetes (PMID: 21115771)
More vigorous activities, such as walking up hills or jogging, can be encouraged for
middle-aged and younger patients. In addition, resistance exercise performed 2 or
3 times per week provides additional benefits that complement those of aerobic
training (eg, increased lean mass and strength, reduced body fat, increased resting
metabolic rate).34,35
It is essential that people with diabetes are actively involved with health profes-
sionals to collaboratively develop appropriate nutrition interventions and an individ-
ualized eating pattern that they can implement. Multiple encounters to provide
education and counseling initially and on a continued basis are also essential.36
Because of the progressive nature of type 2 diabetes, nutrition therapy recommen-
dations often need to be adjusted over time based on changes in life circumstance,
preferences, and disease course. Progression of diabetes complications may be
modified by improving glycemic control, reducing blood pressure, and reducing
fat intake.2
Because cardiovascular disease (CVD) is a common cause of death among individ-
uals with and without diabetes, nutrition recommendations similar to those for the gen-
eral population to manage CVD risk factors should be followed. The Dietary Guidelines
for Americans 2010 recommendations include reducing saturated fats to less than
10% of calories, aiming for 300 mg of dietary cholesterol per day, and limiting trans
fat as much as possible.37 In people with type 2 diabetes, a Mediterranean-style,
monounsaturated fatty acidrich eating pattern may also benefit glycemic control
and CVD risk factors and can, therefore, be recommended as an effective alternative
to a lower-fat, higher-carbohydrate eating pattern.2,14,3840
Evidence from 2 meta-analyses shows no clear benefits for individuals with diabetic
neuropathy on renal parameters from protein-restricted diets.41,42 Therefore reducing
protein intake to less than the usual intake for people with diabetes and diabetic kid-
ney disease (either microalbuminuria or macroalbuminuria) is not recommended
because it does not alter glycemic measures, cardiovascular risk measures, or the
course of glomerular filtration rate decline.2
Although regular physical activity is clearly beneficial for patients with diabetes,
compliance with recommendations is often poor. Compared with physical activity
advice only, supervised programs involving both aerobic and resistance exercise
are associated with better improvements in glycemic control in people with type 2 dia-
betes.43 Supervision helps with instruction, safety, motivation, and the capacity to
overcome any physical barriers. Unsupervised exercise programs usually fail to
improve glycemic control on their own, but can be associated with improved HbA1c
levels if they are done with dietary intervention.43 Exercise dropout remains a major
limitation, with w 60% of patients failing to maintain both aerobic and resistance-
type exercises after a lifestyle intervention.44 However, motivational interviewing
following a lifestyle intervention improves the maintenance of physical activity in peo-
ple with type 2 diabetes.45
Although having diabetes increases the risk of having underlying CVD and other
comorbidities, there is little evidence to suggest that moderate-intensity exercise trig-
gers adverse cardiovascular events or worsens disease complications in people with
diabetes.46 Nonetheless, before beginning a program of vigorous physical activity,
people with diabetes should be assessed for conditions that might increase risks
associated with certain types of exercise or predispose them to injury.33 Before
Lifestyle Intervention 75
or pulmonary disease should take care to avoid heat-related illness. Precautions may
include exercising indoors in cool environments or outdoors in the early or later hours
of the day during hot or sunny days.
For individuals trying to lose weight, a mild to moderate daily energy deficit is
needed (10%25% relative caloric restriction). Modest weight loss (of >6 kg or
w7.0%8.5% loss of initial body weight) may provide clinical benefits such as
improved glycemia, blood pressure, and/or lipid levels in some individuals with
diabetes, especially those early in the disease process. Intensive lifestyle inter-
ventions (counseling about nutrition therapy, physical activity, and behavior
change) with ongoing support are recommended to achieve and sustain a
modest energy deficit until a goal weight is achieved.
Limitation of any caloric sweetener, including high-fructose corn syrup and su-
crose, reduces risk of worsening the cardiometabolic risk profile and weight
gain.2 The term free fructose refers to the consumption of fructose that is natu-
rally occurring in foods such as fruit, and does not include the fructose that is
found in the form of the disaccharide sucrose or the fructose in high-fructose
corn syrup.2 It seems that free fructose is not more harmful than other forms of
sugar unless it is consumed in excessive amounts (>12% of the total caloric
intake).59,60
The selection of lean protein sources and meat alternatives and the substitution
of foods high in unsaturated fat (liquid oils) should be preferred rather than those
high in trans or saturated fats. Fat quality seems to be more in important than
quantity.
Micronutrients, vitamins, herbal products, and supplements are not recommen-
ded for management of diabetes because of a lack of evidence at this time. How-
ever, without well-designed clinical trials to prove efficacy, the benefit of
pharmacologic doses of micronutrients and supplements is unknown, and find-
ings from small clinical and animal studies is frequently extrapolated to clinical
practice.61
Use of nonnutritive sweeteners (NNS), also commonly referred to as artificial
sweeteners, continues to be an area of much debate and misinformation. The
US Food and Drug Administration has reviewed several types of hypocaloric
sweeteners (eg, aspartame, sucralose, saccharin, and sugar alcohols) for safety
and has approved them for consumption by the general public, including people
with diabetes.62 Table 2 shows the acceptable daily intake of popular nonnutri-
tive sweeteners (based on a 70-kg [150-lb] adult). Research supports that nonnu-
tritive sweeteners do not produce a glycemic effect; however, foods containing
Table 2
Acceptable daily intake of popular nonnutritive sweeteners (based on 70-kg [150-lb] adult)
Patients with intermittent claudication are advised to walk at a speed that in-
duces claudication pain within 3 to 5 minutes. Walking should be stopped
when claudication pain is rated as moderate and the patient should rest until
the claudication pain has resolved. At that point, the patient should resume
walking until moderate claudication pain is induced again. The walking exercise
program should begin with exercise and rest cycles of at least 30 minutes and
should progress to 60 minutes.66
Individuals with peripheral neuropathy and without acute ulceration may partic-
ipate in moderate weight-bearing exercise. Comprehensive foot care including
daily inspection of feet and use of proper footwear (correct sizing and with
custom-made foot beds with some cushioning, if feasible) is recommended for
prevention and early detection of sores or ulcers. In general, shoes should:
Fit well
Be made out of breathable material
Have a firm heel
Have hook and loop type fasteners or shoelaces
Have good shock absorption
Not be bent or twisted
Have no seams in the toe box
Stabilize overpronation or oversupination
Moderate walking likely does not increase risk of foot ulcers or reulceration in pa-
tients with peripheral neuropathy.
Individuals with cardiac autonomic neuropathy should be screened and receive
physician approval and possibly an exercise stress test before exercise initiation.
Exercise intensity is best prescribed using the heart rate reserve method with
direct measurement of maximal heart rate.
In individuals with proliferative or preproliferative retinopathy or macular degen-
eration, careful screening and physician approval are recommended before initi-
ating an exercise program. Activities that greatly increase intraocular pressure,
such as high-intensity aerobic or resistance training (with large increases in sys-
tolic blood pressure) and head-down activities, are not advised with uncontrolled
proliferative disease, nor are jumping or jarring activities, all of which increase
hemorrhage risk.
Individuals with nephropathy often have exercise intolerance. However, exercise
training improves cardiovascular risk profile, muscle mass, physical function, and
quality of life in individuals with kidney disease67 and may even be undertaken
during dialysis sessions. Animal models suggest that regular exercise delays
the progression of diabetic nephropathy68,69 although good evidence for this in
humans is currently lacking. The presence of microalbuminuria per se does not
necessitate exercise restrictions.
Patients with knee pain from osteoarthritis and obesity should be encouraged to
participate in modified exercise programs to help with weight loss and improve-
ments in pain, physical function, mental health, and quality of life.70 Walking, if
tolerated, should be encouraged, as should resistance exercise as long as the
affected joints are not overly stressed. Other exercise modes, such as recumbent
cycling and aquatic exercises, may also help limit knee pain.
Efforts to promote physical activity should focus on developing self-efficacy and
fostering social support from family, friends, and health care providers. Encour-
aging mild or moderate physical activity may be most beneficial to adoption and
maintenance of regular physical activity participation. Lifestyle interventions may
have some efficacy in promoting physical activity behavior.
80 Evert & Riddell
Box 2
The 5 As
Assess: establish current physical activity level and readiness for change (consider the
frequency, intensity, duration, and type of activity)
Not active, not thinking about physical activity
Not active, ready for physical activity
Active and ready to maintain or progress
Advise: strongly encourage all patients to get more active by reviewing the health risks of
inactivity and the benefits of physical activity. Advise on the appropriate amount and type of
physical activity.
Agree: collaboratively develop goals and a personalized action plan. Provide individually
relevant exercise prescriptions, time frames, and monitoring of strategies to meet the goals.
Assist: identify personal barriers and strategies to overcome barriers. Identify connections and
resources for exercise and physical activity in the community.
Arrange: specify plan for follow-up at diabetes-focused visits with telephone calls or email
reminders. Review physical activity level at subsequent visits and provide advice to achieve the
next level of activity.
Adapted from Glynn TJ, Manley MW. How to help your patients stop smoking: a National Can-
cer Institute manual for physicians. Bethesda (MD): National Cancer Institute; 1989. NIH publi-
cation no. 89-3064.
To help facilitate changes in physical activity and eating habits, diabetes health
care professionals can incorporate the use of the so-called 5 As (assess, advise,
agree, assist, and arrange). This approach does not require a lot of training and offers
a simple framework that can be integrated with other education and counseling re-
sources. The 5 As concept was introduced by the National Cancer Institute as a
guide to help physicians counsel their patients about smoking cessation.71 This
framework has since been expanded to address broader issues of health behavior
change and to give care providers the flexibility of addressing important lifestyle
topics in a manner ranging from simple to in-depth (depending on time, training,
and resources). Box 2 provides an example of how to use the 5 As for development
of a physical activity prescription71,72:
FUTURE CONSIDERATIONS/SUMMARY
Lifestyle intervention for the treatment of type 2 diabetes should focus on a reduced
energy intake with modification of food choices (increased whole grains, fiber, vege-
tables, and fruit; reduced total and saturated fat, sugar, and refined grains) and
increased physical activity (150 min/wk of aerobic exercise plus strength training 2
3 times per week). In order to be successful another critical component of lifestyle
intervention is the use of behavior modification, such as motivational interviewing,
self-monitoring, and individualized goal setting, to support long-term results.
REFERENCES
1. Centers for Disease Control and Prevention. National diabetes fact sheet, United
States. 2014. Available at: http://www.cdc.gov/diabetes/pubs/statsreport14.
htm. Accessed May 23, 2014.
Lifestyle Intervention 81
2. Evert AB, Boucher JL, Cypress M, et al. Nutrition therapy recommendations for
the management of adults with diabetes. Diabetes Care 2013;36:382142.
3. Franz MJ, Powers MA, Leontos C, et al. The evidence for medical nutrition ther-
apy for type 1 and type 2 diabetes in adults. J Am Diet Assoc 2010;110:185289.
4. Academy of Nutrition and Dietetics. Diabetes type 1 and 2 for adults
evidence-based nutrition practice guidelines. 2008. Available at: http://www.
adaevidencelibrary.com/topic.cfm?cat53253. Accessed May 23, 2014.
5. Diabetes Prevention Program Research Group (DPP). Reduction in the inci-
dence of type 2 diabetes with lifestyle intervention or metformin. N Engl J
Med 2011;346:393403.
6. Ali MK, Bullard KM, Saaddine JB, et al. Achievement of goals in US diabetes
care. 19992010. N Engl J Med 2013;368:161324.
7. Nguyen NT, Nguyen XM, Lane J, et al. Relationship between obesity and dia-
betes in a US adult population: findings from the National Health and Nutrition
Examination Survey, 1999-2006. Obes Surg 2011;21:3515.
8. Clinical guidelines on the identification, evaluation, and treatment of overweight
and obesity in adultsthe evidence report. National Institutes of Health. Obes
Res 1998;6:51S209S.
9. National Heart, Lung, and Blood Institute; Clinical Guidelines on the Identifica-
tion, Evaluation, and Treatment of Overweight and Obesity in Adults. The Evi-
dence Report NHLBI Obesity Education Initiative Expert Panel on the
Identification, Evaluation, and Treatment of Obesity in Adults (US). Bethesda
(MD):1998 Sep. Report No 98-4083.
10. Lindstrom J, Ilanne-Parikka P, Peltonen M, et al, Finnish Diabetes Prevention
Study Group. Sustained reduction in the incidence of type 2 diabetes by lifestyle
intervention: follow-up of the Finnish Diabetes Prevention Study. Lancet 2006;
368:16739.
11. Li G, Zhang P, Wang J, et al. The long-term effect of lifestyle interventions to pre-
vent diabetes in the China Da Qing Diabetes Prevention Study: a 20-year follow-
up study. Lancet 2008;371:17839.
12. Look AHEAD Research Group. Cardio-vascular effects of intensive lifestyle
intervention in type 2 diabetes. N Engl J Med 2013;369:14554.
13. Look AHEAD Research Group. Impact of intensive lifestyle intervention on
depression and health-related quality of life in type 2 diabetes: the Look AHEAD
Trial. Diabetes Care 2014;37:154453.
14. Esposito K, Maiorino MI, Ciotola M, et al. Effects of a Mediterranean-style diet on
the need for antihyperglycemic drug therapy in patients with newly diagnosed
type 2 diabetes: a randomized trial. Ann Intern Med 2009;151:30614.
15. Feldstein AC, Nichols GA, Smith DH, et al. Weight change in diabetes and gly-
cemic and blood pressure control. Diabetes Care 2008;31:19605.
16. Andrews RC, Cooper AR, Montgomery AA, et al. Diet or diet plus physical ac-
tivity versus usual care in patients with newly diagnosed type 2 diabetes: the
early ACTID randomized controlled trial. Lancet 2011;378:12939.
17. Coppell KJ, Kataoka M, Williams SM, et al. Nutritional intervention in patients
with type 2 diabetes who are hyperglycaemic despite optimized drug treat-
mentLifestyle Over and Above Drugs in Diabetes (LOADD) study: random-
ized controlled trial. BMJ 2010;341:c3337.
18. Battista MC, Labonte M, Menard J, et al. Dietitian-coached management in
combination with annual endocrinologist follow up improves global metabolic
and cardiovascular health in diabetic participants after 24 months. Appl Physiol
Nutr Metab 2012;37:61020.
82 Evert & Riddell
19. Banister NA, Jastrow ST, Hodges V, et al. Diabetes self-management training
program in a community clinic improves patient outcomes at modest cost.
J Am Diet Assoc 2004;104:80710.
20. Barratt R, Frost G, Millward DJ, et al. A randomized controlled trial investigating
the effect of an intensive lifestyle intervention v. standard care in adults with type
2 diabetes immediately after initiating insulin therapy. Br J Nutr 2008;99:
102531.
21. Lee DC, Sui X, Church TS, et al. Changes in fitness and fatness on the develop-
ment of cardiovascular disease risk factors hypertension, metabolic syndrome,
and hypercholesterolemia. J Am Coll Cardiol 2012;59:66572.
22. Inzucchi SE, Bergenstal RM, Buse JB, et al, American Diabetes Association
(ADA), European Association for the Study of Diabetes (EASD). Management
of hyperglycemia in type 2 diabetes: a patient-centered approach. Position
statement of the American Diabetes Association (ADA) and the European Asso-
ciation for the Study of Diabetes (EASD). Diabetes Care 2012;35:136479.
23. American Diabetes Association. Standards of medical care in diabetes2014.
Diabetes Care 2014;37(Suppl 1):S1490.
24. Robbins JM, Thatcher GE, Webb DA, et al. Nutritionist visits, diabetes classes,
and hospitalization rates and charges: the Urban Diabetes Study. Diabetes Care
2008;31:65560.
25. Lacey K, Pritchett E. Nutrition care process and model: ADA adopts road map
to quality care and outcomes management. J Am Diet Assoc 2003;103:
106172.
26. Wheeler ML, Dunbar SA, Jaacks LM, et al. Macronutrients, food groups and
eating patterns in the management of diabetes: a systematic review of the liter-
ature, 2010. Diabetes Care 2012;35:43445.
27. Canadian Diabetes Association Clinical Practice Guidelines Expert Committee,
Sigal RJ, Armstrong MJ, et al. Physical activity and diabetes. Can J Diabetes
2013;7(Suppl 1):S404.
28. Steinberg H, Jacovino C, Kitabchi AE. Look inside look ahead: why the glass is
more than half-full. Curr Diab Rep 2014;7:500.
29. Thompson D, Walhin JP, Batterham AM, et al. Effect of diet or diet plus physical
activity versus usual care on inflammatory markers in patients with newly diag-
nosed type 2 diabetes: the Early ACTivity In Diabetes (ACTID) randomized,
controlled trial. J Am Heart Assoc 2014;3:e000828.
30. Herbst A, Kapellen T, Schober E, et al, for the DPV-Science-Initiative. Impact of
regular physical activity on blood glucose control and cardiovascular risk fac-
tors in adolescents with type 2 diabetes mellitus - a multicenter study of 578 pa-
tients from 225 centres. Pediatr Diabetes 2014. http://dx.doi.org/10.1111/pedi.
12144.
31. Balducci S, Sacchetti M, Haxhi J, et al. Physical exercise as therapy for type 2
diabetes mellitus. Diabetes Metab Res Rev 2014;30(Suppl 1):1323.
32. Colberg SR, Sigal RJ, Fernhall B, et al, American College of Sports Medicine,
American Diabetes Association. Exercise and type 2 diabetes: the American
College of Sports Medicine and the American Diabetes Association: joint posi-
tion statement executive summary. Diabetes Care 2010;33:26926.
33. Colberg SR, Sigal RJ. Prescribing exercise for individuals with type 2 diabetes:
recommendations and precautions. Phys Sportsmed 2014;39:1326.
34. Church TS, Blair SN, Cocreham S, et al. Effects of aerobic and resistance
training on hemoglobin A1c levels in patients with type 2 diabetes: a random-
ized controlled trial. JAMA 2010;304(20):225362.
Lifestyle Intervention 83
35. Sigal RJ, Kenny GP, Boule NG, et al. Effects of aerobic training, resistance
training, or both on glycemic control in type 2 diabetes: a randomized trial.
Ann Intern Med 2007;147(6):35769.
36. Pastors JG, Franz MJ. Effectiveness of medical nutrition therapy in diabetes.
In: Franz MJ, Evert AB, editors. American Diabetes Association guide to nutri-
tion therapy for diabetes. Alexandria (VA): American Diabetes Association;
2012. p. 118.
37. US Department of Health and Human Services and US Department of Agricul-
ture. Dietary guidelines for Americans, 2010. [Internet]. Available at: www.
health.gov/dietaryguidelines/. Accessed 12 July 7, 2014.
38. Schwingshackl L, Strasser B, Hoffmann G. Effects of monounsaturated fatty
acids on glycaemic control in patients with abnormal glucose metabolism: a
systematic review and meta-analysis. Ann Nutr Metab 2011;58:2906.
39. Itsiopoulos C, Brazionis L, Kaimakamis M, et al. Can the Mediterranean diet
lower HbA1c in type 2 diabetes? Results from a randomized cross-over study.
Nutr Metab Cardiovasc Dis 2011;21:7407.
40. Brehm BJ, Lattin BL, Summer SS, et al. One-year comparison of a high-
monounsaturated fat diet with a high-carbohydrate diet in type 2 diabetes. Dia-
betes Care 2009;32:21520.
41. Pan Y, Guo LL, Jin HM. Low-protein diet for diabetic nephropathy: a meta-
analysis of randomized controlled trials. Am J Clin Nutr 2008;88:6606.
42. Robertson L, Waugh N, Robertson A. Protein restriction for diabetic renal dis-
ease. Cochrane Database Syst Rev 2007;(4):CD002181.
43. Umpierre D, Ribeiro PA, Kramer CK, et al. Physical activity advice only or struc-
tured exercise training and association with HbA1c levels in type 2 diabetes: a
systematic review and meta-analysis. JAMA 2011;305:17909.
44. Tulloch H, Sweet SN, Fortier M, et al. Exercise facilitators and barriers from
adoption to maintenance in the diabetes aerobic and resistance exercise trial.
Can J Diabetes 2013;37:36774.
45. Armstrong MJ, Campbell TS, Lewin AM, et al. Motivational interviewing-based
exercise counselling promotes maintenance of physical activity in people with
type 2 diabetes. Can J Diabetes 2013;37(Suppl 4):S3.
46. Riddell MC, Burr J. Evidence-based risk assessment and recommendations for
physical activity clearance: diabetes mellitus and related comorbidities. Appl
Physiol Nutr Metab 2011;36(Suppl 1):S15489.
47. Colberg SR, Vinik AI. Exercising with peripheral or autonomic neuropathy: what
health care providers and diabetic patients need to know. Phys Sportsmed
2014;42(1):1523.
48. Armstrong MJ, Martin BJ, Arena R, et al. Patients with diabetes in cardiac reha-
bilitation: attendance and exercise capacity. Med Sci Sports Exerc 2014;46(5):
84550.
49. Rabasa-Lhoret R, Bourque J, Ducros F, et al. Guidelines for premeal insulin dose
reduction for postprandial exercise of different intensities and durations in type 1
diabetic subjects treated intensively with a basal-bolus insulin regimen (ultra-
lente-lispro). Diabetes Care 2001;24:62530.
50. Seaquist ER, Anderson J, Childs B, et al. Hypoglycemia and diabetes: a report
of a workgroup of the American Diabetes Association and the Endocrine Soci-
ety. Diabetes Care 2013;36:138495.
51. Yardley JE, Stapleton JM, Sigal RJ, et al. Do heat events pose a greater
health risk for individuals with type 2 diabetes? Diabetes Technol Ther
2013;15:5209.
84 Evert & Riddell
52. Pi-Sunyer X, Blackburn G, Brancati FL, et al. Reduction in weight and cardiovas-
cular disease risk factors in individuals with type 2 diabetes: on-year results of
the Look AHEAD trial. Diabetes Care 2007;30:137483.
53. Metz JA, Stern JS, Kris-Etherton P, et al. A randomized trial of improved weight
loss with a prepared meal plan in overweight and obese patients: impact on car-
diovascular risk reduction. Arch Intern Med 2000;160:21508.
54. Nield L, Moore HJ, Hooper L, et al. Dietary advice for treatment of type 2 dia-
betes mellitus in adults. Cochrane Database Syst Rev 2007;(3):CD004097.
55. Church TS, LaMonte MJ, Barlow CE, et al. Cardiorespiratory fitness and body
mass index as predictors of cardiovascular disease mortality among men with
diabetes. Arch Intern Med 2005;16:211420.
56. Lyerly GW, Sui X, Lavie CJ, et al. The association between cardiorespiratory
fitness and risk of all-cause mortality among women with impaired fasting
glucose or undiagnosed diabetes mellitus. Mayo Clin Proc 2009;84:7806.
57. McAuley PA, Artero EG, Sui X, et al. Fitness, fatness, and survival in adults with
pre-diabetes. Diabetes Care 2014;37:52936.
58. Hansen D, Peeters S, Zwaenepoel B, et al. Exercise assessment and prescrip-
tion in patients with type 2 diabetes in the private and home care setting: clinical
recommendations from AXXON (Belgian Physical Therapy Association). Phys
Ther 2013;93:597610.
59. Sievenpiper JL, Carleton AJ, Chatha S, et al. Heterogeneous effects of fruc-
tose on blood lipids in individuals with type 2 diabetes: systematic review
and meta-analysis of experimental trials in humans. Diabetes Care 2009;32:
19307.
60. Livesey G, Taylor R. Fructose consumption and consequences for glycation,
plasma triacylglycerol, and body weight: meta-analyses and meta-regression
models of intervention studies. Am J Clin Nutr 2008;88:141937.
61. Nuemiller JJ. Micronutrients and diabetes. In: Franz MJ, Evert AB, editors.
American Diabetes Association guide to nutrition therapy for diabetes. Alexan-
dria (VA): American Diabetes Association; 2012. p. 4168.
62. US Department of Agriculture. Nutritive and nonnutritive sweetener resources
[Internet]. National Agricultural Library, Food and Nutrition Information Center.
2013. Available at: http://fnic.nal.usda.gov/food-composition/nutritive-and-
nonnutritive-sweetener-resources. Accessed May 23, 2014.
63. Gardner C, Wylie-Rosett J, Gidding SS, et al, American Heart Association Nutri-
tion Committee of the Council on Nutrition, Physical Activity and Metabolism,
Council on Arteriosclerosis, Thrombosis and Vascular Biology, Council on Car-
diovascular Disease in the Young, American Diabetes Association. Nonnutritive
sweeteners: current use and health perspectives: a scientific statement from the
American Heart Association and the American Diabetes Association. Diabetes
Care 2012;35:1798808.
64. Miller PE, Perez V. Low-calorie sweeteners and body weight and composition: a
meta-analysis of randomized controlled trials and prospective cohort studies.
Am J Clin Nutr 2014;100:76577.
65. Colberg SR. Exercise and diabetes. A clinicians guide to prescribing physical
activity. Alexandria (VA): American Diabetes Association; 2013.
66. Brunelle CL, Mulgrew JA. Exercise for intermittent claudication. Phys Ther 2011;
91:9971002.
67. Smith AC, Burton JO. Exercise in kidney disease and diabetes: time for action.
J Ren Care 2012;38(Suppl 1):528.
Lifestyle Intervention 85
KEYWORDS
Metformin Sulfonylureas Thiazolidinediones
Sodium-glucose transporter-2 inhibitors (SGLT2 inhibitors) Colesevelam
Bromocriptine Type 2 diabetes mellitus
KEY POINTS
Metformin is the best available combination of low-cost, low-risk, high-efficacy oral
therapy for type 2 diabetes mellitus.
The lowest-cost oral add-on drug to metformin is a sulfonylurea.
A sodium-glucose transporter type 2 inhibitor, an alpha-glucosidase inhibitor, or a thiazo-
lidinedione, is a reasonable second or tertiary add-on option.
Alpha-glucosidase inhibitors, colesevelam, and bromocriptine mesylate are niche drugs
and may have value in cardiovascular risk reduction, but more information from clinical
trials and/or meta-analyses is needed.
INTRODUCTION
The worldwide epidemic of type 2 diabetes mellitus (T2DM) has made diagnosing,
counseling, and prescribing for newly diagnosed patients an almost reflex process
for many primary care physicians. Patients overwhelmingly prefer initial therapy to
be with an oral medication, rather than an injectable (ie, insulin) and, as patient advo-
cates, their treating physicians comply with this request. The past 20 years have trans-
formed oral treatment options for T2DM from a single option (sulfonylureas [SUs]) to at
least 9 different classes of drugs, enabling rational, individually customized combina-
tion therapy. Incretin analogues and dipeptidyl peptidase-4 (DPP-4) inhibitors are
covered in detail elsewhere in this issue. This article reviews the mechanism of action,
efficacy, major untoward effects, and impact of other oral therapies on T2DM and
associated health risks; most notably, cardiovascular disease.
The likelihood of success for prescribed oral therapy can be estimated from simple
observations and measurements at the point of care. Box 1 emphasizes the
Box 1
Predictors of response to oral antihyperglycemic drugs (consider initial therapy with insulin if
multiple points are negative)
characteristics of patients likely to respond well to oral therapy for T2DM; patients who
lack multiples of these characteristics are best served by an initial prescription for
insulin therapy (covered in a separate article by Meah and Juneja in this issue).
Rules of thumb estimating the impact of drug monotherapy, and subsequent add-
on drugs, are highlighted in Box 2. Available drug therapies, by class, are overviewed
individually, with regard to mechanism of action, efficacy, adverse effects, and influ-
ence on cardiovascular disease and neoplasia.
METFORMIN
Metformin was first available in the United States in 1995, and was long delayed
because of fear of fatal lactic acidosis, which had led to market withdrawal of another
biguanide drug, phenformin, in 1970. Practitioners have learned to use the drug
cautiously or not at all in patients thought to be at increased risk for lactic acidosis,
including the elderly, patients with congestive heart failure (CHF), and patients with
chronic kidney disease. However, it has become the number 1 most prescribed oral
antihyperglycemic agent in the world, while also becoming one of the lowest-cost
and lowest-risk agents available. As metformin approaches its 20th anniversary in
the United States, its track record of low cost, low risk, and low frequency of trouble-
some side effects justifies its place as the first choice when oral therapies for T2DM are
prescribed for patients. Many of the original cautions and presumed contraindications
for prescribing should be relearned.
Metformins primary action is suppression of hepatic glucose generation, and the
exact molecular action is still not understood. Enhanced activity of AMP kinase
(AMPK) may be either caused by a direct agonist effect on AMPK, or by suppression
of hepatic mitochondrial oxidation, resulting in a higher AMP/ATP ratio, and thence
secondary activation of AMPK.1,2 An apparent insulin-sensitizing effect of metformin
on muscle glucose uptake may simply be escape from the glucose toxicity phenom-
enon, caused by reduced endogenous glucose production.
Box 2
Anticipated efficacy of initial and add-on oral antihyperglycemic drugs
cases per 100,000 patients treated16; furthermore, a recent Cochrane Review of 347
clinical trials and observational studies concluded that, compared with other treat-
ments for T2DM, metformin was not associated with any risk for lactic acidosis.17 A
comprehensive review by Scheen and Paquot18 identified reduced risk for all-cause
mortality in metformin users versus other T2DM treatment regimens, in the settings
of stable coronary heart disease (relative risk, 0.720.76), following acute coronary
syndrome (relative risk, 0.40.8), and in CHF (relative risk, 0.650.87). In a systematic
review of observational studies numbering more than 34,000 patients with CHF, Eurich
and colleagues19 found metformin use to be associated with reduced (not increased)
risk for mortality (relative risk vs nonusers, 0.80), and even when left ventricular ejec-
tion fraction was severely reduced the relative risk for mortality was not significantly
different than for nonusers (0.91). Among patients with CHF and chronic kidney dis-
ease, metformin use was also associated with reduced mortality risk (relative risk,
0.81 for metformin users vs nonusers). The following recommendations for metformin
use based on renal function have been offered independently by several critical re-
views: no dose adjustment for estimated glomerular filtration rate (eGFR) greater
than or equal to 45 mL/min/1.73 m2; limit dose to 50% of maximum recommended
for eGFR greater than or equal to 30 to less than 45 mL/min/1.73 m2; and discontinue
metformin only for eGFR less than 30 mL/min/1.73 m2.16,20,21 Based on the Eurich and
colleagues19 systematic review, and based on US Food and Drug Administration
(FDA) change in prescribing information for metformin in 2010, CHF independent of
eGFR less than 30 mL/min/1.73 m2 should no longer be considered a contraindication
to metformin use.19
INSULIN SECRETOGOGUES
Sulfonylureas
Until the introduction of metformin in 1995, SUs were the only oral antihyperglycemic
class available in the United States. The SU class might now be considered the Rod-
ney Dangerfield of oral therapies for T2DM. Like the late comedian, whose signature
line bemoaned that he got no respect at all, the SU class has been disrespected over
the years for possibly increasing cardiovascular risk, and possibly accelerating
pancreatic islet cell burnout. Despite the concerns, SUs remain widely prescribed,
because of familiarity, relative lack of nonglycemic adverse effects, very low cost,
and generally good efficacy in controlling glycemia, at least in the early phases of
T2DM. The SUs prevalently used in the United States are the second-generation
SUs glyburide and glipizide, and the third-generation SU, glimepiride.
The mechanism of action common to all the SU drugs involves binding to the
pancreatic islet cell sulfonylurea receptor 1 (SUR1), which results in closure of the
cell membrane ATP-sensitive potassium channel (K1ATP), thereby causing membrane
depolarization, influx of calcium ions, and subsequent release of insulin from storage
vesicles.22,23 A Cochrane Review of clinical trial and observation study data totaling
more than 22,000 patients, and including both first-generation and second-
generation SUs, identified a mean 1.01% reduction in HbA1c with SU monotherapy.24
Initiation of SU monotherapy in previously treatment-naive individuals with T2DM can
be expected to produce a 1% to 2% reduction in HbA1c,25 averaging about 1.5%.26,27
Based on the UKPDS trial results, slightly more than half of patients newly diag-
nosed with T2DM can be expected to attain a goal HbA1c less than 7% on SU mono-
therapy. In the UKPDS, only 24% of patients treated by intent to a goal HbA1c level of
less than 7.0% were achieving that goal with SU alone after 9 years; 50% were failing
to reach goal by 3 years.28 With regard to purported accelerated burnout of islet cells
Oral Antihyperglycemic Treatment 5
with SU therapy, some investigators have pointed out that the rate of monotherapy
failure for metformin in UKPDS was similar to that for SU, suggesting that progressive
loss of islet cell function is simply part of the natural history of T2DM.29,30 In the ADOPT
(A Diabetes Outcome Progression Trial) trial, monotherapy failure after 5 years of treat-
ment was 34% for glyburide, 21% for metformin, and 15% for rosiglitazone.31 Based
on available dose-response curves, many experienced clinicians recommend a
maximum clinical dose of an SU drug of approximately half the US FDA-approved
maximal dose.25,32 In one dose-response trial of glimepiride, the mean reduction in
HbA1c was 1.9% at the maximal dose, 8 mg daily, and 1.8% at 4 mg daily.33 Some
investigators have suggested a tachyphylaxis response to high-dose SU, with down-
regulation of SUR1 binding and signaling transduction.34
Efficacy of SU as add-on therapy to metformin, and thiazolidinedione (TZD) has
been established, with efficacy of DHbA1c 0.47% to 1.3%,27 and 1.76% to
2.68%,35 respectively. In these studies of combination oral therapy including SU,
adverse events except for hypoglycemia were similar: SU-plus groups experienced
hypoglycemia about twice as often as the comparator groups (relative risk, 2.41).27
The most frequent serious adverse effect of SUs is hypoglycemia, occurring at a fre-
quency of 1.7% of glimepiride users and 5% of glyburide users within the first month of
therapy in one study.25 In a German study, glyburide was responsible 6 times as often
as was glimepiride for severe hypoglycemic events requiring professional care,
despite many more active prescriptions in use for glimepiride.36 Because risk for hy-
poglycemia is greater in persons with chronic kidney disease, all of the SUs are consid-
ered contraindicated at serum creatinine greater than 1.8 mg/dL (eGFR <30 mL/min/
1.73 m2); at any degree of impaired renal function, glipizide or glimepiride is preferred
to glyburide, because of its longer half-life and inherently greater risk for hypoglycemia.
Weight gain is also a frequent, possibly ubiquitous occurrence in SU-treated patients;
over a 6-year period in the United Kingdom Prospective Diabetes Study, patients ran-
domized to treatment with an SU gained a mean of 5.3 kg.37 In the UKPDS, the prev-
alent SUs were chlorpropamide and glyburide; there is evidence that glimepiride may
be associated with less weight gain over time than other drugs of the SU class.25,26
Glyburide, glipizide, and glimepiride are all rated as class C in pregnancy, and glybur-
ide has been studied and established as noninferior to insulin therapy in gestational
diabetes, with no evidence of adverse fetal or maternal outcomes.38,39
The cardiovascular safety question that has dogged the SU class remains unre-
solved 43 years after the University Group Diabetes Project (UGDP) study reported
a disproportionate number of acute MIs in patients receiving tolbutamide, a first-
generation SU.40 The UKPDS study partly assuaged concerns, with a nonsignificant
decreased number of cardiovascular events during the original trial,41 and a reduced
rate (vs the nonSU-using usual care group) during the 10-year follow-up study,
including risk ratios of 0.87 for all-cause mortality and 0.85 for MI, versus usual
care.5 However, a large retrospective cohort study of patients attending US Veterans
Administration care facilities compared 98,665 veterans who received SU monother-
apy with 155,025 receiving metformin monotherapy. After adjustment for confounding
factors, a hazard ratio of 1.26 for glyburide versus metformin (95% confidence interval
[CI], 1.161.37), and 1.15 for glipizide versus metformin (CI, 1.061.26) was identified
in this study for the composite end point of acute MI, stroke, or death.42
It is possible that some of the disparity in cardiovascular outcomes with SU drugs
can be explained by different pharmacologic properties of individual SUs. Although
the various SU agents have similar agonist effects on the pancreatic islet SUR1 recep-
tor, they differ in the degree of agonist activity on myocardial and coronary vascular
SUR2 receptors.43,44 Glipizide and glimepiride have low agonist effects on the
6 Brietzke
SUR2 receptor, whereas glyburide has significant agonist effect on SUR2. Opening of
the myocardial K1ATP is important in the ischemic preconditioning phenomena, which
can limit infarct size following the acute ischemic insult. Closure of this channel by acti-
vation of the SUR2 receptor is thought to interfere with ischemic preconditioning,
thereby potentially extending infarct size and adversely affecting prognosis.45 There
is experimental and observational evidence to support a concept that glyburide is
uniquely hazardous among the 3 SUs in common use in the United States with regard
to coronary disease outcomes. In a study conducted in Taiwan, Lee and Chou46 noted
differential response to glimepiride and glyburide in both nondiabetic and diabetic pa-
tients undergoing coronary angioplasty, with lower ischemic burden scores in patients
receiving glimepiride as opposed to glyburide. In a prospective study of 1310 patients
admitted for acute MI over a 1-month period to French hospitals in 2005, SU use at the
time of admission was not associated with an in-hospital increased risk for complica-
tions or mortality. On the contrary, SU use before admission was associated with
lower mortality (3.9%) than was use of other oral agents (mortality 6.4%), insulin (mor-
tality 9.4%), or no T2DM drug therapy (mortality 8.4%). However, the shorter-acting
and more pancreatic isletspecific ATP channel agonists gliclazide and glimepiride
were associated with lower in-hospital mortality (2.7%) than was the longer-acting,
nonorgan-specific K1 ATP channel agonist glyburide (in-hospital mortality, 7.9%).47
There is controversy as to whether or not SUs are associated with increased risk for
common cancers, with data from several studies summarized in Table 1. Taken in the
aggregate, findings from these studies lead to a conclusion that, although SUs may
not definitely increase the risk for malignancies, there is no evidence that they reduce
cancer risk.
Based on low toxicity, low cost, and extensive worldwide experience, SU drugs are
still deserving of a role as add-on therapy for patients failing to achieve treatment goals
on regimens of 1 or 2 drugs that include metformin. Glyburide is associated with both a
greater risk of hypoglycemia and greater association with complications arising from
acute coronary presentations. It therefore seems prudent to preferentially use glipizide
or glimepiride. It is unclear whether glyburide offers any justification for continued use,
given the concerns with disproportionate risk,51,52 except in pregnancy and in coun-
tries in which glyburide is the only available SU.
Glinides
Two drugs of the glinide class, repaglinide and nateglinide, are available for use. Like
SUs, these drugs work as agonists of the SUR1 receptor, but have extremely short
Table 1
Relative risk of incident cancer with sulfonylureas (vs nonusers)
durations of action. They are best considered as non-SU SUs, and use is best
reserved for persons responsive to SU but susceptible to fasting hypoglycemia, or
for persons with true SU allergy.53,54
THIAZOLIDINEDIONES
If SUs are the Rodney Dangerfield, it seems fair to label TZDs as the Warren G. Har-
ding of antihyperglycemic drugs, because Harding was a US President elected
largely on the basis that he looked like a president, and many TZD effects look as if
they should be ideal treatment of T2DM. Rosiglitazone and pioglitazone bind to perox-
isome proliferator activating receptor gamma (PPARg) receptors to form heterodimers
with retinoid-X receptors, which then bind to various response elements of the
genome, resulting in transactivation of gene products enhancing insulin action, and
transrepression of nuclear signal pathways generally unfavorable to insulin action
(notably, nuclear factor kappa B [NF-kB]).55,56 In adipose tissue, PPARg activation
blocks release of free fatty acids (FFAs), reduces tumor necrosis factor alpha (TNF-
a), and increases adiponectin. TZDs promote expansion of the subcutaneous adipose
compartment, and contraction of the visceral adipose compartment.57 The lipid steal
hypothesis suggests that increased uptake of FFAs by adipose tissue allows FFAs to
escape from muscle, liver, and islet cells, resulting in improved insulin action and
increased insulin secretion.55,56
Clinical efficacy trials of the TZD drugs have all shown significant improvement in
HbA1c, as monotherapy versus placebo, or as add-on therapy to metformin, SU,
and insulin regimens. Monotherapy trials of pioglitazone 15 to 45 mg produced
DHbA1c versus placebo of up to 1.6%, at the study end points.58 Compared with
placebo as add-on therapy to metformin, pioglitazone produced DHbA1c up to
1.4%; as add-on therapy to SU, it produced DHbA1c up to 1.6%; and as add-on
to insulin, it produced DHbA1c up to 1.0%.58,59 Monotherapy trials of rosiglitazone
2 to 8 mg daily likewise produced DHbA1c of up to 1.5% versus placebo.58
Compared with placebo as add-on therapy to metformin, SU, and insulin, rosiglitazone
2 to 8 mg daily produced DHbA1c up to 2.3%, 1.0%, and 1.3%, respectively.58,59
TZDs have shown nonglycemic pleiotropic effects on numerous surrogate markers
of atherosclerotic cardiovascular disease, including reduced carotid artery intimal me-
dia thickness on carotid ultrasonography. Because of the numerous salutary effects of
TZDs on markers of inflammation, thrombosis, and endothelial health (summarized in
Box 3), the use of these agents attracted widespread interest among both researchers
and clinicians interested in preventing microvascular and atherosclerotic complica-
tions of T2DM.6065
Pioglitazone has shown some utility in the treatment of nonalcoholic fatty liver dis-
ease (NAFLD), which is frequently associated with T2DM, and is clinically heralded by
variable transaminitis and hepatomegaly. NAFLD is now recognized as a cause of
formerly cryptogenic cirrhosis. Use of both rosiglitazone and pioglitazone have been
associated with net reduction in hepatic fat; in some studies, pioglitazone seems to
reduce hepatic fibrosis in patients with severe NAFLD.70
The favorable pleiotropic effects of TZDs on multiple cardiovascular risk factors
contrasts with a general lack of disease outcomes improvements. By contrast, the ev-
idence is confluent that these drugs cause or aggravate edema and CHF. Overall,
when used as monotherapy, a TZD is associated with edema in 2% to 5% of users;
if combined with another oral agent, the risk increases to 6% to 8%; and, if combined
with insulin, the risk is about 15%.71 Relative risk for CHF from 17,579 patients in 3
rosiglitazone and 2 pioglitazone trials ranges from 1.41 to 7.0 versus a comparator
8 Brietzke
Box 3
Pleiotropic effects of TZDs
Antiinflammatory effects
YhsCRP
YTNF-a
YIL-6
YVascular adhesion molecules
Antithrombotic effects
YPAI-1
YMMP-9
Lipid composition effects
[HDLc
YTG
[LDL particle size (large fluffy LDLc)
Salutary vascular effects
[eNOS
YSmooth muscle proliferation
YSystolic blood pressure
YRestenosis after coronary angioplasty66
Abbreviations: eNOS, endothelial nitric oxide synthase; HDLc, high-density lipoprotein choles-
terol; hsCRP, highly sensitive C-reactive protein; IL-6, interleukin 6; LDL, low-density lipopro-
tein; LDLc, low-density lipoprotein cholesterol; MMP-9, matrix metallopeptidase 9; PAI-1,
plasminogen activator inhibitor-1; TG, triglycerides.
Data from Refs.6769
1.43 (95% CI, 1.031.98; P 5 .03) for MI, and 1.64 (95% CI, 0.982.74; P 5 .06) for
cardiovascular death for rosiglitazone use versus comparator groups in the pooled
trial data.75 With subsequent reviews reaching similar conclusions, albeit at lower
magnitude of risk, rosiglitazone virtually disappeared from clinical use.
The PROspective pioglitAzone clinical trial in macroVascular events (PROActive) trial,
which compared pioglitazone versus placebo as add-on therapy to existing treatment of
T2DM, was specifically designed to measure rate of incident cardiovascular disease
events and cardiovascular mortality in a high-risk group of patients with prior cardiovas-
cular disease events, but there was no difference in the primary outcomes in the piogli-
tazone versus placebo groups.76 Head-to-head comparison seems to favor
pioglitazone rather than rosiglitazone, with regard to cardiovascular outcomes, based
on data from a meta-analysis of 4 case-control and 12 retrospective cohort studies, in
which relative risk for MI was 1.16 (95% CI, 1.071.24; P<.001) and relative risk of death
was 1.14 (95% CI, 1.091.20; P<.001), for rosiglitazone versus pioglitazone.77 Caution in
accepting that conclusion has been urged based on methodologic flaws in many of the
studies.71 Pioglitazone, but not rosiglitazone, has been associated with an increased
risk for bladder cancer; a meta-analysis by Bosetti and colleagues78 identified a relative
risk of 1.42 (95% CI, 1.171.72) for pioglitazone use beyond 2 years, versus never-users.
No other cancer risk has thus far been linked with either rosiglitazone or pioglitazone.
TZD drugs seem to have an adverse effect on bone health. Among 666 participants
with T2DM in the Health, Aging, and Body Composition observational study, self-
reported TZD use in women (but not in men) was associated with annualized bone
loss of 1.23% at the lumbar spine, and 0.65% at the hip by dual-energy x-ray ab-
sorptiometry (DEXA), compared with nonusers.79 Other investigators have identified
increased risk of fracture in TZD users; these studies are summarized in Table 2. In
summary, literature to date establishes that TZD use is associated with bone loss,
which translates into a roughly 50% increased risk of fracture, over time.
The increase and decrease in popularity of the TZD class represents a new age of
awareness in which glycemic efficacy is no longer the sole determinant leading to drug
approval, marketing, and prescribing. Henceforth, cardiovascular safety will be as impor-
tant as blood glucose normalization. The TZD experience is a reminder that favorable ef-
fects on surrogate markers of disease do not necessarily translate to clinical outcomes.
Table 2
Relative risk of TZD use for incident fractures (vs nonusers)
tubule, the SGLT2 is the predominant transport system, normally reclaiming about
144 g of filtered glucose from glomerular filtrate per 24 hours. The avidity of SGLT2-
mediated glucose transport in the kidney is such that normally serum glucose must
exceed 180 mg/dL for the volume of filtered glucose to exceed transport capacity
and produce glucosuria. Inhibition of SGLT2 causes glycosuria at a lower level of
filtered (and hence, serum) glucose and thus lowers serum glucose through increased
selective glycosuria.86
Canagliflozin and dapagliflozin are the first two SGLT2 inhibitor drugs available in
the United States. They are indicated for treatment of T2DM, based on monotherapy
trials versus placebo, and as add-on therapy for patients failing to reach HbA1c treat-
ment goals with metformin monotherapy. Monotherapy with canagliflozin produced
DHbA1c of 0.77% to 1.03%, along with body weight change of 2.5 to 3.4 kg
at doses of 100 mg and 300 mg daily, respectively, versus placebo.87 Canagliflozin
proved equal to glimepiride as add-on therapy for subjects inadequately controlled
on metformin, in the CANagliflozin Treatment And Trial Analysis-Sulfonylurea
(CANTATA-SU) trial, with DHbA1c 0.93% (vs baseline value) in the canagliflozin
add-on group, and DHbA1c 0.81% in the glimepiride group, although on average
weight changed by 3.7 kg in the canagliflozin groups and by 10.7 kg in the glimepir-
ide group.88 Hypoglycemia was more frequent in the glimepiride plus metformin
group, whereas genital mycotic infections were more frequent in the canagliflozin
plus metformin groups. Another trial examining canagliflozin versus sitagliptin as ter-
tiary therapy for patients failing metformin plus SU slightly favored canagliflozin, with
DHbA1c 1.03% in the canagliflozin plus SU plus metformin group, and DHbA1c
0.67% in the sitagliptin plus SU plus metformin group; weight changed 2.3 kg in
the canagliflozin-plus group and by 10.3 kg in the sitagliptin-plus group.89 Dapagliflo-
zin has been studied versus placebo, as add-on therapy to metformin in inadequately
controlled T2DM, with DHbA1c of 0.67% to 0.84% for dapagliflozin doses ranging
from 2.5 to 10 mg daily, versus DHbA1c of 10.3% in the placebo plus metformin
group. Body weight changed by 2.2 to 3.0 kg with canagliflozin plus metformin,
and by 0.9 kg for placebo plus metformin, with similar frequency of adverse events.90
Vasilakou and colleagues91 conducted a meta-analysis of all clinical trial data, to es-
timate the overall efficacy of the SGLT2 drug class, and found an overall DHbA1c of
0.79% in patients treated with SGLT2 monotherapy, and DHbA1c of 0.61% with
SGLT2 as add-on therapy. Other associations with SGLT2 therapy included mean
1.8 kg weight loss, 4.5 mm Hg systolic blood pressure, and up to a 5-fold increased
rate of genital mycotic infections, versus comparator groups. These investigators, and
others, have been critical of missing data in trials and strong possibility of overestima-
tion of benefit, caused by the last observation carried forward when subjects dropped
out or were lost to follow-up in the trials.91,92 It is hoped that an ongoing cardiovascular
safety trial will establish long-term safety for canagliflozin93; dapagliflozin will be moni-
tored closely not only for cardiovascular safety but for incident breast and bladder
cancer, which was noted to have occurred more frequently in dapagliflozin users in
the meta-analysis.91 For now, SGLT2s can be viewed as equivalent to other available
agents as add-on therapy to metformin, albeit at high financial cost and with increased
risk for genital mycotic infections. Small but significant weight loss of up to 5 kg in the
first year of therapy is expected, and risk of hypoglycemia is low. Long-term safety
(benefit or noninferiority with regard to other drug classes) with regard to cardiovascu-
lar disease events and neoplasia has not yet been established.94 Based on relative
absence of long-term safety information, and high financial cost of treatment, it seems
prudent to recommend SGLT2 inhibitors as third-line therapy for T2DM at the present
time.
Oral Antihyperglycemic Treatment 11
ALPHA-GLUCOSIDASE INHIBITORS
COLESEVELAM
Bile acids are involved in glucose homeostasis signal pathways as activators of the
farnesoid X receptor alpha, which is a regulator of gluconeogenesis and glucagon syn-
thesis; bile acids may also induce glucagon-like peptide-1 production.102 The glyce-
mic efficacy of a bile acid sequestrant, colesevelam, was first formally tested in a
randomized, placebo-controlled fashion in the GLOWS Glucose Lowering Effect of
WelChol Study (GLP-1) trial, which showed a DHbA1c of 0.5% versus placebo,
and also showed decreased low-density lipoprotein cholesterol (LDLc) level of
9.6% (vs baseline value), compared with 12.1% (vs baseline value) in the placebo
group. Gastrointestinal symptoms, primarily constipation, were 3 times more frequent
in the colesevelam group than in the placebo group.103
The efficacy of colesevelam as add-on therapy for T2DM was subsequently tested
in clinical trials in patients receiving monotherapy with SUs, metformin, combined oral
12 Brietzke
therapies (excluding DPP-4 inhibitors), and insulin. In a 26-week clinical trial of 316
subjects at multiple centers in the United States and Mexico, patients treated with
metformin or metformin plus combinations of SU, glinides, TZDs, and/or alpha-
glucosidase inhibitors, were randomized to colesevelam 3.75 g per day, or placebo.
At study conclusion, the colesevelam groups HbA1c level was 0.54% lower than
the placebo groups; LDLc, and highly sensitive C-reactive protein (hsCRP) were
also lower in the colesevelam group.104 A 26-week multicenter trial, also including
US and Mexican sites, of 461 subjects with T2DM with baseline HbA1c of 8.2%, ran-
domized patients treated with SU or with SU plus metformin, TZD, and/or alpha-
glucosidase inhibitor to receive either colesevelam 3.75 g daily or placebo. At the
studys conclusion, HbA1c was 0.54% lower in the colesevelam than in the compar-
ator groups, and LDLc level was also significantly lower.105 A 16-week clinical trial
added colesevelam or placebo to patients with mean HbA1c of 8.3% treated with
insulin-based therapies, either as insulin alone or in combination with oral therapies
that included metformin, SUs, or glinides, and/or a TZD. In this study of 287 random-
ized patients, HbA1c changed by 0.41%, and LDLc by 12.3% in the colesevelam
group, whereas HbA1c changed by 10.09% and LDLc by 10.5% in the placebo
group.106
A 2012 Cochrane Review of the available clinical trial data for colesevelam
concluded that the overall strength of evidence supported adjunctive use of coleseve-
lam, but that further research to establish long-term risks and benefits would be
necessary before widespread or early use of colesevelam for glycemic control could
be strongly encouraged.107 Among other concerns, the mechanism by which colese-
velam effects improved glycemia has not been elucidated. Radiolabeled tracer study
of mixed meal feedings has suggested that the major action of colesevelam is to in-
crease splanchnic sequestration of meal-derived glucose,108 which is consistent
with the clinical data from the Zieve and colleagues103 trial, in which postprandial gly-
cemia was significantly reduced in the colesevelam group compared with the placebo
group.103 At the present time, perhaps the best niche for colesevelam in the treatment
arsenal of oral antihyperglycemic therapies is in patients adjudged to have unsatisfac-
tory glycemic control, as well as unsatisfactory LDLc, on other well-tolerated antihy-
perglycemic and lipid-lowering (specifically, statin) drug therapies.102,109,110
BROMOCRIPTINE MESYLATE
Approved by FDA in 2010 for the indication of treatment of T2DM, the mechanism of
action of bromocriptine mesylate (also known as bromocriptine-QR [quick release]) is
largely inferred from animal studies. The drug is ingested within 2 hours of waking in
the morning, with breakfast, and is rapidly cleared by first-pass action of cytochrome
P450 34A (CYP34A) in the liver, with less than 10% of the ingested dose reaching the
systemic circulation. It is thought to increase dopamine in the hypothalamus, thereby
reducing sympathetic nervous activity, hepatic glucose production, and lipolysis, with
resultant improvement in insulin sensitivity.111
Bromocriptine mesylate has been studied as monotherapy versus placebo, and as
add-on therapy to SU, with DHbA1c of 0.5% to 0.7%, and also with lower FFAs
and triglycerides, versus placebo.112,113 Vinik and colleagues114 showed similar effi-
cacy of bromocriptine added to failing monotherapy or combined therapies with
various combinations of metformin, SU, and TZDs, finding DHbA1c of 0.47% in
the bromocriptine group, versus 10.26% in the placebo group, at 24 weeks.
A 52-week safety trial compared bromocriptine mesylate versus placebo, in ran-
domized fashion, in 3095 subjects treated with various monotherapies, oral
Oral Antihyperglycemic Treatment 13
combinations, or insulin alone or in combination with oral therapies, for the purpose of
comparing incidence of serious adverse events in the two groups115 Composite major
adverse cardiovascular events, including MI, stroke, coronary revascularization, or
hospitalization for unstable angina or CHF, occurred in 1.8% of the bromocriptine
group and in 3.2% of the placebo group; a risk reduction of 40% (hazard ratio,
0.61; 95% CI, 0.380.97; P 5 .02).116 Reasons for the apparent risk reduction are
thought to be related to reduced sympathetic nervous system activation or to reduced
circulating inflammatory markers such as hsCRP, and TNF-a, although to date such
markers have not been measured in studies.117,118 The lack of long-term efficacy
data (ie, studies longer than 24 weeks), the high financial cost of bromocriptine mesy-
late, and a high frequency of significant adverse effects (nausea in 26%, asthenia/mal-
aise in 15%) have led some authorities to recommend against widespread use of this
therapy.118,119 As further experience accumulates, the magnitude of benefit may allow
a more optimistic benefit versus risk estimation for select patients.
SUMMARY
Table 3
Oral antihyperglycemic drug: suggested dosing, action, expected efficacy, and cost
REFERENCES
11. Li D, Yeung SC, Hassan MM, et al. Antidiabetic therapies affect risk of pancre-
atic cancer. Gastroenterology 2009;137:4828.
12. Wright JL, Stanford JL. Metformin use and prostate cancer in Caucasian men:
results from a population-based casecontrol study. Cancer Causes Control
2009;20:161722.
13. Bouchoucha M, Uzza B, Cohen R. Metformin and digestive disorders. Diabetes
Metab 2010;37:906.
14. de Jager J, Kooy A, Lehert P, et al. Long term treatment with metformin in
patients with type 2 diabetes and risk of vitamin B-12 deficiency: randomised
placebo controlled trial. BMJ 2010;340:c2181.
15. Anonymous. Metformin for non-insulin-dependent diabetes mellitus. Med Lett
Drugs Ther 1995;37:412.
16. Lipska KJ, Bailey CJ, Inzucchi SE. Use of metformin in the setting of mild-to-
moderate renal insufficiency. Diabetes Care 2011;34:14317.
17. Salpeter SR, Greyber E, Pasternak GA, et al. Risk of fatal and nonfatal lactic
acidosis with metformin use in type 2 diabetes. Cochrane Database Syst Rev
2010;(4):CD002967.
18. Scheen AJ, Paquot N. Metformin revisited: a critical review of the benefit-risk
balance in at-risk patients with type 2 diabetes. Diabetes Metab 2013;39:
17990.
19. Eurich DT, Majumdar SR, McAlister FA, et al. Improved clinical outcomes asso-
ciated with metformin in patients with diabetes and heart failure. Diabetes Care
2005;28:234551.
20. Nye HJ, Herrington WG. Metformin: the safest hypoglycaemic agent in chronic
kidney disease? Nephron Clin Pract 2011;118:c3803.
21. Rocha A, Almeda M, Santos J, et al. Metformin in patients with chronic kidney
disease: strengths and weaknesses. J Nephrol 2013;26:5560.
22. Seino S. Cell signaling in insulin secretion: the molecular targets of ATP, cAMP
and sulfonylurea. Diabetologia 2012;55:2096108.
23. Ashcroft FM. ATP-sensitive potassium channelopathies: focus on insulin secre-
tion. J Clin Invest 2005;115:204758.
24. Hemmingsen B, Schroll JB, Lund SS, et al. Sulphonylurea monotherapy for
patients with type 2 diabetes mellitus (review). Cochrane Database Syst Rev
2013;(4):CD009008.
25. Bell DS. Practical considerations and guidelines for dosing sulfonylureas as
monotherapy or combination therapy. Clin Ther 2004;26:171527.
26. Davis SN. The role of glimepiride in the effective management of type 2
diabetes. J Diabetes Complications 2004;18:36776.
27. Hirst JA, Farmer AJ, Dyar A, et al. Estimating the effect of sulfonylurea on HbA1c
in diabetes: a systematic review and meta-analysis. Diabetologia 2013;56:
97384.
28. Turner RC, Cull CA, Frighi V, et al. Glycemic control with diet, sulfonylurea, met-
formin, or insulin in patients with type 2 diabetes mellitus: progressive require-
ment for multiple therapies (UKPDS 49). UK Prospective Diabetes Study
(UKPDS) Group. JAMA 1999;281:200512.
29. Del Prato S, Pulizzi N. The place of sulfonylureas in the therapy for type 2 dia-
betes mellitus. Metabolism 2006;55(Suppl 1):S207.
30. Holman RR. Long-term efficacy of sulfonylureas: a United Kingdom Prospective
Diabetes Study perspective. Metabolism 2006;55(Suppl 1):S25.
31. Kahn SE, Haffner SM, Helse MA, et al. Glycemic durability of rosiglitazone, met-
formin, or glyburide monotherapy. N Engl J Med 2006;355:242743.
16 Brietzke
50. Thakkar B, Aronis KN, Vamvini MT, et al. Metformin and sulfonylureas in relation
to cancer risk in type 2 diabetes patients: a meta-analysis using primary data of
published studies. Metabolism 2013;62:92234.
51. Riddle MC. Editorial: sulfonylureas differ in effects on ischemic precondition-
ingis it time to retire glyburide? J Clin Endocrinol Metab 2003;88:52830.
52. Riddle MC. Editorial: more reasons to say goodbye to glyburide. J Clin Endocri-
nol Metab 2010;95:486770.
53. Anonymous. Repaglinide for type 2 diabetes. Med Lett Drugs Ther 1998;40:
556.
54. Anonymous. Nateglinide for type 2 diabetes. Med Lett Drugs Ther 2001;43:
2931.
55. Cariou B, Charbonnel B, Staels B. Thiazolidinediones and PPARg agonists: time
for a reassessment. Trends Endocrinol Metab 2012;23:20515.
56. Decker M, Hofflich H, Elias AN. Thiazolidinediones and the preservation of b-cell
function, cellular proliferation and apoptosis. Diabetes Obes Metab 2008;10:
61725.
57. Ovalle F, Ovalle-Berumen JF. Thiazolidinediones: a review of their benefits and
risks. South Med J 2002;95:118894.
58. Diamant M, Heine RJ. Thiazolidinediones in type 2 diabetes mellitus: current
clinical evidence. Drugs 2003;63:1373405.
59. Derosa G, Maffioli P. Thiazolidinediones plus metformin association on body
weight in patients with type 2 diabetes. Diabetes Res Clin Pract 2011;91:
26570.
60. Viberti G. Thiazolidinedionesbenefits on microvascular complications of type
2 diabetes. J Diabetes Complications 2005;19:16877.
61. Riera-Guardia N, Rothenbacher D. The effect of thiazolidinediones on adiponec-
tin serum level: a meta-analysis. Diabetes Obes Metab 2008;10:36775.
62. Quinn CE, Hamilton PK, Lockhart CJ, et al. Thiazolidinediones: effects on insulin
resistance and the cardiovascular system. Br J Pharmacol 2008;153:63645.
63. Lebovitz HE. Rationale for and role of thiazolidinediones in type 2 diabetes mel-
litus. Am J Cardiol 2002;90(Suppl):34G41G.
64. Kendall DM. Thiazolidinedionesthe case for early use. Diabetes Care 2006;
29:1547.
65. Ceriello A. Thiazolidinediones as anti-inflammatory and anti-atherogenic agents.
Diabetes Metab Res Rev 2008;24:1426.
66. Choi D, Kim SK, Choi SH, et al. Preventative effects of rosiglitazone on resteno-
sis after coronary stent implantation in patients with type 2 diabetes. Diabetes
Care 2004;27:265460.
67. Gilling L, Suwattee P, DeSouza C, et al. Effects of thiazolidinediones on cardio-
vascular risk factors. Am J Cardiovasc Drugs 2002;2:14956.
68. Wyne KL. The metabolic syndrome: evolving evidence that thiazolidinediones
provide rational therapy. Diabetes Obes Metab 2006;8:36580.
69. Parulkar AA, Pendergrass ML, Granda-Ayala R, et al. Nonhypoglycemic effects
of thiazolidinediones. Ann Intern Med 2001;134:6171.
70. Yki-Jarvinen H. Thiazolidinediones and the liver in humans. Curr Opin Lipidol
2009;20:47783.
71. Khanderia U, Pop-Busui R, Eagle KA. Thiazolidinediones in type 2 diabetes: a
cardiology perspective. Ann Pharmacother 2008;42:146674.
72. Lago RM, Singh PP, Nesto RW. Congestive heart failure and cardiovascular
death in patients with prediabetes and type 2 diabetes given thiazolidinediones:
a meta-analysis of randomized clinical trials. Lancet 2007;370:112936.
18 Brietzke
109. Aggarwal S, Loomba RS, Arora RR. Efficacy of colesevelam on lowering glyce-
mia and lipids. J Cardiovasc Pharmacol 2012;59:198205.
110. Goldfine AB. Modulating LDL cholesterol and glucose in patients with type 2
diabetes mellitus: targeting the bile acid pathway. Curr Opin Cardiol 2008;23:
50211.
111. DeFronzo RA. Bromocriptine: a sympatholytic, D2-dopamine agonist for the
treatment of type 2 diabetes. Diabetes Care 2011;34:78994.
112. Cincotta AH, Meier AH, Cincotta M Jr. Bromocriptine improves glycaemic con-
trol and serum lipid profile in obese type 2 diabetic subjects: a new approach in
the treatment of diabetes. Expert Opin Investig Drugs 1999;8:1683707.
113. Kerr JL, Timpe EM, Petkewicz KA. Bromocriptine mesylate for glycemic man-
agement in type 2 diabetes mellitus. Ann Pharmacother 2010;44:177786.
114. Vinik AI, Cincotta AH, Scranton RE, et al. Effect of bromocriptine-QR on glyce-
mic control in subjects with uncontrolled hyperglycemia on one or two oral anti-
diabetes agents. Endocr Pract 2012;18:93143.
115. Gaziano JM, Cincotta AH, OConnor CM, et al. Randomized clinical trial of
quick-release bromocriptine among patients with type 2 diabetes on overall
safety and cardiovascular outcomes. Diabetes Care 2010;33:15038.
116. Gaziano JM, Cincotta AH, Vinik A, et al. Effect of bromocriptine-QR (a quick-
release formulation of bromocriptine mesylate) on major adverse cardiovascular
events in type 2 diabetes subjects. J Am Heart Assoc 2012;1:e002279. http://
dx.doi.org/10.1161/JAHA.112.002279.
117. Bell DS. Why does quick-release bromocriptine decrease cardiac events? Dia-
betes Obes Metab 2011;13:8804.
118. Garber AJ, Blonde L, Bloomgarden ZT, et al. The role of bromocriptine-QR in the
management of type 2 diabetes expert panel recommendations. Endocr Pract
2013;19:1006.
119. Anonymous. Bromocriptine (Cycloset) for type 2 diabetes. Med Lett Drugs Ther
2010;52:979.
120. Bennett WL, Maruthur NM, Singh S, et al. Comparative effectiveness and safety
of medications for type 2 diabetes: an update including new drugs and 2-drug
combinations. Ann Intern Med 2011;154:60213.
I n c re t i n - B a s e d T h e r a p i e s
Joshua J. Neumiller, PharmD, CDE
KEYWORDS
Dipeptidyl peptidase 4 DPP-4 inhibitors GLP-1 receptor agonists
Glucagon-like peptide 1 Incretin effect Incretin mimetics Pharmacotherapy
KEY POINTS
Incretin hormones (glucagon-like peptide 1 [GLP-1] and gastric inhibitory peptide) play a
key role in glucose homeostasis.
Two classes of incretin-based therapies are currently available: GLP-1 receptor agonists
and dipeptidyl peptidase 4 (DPP-4) inhibitors.
Potential key benefits of GLP-1 receptor agonist therapy include a low risk of hypoglyce-
mia and a potential for weight loss with treatment.
GLP-1 receptor agonists have variable effects on glycemia, with short-acting agents
having a greater effect on postprandial glucose and longer-acting agents having a rela-
tively greater effect on fasting glucose levels.
Potential key benefits of DPP-4 inhibitor therapy include a low risk of hypoglycemia, a
relatively mild side-effect profile, and simple daily oral administration.
Incretin-based therapies have been associated with rare adverse events such as pancre-
atitis and acute renal failure, and patients should be selected and monitored accordingly.
INTRODUCTION
Disclosure Statement: J.J. Neumiller receives institutional research grant support from Amylin,
AstraZeneca, Johnson & Johnson, Merck, and Novo Nordisk. J.J. Neumiller serves as a consul-
tant to Janssen Pharmaceuticals and Sanofi and serves on the speakers bureau for Janssen
Pharmaceuticals. No financial support was received for writing this article.
Department of Pharmacotherapy, College of Pharmacy, Washington State University, PO
Box 1495, Spokane, WA 99210-1495, USA
E-mail address: [email protected]
As mentioned previously, the incretin effect plays a major role in glucose homeo-
stasis. Although native GLP-1 has been targeted as a therapeutic agent because
Incretin-Based Therapies 3
Fig. 1. Actions of glucagon-like peptide 1 (GLP-1) in peripheral tissues. Most of the effects of
GLP-1 are mediated by direct interaction with GLP-1 receptor agonists on specific tissues.
However, the actions of GLP-1 in liver, fat, and muscle most likely occur through indirect
mechanisms. (From Baggio LL, Drucker DJ. Biology of incretins: GLP-1 and GIP. Gastroenter-
ology 2007;132:213157; with permission.)
of its favorable effects on glycemia, its clinical utility in the ambulatory care
setting is hindered owing to its extremely short half-life.11 Both native GLP-1
and GIP are quickly cleared following release caused by renal clearance and
rapid metabolism by the enzyme dipeptidyl peptidase-4 (DPP-4).23 Owing to
the short half-life of incretin hormones, 2 predominant therapeutic strategies
have been developed and marketed to address the impaired incretin response
(Fig. 2):
1. GLP-1 receptor agonists (RAs) resistant to degradation by DPP-4
2. DPP-4 inhibitors
Although both strategies are used to augment the incretin effect, there are key
differences in clinical outcomes achieved with these 2 medication classes. Table 1
provides a general clinical comparison of GLP-1 RAs and DPP-4 inhibitors for the
treatment of T2DM.24,25
4 Neumiller
Fig. 2. Timeline for the development of incretin-based therapies. DPP-4, dipeptidyl pepti-
dase 4; FDA, Food and Drug Administration; GIP, gastric inhibitory peptide; GLP-1,
glucagon-like peptide 1; GLP-1RA, GLP-1 receptor agonist.
Table 1
Select clinical properties of GLP-1 receptor agonists and DPP-4 inhibitors
a
Short-acting GLP-1 receptor agonist.
Adapted from Campbell RK. Clarifying the role of incretin-based therapies in the treatment of
type 2 diabetes mellitus. Clin Ther 2011;33(5):51127; and Meier JJ. GLP-1 receptor agonists for
individualized treatment of type 2 diabetes mellitus. Nat Rev Endocrinol 2012;8:72842.
Incretin-Based Therapies 5
Table 2
Comparison and contrast of currently available GLP-1 receptor agonists
a
Placebo-subtracted change from baseline for exenatide, liraglutide, and albiglutide, and abso-
lute change from baseline for exenatide extended-release (ER). Baseline characteristics of study
groups and concomitant medications varied from study to study.
Fig. 3. Glycemic and extraglycemic effects of incretins/GLP-1 agents. BP, blood pressure; CNS,
central nervous system; GI, gastrointestinal. (From Mudaliar S, Henry RR. Incretin therapies:
effects beyond glycemic control. Eur J Intern Med 2009;20:S31928; with permission.)
6 Neumiller
Exenatide
Exenatide was the first GLP-1 RA approved by the FDA for the treatment of T2DM.26
Compared with other longer-acting GLP-1 RAs, exenatide has a more robust effect on
postprandial blood glucose excursions (for those meals in which it is administered
prior).39 Select key clinical information for exenatide is provided in Box 1.26
Nausea is the most common dose-limiting adverse event associated with exenatide
therapy, with approximately 48% of participants receiving exenatide at the 10-mg
twice-daily dose reporting nausea during clinical trials.3033 Accordingly, exenatide
therapy should be initiated with caution in individuals with gastrointestinal disease.
The following are select contraindications and warnings/precautions noted with
exenatide.26
Contraindications
A history of severe hypersensitivity to exenatide or any product components.
Warnings/precautions
Pancreatitis
The association between incretin-based medications and pancreatitis is contro-
versial.50 Overall, the incidence of acute pancreatitis in persons with T2DM is
Box 1
Exenatide (Byetta): key clinical information
Liraglutide
Liraglutide is approved for once-daily subcutaneous administration for the treatment
of T2DM. Select clinical information is provided in Box 2.27 Liraglutide has been stud-
ied head-to-head versus exenatide as add-on therapy for persons with T2DM inade-
quately controlled on metformin and a sulfonylurea.53 Once-daily liraglutide compared
favorably with twice-daily exenatide, with similar effects on weight and hemoglobin
A1C observed with both agents (Box 3).53
The nausea associated with liraglutide therapy was reported most commonly during
the initial 4 weeks of therapy in clinical trials, with nausea symptoms improving over
time with continued use.3437 The following are contraindications and warnings/pre-
cautions for consideration with liraglutide.27
Box 2
Liraglutide (Victoza): key clinical information
Adapted from Victoza (liraglutide) [package insert]. Plainsboro, NJ: Novo Nordisk, Inc; 2013.
8 Neumiller
Box 3
Findings from head-to-head study of liraglutide and exenatide
Contraindications
A history of serious hypersensitivity to liraglutide or any product components.
Personal or family history of medullary thyroid carcinoma or in patients with mul-
tiple endocrine neoplasia syndrome type 2.
Warnings/precautions
Thyroid C-cell tumors in animals
An additional concern noted in the prescribing information is a warning of dose-
dependent and treatment-durationdependent thyroid C-cell tumors observed
during preclinical studies with liraglutide. In rodent models, liraglutide was asso-
ciated with an increased risk of thyroid C-cell focal hyperplasia and C-cell tumors
at clinically relevant doses. The true meaning of these findings with regard to hu-
man use is currently unknown. According to the prescribing information for lira-
glutide, clinical trials have generated 4 reported cases of thyroid C-cell
hyperplasia among liraglutide-treated patients, compared with 1 case in a patient
treated with a comparator product. These cases equate to 1.3 versus 0.6 cases
per 1000 patient-years, respectively. Data from long-term studies did not
demonstrate differences in mean calcitonin levels (a surrogate marker for
C-cell hyperplasia) between subjects treated with liraglutide and those in
comparator groups during 2 years of follow-up.54
Pancreatitis
Like exenatide, the labeling for liraglutide includes a warning of pancreatitis.
Seven cases of pancreatitis were reported during the phase 3 clinical trial pro-
gram for liraglutide, compared with 1 case observed within the comparator
groups. Box 4 summarizes key recommendations provided as part of the
REMS (Risk Evaluation and Mitigation Strategy) for liraglutide.55
Hypoglycemia
Similarly to exenatide, caution should be exercised when adding liraglutide in a
patient receiving a sulfonylurea or insulin, and a decrease in the dose of sulfonyl-
urea or insulin may be warranted to avoid hypoglycemic events.27
Renal impairment
Cases of renal impairment, typically associated with nausea, vomiting, and diar-
rhea, have been noted with liraglutide therapy. Caution should be used when
initiating therapy or titrating up the dose of liraglutide in persons with renal
impairment.27
Box 4
FDA recommendations to reduce the risk of pancreatitis in patients using liraglutide
Patients using liraglutide should be counseled about the symptoms of pancreatitis, such
as severe abdominal pain that may radiate to the back, possibly with nausea and
vomiting
If patients experience symptoms of pancreatitis, they should contact their health care
provider immediately
Patients must be provided a Medication Guide that provides information about pancreatitis
that includes the following:
Conditions that may place patients at greater risk for pancreatitis, such as a prior history of
pancreatitis, gallstones, excessive use of alcohol, or very high levels of triglycerides
Symptoms of pancreatitis and what to do if these symptoms occur
If health care professionals suspect a patient has pancreatitis, liraglutide should be stopped
immediately and the patient should undergo testing to confirm a diagnosis of pancreatitis
and, if confirmed, liraglutide should not be resumed
Liraglutide should be used cautiously in those with a history of pancreatitis
Adapted from US Food and Drug Administration. NDA 22-341 Victoza (liraglutide [rDNA origin]
injection) risk evaluation and mitigation strategy (REMS). Available at: http://www.fda.gov/
downloads/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/
UCM202063.pdf. Accessed June 1, 2014.
Contraindications
A history of serious hypersensitivity to exenatide or any product components.
Personal or family history of medullary thyroid carcinoma or in patients with mul-
tiple endocrine neoplasia syndrome type 2.
Warnings/precautions Warnings/precautions for exenatide ER are similar to those
listed for liraglutide, and include:
Thyroid C-cell tumors in animals
Pancreatitis
10 Neumiller
Box 5
Exenatide ER (Bydureon): key clinical information
Hypoglycemia
Renal impairment
Injection-site reactions
Albiglutide
Albiglutide is the newest FDA-approved once-weekly GLP-1 RA. The protracted dura-
tion of action of albiglutide is achieved by fusion of recombinant GLP-1 to human
Table 3
Comparison of exenatide ER with exenatide twice daily (30-week data)
Abbreviations: A1C, hemoglobin A1c; FPG, fasting plasma glucose; PPG, postprandial glucose.
a
P 5 .0023.
b
P<.0001.
c
P 5 .0124.
d
P 5 .0039 versus comparator.
Adapted from Drucker DJ, Buse JB, Taylor K, et al. Exenatide once weekly versus twice daily for
the treatment of type 2 diabetes: a randomized, open-label, non-inferiority study. Lancet
2008;372(9645):124050.
Incretin-Based Therapies 11
Contraindications
A history of serious hypersensitivity to albiglutide or any product components.
Personal or family history of medullary thyroid carcinoma or in patients with mul-
tiple endocrine neoplasia syndrome type 2.
Box 6
Albiglutide (Tanzeum): key clinical information
Adapted from Tanzeum (albiglutide) [package insert]. Wilmington, DE: GlaxoSmithKline, LLC;
2014.
12 Neumiller
Sitagliptin
Sitagliptin, the first DPP-4 inhibitor approved by the FDA, has been studied and used
clinically in combination with numerous other antidiabetic therapies, and has emerged
as a widely used oral antidiabetic medication (Box 7).62 In line with DPP-4 inhibitors
inducing insulin secretion in a glucose-dependent manner, the overall incidence of hy-
poglycemia in subjects receiving sitagliptin was similar to that of placebo controls.
Caution is advised, however, if using sitagliptin in combination with insulin secreta-
gogue medications, owing to an increased risk of hypoglycemia when used
together.6669 Key contraindications, warnings, and precautions for sitagliptin are as
follows.62
Contraindications
A history of a serious hypersensitivity reaction to sitagliptin.
Warnings/precautions
Pancreatitis
The prescribing information for sitagliptin includes information regarding post-
marketing reports of acute pancreatitis.62 The FDA cited 88 cases of acute
pancreatitis reported between October 2006 and February 2009, 2 of which
were cases of hemorrhagic or necrotizing pancreatitis.81 A large retrospective
Table 4
Comparison and contrast of currently available DPP-4 inhibitors
a
Placebo-subtracted change from baseline; baseline characteristics of study groups and concom-
itant medications varied from study to study.
Incretin-Based Therapies 13
Box 7
Sitagliptin: key clinical information
Adapted from Januvia (sitagliptin) [package insert]. Whitehouse Station, NJ: Merck & Co., Inc;
2014.
Saxagliptin
Key clinical information for saxagliptin is summarized in Box 8.63 A differentiating
factor for saxagliptin in comparison with other DPP-4 inhibitors is that it is a
substrate of CYP3A4/5, and a dose reduction is recommended when given in com-
bination with a strong CYP3A4/5 inhibitor such as ketoconazole.63 Similarly to
sitagliptin, a higher risk of hypoglycemia was observed when saxagliptin was
used in combination with an insulin secretagogue. The contraindications, warnings,
and precautions for saxagliptin are similar to those noted for other agents in this
class.63
Contraindications
A history of a serious hypersensitivity reaction to saxagliptin.
14 Neumiller
Box 8
Saxagliptin: key clinical information
Warnings/precautions
Pancreatitis
Overall, the incidence of pancreatitis during clinical trials was 0.2% in the 3422
patients who received saxagliptin, compared with 0.2% in 1066 controls.83
Hypoglycemia
Serious allergic reactions
Linagliptin
In comparison with other currently available DPP-4 inhibitors, linagliptin has a long
half-life (131 hours) owing to its extensive binding to plasma proteins.84 Linagliptin
is primarily eliminated hepatically (w85%), with an estimated 5% of a given dose
undergoing renal elimination (Box 9).64,84 A study of linagliptin use in patients with
renal compromise concluded that dose adjustment is not required in various degrees
of renal impairment,85 a unique trait in comparison with other currently available
DPP-4 inhibitors, which all require renal dose adjustment.
The following are contraindications, warnings, and precautions noted in the labeling
for linagliptin.64
Contraindications
A history of a serious hypersensitivity reaction to linagliptin.
Warnings/precautions
Pancreatitis
Eight of 4687 participants (4311 patient-years of exposure) who received linaglip-
tin experienced pancreatitis while receiving treatment, compared with no cases
in the 1183 participants (433 patient years of exposure) receiving placebo.
Hypoglycemia
Serious allergic reactions
Alogliptin
Alogliptin is the newest DPP-4 inhibitor marketed for the treatment of T2DM. Alogliptin
monotherapy is generally well tolerated, with a generally mild overall side-effect
profile.65 Key clinical information on alogliptin, including the most common side effects
Incretin-Based Therapies 15
Box 9
Linagliptin: key clinical information
Box 10
Alogliptin: key clinical information
Adapted from Nesina (alogliptin) [package insert]. Deerfield, IL: Takeda Pharmaceuticals
American, Inc; 2013.
16 Neumiller
CARDIOVASCULAR SAFETY
Table 5
Select cardiovascular outcome trials (CVOTs) recently completed or in progress with incretin-
based therapies
Adapted from ClinicalTrials.gov. Available at: http://clinicaltrials.gov. Accessed July 28, 2014.
Incretin-Based Therapies 17
SUMMARY
Incretin-based therapies are steadily gaining clinical popularity, with many more prod-
ucts in the developmental pipeline. Current treatment recommendations incorporate
GLP-1 RAs and DPP-4 inhibitors as important agents for consideration in the treat-
ment of T2DM owing to their low hypoglycemia risk, ability to address postprandial
hyperglycemia (DPP-4 inhibitors and short-acting GLP-1 RAs), and potential for
weight reduction (GLP-1 RAs).94,95 These properties may likewise prove advanta-
geous in older adults in whom hypoglycemia is particularly undesirable, although older
adults may be more prone to the nausea and vomiting associated with GLP-1 RA ther-
apy.96 Other safety issues for incretin-based therapies, such as pancreatitis, C-cell
hyperplasia, and renal failure, should be considered when choosing an appropriate
patient to receive such therapies. Ongoing CV outcome studies will further inform
the health care community regarding the CV safety of incretin-based therapies. The
availability of both short-acting and long-acting GLP-1 RAs currently allows practi-
tioners to consider individualized blood glucose trends and therapeutic needs when
choosing an optimal agent.
REFERENCES
1. Baggio LL, Drucker DJ. Biology of incretins: GLP-1 and GIP. Gastroenterology
2007;132:213157.
2. Elrick H, Stimmler L, Hlad CJ, et al. Plasma insulin response to oral and intrave-
nous glucose administration. J Clin Endocrinol Metab 1964;24:107682.
3. Creutzfeldt W. The incretin concept today. Diabetologia 1979;16(2):7585.
4. Dupre J, Ross SA, Watson D, et al. Stimulation of insulin secretion by gastric
inhibitory polypeptide in man. J Clin Endocrinol Metab 1973;37(5):8268.
5. Bell GI, Santerre RF, Mullenbach GT. Hamster preproglucagon contains the
sequence of glucagon and two related peptides. Nature 1983;302(5910):7168.
6. Nauck MA, Homberger E, Siegel EG, et al. Incretin effects of increasing glucose
loads in man calculated from venous insulin and C-peptide responses. J Clin
Endocrinol Metab 1986;63(2):4928.
7. Nauck M, Stockmann F, Ebert R, et al. Reduced incretin effect in type 2 (non-in-
sulin-dependent) diabetes. Diabetologia 1986;29(1):4652.
18 Neumiller
27. Victoza (liraglutide) [package insert]. Plainsboro, NJ: Novo Nordisk, Inc; 2013.
28. Bydureon (exenatide extended-release for injectable suspension) [package
insert]. Wilmington, DE: AstraZeneca Pharmaceuticals LP; 2014.
29. Tanzeum (albiglutide) [package insert]. Wilmington, DE: GlaxoSmithKline, LLC;
2014.
30. DeFronzo RA, Ratner RE, Han J, et al. Effects of exenatide (exendin-4) on
glycemic control and weight over 30 weeks in metformin-treated patients with
type 2 diabetes. Diabetes Care 2005;28(5):1092100.
31. Buse JB, Henry RR, Han J, et al. Effects of exenatide (exendin-4) on glycemic
control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes.
Diabetes Care 2004;27(11):262835, 3.
32. Kendall DM, Riddle MC, Rosenstock J, et al. Effects of exenatide (exendin-4) on
glycemic control over 30 weeks in patients with type 2 diabetes treated with
metformin and a sulfonylurea. Diabetes Care 2005;28(5):108391.
33. Zinman B, Hoogwerf BJ, Duran Garcia S, et al. The effect of adding exenatide to
thiazolidinedione in suboptimally controlled type 2 diabetes: a randomized trial.
Ann Intern Med 2007;146(7):47785.
34. Marre M, Shaw J, Brandle M, et al. Liraglutide, a once-daily human GLP-1 analogue,
added to a sulphonylurea over 26 weeks produces greater improvements in
glycaemic and weight control compared with adding rosiglitazone or placebo in
subjects with Type 2 diabetes (LEAD-1 SU). Diabet Med 2009;26(3):26878.
35. Nauck M, Frid A, Hermansen K, et al. Efficacy and safety comparison of liraglu-
tide, glimepiride, and placebo, all in combination with metformin in type 2
diabetes: the LEAD (liraglutide effect and action in diabetes)-2 study. Diabetes
Care 2009;32(1):8490.
36. Zinman B, Gerich J, Buse JB, et al. Efficacy and safety of the human glucagon-
like peptide-1 analog liraglutide in combination with metformin and thiazolidine-
dione in patients with type 2 diabetes mellitus (LEAD-4 Met 1 TZD). Diabetes
Care 2009;32(7):122430.
37. Russell-Jones D, Vaag A, Schmitz O, et al. Liraglutide vs insulin glargine and pla-
cebo in combination with metformin and sulfonylurea therapy in type 2 diabetes
mellitus (LEAD-5 met 1 SU): a randomized controlled trial. Diabetologia 2009;
52(10):204655.
38. Drucker DJ, Buse JB, Taylor K, et al. Exenatide once weekly versus twice daily
for the treatment of type 2 diabetes: a randomized, open-label, non-inferiority
study. Lancet 2008;372(9645):124050.
39. Buse JB, Drucker DJ, Taylor KL, et al. DURATION 1: exenatide once weekly pro-
duces sustained glycemic control and weight loss over 52 weeks. Diabetes
Care 2010;33(6):125561.
40. Bergenstal RM, Wysham C, Macconell L, et al. Efficacy and safety of exenatide
once weekly versus sitagliptin or pioglitazone as an adjunct to metformin for
treatment of type 2 diabetes (DURATION-2): a randomized trial. Lancet 2010;
376(9739):4319.
41. Diamant M, Van Gaal L, Stranks S, et al. Once weekly exenatide compared with
insulin glargine titrated to target in patients with type 2 diabetes (DURATION-3):
an open-label randomised trial. Lancet 2010;375(9733):223443.
42. Blevins T, Pullman J, Malloy J, et al. DURATION-5: exenatide one weekly resulted
in greater improvements in glycemic control compared with exenatide twice daily
in patients with type 2 diabetes. J Clin Endocrinol Metab 2011;96(5):130110.
43. Reusch J, Stewart M, Perkins C, et al. HARMONY 1 week 52 results: albiglutide
vs. placebo in patients with type 2 diabetes mellitus not controlled on
20 Neumiller
58. Pratley RE, Nauck MA, Barnett AH, et al. Once-weekly albiglutide versus once-
daily liraglutide in patients with type 2 diabetes inadequately controlled on oral
drugs (HARMONY 7): a randomised, open-label, multicentre, non-inferiority
phase 3 study. Lancet Diabetes Endocrinol 2014;2(4):28997.
59. Ahren B. Clinical results of treating type 2 diabetic patients with sitagliptin, vilda-
gliptin or saxagliptindiabetes control and potential adverse events. Best Pract
Res Clin Endocrinol Metab 2009;23(4):48798.
60. Deacon CF. Therapeutic strategies based on glucagon-like peptide 1. Diabetes
2004;53(9):21819.
61. Fadini GP, Avogaro A. Cardiovascular effects of DPP-4 inhibition: beyond GLP-1.
Vascul Pharmacol 2011;55:106.
62. Januvia (sitagliptin) [package insert]. Whitehouse Station, NJ: Merck & Co., Inc;
2014.
63. Onglyza (saxagliptin) [package insert]. Princeton, NJ: Bristol-Myers Squibb
Company; 2013.
64. Tradjenta (linagliptin) [package insert]. Ridgefield, CT: Boehringer Ingelheim
Pharmaceuticals, Inc; 2014.
65. Nesina (alogliptin) [package insert]. Deerfield, IL: Takeda Pharmaceuticals
American, Inc; 2013.
66. Aschner P, Kipnes M, Lunceford M, et al. Effect of the dipeptidyl peptidase-4
inhibitor sitagliptin as monotherapy on glycemic control in patients with type 2
diabetes. Diabetes Care 2006;29(12):26327.
67. Charbonnel B, Karasik A, Liu J, et al. Efficacy and safety of the dipeptidyl
peptidase-4 inhibitor sitagliptin added to ongoing metformin therapy in patients
with type 2 diabetes inadequately controlled with metformin alone. Diabetes
Care 2006;29(12):263843.
68. Hermansen K, Kipnes M, Luo E, et al. Efficacy and safety of the dipeptidyl
peptidase-4 inhibitor, sitagliptin, in patients with type 2 diabetes mellitus inade-
quately controlled on glimepiride alone or on glimepiride and metformin.
Diabetes Obes Metab 2007;9(5):73345.
69. Rosenstock J, Brazg R, Andryuk PJ, et al. Efficacy and safety of the di-
peptidyl peptidase-4 inhibitor sitagliptin added to ongoing pioglitazone ther-
apy in patients with type 2 diabetes: a 24 week, multicenter, randomized,
double-blind, placebo-controlled, parallel-group study. Clin Ther 2006;
28(10):155668.
70. Rosenstock J, Aguilar-Salinas C, Klein E, et al. Effect of saxagliptin monotherapy
in treatment-naive patients with type 2 diabetes. Curr Med Res Opin 2009;
25(10):240111.
71. DeFronzo RA, Hissa MN, Garber AJ, et al. The efficacy and safety of saxagliptin
when added to metformin therapy in patients with inadequately controlled type 2
diabetes on metformin alone. Diabetes Care 2009;32(9):164955.
72. Hollander P, Li J, Allen E, et al. Saxagliptin added to a thiazolidinedione
improves glycemic control in patients with type 2 diabetes and inadequate
control on thiazolidinedione alone. J Clin Endocrinol Metab 2009;94(12):
48109.
73. Del Prato S, Barnett AH, Huisman H, et al. Effect of linagliptin monotherapy on
glycaemic control and markers of beta-cell function in patients with inade-
quately controlled type 2 diabetes: a randomized controlled trial. Diabetes
Obes Metab 2011;13(3):25867.
74. Taskinen MR, Rosenstock J, Tamminen I, et al. Safety and efficacy of linagliptin
as add-on therapy to metformin in patients with type 2 diabetes: a randomized,
22 Neumiller
88. Nissen SE, Wolski K, Topol EJ. Effect of muraglitazar on death and major
adverse cardiovascular events in patients with type 2 diabetes mellitus. JAMA
2005;294:25816.
89. Food and Drug Administration, Center for Drug Evaluation and Research. Guid-
ance for industry: diabetes mellitus-evaluating cardiovascular risk in new antidi-
abetic therapies to treat type 2 diabetes. Available at: http://www.fda.gov/
downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm
071627.pdf. Accessed July 28, 2014.
90. Scirica BM, Bhatt DL, Braunwald E, et al. Saxagliptin and cardiovascular out-
comes in patients with type 2 diabetes mellitus. N Engl J Med 2013;369:131726.
91. Monami M, Dicembrini I, Mannucci E. Dipeptidyl peptidase-4 inhibitors and heart
failure: a meta-analysis of randomized clinical trials. Nutr Metab Cardiovasc Dis
2014;24(7):68997.
92. Pratley R, Nauck M, Bailey T, et al. Liraglutide versus sitagliptin for patients with
type 2 diabetes who did not have adequate glycaemic control with metformin: a
26-week, randomised, parallel-group, open-label trial. Lancet 2010;375(9724):
144756.
93. ClinicalTrials.gov. Available at: http://clinicaltrials.gov. Accessed July 28, 2014.
94. Inzucchi SE, Bergenstal RM, Buse JB, et al. Management of hyperglycemia in
type 2 diabetes: a patient-centered approach. Diabetes Care 2012;35:136479.
95. Garber AJ, Abrahamson MJ, Barzilay JI, et al. American Association of Clinical
Endocrinologists comprehensive diabetes management algorithm 2013
consensus statement. Endocr Pract 2013;19(Suppl 2):148.
96. Kirkman MS, Briscoe VJ, Clark N, et al. Diabetes in older adults: a consensus
report. J Am Geriatr Soc 2012;35(12):265064.
Sodium Glucose
Cotransporter 2 Inhibitors
John R. White Jr, PA-C, PharmD
KEYWORDS
Sodium glucose cotransporter 2 SGLT2 SGLT2 inhibitors Type 2 diabetes
Antihyperglycemic agents
KEY POINTS
Sodium glucose cotransporter 2 (SGLT2) inhibition offers a novel mechanism to mitigate
hyperglycemia in patients with diabetes.
SGLT2 inhibitors are generally associated with a reduction in hemoglobin A1c of between
0.5% and 1%.
The mechanism of action and efficacy of SGLT2 inhibitors are not linked to insulin and are
associated with an exceedingly low incidence of hypoglycemia when used independently
of exogenous insulin or secretagogues.
SGLT2 inhibitors are associated with an increased incidence of urinary tract and genital
infections but these infections are typically mild, responsive to treatment, and are not
use limiting.
INTRODUCTION
For much of the history of modern medicine the kidney has been thought of as primar-
ily an organ of elimination of waste materials and a regulator of ion balance.1 The
impact of the kidney on glucose homeostasis was for the most part unrecognized until
it was incorrectly implicated as the structural cause of diabetes in the late 1800s. It is
now known that the kidney plays other roles and is involved intimately in glucose
metabolism and homeostasis. Advances in the recognition of the role that the kidney
plays in glucose homeostasis and metabolism has over the past few decades fueled
an interest in modulation of these systems for therapeutic reasons. One area of partic-
ular interest has been the sodium glucose cotransporters (SGLTs). At present, several
medications for the management of type 2 diabetes are on the market that inhibit
SGLTs (specifically SGLT2).
This article reviews the role of the kidney in glucose regulation in nondiabetic and
diabetic patients. It also discusses the therapeutic modulation of SGLT for therapeutic
Disclosure: None.
Department of Pharmacotherapy, Washington State University, Health Sciences Building, Suite
210, PO Box 1459, Spokane, WA 99210, USA
E-mail address: [email protected]
reasons and specifically review the development of the SGLT2 inhibitors. Individual
SGLT2 inhibitors, their use in patients with renal disease, and drug-drug interactions
with these agents are discussed, as well as the overall potential benefits and adverse
effects.
The kidney has not always been thought of as one of the major organs responsible for
glucose homeostasis. However, the kidney plays a major role in glucose metabolism
and homeostasis via at least 3 processes: (1) gluconeogenesis, (2) glucose use, and (3)
glomerular filtration and reabsorption of glucose in the proximal convoluted tubules.2
In addition, there are significant perturbations in each of these key processes in pa-
tients who have diabetes.
Renal Gluconeogenesis
The endogenous production and release of glucose into the circulation occurs either
by gluconeogenesis (GNG) or glycogenolysis. In individuals who have fasted for
greater than 14 hours, about half of the endogenously produced glucose released
into the circulation comes from the production of glucose by the kidney or liver
(GNG) and about half comes from the breakdown of glycogen stores in the liver (glyco-
genolysis).2,3 It has also been suggested that the small intestines may play role in GNG
in some species.4 In humans, the liver and the kidney are the only organs that possess
sufficient quantities of glucose-6-phosphatase and other enzymes needed to drive
gluconeogenesis. The kidney is important in this regard because renal glucose pro-
duction accounts for about 20% to 25% of glucose released into the circulation after
a fast of 12 to 16 hours. The kidney is responsible for one-fifth of overall endogenous
glucose release and is responsible for approximately 40% of glucose released specif-
ically by gluconeogenesis.2,3
Endogenous glucose liberation is reduced by about 60% overall in the postprandial
state.5 Hepatic glycogenolysis is essentially extinguished several hours after a meal
and hepatic gluconeogenesis reduced by about 80%. In the postprandial state, renal
gluconeogenesis is increased by 100% and accounts for 60% of endogenous glucose
release. One theory suggests that this increase in postprandial renal gluconeogenesis
is directed toward building hepatic glycogen stores.
The role of gluconeogenesis as a factor in worsening hyperglycemia in patients with
both types 1 and 2 diabetes has been documented.3 Significant increases in renal gluco-
neogenesis have been shown in animal diabetes models and in human studies. Studies
in patients with type 1 and type 2 diabetes have shown that renal glucose release in-
creases in about the same proportion as hepatic glucose production does in these pa-
tients. In patients with type 2 diabetes an increase (compared with people with normal
glucose tolerance) in both fasting and postprandial gluconeogenesis has been shown.2
Fig. 1. Glucose reabsorption from glomerular filtrate through the proximal tubule epithelial
cell into the blood. GLUT, glucose transporter protein. (From Bakris GL, Fonseca V, Sharma K,
et al. Renal sodium-glucose transport: role in diabetes mellitus and potential clinical impli-
cations. Kidney Int 2009;75:1273; with permission.)
134 White Jr
gastrointestinal tract and in the S3 segment of the proximal tubule. Although SGLT1 ac-
counts for only about 10% of glucose reabsorption in the kidney it is the key transporter for
glucose absorption in the gastrointestinal tract. SGLT2 is a high-capacity, low-affinity
transporter found primarily in the kidney. It is the most prevalent and functionally important
SGLT transporter in the kidney and accounts for approximately 90% of glucose reabsorp-
tion. This transporter is found at a high density on the lumen (brush border) membrane of
the S1 segment of the proximal convoluted tubule (PCT).1 SGLT2 binds with glucose
and Na1 in the tubular filtrate and actively transports glucose across the membrane via
coupling with the transport of Na1. This process is driven by the electrochemical Na1
gradient between the tubular filtrate and the cell (secondary active transport).6
After glucose is transported via SGLT2 into the luminal epithelium it is then trans-
ported through the basolateral membrane and back into the peritubular capillary.
This process of facilitated diffusion of glucose depends on another family of glucose
transporter proteins (GLUTs).3 This basolateral membraneperitubular capillary trans-
fer uses GLUT1 transporters in the late proximal tubule and GLUT2 transporters in the
early proximal tubule.
One study evaluating the maximum rate of renal glucose reabsorption in insulin-
treated patients with diabetes reported that most of the patients with diabetes (10
of 12) had higher rates of glucose reabsorption than healthy subjects.10 One study
has also suggested that there is an increase in both expression and activity of
SGLT2 transporters in renal proximal tubular cells from patients with type 2 diabetes.11
Other SGLTs include SGLT3, SGLT4, SGLT5, and SGLT6.1 SGLT3 is found
throughout the body in skeletal muscle and the nervous system and is thought to
act as a glucose sensor. Other members of this family have been identified (SGLT4,
SGLT5, and SGLT6) but their function in humans is still being elucidated.
Several SGLT2 inhibitors are already on the market or are being developed. These
agents increase UGE by lowering the renal threshold for glucose excretion.8 There
are several reasons that make this approach appealing and several that may be cause
for concern. This increase in UGE is linked to a reduction in hyperglycemia, as is dis-
cussed later. Overall, the hemoglobin A1c (A1C) reduction (difference from placebo)
when used as monotherapy for the SGLT2 inhibitors was 0.79% (weighted mean dif-
ference) and when used as add-on therapy was 0.61% (weighted mean differ-
ence).12 This meta-analysis also reported that SGLT2 inhibitors had similar glycemic
efficacy compared with other antihyperglycemic agents. Unlike agents that stimulate
secretion of insulin or alter the sensitivity of insulin the effects of SGLT2 inhibitors are
independent of beta cell function and insulin resistance.2 Thus as beta cell function
and insulin resistance worsen over time, these agents are likely to continue to be effec-
tive, which would prove to be a benefit if verified in long-term studies. Studies have
shown continued efficacy for up to 104 weeks.8 These agents are also less likely to
be linked directly to hypoglycemia, in part because they do not completely block renal
glucose reabsorption. They inhibit reabsorption of 30% to 50% of filtered glucose.8
The reasons for this are not completely understood but it may be caused by a satura-
tion in the transport mechanism that delivers the medication to the active site. Very low
rates of hypoglycemia have been reported in clinical trials with SGLT2 inhibitors
except in patients receiving background insulin or sulfonylureas (SUs). A meta-
analysis reported that the odds ratio for hypoglycemia in patients treated with
SGLT2 inhibitors was 0.44 compared with other antihyperglycemic medications.12
SGLT2 Inhibitors 135
The SGLT2 inhibitors have also been linked to weight loss. The loss in weight has been
reported to be as much as 4.7 kg. Although the magnitude of weight loss varies
depending on the trial, a positive effect on weight (ie, loss) has been consistently
observed in multiple studies. In a trial with the thiazolidinedione (TZD) pioglitazone
(which is linked to weight gain), dapagliflozin was reported to attenuate this side ef-
fect.13 A study evaluating weight loss with SGLT2 inhibitors reported that about
66% of the weight loss linked to dapagliflozin was from fat (both visceral and subcu-
taneous fat).14 The beneficial implications of weight loss in this milieu that is rich in car-
diovascular disease and insulin resistance are obvious. Another potential positive
aspect of SGLT2 inhibition is a mild reduction in blood pressure. A range in reduction
of systolic blood pressure from 2 to 10 mm Hg has been reported in clinical trials with
these agents.8 A meta-analysis reported a weighted mean difference of 3.77 mm Hg
compared with placebo and 4.45 mm Hg in evaluation against active comparators.12
The primary adverse events associated with SGLT2 inhibitors are urinary tract infec-
tions (UTIs), vulvovaginitis, and balanitis. In addition, because of the mechanisms of
action of these agents, there was anticipation of and vigilance regarding their potential
for causing hypotension secondary to osmotic diuresis.
Side effects that have been encountered in patients with glucosuria include urinary
tract and other genital infections. These potential adverse events were anticipated
with the SGLT2 inhibitors and have been documented. UTIs have occurred at a higher
rate in patients treated with SGLT2 inhibitors in most studies.2,8,12,15,16 The incidence
of UTIs in patients treated with SGLT2s varied greatly across the published studies
and was similar to placebo in some.8 A meta-analysis of SGLT2 studies reported an
odds ratio of 1.34 for the development of UTIs in patients treated with SGLT2 inhibitors
versus placebo and an odds ratio of 1.42 in patients treated with SGLT2 inhibitors
versus other antihyperglycemic agents.12 Another study evaluated the overall rates
of UTIs reported in 12 randomized placebo controlled trials involving dapagliflozin.
The overall rates of UTIs in 3152 patients treated with dapagliflozin 2.5, 5, 10 mg, or
placebo were 3.6%, 5.7%, 4.3%, and 3.7% respectively.17 The overall rates of UTIs
in 2313 patients treated with canagliflozin 100 mg, 300 mg, or placebo were 5.9%,
4.3%, and 4% respectively.16 Across the SGLT2 inhibitors, women are linked to a
higher incidence of UTIs than are men.8 Genital infections (vulvovaginitis, balanitis,
and others) also occur at a higher rate in patients treated with SGLT2 inhibitors than
in those treated with placebo.2,8,12,15,16 A meta-analysis of SGLT2 inhibitors reported
an odds ratio of 3.5 for the development of genital infections in patients treated with
SGLT2 inhibitors versus placebo and an odds ratio of 5.06 for the development of gen-
ital infections in patients treated with SGLT2 inhibitors versus active comparators.12
The overall rates of genital infections in 3152 patients treated with dapagliflozin 2.5
mg, 5 mg, 10 mg, or placebo were 4.1%, 5.7%, 4.8%, and 0.9% respectively.18
The overall rates of genital infections in 2313 patients treated with canagliflozin 100
mg, 300 mg, or placebo were 10.4%, 11.4%, and 3.2% respectively in women and
4.2%, 3.7%, and 0.6% respectively in men.16 Overall, both UTIs and genital infections
were mild and rarely resulted in discontinuation of participation from trials.15,16
Volume depletion leading to hypotension has also been a concern with these med-
ications. Both package inserts from the currently marketed SGLT2 inhibitors contain
warnings about this potential adverse event and suggest care with patients at high
risk for side effects related to intravascular volume contraction.15,16 The greatest in-
crease in incidence of volume contractionrelated events occurred in patients 75
136 White Jr
years of age or older, in patients with reduced glomerular filtration rates (GFRs), and in
patients treated with loop diuretics.
Canagliflozin was approved by the US Food and Drug Administration (FDA) in March
2013 and was the first SGLT2 inhibitor to be approved in the United States.2 Canagli-
flozin is indicated as an adjunct to improve glycemic control in adult patients with type
2 diabetes.16 It has been studied in patients with type 2 diabetes as monotherapy, as
an add-on to metformin, in a comparison trial versus glimepiride as an add-on to met-
formin, as an add-on to sulfonylurea, as an add-on to sulfonylurea and metformin, in a
comparison trial versus sitagliptin, as an add-on to sulfonylurea and metformin, as an
add-on to metformin and pioglitazone, and as an add-on to insulin (with and without
other antihyperglycemic agents). The A1C levellowering results of some of those tri-
als are listed in Table 1.16 The baseline A1C in these trials varied but was approxi-
mately 8% in all of these phase III trials. In general, canagliflozin monotherapy as a
first-line pharmacotherapeutic agent lowered A1C levels approximately 1%
(compared with placebo), whereas the A1C level lowering encountered when canagli-
flozin was added to other agents was between 0.6% and 0.9% (compared with pla-
cebo). Its A1C level lowering was similar to that observed with glimepiride (added to
metformin) and greater ( 0.37% difference from sitagliptin) than that of sitagliptin
Table 1
A1C reduction: adjusted means
Data from INVOKANA-canagliflozin tablet, film coated [package insert]. Janssen Pharmaceuticals;
2014. Available at: https://www.invokanahcp.com/prescribing-information.pdf. Accessed June 19,
2014.
SGLT2 Inhibitors 137
(added to metformin and SU). It effectively lowered glycemic indices in all of the iter-
ations of combinations studied in phase III trials.
Dapagliflozin was approved by the FDA in January 2014 for use in adults with type 2
diabetes.2 This compound has been approved and in use in Europe since 2012. Dapa-
gliflozin is indicated for use as an adjunct to diet and exercise in the management of
type 2 diabetes. It has been studied as monotherapy and in combination with pioglita-
zone, metformin, glimepiride, sitagliptin (with or without metformin), and insulin (with or
without other antihyperglycemic therapy). In addition, it has been evaluated in a com-
parison with an SU, each added to metformin. A1C results from some of these studies
are presented in Table 2. The baseline A1C levels in these trials varied and ranged from
7.9 to 9.2 in the phase III trials. Dapagliflozin monotherapy as a first-line pharmacother-
apeutic agent lowered A1C levels by approximately 0.6% (compared with placebo),
whereas the A1C reduction encountered when dapagliflozin was added to other agents
ranged from 0.4% to 0.7% (compared with placebo or comparator). It effectively low-
ered glycemic indices in all of the iterations of combinations studied in phase III trials.
EMPAGLIFLOZIN
Table 2
A1C reduction: adjusted means
can reduce glomerular hyperfiltration.27 One study in 40 patients with type 1 diabetes
showed that empagliflozin was associated with a reduction in GFR in hyperfiltering pa-
tients but was associated with no change in GFR in normal-filtering patients.29 The in-
vestigators suggested that SGLT2 inhibition may be useful in the management of
diabetes-related renal disease. The SGLT2 inhibitors may be useful in this regard for
several reasons. First, as mentioned earlier, they are associated with a reduction in
glomerular hyperfiltration (similar to but via a different mechanism than angiotensin-
converting enzyme inhibitors). Second, they are typically associated with a modest
reduction in blood pressure. Third, by reducing the uptake of glucose they may protect
the proximal convoluted tubules.30 This line of investigation probably warrants more
clinical trials in order to evaluate the potential efficacy and safety of this approach.
SGLT2 inhibitors are likely to be frequently used with multiple other medications thus
the potential for drug-drug interactions (as with all medications) is present. The 3 most
salient SGLT2 inhibitors (canagliflozin, dapagliflozin, and empagliflozin) have been
evaluated for potential interactions with multiple medications. A review of this work
was recently published.31 These studies were in most cases performed on healthy vol-
unteers and evaluated the potential impact of interactions after the administration of a
single dose of an SGLT2 inhibitor. The exposure (as shown by concentration
maximum [Cmax] and area under the curve [AUC]) to each SGLT2 inhibitor tested
was not clinically significantly altered by the concomitant administration of cardiovas-
cular agents or antihyperglycemic medications commonly encountered in patients
with type 2 diabetes (ie, metformin, glimepiride, pioglitazone, sitagliptin, linagliptin,
voglibose, simvastatin, valsartan, ramipril, hydrochlorothiazide, torasemide, verap-
amil, warfarin; note that not all of these medications was evaluated with all three
SGLT2 inhibitors). In contrast, the SGLT2 inhibitors studied did not significantly affect
the pharmacokinetic parameters of the second drug studied. Dapagliflozin undergoes
its primary metabolism through the UGT1A9 pathway. Because of this, dapagliflozin
pharmacokinetics were evaluated with 2 potential UGT1A9 pathway modulators:
rifampicin, an inducer, and mefenamic acid, an inhibitor. Rifampin coadministration
with dapagliflozin resulted in a significant reduction in dapagliflozin exposure (AUC
reduction of 22%). Mefenamic acid coadministration with dapagliflozin resulted in a
significant increase in dapagliflozin exposure (AUC increase of 51%). Canagliflozin
was evaluated in combination with rifampicin (600 mg/d for 8 days). Canagliflozin
exposure was significantly reduced (AUC reduction, 51%; Cmax reduction, 28%) after
exposure to rifampin. Canagliflozin was shown to increase the AUC (20%) and the
Cmax (36%) of digoxin when the two were coadministered.16
In general, the SGLT2 inhibitors seem to be subject to clinically significant interac-
tions (except for canagliflozin and digoxin) with commonly used medications. How-
ever, care should be taken when coadministering these agents with modulators of
UGT1A9. Upper-dose adjustment of the SGLT2 inhibitors dapagliflozin and canagliflo-
zin may be needed if the patient is also treated with UGT1A9 inducers such as
rifampin, phenytoin, phenobarbital, or ritonavir. It is unclear at this time whether or
not UGT is involved in the metabolism of empagliflozin.
As with all new antihyperglycemic medications the FDA is requiring that SGLT2 inhib-
itors undergo cardiovascular outcomes trials. Dapagliflozin is being evaluated in the
140 White Jr
In addition to the SGLT2 inhibitors mentioned earlier, several others are in develop-
ment. Ipragliflozin and ertugliflozin are currently in phase III trials.34 Three so far un-
named compounds (LX 4211, EGT0001442, GW 869682) are in phase II trials and 1
compound (ISIS 388626) is in phase 1 of development. LX 4211 is a novel agent
that inhibits both SGLT1 and SGLT2.2 Its dual mechanism, inhibition of small intestine
glucose absorption and/or glucose reabsorption in the kidney, may offer benefits to
SGLT2 inhibition if it is well tolerated. Studies thus far have suggested that it is well
tolerated.36,37
SUMMARY
associated with a reduction in A1C of between 0.5% and 1%. SGLT2 inhibitors are
associated with an increased incidence of urinary tract and genital infections but these
infections are typically mild, responsive to treatment, and are not use limiting.
REFERENCES
KEYWORDS
Insulin Diabetes Glucose monitoring Hypoglycemia Carbohydrate counting
KEY POINTS
Intensive glucose control reduces microvascular and cardiovascular complications in
those with type 1 diabetes.
Management of type 1 diabetes requires a combination of basal and bolus insulin, admin-
istered either by injection or by continuous insulin infusion.
Adequate glucose control requires education around the relationship between insulin, ac-
tivity, food, and blood glucose levels.
An interdisciplinary team keeps patients motivated and engaged and provides the great-
est likelihood of attaining optimal glucose control.
INTRODUCTION
Multiple factors underlie the increasing importance for primary care physicians to
expand their knowledge and skills in managing patients with type 1 diabetes mellitus.
First, The National Health and Nutrition Examination Survey (NHANES) estimates that
type 1 and type 2 diabetes now affects 21 million people in the United States; this
number represents an increase in diabetes prevalence from 6.2% to 9.9% between
the periods of 1988 to 1994 and 2005 to 2010 respectively.1 The incidence of type
1 diabetes was estimated to be 40% higher in 2010 compared with 1997.2 Because
of the anticipated workforce shortage of endocrinologists, primary care physicians,
who already manage nearly 40% of patients with type 1 diabetes in the United States,3
will fill an expanded role both in initial diagnosis and care and in long-term prevention
and management of diabetic complications.
Another factor important in primary care relates to the understanding of dosing of
insulin in type 1 diabetes in light of the increasing complexity of insulin and delivery
mechanisms. As an autoimmune disorder, type 1 diabetes destroys pancreatic beta
cells, which causes children to present typically with complete beta cell failure and
acute, severe hyperglycemia. In contrast, individuals with type 1 diabetes who present
Providence Medical Group NE-Medical Education, 5050 Northeast Hoyt, Suite 540, Portland, OR
97213, USA; Department of Internal Medicine, Oregon Health and Sciences University, Port-
land, OR, USA
E-mail address: [email protected]
in adulthood often follow a smoldering course with adequate glucose control main-
tained if physicians can carefully adjust low-dose insulin regimens. Eventually, howev-
er, complete insulin deficiency requires insulin replacement therapy with the twin goals
of normalizing blood glucose levels while avoiding hypoglycemic episodes. The Dia-
betes Complications and Control Trial (DCCT) underscored the critical importance
of precise insulin dosing to achieve these goals.4 The study randomized subjects
with type 1 diabetes to intensive control (target A1c 7%) or conventional treatment
(target A1c 9%). After 6.5 years, the intensive therapy group had a reduced relative
risk of diabetic retinopathy of 76%; for nephropathy, the same group had a reduced
relative risk of 56%, and for neuropathy, it was 69%.5 Long-term follow up of these
subjects for an additional 11 years reported in the Epidemiology of Diabetes Interven-
tions and Complications (EDIC) trial found that intensive therapy during the initial
6.5 years resulted in a long-term 42% risk reduction for any cardiovascular event
and a 57% risk reduction of nonfatal myocardial infarction, stroke, or death from car-
diovascular disease.6 Unfortunately, these gains need to be balanced against the risk
of hypoglycemia, which is a critical limiting factor in attaining tight glucose control in
those with type 1 diabetes. Although the benefits of the DCCT were impressive, it is
important to note that participants were relatively new to the diagnosis of diabetes.
Severe hypoglycemia leading to seizure and loss of consciousness is strongly associ-
ated with diabetes duration7 and necessitates less stringent glycemic targets in those
with limited symptoms of hypoglycemia, especially if diabetes has been present for
over 20 years.
The insulin regimens used in the DCCT and EDIC studies require primary care phy-
sicians to understand how to replicate normal insulin secretory patterns using multiple
daily injections (MDI) or insulin pumps. Although these approaches are variably termed
basalbolus therapy, intensive insulin therapy (IIT), and physiologic insulin therapy,
they share a common goal of dosing insulin based on glucose levels and food intake
in addition to other variables, such as activity, stress, and absorption of insulin.
Although seemingly complex, primary care physicians can master these advanced
regimens in order to normalize glucose levels while avoiding hypoglycemia.
MANAGEMENT FRAMEWORK
INSULIN THERAPY
insulin deficiency. Early in the disease, patients may require total daily doses (TDD)
of only .2 to .4 U/kg/d of insulin, to supplement partially impaired insulin secretion.
The longer patients remain able to secrete endogenous insulin, the less subject
they are to hypoglycemic episodes and the development of retinopathy.8 Time to
complete loss of insulin secretion varies. When it occurs, patients require a TDD
.5 to 1.0 U/kg/d.9 To mimic physiologic insulin secretion, both long- and short-
acting insulins are used. Long-acting insulin suppresses glucose output from the
liver overnight and provides basal insulin between meals; bolus doses of short-
acting insulin modulate glucose excursions associated with carbohydrate con-
sumption. See Table 1 and Fig. 1 for a description of currently available basal
and bolus insulins and their action profiles.
Basal Insulin
The availability of multiple basal insulin formulations with varied pharmacokinetic fea-
tures requires a clear understanding of their use to allow safe and effective glucose con-
trol. Although lente and ultralente were previously mainstays of therapy, they are no
longer manufactured because of variable absorption and glucose effects, and the
advent of more effective basal insulins. Available since 1946,10 neutral protamine Hage-
dorn (NPH) remains in use, although primarily for those with type 2 diabetes. As an
intermediate-acting insulin with a peak effect 6 to 10 hours after injection, NPH serves
as both bolus and basal insulin. Morning NPH injections affect breakfast and lunchtime
glucose levels and glucose release between meals. Evening injections provide over-
night basal control, with bedtime administration reducing the risk of nocturnal hypogly-
cemia, as well as hyperglycemia associated with the dawn phenomenon.11,12 Many
challenges exist with NPH, including midday hypoglycemia if lunch is delayed, hyper-
glycemia with excessive ingestion of carbohydrate at mid-day, and predinner hypergly-
cemia due to the waning effect of morning NPH injection. Despite these limitations, NPH
remains an acceptable alternative for patients who cannot afford newer insulin analogs.
The introduction to the United States in 2001 of glargine as a basal insulin provided a
more stable and physiologic insulin effect as compared with NPH. The onset of action
occurs 2 to 3 hours after injection, but glargine is notable for not having a peak effect,
thereby reducing risk of nocturnal hypoglycemia, especially when dosed at bedtime.
Table 1
Currently available insulin options
Cost-Pens
Onset Peak Duration Costa-Vial (10 mL) (5 Pens/15 mL)
Basal insulin options
NPH 12 h 410 h 1016 h $100 ($25 at $330
Walmart)
Detemir 24 h No peak 1420 h $203 $318
Glargine 24 h No peak 2024 h $207 $337
Bolus insulin options
Regular 3060 min 24 h 48 h $100 ($25 at N/A
Walmart)
Aspart, glulisine, 515 min 12 h 35 h $180 $340
lispro
a
Costs are approximate from Costco.com and GoodRx.com.
Courtesy of Jonathan R. White, PharmD, BCPS, BCACP, Clinical Pharmacy Specialist, Providence
Medical Group.
148 Stephens
Fig. 1. Action profiles of insulins. (From Inzucchi SE, Bergenstal RM, Buse JB, et al. Manage-
ment of hyperglycemia in type 2 diabetes: A patient-centered approach. Diabetes Care
2012;35:136479 [data supplement]; with permission.)
Compared with NPH, studies of subjects with type 1 diabetes note decreased
frequency of hypoglycemia and less weight gain with glargine1316 but similar effects
on A1c.13 Insulin glargines peakless profile provides a cleaner basal effect, which prob-
ably limits weight gain by decreasing a need for snacking between meals and at
bedtime, which is needed in response to the relative hyperinsulinemia from NPH.
Insulin detemir is the second available long-acting insulin analog, which also re-
duces hypoglycemia risk compared with NPH.17 Acylated with a fatty acid chain, in-
sulin detemir binds to albumin, prolonging its effect compared with other analogs,18
while also leading to weaker effects on glucose and lipid metabolism compared
with glargine.19 The binding of detemir leads to a shorter effect and higher dosing
requirements; some patients may need twice-daily administration.20
Bolus Insulin
Many options exist for bolus insulin. Regular insulin has been a mainstay for decades
but has significant limitations. Hampered by its tendency to self-associate into hex-
amers after injection, regular insulin diffuses slowly into the circulation,21 necessi-
tating injections 20 to 30 minutes before meals in order to match insulin action to
carbohydrate absorption. In real life, this 30-minute lag time is inconvenient for pa-
tients who do not adhere to consistent mealtimes, which is the reality for 30% to
70% of patients.22,23
Consequently, the rapid-acting insulin analogs, which include insulins lispro, aspart,
and glulisine, are generally preferred in type 1 diabetes. These insulins, by virtue of
their amino acid structural changes, remain monomeric following injection, giving
them a more rapid onset of effect that allows their injection 10 to 15 minutes before,
during, or immediately after meals.21 One meta-analysis of 1400 patients demon-
strated that insulin lispro reduces the frequency of severe hypoglycemic events by
25% compared with regular insulin.24 Insulins lispro and aspart also provide better
control of postprandial hyperglycemia and glucose variability compared with regular
insulin.21 Interestingly, despite these improvements in convenience and glucose con-
trol, meta-analyses have reported only a small benefit in A1c with use of rapid-acting
insulin analogs.25
Insulin Therapy in Type 1 Diabetes 149
Dosing Regimens
Determination of initial insulin doses for a newly diagnosed patient with type 1 dia-
betes starts with estimation of the TDD, provided as 50% basal and 50% bolus in-
sulin.26 Initially, most patients require low doses of .2 to .4 U/kg/d, which increase
over time as endogenous insulin secretion declines so that ultimately doses of .5
to 1.0 U/kg/d comprise the average TDD. Basal insulin with insulin glargine or dete-
mir is dosed once or twice daily. Previously administered at night to better match
glucose elevations with the dawn phenomenon, recent studies note that basal dosing
can be equally effective when given either in the morning, evening, or as a split
dose,27 providing flexibility of dosing and promoting adherence. For insulin-
sensitive patients, splitting basal insulin into twice-daily dosing may reduce the risk
of hypoglycemia that could occur with a single larger dose. When transitioning
from NPH to a long-acting analog, decreasing the basal dose by 20% to reduce
the risk of hypoglycemia is worth considering.3 Physicians must remind patients
that the long-acting analogs cannot be mixed with other bolus insulins.
Many alternative strategies exist for determining bolus insulin doses. One option is
carbohydrate counting, which is the most physiologic approach. Using this method,
individuals are taught how to estimate carbohydrate content in certain foods by either
reading labels or measuring. Estimation of a carbohydrate ratio is the next step, where
insulin is taken for a certain number of carbohydrate grams. A typical algorithm uses a
factor of 1 U of insulin for every 15 g of carbohydrate consumed, with the patient then
dividing the total amount of carbohydrate in a meal by the factor to determine the dose
of insulin. Dosing insulin in this manner provides flexibility to meet variation in meal
timing and content and has been shown to reduce A1c by 0.7%, and the frequency
of severe hypoglycemic events.28 For patients who find this strategy too complex,
an alternative approach is to maintain a consistent carbohydrate diet and match the
meal insulin dose to the carbohydrate consumed. This method has also been shown
to improve glucose control.29
Patients should also receive education around on how to add an extra amount of
bolus insulin to their calculated premeal insulin doses in response to elevated blood
glucose levels measured before meals or snacks. Commonly this extra dose, called
supplemental or correctional insulin, is a ratio of 1 U for every 50 mg/dL. Effective
use of supplemental insulin also requires a targeted premeal glucose goal, which is
often set at 100 mg/dL. See Table 2 for an example of dosing insulin using these
factors.
Patients should also receive education in avoiding insulin stacking, which is the
administration of any insulin doses at too short of intervals in response to between
meal elevations in blood glucose.26 Generally, glucose levels increase 30 to 50 mg/dL
above the premeal level in the 2 hours after eating if the insulin dose is correct for the
meal. When the measured glucose between meals is higher than anticipated, patients
may incorrectly administer a full dose of supplemental insulin calculated by the desired
reduction in blood glucose. Because the insulin administered before the meal has a
duration of action of 4 to 6 hours, this supplement after the meal may stack onto the re-
sidual premeal insulin dose, causing hypoglycemia. Patients may reduce this risk by
decreasing the calculated correctional insulin dose by 50% when it is administered
less than 3 hours after the premeal bolus dose.3 Table 2 includes an example of this
adjustment for review.
Exercise presents a special challenge in type 1 diabetes, because strenuous activity
during severe insulin deficiency can cause hyperglycemia due to release of counter-
regulatory hormones, as well as delayed hypoglycemia due to increased insulin
150 Stephens
Table 2
Examples of insulin dosing calculations
sensitivity in the hours after activity.30 Because patients are encouraged to exercise
for better glucose control, they may become frustrated by these exercise-related
glucose excursions. Weight loss can also be a struggle due to more frequent hypogly-
cemia following exercise. Adjustments in meal insulin can be helpful, with 1 option be-
ing a decrease in the premeal dose by 50% to 75% if the exercise occurs in the 1 to
3 hours after a meal. No adjustment may be necessary if the activity is later in the post-
prandial period.31,32
with MDI, and also resulted in a 10% to 20% reduction in insulin doses.34,36 Hypogly-
cemia frequency is reduced with CSII,37 likely because of more consistent insulin ab-
sorption from infusion sites compared with MDI,38 as well as the ability to deliver more
accurate, small insulin doses for insulin-sensitive patients. Pumps may also better
match insulin dosing with changing schedules, activity, and mealtimes.38 A 2010
Cochrane review noted that CSII showed improvements in quality of life, overall health,
and satisfaction compared with MDI.39 A review of indications for pump therapy is
listed in Box 1.
Before making the transition to a pump, patient expectations need clarification.
Blood glucose monitoring still needs to occur, and patients need to carry supplies
in the event of pump malfunction. Concerns regarding an increased risk for diabetic
ketoacidosis with pump diminish with appropriate patient education. Infusion site in-
fections are uncommon with adequate site preparation.40 Cost of insulin pump ther-
apy represents is a prominent limitation, with current insulin pumps costing $5000
to $7000, and pump supplies costing up to $2500 per year.34 Despite this, compared
with MDI, CSII has been shown to be a cost-effective option.
Box 1
Indications for insulin pump therapy in type 1 diabetes
1. Persistent elevation in A1c despite adjustments in MDI and ongoing patient education
2. Continued hypoglycemia despite adjustments in MDI and ongoing patient education
3. Significant insulin sensitivity, where .5 to 1 U dosing amounts often result in significant
glucose excursions/hypoglycemia
4. To get to glucose/A1c goal in those attempting pregnancy, who are unable with MDI
152 Stephens
is provided about food choices, reduction in hypoglycemia frequency, and use of in-
sulin analogs such as insulin detemir, which has been associated with slightly less
weight gain.16
Diabetic retinopathy may progress after rapid correction of hyperglycemia, with the
greatest risk seen in those with A1c greater 10% when there is underlying retinopathy.
To prevent deterioration of retinopathy, a gradual correction in A1c by 2% per year
and twice-yearly evaluation by an ophthalmologist to monitor for changes should be
considered.3
MONITORING
Monitoring allows patients to achieve their glucose goals. The American Diabetes As-
sociation (ADA) recommends that individuals on MDI or CSII consider monitoring
glucose levels before meals and snacks, occasionally postprandially, at bedtime, prior
to exercise, in response to suspected hypoglycemia, and prior to tasks such as
driving.44 Adherence to these recommendations may require monitoring glucose
levels up to 6 to 10 times per day. To ensure the value of this time-consuming and
expensive effort, patients need to know how to respond to the glucose data. The
ADA guidelines recommend a preprandial glucose goal of 70 to 130 mg/dL, and a
glucose goal 1 to 2 hours after a meal of less than 180 mg/dL. Controversy exists how-
ever, regarding postprandial monitoring. Although postprandial hyperglycemia is
associated with endothelial dysfunction, which is a surrogate marker for vascular dis-
ease,45 glucose corrections with supplemental insulin after meals often lead to hypo-
glycemia. Encouraging patients to eat more complex carbohydrates may reduce the
postprandial hyperglycemia associated with eating simple starches. Also, patients
should consider postprandial glucose monitoring when they are uncertain about the
carbohydrate amount in a meal, and administer supplemental insulin cautiously.
Variability of glucose levels can be identified and managed more efficiently with the
use of CGM. CGM includes a sensor that is inserted subcutaneously to measure inter-
stitial glucose levels every 5 minutes and transmits the data either to a separate
receiver or insulin pump. These data are available to the user, who can anticipate
changes missed with traditional SMBG, and respond to set alarms when glucose
levels rise above or drop below preset targets. Studies comparing these devices
with SMBG report variable results, with A1c improvements of .53% shown in 1
study,46 and a small, but significant reduction of A1c by .26% without reductions in
hypoglycemia frequency in another meta-analysis.47 Currently a CGM-augmented
pump is available, bringing a closed-loop system closer. This device will suspend in-
sulin delivery for up to 2 hours, when persistent hypoglycemia occurs. Use of these
augmented pumps has been shown to be effective in reducing the duration and fre-
quency of severe hypoglycemia.48,49
Finally, in regards to monitoring, the A1c should be measured 2 to 4 times per year
depending on patient status, glucose levels, and changes in therapy. A goal of less
than 7% is recommended for most patients with type 1 diabetes given the findings
from the DCCT and EDIC that showed reductions in complications with this level of
control.6 A higher A1c target for patients with frequent hypoglycemia and longer dura-
tion of diabetes should be considered.7
A diabetes team assists in the management of patients with type 1 diabetes. Ideally
the team should include a provider with experience in IIT, a dietitian to provide educa-
tion around carbohydrate counting, and a mental health provider to identify and
Insulin Therapy in Type 1 Diabetes 153
SUMMARY
Although not curable, type 1 diabetes is eminently controllable. IIT, as guided by the
results of landmark studies such as the DCCT, provides primary care providers with
a blueprint for reducing the frequency of the devastating complications of diabetes
that were all too common in the recent past. Considering the remarkable advances
in contemporary therapy, including MDI and CSII, the likelihood of even greater future
improvements in quality of life and survivability can be anticipated. Success requires
patient engagement and education, an informed primary care provider, and an inter-
disciplinary team to maximize the benefits of insulin therapy and avoid the risks of
hypoglycemia.
REFERENCES
and improve control. A randomized, controlled trial. Ann Intern Med 2002;
136(7):50414.
12. Pampanelli S. Long-term intensive insulin therapy in IDDM: effects on HbA1c,
risk for severe and mild hypoglycaemia, status of counterregulation and aware-
ness of hypoglycaemia. Diabetologia 1996;39(6):67786.
13. Ratner RE. Less hypoglycemia with insulin glargine in intensive insulin therapy
for type 1 diabetes. U.S. Study Group of Insulin Glargine in Type 1 Diabetes.
Diabetes Care 2000;23(5):63943.
14. Vague P. Insulin detemir is associated with more predictable glycemic control
and reduced risk of hypoglycemia than NPH insulin in patients with type 1 dia-
betes on a basal-bolus regimen with premeal insulin aspart. Diabetes Care
2003;26(3):5906.
15. Rosenstock J. Basal insulin therapy in type 2 diabetes: 28-week comparison of in-
sulin glargine (HOE 901) and NPH insulin. Diabetes Care 2001;24(4):6316.
16. De Leeuw I. Insulin detemir used in basal-bolus therapy in people with type 1
diabetes is associated with a lower risk of nocturnal hypoglycaemia and less
weight gain over 12 months in comparison to NPH insulin. Diabetes Obes Metab
2005;7(1):7382.
17. Owens DR, Bolli GB. Beyond the era of NPH insulinlong-acting insulin analogs:
chemistry, comparative pharmacology, and clinical application. Diabetes Tech-
nol Ther 2008;10(5):33349.
18. Havelund S. The mechanism of protraction of insulin detemir, a long-acting,
acylated analog of human insulin. Pharm Res 2004;21(8):1498504.
19. Porcellati F. Comparison of pharmacokinetics and dynamics of the long-acting
insulin analogs glargine and detemir at steady state in type 1 diabetes: a
double-blind, randomized, crossover study. Diabetes Care 2007;30(10):
244752.
20. Heller S, Koenen C, Bode B. Comparison of insulin detemir and insulin glargine
in a basalbolus regimen, with insulin aspart as the mealtime insulin, in patients
with type 1 diabetes: a 52-week, multinational, randomized, open-label, parallel-
group, treat-to-target noninferiority trial. Clin Ther 2009;31(10):208697.
21. Hirsch IB. Insulin analogues. N Engl J Med 2005;352(2):17483.
22. Lean ME, Ng LL, Tennison BR. Interval between insulin injection and eating in
relation to blood glucose control in adult diabetics. Br Med J (Clin Res Ed)
1985;290(6462):1058.
23. Sackey AH, Jefferson IG. Interval between insulin injection and breakfast in dia-
betes. Arch Dis Child 1994;71(3):24850.
24. Brunelle BL. Meta-analysis of the effect of insulin lispro on severe hypoglycemia
in patients with type 1 diabetes. Diabetes Care 1998;21(10):172631.
25. Siebenhofer A. Short acting insulin analogues versus regular human insulin in pa-
tients with diabetes mellitus. Cochrane Database Syst Rev 2006;(2):CD003287.
26. DeWitt DE, Dugdale DC. Using new insulin strategies in the outpatient treatment
of diabetes: clinical applications. JAMA 2003;289(17):22659.
27. Garg SK. Improved glycemic control without an increase in severe hypoglyce-
mic episodes in intensively treated patients with type 1 diabetes receiving morn-
ing, evening, or split dose insulin glargine. Diabetes Res Clin Pract 2004;66(1):
4956.
28. Samann A. Glycaemic control and severe hypoglycaemia following training in
flexible, intensive insulin therapy to enable dietary freedom in people with
type 1 diabetes: a prospective implementation study. Diabetologia 2005;
48(10):196570.
Insulin Therapy in Type 1 Diabetes 155
KEYWORDS
Type 2 diabetes Insulin secretion Exogenous insulin profiles
Insulin administration Insulin adjustment Noninsulin therapy
KEY POINTS
Type 2 diabetes is a multifactorial disease comprising insulin resistance, relative insulin
deficiency, increased hepatic glucose output, and increased renal glucose reabsorption,
which together result in failure to maintain normal glucose homeostasis.
Therapeutic interventions for Type 2 diabetes include lifestyle modifications, noninsulin
drugs, and insulin therapy.
Although insulin can be used as stand-alone therapy, it is more commonly used as add-on
to other noninsulin agents.
Insulin treatment in Type 2 diabetes is generally instituted with basal insulin alone and
intensified to basal plus bolus insulin regimens if glycemic goals are not achieved.
Self-monitored blood glucose (SMBG) testing is critical in guiding the titration of insulin
treatment.
The addition of newer noninsulin drugs to previous insulin treatment may allow for partial
or complete reduction of the insulin.
Patient education by a multidisciplinary treatment team that includes diabetes educators is
helpful in maximizing efficacy and minimizing adverse events related to the use of insulin.
INTRODUCTION
Disclosures: Past speaker for Astra Zeneca, Boehringer Ingelheim, Eli Lilly, Merck, Janssen
(R. Juneja); Nothing to disclose (F. Meah).
Division of Endocrinology, Indiana University School of Medicine, 541 Clinical Drive, CL 365,
Indianapolis, IN 46202, USA
* Corresponding author.
E-mail address: [email protected]
resulting in decreased postprandial insulin release by the beta (b) cells accompanied
by a failure to suppress glucagon by the alpha (a) cells, resulting in postprandial hyper-
glycemia and continued release of glucose from hepatic glycogen stores (glycogenol-
ysis).1 Furthermore, there is increased renal tubular reabsorption of glucose due to
upregulation of sodium glucose co-transporters-2 (SGLTs-2) and a b-cell deficiency
secondary to a decrease in its numbers, mass, and function.1,2 All these factors
together increase the workload of the b cell, which can, over time, lead to its exhaus-
tion, implying that insulin therapy might be an inevitable consequence of long-
standing T2D.35
Therapy with insulin, however, has challenges, because unlike most other drugs, it
needs to be dosed in synergy with the peaks and troughs of glucose. Commercially
available insulin, however, does not share the physiologic properties of endogenous
insulin. It is therefore important to understand the pharmacokinetic properties of insu-
lin preparations and to time the dose of the insulin to meet the needs of the patient. In
this article, we discuss strategies of how to introduce insulin as a treatment option in
patients with T2D and how to decrease it when other noninsulin drugs are added to the
treatment.
Fig. 2. Endogenous glucose production of the nondiabetic and the diabetic individual.
Compared with nondiabetic individuals who produce glucose at a rate of 2.0 mg/kg/min, he-
patic glucose output in diabetic individuals is increased to a rate of 2.5 mg/kg/min. In addi-
tion, in response to an oral glucose load, diabetic individuals experience a greater rise in
glucose related to insufficient insulin production. B, breakfast; L, lunch; S, supper/dinner;
HS, bedtime.
Fig. 3. Endogenous insulin production of the nondiabetic and the diabetic individual. Pul-
satile endogenous insulin production in the nondiabetic individual (gray shaded areas)
closely maintains euglycemia during and between meals. In the diabetic individual (black
lines), FPG is elevated, as there is insufficient basal insulin production by the pancreatic b
cell. In addition, there is insufficient mealtime insulin production due to a blunted FPIR
and incretin hormone defects. B, breakfast; L, lunch; S, supper/dinner; HS, bedtime.
4 Meah & Juneja
Fig. 4. The first and second phases of insulin secretion. Insulin (D) is packaged in membrane-
bound insulin secretory granules in the pancreatic b cell. (A, B) The steep first-phase insulin
response reflects the immediate discharge of primed and docked insulin from secretory ves-
icles due to direct stimulation by glucose and indirectly through intestinal incretin hor-
mones. The second phase of insulin release is gradual and requires mobilization of insulin
secretory granules to the cell membrane before their discharge (C).
glucose production.9 This explains why high doses of exogenous insulin are often
required in patients with insulin resistance.
Fig. 5. Insulin sensitivity and insulin secretion. At any given insulin sensitivity, the residual
capacity of the b cell can be measured by exposing it to an intravenous glucose challenge
called the Acute Insulin Response to Glucose (AIRglucose). If the AIRglucose decreases
with increasing insulin resistance, patients progress from normal glucose tolerance to
impaired glucose tolerance, and eventually T2D. Patients who can maintain adequate
b-cell secretion, such as those with polycystic ovarian syndrome, might not progress to hy-
perglycemia despite substantial insulin resistance. (From Kahn SE. The relative contributions
of insulin resistance and beta-cell dysfunction to the pathophysiology of Type 2 diabetes.
Diabetologia 2003;46(1):7; with permission.)
Before one can initiate insulin (or any drug therapy) in a patient with diabetes, it is crit-
ical that goals of treatment are established. The first of these goals is the trigger for
initiation of a new drug. The second goal is to set parameters under which therapy
needs to be advanced either with the same drug or with the addition of new agents.
The trigger to initiate drug therapy can be either the hemoglobin A1c (HbA1c) or self-
monitored blood glucose values (SMBG). In general, it is easiest to use HbA1c as the
trigger for initiation of therapy; a parameter used by most guidelines. SMBG can then
be used to modify the initiated therapy.
The most commonly used guidelines for the treatment of T2D used in the United
States come from the American Diabetes Association (ADA) (Fig. 6)14 and the Amer-
ican Association of Clinical Endocrinologists (AACE) (Fig. 7).15 The ADA guidelines
recommend a target HbA1c of 7.0% or lower in most patients. More stringent
HbA1c targets of 6.0% to 6.5% are recommended in patients with short disease dura-
tion, long life expectancy, and no significant history of cardiovascular disease;
provided these goals can be achieved without adverse effects (particularly hypoglyce-
mia). Less-stringent HbA1c targets of 7.5% to 8.0% are recommended in patients with
long disease duration, short life expectancy, history of severe hypoglycemia,
advanced complications, extensive comorbid conditions, and in patients difficult to
control despite intensive education (see Fig. 6). With these guidelines, following met-
formin (MET) monotherapy as first line, the addition of a second drug is recommended
if HbA1c is not at goal after 3 months. Importantly, besides HbA1c-lowering ability, the
ADA guidelines recommend consideration to cost, effect on weight, hypoglycemia
risk, and potential for side effects when making the choice of second agent, with basal
6 Meah & Juneja
Fig. 6. The ADA treatment algorithm for T2D. These guidelines recommend MET monother-
apy followed by addition of agents every 3 months if HbA1c is not at goal. Basal insulin can
be used as a second-line agent. The guidelines recommend taking into consideration effi-
cacy, hypoglycemia risk, effect on weight, side-effect profile, and cost when making a choice
of drug. (From the American Diabetes Association. Standards of medical care in diabetes
2014. Diabetes Care 2014;37(Suppl 1):S14; with permission.)
insulin being one of the choices (see Fig. 6). After 3 to 6 months of a 2-drug regimen, if
HbA1c targets are still not achieved, the guidelines recommend addition of a third
noninsulin agent or intensification of insulin therapy if already initiated.14
The AACE treatment algorithm also uses HbA1c as a guide to therapy; however,
they recommend a more stringent goal of 6.5% or lower for most patients. In addition,
these guidelines use baseline HbA1c itself as the trigger for choosing the number of
drugs with which to start therapy (see Fig. 7). With the AACE guidelines, for patients
with baseline HbA1c less than 7.5%, monotherapy with any of the approved noninsu-
lin agents is considered appropriate. For patients with baseline HbA1c between 7.5%
and 9.0%, these guidelines recommend a 2-drug approach with MET plus another
agent from a different class, including basal insulin. For patients with a baseline
HbA1c higher than 9.0%, the AACE guidelines recommend initiating therapy with an
aggressive 2-drug or in some cases even a 3-drug approach, and in severely symp-
tomatic patients they recommend having insulin be one of these agents. Once treat-
ment is initiated, these guidelines go on to recommend an aggressive 3-monthly
up-titration of therapy with the addition of additional drugs if HbA1c targets of 6.5%
or lower are not achieved.15
Our own approach is a hybrid of the ADA and AACE guidelines. As initial therapy, we
prefer a MET Plus approach; maximizing MET over a period of 1 month to 2000 mg per
day or the maximum tolerated dose followed by the addition of a second noninsulin
agent in 1 to 3 months irrespective of HbA1c. If MET is contraindicated or not tolerated,
Insulin Tactics in Type 2 Diabetes 7
Fig. 7. The AACE treatment algorithm for T2D. These guidelines make recommendations on
the choice and number of agents based on baseline HbA1c. (From American Association of
Clinical Endocrinologists. Garber AJ, Abrahamson MJ, Barzilay JI, et al. AACE comprehensive
diabetes management algorithm. Endocr Pract 2013;19:6; with permission.)
we use one of the other noninsulin oral agents from the AACE guidelines as first line.15
We use this approach to address the multiple pathophysiological defects of T2D1
because we have found that single-drug approaches generally fail to maintain HbA1c
over time similar to what has been observed in the UK Prospective Diabetes Study
and A Diabetes Outcome Progression Trial (ADOPT) Study.16,17 Our choice of second
drug is based on the criteria of cost, hypoglycemia risk, weight-losing properties, and
side-effect profiles as proposed by the ADA (Fig. 8).14 If a 2-drug regimen is ineffective
in maintaining HbA1c, a third drug from a different class can be added. We, however,
wait 6 to 12 months before proceeding from a 2-drug to a 3-drug regimen. Waiting
for this period is particularly helpful when using agents that can result in weight loss;
therapies that have the potential to continue to modify the diabetes disease process
by reducing insulin resistance. In addition, it can take up to 6 months or longer for a
newly diagnosed patient to truly affect lifestyle changes, which may also alter the
need for additional medications. Unless there is severe and symptomatic hyperglyce-
mia, we try different combinations of noninsulin agents for a period of 12 to 24 months
before considering insulin. We initiate insulin therapy earlier if weight loss has stabilized
but hyperglycemia persists or if weight loss continues in the setting of sustained hyper-
glycemia, indicating an insulin-deficient, catabolic state. We also consider insulin as a
treatment option at the time of diagnosis of T2D for those patients who have severe
symptoms of polyuria and polydipsia and especially those with excessive weight
loss. In these individuals and in patients who do not manifest the typical features of
metabolic syndrome, such as low high-density lipoprotein levels, high triglycerides,
or hypertension, it may be appropriate to test for immune markers of Type 1 diabetes,
8 Meah & Juneja
such as Glutamic Acid Decarboxylase (GAD) antibodies, to rule out the possibility of
Latent Autoimmune Diabetes of the Adult (LADA), a condition not typically prone to
ketoacidosis that can be managed initially with noninsulin therapy but may, in 6 to
12 months after diagnosis, require insulin to maintain glycemic goals.18,19
Although HbA1c is typically measured every 90 days, it can be checked every 30 days
in the early stages of therapy to monitor response. However, once insulin (or any non-
insulin therapy) has been initiated, we find SMBG to be most helpful in guiding titration.
Particularly in the early stages of insulin therapy, it is helpful for patients to monitor
glucose fasting, before meals, and at bedtime to gauge an understanding of glycemic
control. The ADA guidelines recommend a goal fasting plasma glucose (FPG) of less
than 130 mg/dL and 2-hour post-prandial glucose (2h-PPG) less than 180 mg/dL14
whereas the AACE guidelines recommend a goal FPG less than 110 mg/dL and
2h-PPG less than 140 mg/dL,15 if these goals can be achieved safely without hypogly-
cemia. Once glycemic goals have been achieved, then checking SMBG 2 to 3 times
daily (one must be fasting) may be adequate. PPG testing may be helpful in individuals
on basal-bolus insulin therapy to help assess the adequacy of the chosen insulin-to-
carbohydrate ratio (ICR) (discussed later).
It is important to keep in mind that SMBG goals chosen for the patient must be
congruent with HbA1c targets for that patient. As seen in Table 1, for every 29-mg/dL
Insulin Tactics in Type 2 Diabetes 9
Table 1
Estimated average blood glucose (eAG) and hemoglobin A1c (HbA1c)
Hemoglobin A1c, % Blood Glucose (range), mg/dL Blood Glucose (range), mmol/L
5 97 (76120) 5.4 (4.26.7)
6 126 (100152) 7.0 (5.58.5)
7 154 (123185) 8.6 (6.810.3)
8 183 (147217) 10.2 (8.112.1)
9 212 (170249) 11.8 (9.413.9)
10 240 (193282) 13.4 (10.715.7)
11 269 (217314) 14.9 (12.017.5)
12 298 (240347) 16.5 (13.319.3)
Adapted from Nathan DM, Kuenen J, Borg R, et al. Translating the A1C assay into estimated
average glucose values. Diabetes Care 2008;31(8):14738.
increase in blood glucose (BG), HbA1c goes up by approximately 1%.20 This relation-
ship between HbA1c and BG is referred to as the estimated Average Glucose (eAG),
and most validated laboratory assays for HbA1c now report an eAG result as well.
Explaining this relationship to patients is helpful, because they can correlate their
SMBG data with HbA1c goals.20
Because the basis of insulin therapy is to try to match the onset of insulin action, its
peak, and duration with the onset, peak, and duration of its need to metabolize
glucose, if there is a mismatch between glucose levels and the actions of the injected
insulin, either hyperglycemia persists or hypoglycemia can result. Because the phar-
macokinetic properties of exogenously administered insulin (when the insulin peaks)
do not always match the pharmacodynamic needs of the body (when the insulin
should peak), it is critical to understand the properties of different insulin preparations
and choose a product based on the glycemic needs of the patient (Fig. 9, Tables 2
and 3).2123
Human Insulin Preparations
The earliest insulins were derived from animal pancreas. These extracts had signifi-
cant variability in their onset, peak, and duration of action depending on purification
Abbreviations: NPA, neutral protamine aspart; NPH, neutral protamine Hagedorn; NPL, neutral protamine Lispro; U, refrigerate; J, room temperature.
11
12
Table 3
Important facts and caveats regarding insulin preparations
techniques. They also had a propensity to induce anti-insulin antibodies24 and have
since been phased out in the United States. Now, with recombinant DNA technology,
the human insulin gene can be introduced into yeast or Escherichia coli, which then
secrete insulin with the same amino acid sequence as native human insulin; this is
the predominant form of insulin in the world. These recombinant DNAproduced insu-
lins are collectively referred to as Human Insulin and broadly, there are 2 types: a
short-acting product called human regular insulin (Regular) and an intermediate-
acting product called neutral protamine Hagedorn (NPH) insulin (see Fig. 9, Tables
2 and 3).
Short-acting human regular insulin
Human regular insulin is a short-acting insulin that, when injected, tends to self-
associate to form hexameric aggregates in the presence of zinc.25 These hexamers
slowly disassociate into dimers, then monomers, which are the active form of the in-
sulin (Fig. 10). This disassociation takes time, which explains the need to administer
this insulin approximately 30 to 45 minutes before meals. The typical activity profile
of human regular insulin is displayed in Fig. 9. However, it is important to keep in
mind that the activity profile of human regular insulin is also dose-dependent; the
higher the dose, the slower is the onset of action (sometimes up to 60 minutes), the
broader the peak (23 hours), and the longer the duration of action (up to 36 hours).
Because the time to peak and duration of action do not replicate endogenous bolus
insulin secretion, it is a disadvantage for most patients when used at mealtimes.
Intermediate-acting neutral protamine Hagedorn insulin
NPH is an intermediate-acting insulin that has delayed absorption kinetics due to the
addition of protamine and zinc. It has an onset of action in 1 to 2 hours, broad peak at 6
to 12 hours, and duration of action of 12 to 16 hours. It is a cloudy suspension and, to
prevent variability in its absorption, it must be gently rolled in the palms of the hands 15
to 20 times to resuspend it before injection.
Fig. 10. Dissociation and absorption of human regular compared with rapid-acting analog
insulin. Human regular insulin tends to self-associate to form hexameric aggregates in the
presence of zinc. After subcutaneous injection, these hexamers slowly disassociate into di-
mers, then monomers, which are the active form of insulin. The onset of action is slow
and human regular insulin must be administered approximately 30 to 45 minutes before
meals. Rapid-acting insulin analogs also exist in hexameric aggregates in solution; however,
have a low tendency to self-aggregate subsequent to subcutaneous injection. Once injected,
they quickly disassociate into the active monomeric form. The onset of action is therefore
quick, allowing this insulin to be given approximately 15 minutes before and up to approx-
imately 15 minutes after the meal is consumed.
14 Meah & Juneja
NPH should typically be dosed twice daily, once with breakfast and again with din-
ner or at bedtime to provide continuous basal coverage, although it is sometimes used
only once a day in clinical practice. When used twice a day, the morning dose peaks in
the afternoon, which can result in hypoglycemia, particularly if lunch is delayed or skip-
ped. The dinner or bedtime dose peaks during sleep. This nocturnal peak is a reason
to recommend SMBG testing at approximately 3 AM, especially when a dose change is
made.
INSULIN-DELIVERY DEVICES
Insulin can be dispensed in vials, pens, or with pumps. When dispensed in a vial, there
is usually 1000 units/10 mL; whereas in pens, 300 units per device. Table 4 summarizes
the advantages and disadvantages of the various insulin-administration devices.31,32
The overarching goal with insulin therapy is to mimic physiologic insulin profiles, with
basal insulin to suppress overnight and between-meal hepatic glucose production and
bolus insulin to account for meal excursions (Figs. 1117).33 Much of the actual insulin
tactics discussed here are anecdotal, although more recently some guidelines are
evolving from experience in clinical trials.14,15,34,35
Approaches Using Basal Insulin
We generally follow the ADA guidelines for the introduction of basal insulin after failure
of 2 or more noninsulin agents, as discussed previously, and AACE guidelines on titra-
tion/intensification, as shown in Fig. 11.14,15 These guidelines have been developed
from studies such as the treat-to-target trial, which showed that the addition of a single
dose of basal insulin (NPH or glargine) was effective in achieving a target HbA1c of less
than 7.0%. One critical element of the treat-to-target trial was a forced titration algo-
rithm,36 which highlighted the importance of regular and sustained efforts at adjusting
doses of the insulin to predetermined glycemic goals. We prefer a long-acting basal
analog over NPH insulin because of its sustained action over 24 hours and less risk
of afternoon and nocturnal hypoglycemia (see Figs. 12 and 13). If there is concern
for nocturnal hypoglycemia, 3 AM SMBG values should be checked, especially when
using NPH insulin. In most circumstances, at the time of basal insulin initiation, ongoing
noninsulin therapies are not discontinued. Although there is some controversy whether
secretagogues, especially sulfonylureas should be continued when insulin is started,
our approach is to stop these medications only when we introduce bolus insulin.
Numerous studies have shown that glycemic goals can be achieved when patients
are given guidance and autonomy in managing their own insulin dose titration.3739 We
strongly endorse such empowerment. We however feel the 2-day to 3-day schedule
suggested in the AACE guidelines (see Fig. 11)15 is too aggressive for self-titration
16
Meah & Juneja
Table 4
Advantages and disadvantages of insulin delivery devices
Fig. 11. AACE algorithm for initiation and modification of insulin therapy. These guidelines
provide guidance on the starting dose of basal insulin based on body weight. In the event of
hypoglycemia, a decrease of the total daily dose is recommended. If glycemic goals are be-
ing achieved, intensification to a basal-bolus regimen with titration based on SMBG is the
next step. (From American Association of Clinical Endocrinologists, Garber AJ, Abrahamson
MJ, Barzilay JI, et al. AACE comprehensive diabetes management algorithm. Endocr Pract
2013;19:7; with permission.)
and prefer a 5-day to 7-day schedule instead. Like the treat-to-target trial, we use a
mean of the last 3 days of FPG as a guide to dose adjustment.36 Once insulin is initi-
ated, it is important for the physician to monitor the patients progress every 1 to
2 weeks for the first month and then biweekly for the next 1 to 2 months, at which
time the patient should be reevaluated in the clinic. We pick a maximum daily basal
insulin dose, generally 30 to 40 units a day, at which time if FPG goals have not
been achieved, we ask the patient to return to the clinic for an evaluation. At the visit,
we reassess the patients understanding of self-management, with particular attention
to insulin-injection techniques and compliance. We then determine if therapy needs to
be modified with the addition of or changes to noninsulin drugs or if the addition of
bolus insulin is necessary.
Fig. 12. Basal and basal-bolus insulin regimens using human insulin preparations. B, break-
fast; L, lunch; S, supper/dinner; HS, bedtime. (A) NPH insulin alone at bedtime. As seen in this
figure, NPH alone has the potential to cause nocturnal hypoglycemia at its peak action and
it does not provide coverage for the entire 24-hour period. (B) Addition of 1 dose of human
regular insulin with the largest meal to bedtime NPH. This regimen helps cover dinner and
also helps with bedtime targets. However, the human regular insulin must be dosed 30 to
45 minutes before the meal. (C) Addition of 2 fixed doses of human regular insulin with
NPH before breakfast and supper. As seen in the figure, this regimen produces a gap in
coverage if the patient were to consume lunch. In addition, because the dose of the meal-
time insulin is fixed, the amount of carbohydrate consumed also needs to be fixed to match
the injected insulin dose. (D) Addition of flexible (carbohydrate-based) doses of human reg-
ular insulin with each meal with NPH before breakfast and supper. Although this regimen
allows for variable amounts of carbohydrates with each meal, the protracted duration of ac-
tion of the regular insulin results in an overlap (stacking) of the insulin doses. Patients also
need to learn to count carbohydrates.
Generally, the total daily dose consists of 50% basal and 50% bolus insulin. With the
initiation of bolus insulin, therefore, the basal insulin may need to be decreased by
10% to 20% to prevent fasting hypoglycemia. If FPG is already at target, a greater
reduction in the basal insulin may be necessary.
There are 2 broad approaches to bolus insulin therapy in T2D. The first approach is
to start with fixed doses of mealtime insulin and then adjust based on 2h-PPG or the
blood glucose immediately before the next meal. For this fixed dose approach, we
follow AACE guidelines for initiation, as shown in Fig. 11. The second approach is
based on counting carbohydrates, which is more complex but provides more precise
mealtime insulin dosing and allows patients the flexibility to adjust insulin to varying
amounts of carbohydrates (see Figs. 12D and 13D). Although the complexity of the
carbohydrate-counting approach has been called into question in patients with T2D,
in our clinical experience it remains a valuable tool for patients and both this approach
and the fixed-dose approach can achieve similar glycemic goals.42 With either
approach it is important to assess meal patterns so as to choose the best initial
regimen.
Fig. 13. Basal and basal-bolus regimens using analog insulin preparations. B, breakfast; L,
lunch; S, supper/dinner; HS, bedtime. (A) Long-acting basal insulin analog alone at bedtime.
As seen in this figure, unlike with NPH insulin (see Fig. 12A), a single dose of a long-acting
analog insulin given once a day has the potential to provide consistent basal insulin
coverage for the entire day. (B) Addition of 1 dose of rapid-acting analog insulin with the
largest meal to bedtime long-acting analog insulin. Unlike with human regular insulin
(see Fig. 12B), a rapid-acting analog can be administered with the meal and also helps
achieve bedtime targets. (C) Addition of fixed doses of rapid-acting analog insulin with
each meal to bedtime long-acting analog insulin. Due to the shorter duration of action
of rapid-acting analogs, this regimen highlights the need for continuous basal insulin
coverage. There is, however, less potential for insulin stacking. (D) Addition of flexible
(carbohydrate-based) doses of rapid-acting analog insulin with each meal to bedtime
long-acting analog insulin. This is the ideal basal-bolus insulin regimen with multiple daily
injections. The analog rapid-acting insulin can be dosed with meals based on carbohydrates
consumed again with little risk for insulin stacking. However, this regimen does require the
patient to be well versed with self-management skills, including carbohydrate counting.
Carbohydrate-counting approach
The patient learns how to count carbohydrates using an Insulin:Carbohydrate Ratio
(ICR). An ICR is calculated using the formula 500/TDD of insulin. For example, if the
TDD is 50 units, 1 unit of rapid-acting analog insulin is required for every 10 g of car-
bohydrates consumed (500/50 5 10). Another method is to use TDD/3 to approximate
the amount of bolus insulin for each meal. This is particularly helpful for patients who
eat fixed amounts of carbohydrates with each meal.
With the addition of rapid-acting insulin, a correction dose, known as the Insulin
Sensitivity Factor (ISF) should be added to the insulin regimen. The ISF is a dose of
rapid-acting insulin given at meal times along with the meal dose of the same rapid-
acting insulin to account for glucose that is out of target before the meal is consumed.
This corrective dose of insulin is calculated using the 1800 rule, (1800/TDD) for
rapid-acting analogs, or the 1500 rule (1500/TDD) for human regular insulin. The
actual calculation can be written for the patient as follows: X (Target BG)/ISF; X
20 Meah & Juneja
Fig. 14. Insulin regimen for exogenous glucocorticoids. B, breakfast; L, lunch; S, supper/din-
ner; HS, bedtime. (A) The addition of exogenous glucocorticoids leads to postprandial hy-
perglycemia, thus more insulin is required with meals. (B) One solution with human
insulin preparations is to use NPH and regular insulin with breakfast and dinner. In this
regimen, 60% of the NPH dose is administered with breakfast and 40% with dinner. For
the regular insulin, the proportions are reversed, with 40% of the dose given 30 to 45 mi-
nutes before breakfast and 60% of the dose 30 to 45 minutes before dinner to try to match
the expected glucose excursions, as seen in (A). (C) Another solution with analog insulin is to
give 1 dose of long-acting analog basal insulin with breakfast and mealtime analog rapid-
acting insulin with each meal, the highest dose administered with dinner again to match
glucose excursions, as shown in (A). We prefer to administer the long-acting basal with
breakfast in patients on steroids, because their glucose nadir occurs in the morning just
before breakfast. (D) For patients already on a basal-bolus insulin with analog long-
acting basal insulin at bedtime and mealtime, analog rapid-acting insulin, insulin NPH can
be added at breakfast to account for the afternoon BG rise that occurs with glucocorticoids.
Fig. 16. Humulin R U-500 insulin-based regimens. As seen in the figure, U-500 insulin in-
jected twice has the effect of overlapping of the doses. In effect, therefore, the pharmaco-
kinetic profile of this insulin is similar to basal insulin. Typically 60% of the dose is
administered before breakfast and 40% before supper. B, breakfast; L, lunch; S, supper/din-
ner; HS, bedtime.
represents the patients BG. For example, with a premeal BG of 230 mg/dL, target BG
of 130 mg/dL, and an ISF of 50, the patient will require (230 130)/50 5 2 units of
rapid-acting insulin added to the meal dose.
Insulin stacking
Insulin stacking refers to situations in which a previously injected insulin still has a re-
sidual effect due to its protracted duration of action. It is generally a problem with
short-acting human regular insulin (see Fig. 12C, D), because these are dosed more
Fig. 17. Insulin regimen with CSII, using a pump. B, breakfast; L, lunch; S, supper/dinner; HS,
bedtime. CSII therapy uses only rapid-acting analog insulin, delivered at preset basal rates
with a mealtime bolus based on the ICR plus the ISF.
22 Meah & Juneja
frequently, although it can occur with any type of insulin. If a subsequent short-acting
insulin injection does not take the residual insulin from the previous dose into account,
the two can add on to each other, resulting in hypoglycemia.43 For this reason, short-
acting insulins are typically administered at least 4 hours apart.
Table 5
Calculating U-500 insulin dose (mL) based on U-100 insulin dosage (Units)
Adapted from Lane WS, Cochran EK, Jackson JA, et al. High-dose insulin therapy: is it time for U-500
insulin? Endocr Pract 2009;15(1):719.
Insulin Tactics in Type 2 Diabetes 23
syringe or a tuberculin syringe. Care should be taken in using only 1 of these 2 injection
devices and patients should be retrained in the use of the device even if they have
used a U-100 syringe before. The prescription for U-500 insulin should always clearly
state the device type to be used. If prescribed with a U-100 insulin syringe, the amount
of insulin drawn into the syringe should be written in units and if prescribed with a tu-
berculin syringe the amount should be written in milliliters (see Table 5). In the case of
the patient described previously who is transitioning from 300 units of U-100 to U-500
insulin, the prescription should read: Humulin R U-500 (500 units/mL), inject 36 units
30 minutes before breakfast and 24 units before supper with an insulin syringe. If using
a tuberculin syringe, the same prescription should read: Humulin R U-500 (500 units/
mL), inject 0.36 mL 30 minutes before breakfast and 0.24 mL before supper with a tu-
berculin syringe. Our preferred administration device is the tuberculin syringe with
dose written in milliliters so there is no confusion of the actual insulin dose adminis-
tered with the unit markings of an insulin syringe.
Although insulin is the most powerful agent to correct hyperglycemia, its use is not
without risk. Besides weight gain, treatment with insulin can produce lipohypertrophy
(deposition of fat) at the site of injections due to local anabolic effects of the drug. The
absorption, and hence the kinetics, of insulin action can become erratic if the drug is
injected into these hypertrophied areas. It is, therefore, important to rotate injection
sites.
By far, however, the greatest risk associated with insulin use is that of hypoglyce-
mia. Individuals should be counseled on the clinical manifestations of hypoglycemia,
as well as treatment. We educate patients on the rule of 15; on noting the symptoms
of hypoglycemia, the patient performs a BG to confirm hypoglycemia. If hypoglycemia
is confirmed, the patient is to consume 15 g of carbohydrates (eg, 3 glucose tablets, 4
oz fruit juice) and then recheck BG 15 minutes later to ensure BG is trending up. The
process should be repeated until the BG is greater than 100 mg/dL. Because of the
potential risk of hypoglycemia with insulin therapy, we believe that all patients pre-
scribed this drug should be given a prescription for glucagon and a family member
or person who has close and constant contact with the patient should be trained in
its use. All patients on insulin therapy should also be encouraged to wear a medical
alert bracelet and always check their BG before driving and frequently when driving
for long periods of time. In certain high-risk occupations (eg, drivers of commercial ve-
hicles, pilots, and those operating dangerous machinery), workers who use insulin
must provide detailed glucose logs and paperwork from their physicians regarding
their history of diabetes and its management. Awareness of the risk of hypoglycemia
24 Meah & Juneja
There are circumstances in which a need to deescalate previously started insulin ther-
apy might arise. One such circumstance is following a new diagnosis of T2D with
glucose toxicity, where insulin was initiated at the time of diagnosis. As glucose
toxicity abates with treatment, it may be possible to taper off insulin while at the
same time introducing other noninsulin therapy. Similarly, insulin-sparing agents,
such as incretin mimetics or SGLT-2 inhibitors, might be introduced in patients already
on insulin. The introduction of these agents could precipitate hypoglycemia if the insu-
lin (or sulfonylurea) doses are not adjusted downward. Because there are no published
guidelines on strategies for reducing insulin in such circumstances, we present our
approach to insulin adjustment in the presence of such agents.16,4663 The approach
presented is an amalgamation of our clinical experience and insulin dose titrations
used in clinical trials where new therapeutic agents were used on a background of in-
sulin therapy. We have summarized the mechanism of action of drugs from different
therapeutic classes used for T2D in Table 6 to help determine when insulin deescala-
tion might be appropriate to consider.
For patients on basal insulin alone:
In such circumstances, our strategy is to reduce the basal insulin as follows:
HbA1c 8%: Basal insulin is reduced by 20% on initiation of the new agent.
HbA1c >8%: Basal insulin is reduced by 0% to 10% on initiation of the new agent.
The patient continues to monitor SMBG, and if any 2 values in 1 week are less than
100 mg/dL (or <80 mg/dL if tighter control is desired), basal insulin should be reduced
by another 10% to 20%. Such reductions occur weekly until the patient is taking less
than 10 to 20 units of basal insulin. At this time, the need for continuing basal insulin
needs to be reassessed. For the management of hyperglycemia, if 3 BG values in
1 week are greater than 250 mg/dL, we recommend the patient contact the physician
to assess if the dose of the newly introduced agent or insulin needs modification.
For patients on basal 1 bolus insulin (or bolus insulin alone):
In such circumstances, our strategy is to reduce the bolus insulin first, as follows:
HbA1c 8%: Bolus insulin is reduced by 30% to 50% on initiation of the new
agent.
HbA1c >8%: Bolus insulin is reduced by 0% to 20% on initiation of the new agent.
The patient continues to monitor SMBG, and if any 2 values in 1 week are less than
100 mg/dL (or <80 mg/dL if tight control is desired), bolus insulin should be reduced by
another 30% to 50%. Such reductions occur weekly until adequate glycemic control is
achieved or the bolus insulin is tapered off entirely. Once bolus insulin has been
tapered off completely and if the patient continues to have any 2 SMBG values in a
week less than 100 mg/dL, we recommend basal insulin reductions as described pre-
viously. For the management of hyperglycemia, if 3 SMBG values in 1 week are greater
than 250 mg/dL, we recommend that the patient contact the physician to assess if
therapy with the noninsulin agent or insulin needs modification.
For patients on premixed insulin, we generally follow the parameters for basal insulin
alone. For patients on insulin plus a sulfonylurea, our approach is to try to reduce the
insulin before the sulfonylurea, because in our experience patients prefer to remain on
oral agents over injectable ones.
Table 6
Mechanisms of action of currently available agents for type 2 diabetes
N/A, not used as monotherapy; 0, no effect; 1, small effect; 11, moderate effect; 111, marked effect.
a
Vildagliptin is not yet approved for use in the United States.
25
26 Meah & Juneja
THE ABCS OF DIABETES CARE AND THE DIABETES CARE T.E.A.M. APPROACH
When managing the patient with diabetes, it is important to not only emphasize glyce-
mic goals as measured by HbA1c, but also Blood Pressure and Cholesterol targets,
collectively referred to as the ABCs of diabetes.64 Addressing these helps reduce
the risk of both microvascular and macrovascular complications. This is best accom-
plished using what we call the T.E.A.M. approach. The most critical member of the
T.E.A.M. is the patient; other members include the physician, a certified diabetes
educator (CDE) dietician, nurse CDE, pharmacist, optometrist/ophthalmologist, podi-
atrist, behavioral psychologist, social worker, and the family of the patient. All mem-
bers of the team help in achieving goals for diabetes. The T.E.A.M. approach itself
consists of the following:
Talking with the patient: Clearly communicating goals and roles and responsibil-
ities of each member of the team with the patient is key in overcoming barriers to
optimal glycemic control. This communication should occur with and from all
team members.
Exercise and nutrition: Addressing pertinent lifestyle issues.
Attitude: Help the patient deal with psychological, social, and financial issues that
could become barriers to achieving control.
Medications: Choosing the correct medications in discussion with the patient.
SUMMARY
Insulin is the most powerful glycemic control agent available. However, its use as a
therapeutic modality requires education of the patient and regimentation of food
intake, exercise, and frequent glucose monitoring. Such regimentation is particularly
important when using a basal-bolus therapy approach.
The introduction of many novel noninsulin drugs in the past decade has resulted in
better glycemic control and often a need to reduce previously instituted insulin ther-
apy. Although many of these novel therapies by themselves do not cause hypoglyce-
mia, by reducing the overall glycemic burden through a myriad of mechanisms, they
function in an insulin-sparing fashion. The doses of exogenously administered insulin
may therefore need to be reduced in the presence of these new drugs to mitigate
hypoglycemia.
For insulin therapy (or any other drug treatment) to be successful, it is critical that the
physician not only establish glycemic goals, but communicate these goals to the pa-
tient. The measurement of HbA1c helps in achieving a long-term goal, but on a day-to-
day basis, patients need to be cognizant of their own BG goals and what they need to
do if falling outside of target. The patients understanding of self-management skills
and empowerment are therefore foundational to insulin therapy.
REFERENCES
1. Defronzo RA. Banting Lecture. From the triumvirate to the ominous octet: a new
paradigm for the treatment of type 2 diabetes mellitus. Diabetes 2009;58(4):
77395.
2. Butler AE, Janson J, Bonner-Weir S, et al. Beta-cell deficit and increased beta-
cell apoptosis in humans with type 2 diabetes. Diabetes 2003;52(1):10210.
3. Weng J, Li Y, Xu W, et al. Effect of intensive insulin therapy on b-cell function and
glycaemic control in patients with newly diagnosed type 2 diabetes: a multi-
centre randomised parallel-group trial. Lancet 2008;371(9626):175360.
Insulin Tactics in Type 2 Diabetes 27
24. Retnakaran RZ, Zinman B. Treatment of type 1 diabetes mellitus in adults. In:
Jameson JL, Grott LJ, editors. Endocrinology, 2 Volume-Set: adult and pediatric.
6th edition. Philadelphia(PA): Saunders Elsevier; 2010. p. 84057.
25. Hirsch IB. Intensive treatment of type 1 diabetes. Med Clin North Am 1998;
82(4):689719.
26. Baxter MA. The role of new basal insulin analogues in the initiation and optimi-
sation of insulin therapy in type 2 diabetes. Acta Diabetol 2008;45(4):25368.
27. Owens DR, Matfin G, Monnier L. Basal insulin analogues in the management of
diabetes mellitus: what progress have we made? Diabetes Metab Res Rev
2014;30(2):10419.
28. Heise T, Weyer C, Serwas A, et al. Time-action profiles of novel premixed prep-
arations of insulin lispro and NPL insulin. Diabetes Care 1998;21(5):8003.
29. Weyer C, Heise T, Heinemann L. Insulin aspart in a 30/70 premixed formulation.
Pharmacodynamic properties of a rapid-acting insulin analog in stable mixture.
Diabetes Care 1997;20(10):16124.
30. Banting FG, Collip JB, MacLeod JJ, et al. The effect of pancreatic extract (insu-
lin) on normal rabbits. Am J Phys 1922;62:16276.
31. Rosenfeld CR, Bohannon NJ, Bode B, et al. The V-Go insulin delivery device
used in clinical practice: patient perception and retrospective analysis of glyce-
mic control. Endocr Pract 2012;18(5):6607.
32. Neithercott T. The basics of insulin pumps: these devices are the closest thing to
a pancreasso far. Diabetes Forecast 2014;67(1):58.
33. Bergenstal RM, Buse JB, Peters AL, et al. Endocrinology (3-volume set). In:
Jameson JL, Degroot LJ, editors. 4th edition. Philadelphia: W.B. Saunders; 2001.
34. Leahy JL. Insulin therapy in type 2 diabetes mellitus. Endocrinol Metab Clin
North Am 2012;41(1):11944.
35. Hirsch IB, Bergenstal RM, Parkin CG, et al. A real-world approach to insulin ther-
apy in primary care practice. Clinical Diabetes 2005;23:7886.
36. Riddle MC, Rosenstock J, Gerich J. The treat-to-target trial: randomized addi-
tion of glargine or human NPH insulin to oral therapy of type 2 diabetic patients.
Diabetes Care 2003;26(11):30806.
37. Meneghini L, Koenen C, Weng W, et al. The usage of a simplified self-titration
dosing guideline (303 Algorithm) for insulin detemir in patients with type 2 dia-
betesresults of the randomized, controlled PREDICTIVE 303 study. Diabetes
Obes Metab 2007;9(6):90213.
38. Edelman SV, Liu R, Johnson J, et al. AUTONOMY: the first randomized trial
comparing two patient-driven approaches to initiate and titrate prandial insulin
lispro in type 2 diabetes. Diabetes Care 2014;37(8):213240.
39. Davies M, Storms F, Shutler S, et al. Improvement of glycemic control in subjects
with poorly controlled type 2 diabetes: comparison of two treatment algorithms
using insulin glargine. Diabetes Care 2005;28(6):12828.
40. Monnier L, Colette C, Rabasa-Lhoret R, et al. Morning hyperglycemic excur-
sions: a constant failure in the metabolic control of non-insulin-using patients
with type 2 diabetes. Diabetes Care 2002;25(4):73741.
41. Monnier L, Lapinski H, Colette C. Contributions of fasting and postprandial
plasma glucose increments to the overall diurnal hyperglycemia of type 2 dia-
betic patients: variations with increasing levels of HbA(1c). Diabetes Care
2003;26(3):8815.
42. Bergenstal RM, Johnson M, Powers MA, et al. Adjust to target in type 2 dia-
betes: comparison of a simple algorithm with carbohydrate counting for adjust-
ment of mealtime insulin glulisine. Diabetes Care 2008;31(7):130510.
Insulin Tactics in Type 2 Diabetes 29
43. Heise T, Meneghini LF. Insulin stacking versus therapeutic accumulation: under-
standing the differences. Endocr Pract 2014;20(1):7583.
44. Lane WS, Cochran EK, Jackson JA, et al. High-dose insulin therapy: is it time for
U-500 insulin? Endocr Pract 2009;15(1):719.
45. Reznik Y, Cohen O. Insulin pump for type 2 diabetes: use and misuse of contin-
uous subcutaneous insulin infusion in type 2 diabetes. Diabetes Care 2013;
36(Suppl 2):S21925.
46. Riddle M. Combination therapies with oral agents or oral agents and insulin. In:
Lebovitz HE, editor. Therapy for diabetes mellitus and related disorders. 5th edi-
tion. Alexandria (Egypt): American Diabetes Association; 2009. p. 33241.
47. Hambrock A, de Oliveira Franz CB, Hiller S, et al. Glibenclamide-induced
apoptosis is specifically enhanced by expression of the sulfonylurea receptor
isoform SUR1 but not by expression of SUR2B or the mutant SUR1(M1289T).
J Pharmacol Exp Ther 2006;316(3):10317.
48. Wright A, Burden AC, Paisey RB, et al. Sulfonylurea inadequacy: efficacy of
addition of insulin over 6 years in patients with type 2 diabetes in the UK Pro-
spective Diabetes Study (UKPDS 57). Diabetes Care 2002;25(2):3306.
49. Johnson JA, Majumdar SR, Simpson SH, et al. Decreased mortality associated
with the use of metformin compared with sulfonylurea monotherapy in type 2
diabetes. Diabetes Care 2002;25(12):22448.
50. Evans JM, Ogston SA, Emslie-Smith A, et al. Risk of mortality and adverse car-
diovascular outcomes in type 2 diabetes: a comparison of patients treated with
sulfonylureas and metformin. Diabetologia 2006;49(5):9306.
51. Monami M, Genovese S, Mannucci E. Cardiovascular safety of sulfonylureas: a
meta-analysis of randomized clinical trials. Diabetes Obes Metab 2013;15(10):
93853.
52. Gastaldelli A, Ferrannini E, Miyazaki Y, et al. Thiazolidinediones improve beta-
cell function in type 2 diabetic patients. Am J Physiol Endocrinol Metab 2007;
292(3):E87183.
53. DeFronzo RA, Triplitt C, Qu Y, et al. Effects of exenatide plus rosiglitazone on
beta-cell function and insulin sensitivity in subjects with type 2 diabetes on met-
formin. Diabetes Care 2010;33(5):9517.
54. Mari A, Nielsen LL, Nanayakkara N, et al. Mathematical modeling shows exena-
tide improved beta-cell function in patients with type 2 diabetes treated with
metformin or metformin and a sulfonylurea. Horm Metab Res 2006;38(12):
83844.
55. Astrup A, Rossner S, Van Gaal L, et al. Effects of liraglutide in the treatment of
obesity: a randomised, double-blind, placebo-controlled study. Lancet 2009;
374(9701):160616.
56. Mari A, Sallas WM, He YL, et al. Vildagliptin, a dipeptidyl peptidase-IV inhibitor,
improves model-assessed beta-cell function in patients with type 2 diabetes.
J Clin Endocrinol Metab 2005;90(8):488894.
57. Polidori D, Mari A, Ferrannini E. Canagliflozin, a sodium glucose co-transporter
2 inhibitor, improves model-based indices of beta cell function in patients with
type 2 diabetes. Diabetologia 2014;57(5):891901.
58. Neal B, Perkovic V, de Zeeuw D, et al. Rationale, design, and baseline charac-
teristics of the Canagliflozin Cardiovascular Assessment Study (CANVAS)a
randomized placebo-controlled trial. Am Heart J 2013;166(2):21723.e11.
59. Stenlof K, Cefalu WT, Kim KA, et al. Efficacy and safety of canagliflozin mono-
therapy in subjects with type 2 diabetes mellitus inadequately controlled with
diet and exercise. Diabetes Obes Metab 2013;15(4):37282.
30 Meah & Juneja
KEYWORDS
Diabetes guidelines Diabetes treatment targets Lipids Hypertension
Mental health Nephropathy
KEY POINTS
Blood pressure targets for all patients with diabetes are now less than 140/90 regardless
of diabetic nephropathy. Geriatric guidelines concur with this target.
All patients between 40 and 75 years of age should be considered for moderate- to high-
intensity statin therapy. Patients older than 75 years should be preferentially treated with a
statin if appropriate after lipid levels, risk, and longevity are considered and at doses that
minimize side effects.
Diabetes-related stress and depression has been identified as a major treatable factor that
will improve outcomes.
For medically obese patients with diabetes, there is increasing evidence that bariatric sur-
gery decreases morbidity and mortality significantly and may be an appropriate treatment
option.
INTRODUCTION
Diabetes care and, subsequently, diabetes morbidity and mortality have changed
dramatically in the last decades. In addition to new agents and methods for glycemic
control, newer agents to control the progression of renal disease and knowledge
about interventions to improve cardiovascular outcomes are now available. Impor-
tantly, we have learned much about the importance and primacy of diet, weight
loss, exercise, and mental health as they affect the risk of and progression of diabetes,
the last through the critical lens of compliance and self-care. We also have better
Disclosures: None.
a
Department of Medicine, University of British Columbia, Vancouver, British Columbia,
Canada; b Division of Internal Medicine, Department of Medicine, University of Washington,
Seattle, WA, USA; c Rural Health Academic Centre, Melbourne Medical School, Parkville,
Graham St. Shepparton, Victoria, Australia
* Corresponding author.
E-mail address: [email protected]
Diabetic renal disease commonly involves multiple primary and secondary pathologic
processes that lead to a limited variety of clinical manifestations (Box 1). Genetic sus-
ceptibility to diabetic nephropathy, suggested by familial clustering of nephropathy,1,2
is complex because of ill-defined pathophysiology and variable genetic expression.3
Classic diabetic nephropathy, with microalbuminuria progressing to macroalbumi-
nuria and a decreased glomerular filtration rate (GFR), is common and easy to diag-
nose in type 1 diabetes but is responsible for less than 50% of cases of renal
disease in type 2 diabetes. Renal biopsies from patients with type 2 diabetes (eg, he-
maturia, decreased GFR without significant albuminuria, absence of microvascular
disease, and so forth) show changes consistent with diabetic nephropathy, other renal
diseases, or a combination in roughly equal numbers.4
Indications for a renal biopsy in patients with diabetes and evidence of renal disease
include the likelihood of other treatable renal disease and the patients tolerance for any
needed immunosuppressive therapy. Indications for renal biopsy include nephrotic
range proteinuria in the absence of other microvascular disease or the combination of
glomerular hematuria, significant proteinuria (>1 g/d), and renal impairment, particularly
with clinical or serum biomarker evidence of diffuse immune-mediated diseases (anti-
neutrophil cytoplasmic antibodies, double-stranded DNA).
The early diagnosis of diabetic nephropathy is even more problematic based as it is
on the development of microalbuminuria, which is also associated with exercise, in-
fections, and other renal diseases. These other causes of microalbuminuria probably
explain transient microalbuminuria in 50% of the initial diagnoses of diabetic
Box 1
Pathophysiology, anatomical pathology, and clinical manifestations of renal disease in
patients with diabetes
Table 1
Recommendations on target BP in patients with diabetes based on JNC 8 guidelines
Alternative approaches suggested when JNC 8 guidelines rated as soft or unhelpful. JNC 8 guide-
lines for initial and second-line treatment in nonblack patients: a thiazide diuretic, a calcium chan-
nel blocker, or either an ACEI or angiotensin receptor blocker. Initial choice in black patients: a
thiazide diuretic or calcium channel blocker (JNC 8 and American Society of Hypertension).
Abbreviations: AGS, American Geriatrics Society; ARB, angiotensin receptor blocker; ASH, Amer-
ican Society of Hypertension; BP, blood pressure; HYVET, Hypertension in the Very Elderly Trial;
KDIGO, Kidney Disease Improving Global Outcomes; U Alb, urinary albumin.
reflecting opinion rather than compelling evidence. The justification for treating pa-
tients with type 2 diabetes and a urine microalbumin less than 30 mg/g as if they
had diabetic renal disease (see Table 1) is based on the reduced incidence of new
microalbuminuria in such patients treated with an ACEI,5 with a likely period of silent
diabetes-related renal disease before microalbuminuria.
The KDIGO guidelines also recommend an initial treatment choice of RASIs in dia-
betes. The rationale for the preferred use of RASIs is based on the RAS role in the
development of diabetic nephropathy and the effect of RASIs on reducing the inci-
dence of microalbuminuria,5 the degree of proteinuria, and the rate of loss of GFR.8
Two recent systematic reviews and meta-analyses, although supporting the preferred
use of RASIs in the management of high blood pressure in diabetes, provide less
compelling evidence of a specific benefit.14,15 One of the 2 showed a reduction in mor-
tality with ACEI compared with placebo in patients with diabetes14; neither trial
showed a mortality benefit with an ARB. Renal outcomes were only studied in one
meta-analysis,15 which showed a reduction in the incidence of a doubling of plasma
creatinine (but not the rarer event of end-stage renal disease), with ACEI and, to a
lesser extent, ARB, when compared with placebo; an effect not seen with other anti-
hypertensive; Importantly, b-blockers were considered least effective.15 Unfortu-
nately, the analysis did not study the differences between black and nonblack
populations, leaving the JNC 8 recommendations for the black population with dia-
betes as the preferred option (see Table 1).
Recommendations for the treatment of high blood pressure in elderly diabetic pa-
tients are also problematic because of the lack of evidence. Although JNC 8,8
ASH,12 AGS,13 and KDIGO11 recommend a target of less than 140/90 mm Hg, the re-
sults of the Hypertension in the Very Elderly Trial (<10% diabetes) make a general case
for a target of less than 150/80 mm Hg in patients aged greater than 80 years.16 KDIGO
also suggests that blood pressure should not be allowed to decrease much less than
140/90 mm Hg in the elderly.17 A commonsense approach to likely long-term benefits,
and the side-effect profile of individual patients, is likely to play a significant role in
determining target blood pressure in the elderly with a decreased life expectancy.
Nonglycemic Targets in Diabetes 191
If ACEI or ARB is used in the treatment of high blood pressure in diabetes, the
consequent questions are as follows:
1. What is the best antihypertensive combination? There is now clear evidence that
combinations of an ACEI and ARB are associated with an increased risk of hyper-
kalemia (3.7 cases per 100 person-years) and acute renal failure (5.5 cases per 100
person-years), without additional renal protection.18 The choice between diuretics
and CCBs as the next medication will depend on factors such as the benefits of
other agents for the management of coincident issues (eg, diuretics in heart failure
or hyperkalemia) and likely compliance, including the availability/affordability of
combined antihypertensive tablets.
2. What is an acceptable acute deterioration in GFR when starting an ACEI or ARB?
An acute decrease of 30% or less of the estimated GFR has been considered
acceptable because of reversibility and an association with slower progression
of kidney disease.19 A decreased GFR may cause metabolic abnormalities and
symptoms and is associated with an increased cardiovascular mortality.20 There-
fore, the life expectancy of patients, as a predictor of the likely long-term benefits
in renal function compared with the possible short-term increased risk of cardio-
vascular or other symptoms, should influence the acceptability of an acute short-
term decrease in GFR following an ACEI or ARB. There are no data to support
any recommendation, but a life expectancy of less than 5 years would make
one doubt the benefits of an acute decrease of 30% in GFR following an ACEI
or ARB.
3. What level of hyperkalemia is acceptable on an ACEI or ARB? Hyperkalemia
poses a cardiovascular risk. Surveillance after publication of the Randomized Al-
dactone Evaluation Study21 showed an increased hospitalization rate and mortal-
ity for hyperkalemia (2.6 and 0.5 per 100 person-years). In dialysis patients,
hyperkalemia is associated with an excess mortality of 2 per 100 person-years
(plasma potassium >6 mmol/L) and 4 to 7 per 100 person-years (plasma
potassium >6.5 mmol/L).22 Consistent with other recommendations,23 these
data suggest a plasma potassium target of 6 mmol/L or less, achieved through
dietary modification, diuretics, or by cessation of the ACEI or ARB.
PROTEINURIA
LIPID TARGETS
In 2013, the American College of Cardiology (ACC) and the American Heart Associ-
ation (AHA) jointly released new, highly controversial guidelines for lipid targets and
treatment. Although the ACC/AHAs review of the evidence shows that high-intensity
therapy (lowering low-density lipoprotein [LDL] by 50%) or moderate-intensity ther-
apy (30%) changes atherosclerotic cardiovascular diseases (ASCVD) outcomes,
the new guidelines focus on treatment initialization for patients with a 10-year
ASCVD risk of 10% or more (with the new risk calculator) rather than target levels
of lipids, with treatment, as has been common practice for the last 2 decades.24
192 DeWitt et al
The clinical bottom line is that all patients with diabetes between 40 and 75 years of
age are assumed to have vascular disease and a risk of 7.5% or more, with the
same treatment recommendations for this group with diabetes. In such patients,
the evidence supports treatment with moderate- to high-intensity statins for primary
and secondary prevention (for any LDL cholesterol [LDL-C] 70 mg/dL). It is ex-
pected that moderate-intensity statin will lower LDL-C 30% to 50% from the base-
line and high-intensity statins will lower LDL-C more than 50%, including appropriate
lifestyle measures in the treatment effect. Monitoring of fasting lipids should be un-
dertaken 4 to 12 weeks after changes in therapy and every 3 to 12 months there-
after. In general, fasting LDL-C levels on treatment should only be used to assess
for anticipated reductions and, thus, for adherence to medication and lifestyle
changes or to signal secondary or genetic dyslipidemias for further evaluation.
The ACC/AHA guidelines only give a brief mention of nonstatin therapies. However,
there is a school of thought that nonfasting LDL-C values differ little from fasting
levels and that nonfasting or postprandial triglycerides are a significant predictor
of CV risk and may trump high-density lipoprotein for prognostic value.25,26 Thus,
clinicians should consider whether, given compliance and diagnostic issues,
nonfasting lipid profiles may be indicated or even be preferable to fasting levels.
Evaluation for safety (eg, transaminases) is recommended only as needed in patients
with hepatic or muscle symptoms. Statins should not be prescribed for pregnant or
nursing women.
Adding a nonstatin agent is only recommended for patients who do not have ex-
pected reductions in LDL-C (w14% of patients)27 or have an LDL-C greater than
190 mg/dL on maximum tolerated statin therapy and who have active arteriosclerotic
cardiovascular disease (ASCVD) or diabetes. Large recent studies, action to control
cardiovascular risk in diabetes (ACCORD) and Aim-High Atherothrombosis interven-
tion in metabolic syndrome with low high density lipoprotein/high triglyceride, impact
on global health outcomes (AIM-HIGH), have not shown improved outcomes with
added fibrates or niacin and have confirmed the well-known risk of liver function tests
(LFT) elevations.28,29 However, many patients are intolerant to statins, with patients on
high-intensity statins having an adjusted odds ratio (OR) of 50% for musculoskeletal
pain compared with controls27; no good long-term outcome data exist for other
agents. An Agency for Healthcare Research and Qualityfunded 2014 meta-analysis
showed that the combination of a low-intensity statin with ezetimibe or a bile-acid
resin could be used with fewer side effects and better LDL-C results in patients with
diabetes; but there are no long-term, hard-outcome data; the data for other lipid-
lowering agents were insufficient for analysis.27 It remains to be seen whether the
newer fibrates will address the fasting and/or postprandial CV risk associated with
high triglycerides.30 The ACC/AHAs report mentions safety and prescribing parame-
ters for nonstatin agents if they are required.24
The 2013 guidelines also recommend shared decision making; it is important to
note, for example, that the benefit of quitting smoking far outweighs the benefit
from starting a statin. Thus, provider time might be better spent understanding and
encouraging a patients motivation to quit smoking as a priority before, or in parallel
with, discussing and beginning another expensive medication.31 Patients younger
than 40 years or older than 75 years, with or without diabetes, should be treated using
risk estimates and shared decision making.13 When considering statin therapy, pro-
viders should be aware that the recent NAVIGATOR trial confirms that statins increase
the risk of developing diabetes (number needed to harm 5 1 out of 12 patients every
5 years; HR 5 1.32); thus, patients with prediabetes who are started on statins should
be monitored closely for hyperglycemia.
Nonglycemic Targets in Diabetes 193
In its 2014 Standard of Care, the American Diabetes Association recommends the
assessment of patients psychological and social situation as an ongoing part of the
medical management of diabetes.32 Several mental health conditions can affect the
care of patients with diabetes. In addition, some mental health conditions are associ-
ated with an increase in diabetes incidence or diabetes-related complications.
The depressive disorders have a prevalence of up to 25% in people with dia-
betes,32,33 much higher than the general population prevalence of 2% to 14%. Dia-
betes is a risk factor for developing depression in adults, with a 24% to 43%
increase in relative risk.34,35 Conversely, depression is associated with a relative risk
of incidence of diabetes of 1.37 to 2.02.35,36 Depression is also associated with an
increased incidence of the metabolic syndrome.37
Diabetes-related emotional distress is associated with reduced care plan adher-
ence and worse diabetes control.38 Depression is further associated with worse
adherence to diabetes care plans, with the largest effect sizes being for missed med-
ical appointments and a self-care composite score.39 Depression increases the risk of
diabetes-related microvascular and macrovascular complications,40 myocardial
infarction,41 and death.42
Given the prevalence of depression and the well-known difficulties of recognizing it
in medical practice, universal screening for depression in people with diabetes is a
logical approach that will yield undiagnosed patients with active depression for
whom treatment will be effective, thus, potentially decreasing morbidity. Two easily
available assessment tools for measuring emotional well-being or diabetes-related
distress are the World Health Organization-5 (WHO-5) Well-being Index and the Prob-
lem Areas in Diabetes Questionnaire. These tools ask a limited set of questions about
mental health but are not typically used for definitive assessment of possible mental
health conditions.43 Validated screening tests are available for the common mental
health conditions affecting diabetes care (Table 2).
The choice to treat or refer will be determined by the available resources. Most
mental health conditions are initially or fully treated in primary care or general medical
settings where the use of the Patient Health Questionnaire 9 and the Generalized Anx-
iety Disorder 7 (see Table 2) aid in the assessment and management of depressive
and anxiety disorders. A systematic review shows that psychosocial interventions
can improve A1c ( 0.3%).44 Collaborative care models for diapression involving
mental health and medical providers in a multidisciplinary team show promise.45 In
general medical settings, the collaborative care model with colocated medical and
mental health care provides superior outcomes when compared with more frag-
mented care systems.
The healthy weight target of a body mass index (BMI) less than 25 is well established,
but the difficulty of weight loss has been a persistent problem (see the article by Evert
and Riddell elsewhere in this issue for further exploration of this topic). Although there
is plentiful evidence that exercise is beneficial, the recent Look AHEAD (Action for
Health in Diabetes) trial46 was stopped early, at 9.6 years, because of futility. The bot-
tom line from this intensive lifestyle intervention trial (cardiovascular outcomes in 5145
overweight/obese patients with type 2 diabetes undergoing 175 minutes of exercise
per week and a diet with <30% fat and >15% protein, resulting in a mean weight
loss of 8.6%) is that it was ineffective in reducing cardiovascular events. However,
study participants had already achieved reasonable cardiovascular targets for blood
194 DeWitt et al
Table 2
Screening and assessment tools for well-being and mental health conditions
pressure, glycemia, lipids etc, and mean weight loss at the end of the trial differed by
only 2.6% from the control group. However, study participants already had reasonable
CV targets for blood pressure, glycemia, lipids, and so forth, with mean weight loss at
the end of the trial differing by only 2.5%. Only a few conclusions can be drawn from
the many studies on diet and weight loss (see paper on Lifestyle for details): (1) Med-
iterranean diets with olive oil improve cardiovascular outcomes. (2) Dietary targets of
less than 30% fat and less than 20% carbohydrate intake may facilitate weight loss
and improve glycemic and lipid control. (3) One trial showed that low-carbohydrate di-
ets are probably more effective than very-low-calorie diets alone for weight loss.4752
Increasing evidence points to at least 7% of body weight loss to significantly delay
or prevent diabetes in those at risk. Numerous studies and several meta-analyses
Box 2
Evaluation and targets for safe driving (in any patients at risk for hypoglycemia)
Review the driving history and risk of disruptive hypoglycemia at least every 2 years.
Evaluate for severe hypoglycemia in the past 2 years and, if present, ask whether
hypoglycemia is explained and correctable. The target is 3 or less disruptive hypoglycemic
events per year.
If patients are at risk for disruptive hypoglycemia, the target glucose is greater than 90 mg/dL
(5.0 mmol/L) before extended driving.
If the patients license is suspended, reevaluate at no more than 6 months.
Nonglycemic Targets in Diabetes 195
Box 3
Summary of nonglycemic targets for adults with diabetes
Abbreviations: BP, blood pressure; IFG, impaired fasting glucose; IGT, impaired glucose toler-
ance; MRSA, methicillin-resistant Staphylococcus aureus.
196 DeWitt et al
have supported that bariatric surgery, including bypass surgery, laparoscopic band-
ing, and gastric sleeve surgery, can induce remission of diabetes and improve long-
term outcomes for patients with a BMI of 30 or more. Virtually all trials have shown
that bariatric surgery is more effective than medical therapy, and a recent meta-
analysis showed a 50% decrease in CV events and a 40% reduction in mortality
compared with medical therapy, albeit with 15% of patients having malabsorptive sur-
gery developing iron deficiency and 8% of patients requiring reoperation.53,54
DRIVING TARGETS
Targets for the evaluation of safe driving should include regular (approximately every
2 years) clinical assessments for increased risk.55 Although driving is relatively safe for
most patients with diabetes, the issue is not without controversy. Commercial drivers
with diabetes are legally required to undergo medical evaluation periodically. See the
National Institutes of Healths evaluation site www.diabetesdriving.com. The
estimated HR for accidents while driving in those with diabetes is approximately 2,
though patients with diabetes differ dramatically in their individual risk, with the great-
est risks, excluding eyesight issues, being disruptive hypoglycemia (requiring the
assistance of another person to normalize glucose and cognitive function) and sleep
apnea (OR 5 6.3 of an accident with an apnea-hypopnea index greater than 10).56
Lesser risks include numbness in the right foot (accelerator/brake foot) (Box 2).55
SUMMARY
In conclusion, targets for patients with diabetes have actually become simpler with the
release of new guidelines. The targets discussed in this article are summarized in
Box 3. Finally, as clinicians and patients with diabetes struggle with the overwhelming
burden of care, clinicians should consider the increasingly codified ethic of minimally
disruptive medicine, which considers not just what patients and doctors can do but
what patients priorities, wishes, and needs are rather than the many specialist tests
and treatment options available.57,58 Finding the balance may be easier with the
new evidence-based and more straightforward guidelines.
REFERENCES
1. Orchard TJ, Chang YF, Ferrell RE, et al. Nephropathy in type 1 diabetes: a mani-
festation of insulin resistance and multiple genetic susceptibilities? Further evi-
dence from the Pittsburgh Epidemiology of Diabetes Complication Study.
Kidney Int 2002;62(3):96370.
2. Freedman BI, Bostrom M, Daeihagh P, et al. Genetic factors in diabetic ne-
phropathy. Clin J Am Soc Nephrol 2007;2(6):130616.
3. Divers J, Freedman BI. Genetics in kidney disease in 2013: susceptibility genes
for renal and urological disorders. Nat Rev Nephrol 2014;10(2):6970.
4. Mazzucco G, Bertani T, Fortunato M, et al. Different patterns of renal damage in
type 2 diabetes mellitus: a multicentric study on 393 biopsies. Am J Kidney Dis
2002;39(4):71320.
5. Roscioni SS, Heerspink HJ, de Zeeuw D. The effect of RAAS blockade on the
progression of diabetic nephropathy. Nat Rev Nephrol 2014;10(2):7787.
6. Gregg EW, Li Y, Wang J, et al. Changes in diabetes-related complications in the
United States, 1990-2010. N Engl J Med 2014;370(16):151423.
Nonglycemic Targets in Diabetes 197
7. Hermida RC, Ayala DE, Mojon A, et al. Influence of time of day of blood
pressure-lowering treatment on cardiovascular risk in hypertensive patients
with type 2 diabetes. Diabetes Care 2011;34(6):12706.
8. James PA, Oparil S, Carter BL, et al. 2014 evidence-based guideline for the
management of high blood pressure in adults: report from the panel members
appointed to the Eighth Joint National Committee (JNC 8). JAMA 2014;311(5):
50720.
9. Arguedas JA, Leiva V, Wright JM. Blood pressure targets for hypertension in peo-
ple with diabetes mellitus. Cochrane Database Syst Rev 2013;(10):CD008277.
10. Shen L, Shah BR, Reyes EM, et al. Role of diuretics, beta blockers, and statins in
increasing the risk of diabetes in patients with impaired glucose tolerance: rean-
alysis of data from the NAVIGATOR study. BMJ 2013;347:f6745.
11. Blood pressure management in CKD ND patients with diabetes mellitus. Kidney
Int Suppl 2012;2:3639.
12. Weber MA, Schiffrin EL, White WB, et al. Clinical practice guidelines for the man-
agement of hypertension in the community: a statement by the American Soci-
ety of Hypertension and the International Society of Hypertension. J Clin
Hypertens 2014;16(1):1426.
13. American Geriatrics Society Expert Panel on Care of Older Adults with Diabetes
Mellitus, Moreno G, Mangione CM, et al. Guidelines abstracted from the Amer-
ican Geriatrics Society guidelines for improving the care of older adults with dia-
betes mellitus: 2013 update. J Am Geriatr Soc 2013;61(11):20206.
14. Cheng J, Zhang W, Zhang X, et al. Effect of angiotensin-converting enzyme
inhibitors and angiotensin II receptor blockers on all-cause mortality, cardio-
vascular deaths, and cardiovascular events in patients with diabetes mellitus:
a meta-analysis. JAMA Intern Med 2014;174(5):77385.
15. Wu HY, Huang JW, Lin HJ, et al. Comparative effectiveness of renin-angiotensin
system blockers and other antihypertensive drugs in patients with diabetes: sys-
tematic review and bayesian network meta-analysis. BMJ 2013;347:f6008.
16. Beckett N, Peters R, Tuolilehto J, et al. Immediate and late benefits of treating very
elderly people with hypertension: results from active treatment extension to Hy-
pertension in the Very Elderly randomised controlled trial. BMJ 2012;344:d7541.
17. Blood pressure management in elderly persons with CKD ND. Kidney Int Suppl
2012;2:37781.
18. Fried LF, Emanuele N, Zhang JH, et al. Combined angiotensin inhibition for the
treatment of diabetic nephropathy. N Engl J Med 2013;369(20):1892903.
19. Bakris GL, Weir MR. Angiotensin-converting enzyme inhibitor-associated eleva-
tions in serum creatinine: is this a cause for concern? Arch Intern Med 2000;
160(5):68593.
20. Go AS, Chertow GM, Fan D, et al. Chronic kidney disease and the risks of death,
cardiovascular events, and hospitalization. N Engl J Med 2004;351(13):
1296305.
21. Juurlink DN, Mamdani MM, Lee DS, et al. Rates of hyperkalemia after publica-
tion of the Randomized Aldactone Evaluation Study. N Engl J Med 2004;351(6):
54351.
22. Adam WR. Plasma and dialysate potassium concentrations and haemodialysis
associated mortality. Nephrology 2013;18(10):6556.
23. Weir MR, Rolfe M. Potassium homeostasis and renin-angiotensin-aldosterone
system inhibitors. Clin J Am Soc Nephrol 2010;5(3):53148.
24. Stone NJ, Robinson J, Lichtenstein AH, et al. 2013 ACC/AHA guideline on the treat-
ment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults: a
198 DeWitt et al
61. Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of
America clinical practice guideline for the diagnosis and treatment of diabetic
foot infections. Clin Infect Dis 2012;54(12):e13273.
62. Sigal M. Comment on Evert et al. Nutrition therapy recommendations for the
management of adults with diabetes. Diabetes care 2013;36:3821-3842. Dia-
betes Care 2014;37(5):e100.
63. Evert AB, Boucher JL, Cypress M, et al. Nutrition therapy recommendations for
the management of adults with diabetes. Diabetes Care 2014;37(Suppl 1):
S12043.
S cree ning an d Treat me nt
b y t h e Pr i m a r y C a re
P ro v i d e r o f C o m m o n D i a b e t e s
Complications
Matthew P. Gilbert, DO, MPH
KEYWORDS
Microvascular complications Diabetic retinopathy Diabetic nephropathy
Macrovascular complications Diabetic peripheral neuropathy
Cardiovascular disease
KEY POINTS
Diabetes is the leading cause of end-stage renal disease, blindness, and nontraumatic
lower-limb amputation.
The largest reductions in cardiovascular events are seen when multiple risk factors such
as hypertension, dyslipidemia, and hyperglycemia are addressed simultaneously.
The benefit of aspirin as secondary prevention in patients with previous stroke or myocar-
dial infarction has been well established.
Regular, dilated eye examinations are effective in detecting sight-threatening diabetic reti-
nopathy and have been shown to prevent blindness.
The combined use of appropriate tools and clinical examination/inspection has been
shown to provide greater than 87% specificity in the detection of diabetic peripheral
neuropathy.
Early treatment of risk factors, including hypertension, hyperglycemia, and dyslipidemia
can delay or prevent diabetic nephropathy.
INTRODUCTION
Diabetes is the leading cause of end-stage renal disease, blindness, and nontraumatic
lower-limb amputation. It is also a major cause of cardiovascular morbidity and mor-
tality and the seventh leading cause of death in the United States. The economic cost
of diabetes in the United States in 2012 was estimated to be $245 billion, of which
$176 billion were direct medical costs related to diabetes.1 Much of the disability
and cost associated with diabetes are related to the care of chronic complications.
Recent advances in knowledge, therapies, and technology have enhanced the ability
to effectively care for patients with diabetes. In spite of these advances, patients with
diabetes still experience suboptimal glucose, blood pressure, and cholesterol levels,
putting them at risk for the development of acute and chronic complications.
CARDIOVASCULAR DISEASE
to reduce the risk of vascular events by 12%, with the largest reduction seen in
nonfatal MI. The effect of aspirin on cardiovascular events was similar for patients
with and without diabetes. Two randomized controlled clinical trials of aspirin failed
to show a reduction in cardiovascular events in patients with diabetes.31,32 Clinicians
should consider treatment with aspirin (75162 mg/d) for primary prevention of CVD in
patients with type 1 and type 2 diabetes at increased cardiovascular risk (10-year
risk >10%) and who are not at increased risk for bleeding. Treatment with aspirin is
not recommended as primary prevention in patients with diabetes and low cardiovas-
cular risk (10-year risk <5%). The American Diabetes Association recommends use of
clinical judgment for those at intermediate risk (10-year risk 5%10%) until further
research is available regarding the risks and benefits of aspirin therapy. Aspirin ther-
apy is recommended for all patients with diabetes and a history of CVD as secondary
prevention. Aspirin use in patients less than 21 years of age is contraindicated.
Physical activity can improve insulin sensitivity and lower total cholesterol levels,
LDL cholesterol levels, and triglyceride levels, as well as raising HDL cholesterol
levels. In addition, exercise may further decrease the risk of CVD by improving overall
cardiovascular fitness and function. Even patients with diabetes who are not obese
can benefit from physical activity. Adults with diabetes should be advised to obtain
at least 150 minutes per week of moderate-intensity, aerobic activity with no more
than 2 consecutive days without exercise. Smoking is an independent risk factor for
the development of CVD. A recent study found that smoking cessation was associated
with reduction in blood pressure and albuminuria in patients with newly diagnosed
type 2 diabetes.33 All patients with diabetes should be encouraged not to smoke or
use tobacco products and smoking cessation counseling should be part of routine
diabetes care.
Retinopathy
Diabetic retinopathy is the most frequent cause of blindness among adults 20 to
74 years of age. The pathophysiology, natural history, and clinical presentation of dia-
betic retinopathy are well understood with recognizable stages of the disease. Early
clinical signs of retinopathy include small outpouchings from the retinal capillaries
called microaneurysms and dot intraretinal hemorrhages. As the disease progresses,
macular edema, ischemic changes, collateralization, and proliferative changes may
lead to visual impairment or vision loss. Risk factors for developing diabetic retinop-
athy include duration of diabetes,34,35 severity of hyperglycemia,8,36,37 hypertension,16
and dyslipidemia.38
Twenty years after the diagnosis of diabetes, almost all patients with type 1 diabetes
and approximately 80% of patients with type 2 diabetes have some degree of diabetic
retinopathy.35 Over the last 30 years there has been a decline in both the incidence
and risk of progression of diabetic retinopathy.39 The Wisconsin Epidemiologic Study
of Diabetic Retinopathy reported a 77% decline in the annual incidence of proliferative
retinopathy in patients with type 1 diabetes mellitus (T1DM) from 1980 to 2007.40
There are precise, safe, and accepted screening tests (ophthalmoscopy and retinal
photography) for diabetic retinopathy.41 Regular dilated eye examinations are effec-
tive in detecting sight-threatening diabetic retinopathy and have been shown to pre-
vent blindness.42,43 Patients with macular edema and diabetic retinopathy may be
asymptomatic at the time of diagnosis, so all patients with diabetes should undergo
comprehensive screening. Screening for diabetic retinopathy in patients with type 1
diabetes should be started within 5 years following the diagnosis. This screening
recommendation is supported by evidence that retinopathy is estimated to take
5 years to develop after the onset of hyperglycemia.44 Patients with newly diagnosed
Common Diabetes Complications 205
type 2 diabetes may have had asymptomatic hyperglycemia for several years before
the diagnosis and thus have a significant risk of diabetic retinopathy at the time of
diagnosis. Therefore, patients with type 2 diabetes should have an initial dilated and
comprehensive eye examination at the time of diagnosis. An optometrist or an
ophthalmologist with experience in the diagnosis of diabetic retinopathy should
perform the comprehensive examination. Dilated and comprehensive eye examina-
tions should be repeated on an annual basis for patients with type 1 and type 2 dia-
betes. However, there is evidence to suggest that, in patients with well-controlled
type 2 diabetes, a comprehensive evaluation every 2 years may be cost-effective
with little risk of development of diabetic retinopathy.45
Ophthalmoscopy remains the most common technique for monitoring diabetic reti-
nopathy. However, the use of nondilated ophthalmoscopy by noneye care providers
has been shown to have poor sensitivity compared with retinal photography.41
Screening for diabetic retinopathy using a nonmydriatic camera (eg, without dilating
the pupils) has become more popular. Several studies have examined the efficacy
of digital retinal photographs as a screening tool for retinopathy. A recent meta-
analysis of 20 studies using nonmydriatic digital retinal photographs showed 82.5%
sensitivity and 88.5% specificity for the diagnosis of diabetic retinopathy.46 The use
of retinal photography, with remote reading by an ophthalmologist, has been pro-
moted as a way to improve the diagnosis and treatment of patients with retinopathy,
particularly in rural areas where eye care professionals may not be readily available.
Retinal photographs may be a useful screening tool for diabetic retinopathy, but
should not be a substitute for a comprehensive eye examination. Fig. 1 shows the
effectiveness of retinal photographs in identifying retinopathy.
Changes in glycemic control or other hormonal factors during pregnancy may accel-
erate diabetic retinopathy. Patients enrolled in the DCCT had transient worsening of
retinopathy during pregnancy.47 The American Diabetes Association recommends
that women with preexisting diabetes who are pregnant should have comprehensive
eye examination during the first trimester with close follow-up for 1 year postpartum.
Large randomized controlled trials have shown that intensive glycemic manage-
ment, with a goal of normoglycemia, can prevent the onset and delay the progression
of diabetic retinopathy.8,4749 The UKPDS reported the effectiveness of tight (<150/
85 mm Hg) blood pressure control in reducing the progression of diabetic retinopathy.
Fig. 1. (A) Normal and (B) diabetic retinopathy. (Courtesy of Brian Kim, MD, Burlington, VT.)
206 Gilbert
However, the ACCORD study failed to show that reducing blood pressure to less than
120 mm Hg offered further benefit.29
Retinal photocoagulation for the treatment of diabetic retinopathy was introduced in
the 1960s. The effectiveness of photocoagulation in the treatment of diabetic retinop-
athy has been shown in several clinical trials. The Diabetic Retinopathy Study (DRS)
concluded that retinal photocoagulation reduced the risk of severe vision loss to
6.4% of treated eyes compared with 15.9% of untreated eyes.50 The Early Treatment
Diabetic Retinopathy Study (ETDS) showed that focal retinal photocoagulation was
effective in reducing macular edema.50 Both the DRS and the ETDS showed the effi-
cacy of retinal photocoagulation in the reduction of further vision loss from diabetic
retinopathy, but did not show that photocoagulation could reverse retinopathy.
An active factor in the pathophysiology of diabetic retinopathy is inflammation,
which leads to macular edema, ischemia, and neovascularization.51 Vascular endo-
thelial growth factor is one of many proinflammatory mediators that have been shown
to induce angiogenesis and vascular permeability.51 Treatment with vascular endothe-
lial growth factor inhibitors (ranibizumab and bevacizumab) has been shown to
improve vision and reduce further need for photocoagulation in patients with clinically
significant diabetic macular edema.52 These intravitreal drug therapies are typically
injected every 4 to 6 weeks.
The EURODIAB controlled trial of lisionpril in insulin-dependent diabetes mellitus
(EUCLID) study reported that use of an ACE inhibitor may reduce the progression of
diabetic retinopathy and the incidence of proliferative diabetic retinopathy in normo-
tensive patients with type 1 diabetes.53 The more recent ADVANCE/the action in
diabetes and vascular disease controlled evaluation retinal measurement (ADREM)
trial seemed to show some protective effect of ACE inhibitors on the progression of
retinopathy in patients with type 2 diabetes, although the data were not statistically
significant.54 The Diabetic Retinopathy Candesartan Trials (DIRECT) were a group of
3 multicenter, randomized, placebo-controlled studies design to determine whether
pharmacologic blockade of the renin-angiotensin system by candesartan could
prevent the onset (DIRECT-Prevent 1)55 or progression (DIRECT-Protect 1)55 of dia-
betic retinopathy in patients with type 1 diabetes or promote regression of diabetic
retinopathy in type 2 diabetes (DIRECT-Protect 2).56 The severity of retinopathy at
the end of the study was significantly more favorable in patients treated with cande-
sartan in DIRECT-Prevent 1, DIRECT-Protect 1, and DIRECT-Protect 2. The results
of DIRECT-Protect 2 showed a statistically significant 34% increase in the probability
of regression of diabetic retinopathy in patients with type 2 diabetes treated with
candesartan.
Lipid levellowering agents may also decrease the risk of vision loss in patients with
diabetic retinopathy. The fenofibrate intervention and event lowering in diabetes
(FIELD) study reported a 30% reduction in the need for laser treatment of diabetic
macular edema and proliferative diabetic retinopathy in patients treated with a fenofi-
brate.57 The ACCORD Eye Study Group also reported a reduction in the progression of
diabetic retinopathy in patients with type 2 diabetes treated with a fenofibrate and
statin compared with patients treated with statin alone.49
neuropathy is typically divided into diabetic peripheral neuropathy (DPN) and auto-
nomic neuropathy. DPN has been defined as the presence of symptoms and/or signs
of peripheral nerve dysfunction after the exclusion of other causes (ie, traumatic,
compressive, neoplastic, metabolic, or other systemic illnesses).58,59 The prevalence
of diabetic neuropathy in newly diagnosed patients with diabetes is estimated to be
8% and greater than 50% in patients with long-standing disease.60 Diabetic neurop-
athy remains the leading cause of nontraumatic limb amputations.61 Several epidemi-
ologic studies have shown that duration and severity of diabetes are significant risk
factors for the development of diabetic neuropathy in patients with type 1 and type
2 diabetes.62 Additional investigations have also shown that smoking, dyslipidemia,
and hypertension increase an individuals risk of developing neuropathy.63,64
Symptoms such as burning, tingling, numbness, shooting (electric shock), and
stabbing are present in 33% of patients with DPN.65,66 Patients may first experience
symptoms in their toes that gradually move proximally. These symptoms are most
often worst at night and can disrupt sleep.67 The high prevalence of diabetic neu-
ropathy results in significant morbidity, including an increased risk of recurrent
lower-extremity infections, ulcerations, depression, foot and ankle fractures, and
lower-limb amputations.6871
The pathogenesis of DPN is multifactorial and includes a combination of metabolic,
vascular, and hormonal factors that shift the balance between nerve fiber damage and
repair. The combination of direct nerve injury caused by hyperglycemia, endothelial
injury, and microvascular dysfunction leads to nerve ischemia.72 In addition to nerve
ischemia and hypoxia, increased cytokine levels also play a role in the formation of
DPN.7375
Several questionnaires have been developed to assist clinicians in the diagnosis of
DPN.76 The douleur neuropathique 4 questions (DN4) questionnaire can be completed
rapidly and is easy to use, with reported good specificity (83%) and sensitivity (90%).77
There are several simple clinical tests that should be used to screen patients for DPN.
Patients with type 1 and type 2 diabetes should be screened for DPN on an annual ba-
sis. Pinprick sensation and light touch perception should be assessed using a 10-g
monofilament. In addition, vibratory threshold should be assessed using a 128-Hz tun-
ing fork. The combined use of appropriate tools and clinical examination/inspection
has been shown to provide greater than 87% specificity in the detection of DPN.7880
Improved glycemic control has been shown to improve nerve function in patients
with diabetes.8183 Intensive glycemic control has also been shown to reduce the
risk of developing diabetic neuropathy in patients with type 1 diabetes and may reduce
the risk in patients with type 2 diabetes.84,85 The evidence for glycemic control and the
prevention of neuropathy in patients with type 2 diabetes is not as strong. The UKPDS
investigators reported a 25% risk reduction in microvascular complications after
10 years of intensive treatment. However, most of the risk reduction was driven by
the reduction in retinopathy. Some studies have shown a slowing of the progression
of diabetic neuropathy with improved glycemic control in patients with type 2 dia-
betes. Intensive glycemic control, particularly early in the disease, seems to provide
a long-term benefit for the prevention of diabetic neuropathy. The EDIC trial followed
approximately 95% of the subjects enrolled in the DCCT cohort for several years.7
During the EDIC trial, the glycemic separation between the intensively treated group
and the standard treatment group disappeared. Patients with previous intensive treat-
ment of their type 1 diabetes had a decrease in the prevalence of neuropathy that per-
sisted through the EDIC follow-up despite deterioration of their glycemic control.78
There are no treatments currently available to repair the underlying nerve damage in
diabetic neuropathy; however, there are effective symptomatic treatments for the
208 Gilbert
neuropathic pain associated with DPN. Patients with painful neuropathy should be
treated with a systematic, stepwise approach. Treatments that may be beneficial
include several antidepressants (eg, amitriptyline, duloxetine, venlafaxine) and anti-
convulsants (eg, pregabalin, sodium valproate). Effective treatment of painful diabetic
neuropathy includes a balance between pain relief and medication side effects
(Table 1). General principles regarding pharmaceutical management include careful
selection of initial drug therapy and titration based on efficacy and side effects.
Several randomized, placebo-controlled trials have shown the effectiveness of tricy-
clic antidepressant drugs in the treatment of painful diabetic neuropathy8689; how-
ever, use is often limited by significant side effects. Serotonin-noradrenaline
reuptake inhibitors have been shown to be effective treatments for painful diabetic
neuropathy. Medications in this class include venlafaxine, milnacipran, and duloxe-
tine. These drugs block reuptake of both serotonin and norepinephrine with differing
selectivity. The extended-release version of venlafaxine (doses of 150225 mg daily)
was superior to placebo in nondepressed patients with diabetic neuropathy.90 The
most common side effects of venlafaxine were nausea and fatigue. Given reports of
seizures with this medication it should be used with caution in patients with a history
of frequent hypoglycemic seizures. Duloxetine has been licensed in the United States
for treatment of painful diabetic neuropathy. The benefit of duloxetine was established
in 3 separate 12-week randomized controlled investigations involving more than 1100
patients. In these 3 trials, pain control was better with duloxetine 60 or 120 mg daily
than with placebo.9193
Antiepileptic drugs have a long history of effectiveness in the treatment of neuro-
pathic pain. Gabapentin is a anticonvulsant medication whose structure is similar to
gamma-aminobutyric acid. The exact mechanism of action of gabapentin with regard
to treatment of neuropathic pain is not fully understood. In an 8-week, multicenter,
Table 1
Treatment options for painful, diabetic neuropathy
Abbreviations: BID, twice a day; QID, 4 times a day; SNRI, serotonin-noradrenaline reuptake inhib-
itor; TCAs, tricyclic antidepressants; TID, 3 times a day.
Common Diabetes Complications 209
randomized controlled trial of 165 patients with diabetes gabapentin had moderate
pain relief compared with placebo.94 However, the overall evidence regarding gaba-
pentin as an effective treatment of painful diabetic retinopathy has been described
as weak.95 Gabapentin has been shown to improve sleep, which is often disturbed
in patients with chronic pain and particularly with diabetic neuropathy.96 Lightheaded-
ness and fatigue were the most common adverse events reported in approximately
23% patients in the randomized controlled trial. Weight gain has also been reported
with use of gabapentin. Several clinical trials have investigated the effectiveness of
pregabalin in the treatment of painful diabetic neuropathy.97100 In a pooled analysis
from 7 randomized, placebo-controlled trials, pregabalin was shown to relieve pain
and improve quality-of-life measures, social functioning, and mental health as well
as improve sleep.101 The most common adverse events seen in the clinical trials
were dizziness, fatigue, and peripheral edema. Pregabalin has also been shown to
cause vertigo, incoordination, ataxia, diplopia, blurred vision, sedation, and confu-
sion.102 Pregabalin may also be habit forming.
For patients who are unable to tolerate any of the pharmaceutical treatments for
painful diabetic neuropathy, alternative treatments include capsaicin cream,103,104
lidocaine patch,105 alpha-lipoic acid,106,107 and transcutaneous electrical nerve stim-
ulation.108 The use of opioids for chronic management remains controversial. Several
trials have shown relief of symptoms following treatment with controlled-release oxy-
codone in patients whose pain was not well controlled on standard treatment.109,110
However, opioid-related side effects were common among participants in these trials.
Treatment of painful diabetic neuropathy with opioid medications should be reserved
for patients who have failed to respond or cannot tolerate several first-line medications
used in combination.
Diabetic Nephropathy
Nephropathy is a common complication of both type 1 and type 2 diabetes, occurring
in 15% to 25% and 30% to 40% of patients, respectively.111113 In the analysis of pa-
tients enrolled in the UKPDS trial, 24.9% of patients with type 2 diabetes developed
microalbuminuria, 5.3% developed microalbuminuria, and 0.8% showed increased
creatinine levels or required dialysis within the first 10 years after diagnosis.114 Dia-
betes is the leading cause of end-stage renal disease (ESRD) in both developed
and emerging countries.115 The clinical manifestations of diabetic nephropathy,
including proteinuria, increased blood pressure, and decreased glomerular filtration
rate (GFR), are the same in patients with type 1 and type 2 diabetes.116 However,
by the time the laboratory or clinical abnormalities of diabetic nephropathy become
evident, significant pathologic changes are already present within the kidney. Glomer-
ulosclerosis, thickening of the glomerular basement membrane, mesangial cell expan-
sion, loss of podocytes, renal cell hypertrophy, and tubulointerstitial fibrosis are the
major pathologic changes that occur during the progression of diabetic nephropa-
thy.116119 These changes lead to progressive albuminuria, reduction in GFR, increase
in blood pressure, and fluid retention. Chronic kidney disease is associated with a sub-
stantially increased risk for CVD that is independent of the traditional CVD risk
factors.120,121
Screening for diabetic nephropathy should include the evaluation for increased uri-
nary albumin excretion using an albumin/creatinine ratio on a random spot urine
collection (Fig. 2). An albumin/creatinine ratio should be performed on patients with
type 1 diabetes for more than 5 years and in all patients with type 2 diabetes at the
time of diagnosis. There may be significant variability in urine albumin excretion. Exer-
cise within 24 hours of collection, infection, fever, congestive heart failure, marked
210 Gilbert
Yes
Yes
Yes
Yes
Begin treatment Repeat screening
in one year
hyperglycemia, menstrual blood, and hypertension have all been shown to increase
urinary albumin excretion to more than baseline values. Therefore 2 of 3 specimens
collected within a period of 3 to 6 months should be abnormal before diagnosing
the patient with increased urinary albumin excretion. Clinicians should obtain a serum
creatinine level with estimated GFR on a yearly basis in all patients with diabetes
regardless of the degree of urine albumin excretion. Clinical studies have found
decreased GFR in patients without evidence of increased urine albumin excretion
(Table 2).122,123 The role of continued annual assessment of urine albumin excretion
after the diagnosis of albuminuria has been made remains unclear. The American Dia-
betes Association recommends continued monitoring of urine albumin excretion to
assess both response to therapy and progression of disease. The development of
complications from chronic kidney disease correlates with level of kidney function,
particularly GFR. It is recommended that clinicians begin screening for complications
of chronic kidney disease in patients with estimated GFR less than 60 mL/min/1.73 m2.
The optimal approach to therapy in patients with diabetic nephropathy includes tar-
geting multiple factors, such as hypertension, hyperglycemia, and dyslipidemia. Early
Table 2
Stages of chronic kidney disease
treatment of risk factors can delay or prevent diabetic nephropathy. In the UKPDS trial,
intensive blood pressure control was associated with a 30% risk reduction for the
development of microalbuminuria.8 The optimal lower limit for systolic blood pressure
for the prevention of diabetic nephropathy has not yet been established. Adequate
blood pressure control with drugs that modulate the renin-angiotensin system has
been shown to reduce the incidence and progression of diabetic nephropathy.115
Among patients with type 1 diabetes and diabetic nephropathy, remission or regres-
sion may occur with control of systemic blood pressure, particularly with ACE inhibi-
tors.124 Several large, prospective, randomized trials in patients with type 1 diabetes
have shown that reduction of systolic blood pressures (<140 mm Hg) as a result of
treatment with an ACE inhibitor delayed the progression of microalbuminuria and
slowed the reduction in GFR in patients with proteinuria.125,126 The ADVANCE trial
compared the use of an ACE inhibitor with placebo in 11,000 patients with type 2 dia-
betes. After 4.3 years of follow-up there was a significant reduction in blood pressure
and in the rate of new-onset microalbuminuria.12 The effects of ACE inhibitors and
ARBs seem to be independent of blood pressure reduction, suggesting a direct reno-
protective effect.127,128
Several large, randomized, clinical trials have shown that ARBs reduced the pro-
gression of albuminuria as well as ESRD in patients with type 2 diabetes and diabetic
nephropathy.129136 Other classes of antihypertensive agents can be used in addition
to ACE inhibitors and/or ARBs to further reduce blood pressure or in patients who
cannot tolerate an ACE inhibitor or ARB.
Intensive glucose control has been shown to decrease the risk of development and
delay or prevent progression of diabetic nephropathy. The DCCT and its long-term
follow-up, the EDIC trial, showed that intensive glucose control prevented the devel-
opment of microalbuminuria in patients with type 1 diabetes.7,47 In patients with type 2
diabetes, the UKPDS showed that intensive glucose control reduced the risk of micro-
albuminuria or proteinuria by 33%.137 More recently, the ADVANCE trial confirmed the
benefits of intensive glucose control in the landmark clinical trials discussed earlier.12
Table 3
Screening recommendations for microvascular complications of diabetes mellitus
Microvascular Frequency of
Complication Screening Method Timing of Initial Screening Screening
Retinopathy Dilated and comprehensive T1DM: within 5 y of Annually
eye examination diagnosis
T2DM: at the time of Annually
diagnosis
DPN Pinprick sensation and light At the time of diagnosis Annually
touch perception using a
10-g monofilament and
vibratory threshold
should be assessed using
a 128-Hz tuning fork
Diabetic Albumin/creatinine ratio T1DM: duration of Annually
nephropathy disease >5 y
T2DM: at the time of
diagnosis
Serum creatinine for At the time of diagnosis Annually
estimation of GFR
ACKNOWLEDGMENTS
The author would like to acknowledge Brian Kim, MD, for supplying the retinal pho-
tographs and Annis Marney, MD, for editorial support.
REFERENCES
15. Stamler J, Vaccaro O, Neaton JD, et al. Diabetes, other risk factors, and 12-yr
cardiovascular mortality for men screened in the Multiple Risk Factor Interven-
tion Trial. Diabetes Care 1993;16(2):43444.
16. Tight blood pressure control and risk of macrovascular and microvascular com-
plications in type 2 diabetes: UKPDS 38. UK Prospective Diabetes Study Group.
BMJ 1998;317(7160):70313.
17. Hansson L, Zanchetti A, Carruthers SG, et al. Effects of intensive blood-pressure
lowering and low-dose aspirin in patients with hypertension: principal results of
the Hypertension Optimal Treatment (HOT) randomised trial. HOT Study Group.
Lancet 1998;351(9118):175562.
18. Adler AI, Stratton IM, Neil HA, et al. Association of systolic blood pressure with
macrovascular and microvascular complications of type 2 diabetes (UKPDS
36): prospective observational study. BMJ 2000;321(7258):4129.
19. Baigent C, Keech A, Kearney PM, et al. Efficacy and safety of cholesterol-
lowering treatment: prospective meta-analysis of data from 90,056 participants
in 14 randomised trials of statins. Lancet 2005;366(9493):126778.
20. Cholesterol Treatment Trialists Collaborators, Mihaylova B, Emberson J, et al.
The effects of lowering LDL cholesterol with statin therapy in people at low
risk of vascular disease: meta-analysis of individual data from 27 randomised
trials. Lancet 2012;380(9841):58190.
21. Knopp RH, dEmden M, Smilde JG, et al. Efficacy and safety of atorvastatin in
the prevention of cardiovascular end points in subjects with type 2 diabetes:
the Atorvastatin Study for Prevention of Coronary Heart Disease Endpoints in
Non-Insulin-Dependent Diabetes Mellitus (ASPEN). Diabetes Care 2006;29(7):
147885.
22. Colhoun HM, Betteridge DJ, Durrington PN, et al. Primary prevention of cardio-
vascular disease with atorvastatin in type 2 diabetes in the Collaborative Ator-
vastatin Diabetes Study (CARDS): multicentre randomised placebo-controlled
trial. Lancet 2004;364(9435):68596.
23. Cannon CP, Braunwald E, McCabe CH, et al. Intensive versus moderate lipid
lowering with statins after acute coronary syndromes. N Engl J Med 2004;
350(15):1495504.
24. de Lemos JA, Blazing MA, Wiviott SD, et al. Early intensive vs a delayed conser-
vative simvastatin strategy in patients with acute coronary syndromes: phase Z
of the A to Z trial. JAMA 2004;292(11):130716.
25. Nissen SE, Tuzcu EM, Schoenhagen P, et al. Effect of intensive compared with
moderate lipid-lowering therapy on progression of coronary atherosclerosis: a
randomized controlled trial. JAMA 2004;291(9):107180.
26. Stone NJ, Robinson JG, Lichtenstein AH, et al. 2013 ACC/AHA guideline on the
treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in
adults: a report of the American College of Cardiology/American Heart Associa-
tion Task Force on Practice Guidelines. Circulation 2014;129(25 Suppl 2):S145.
27. Rubins HB, Robins SJ, Collins D, et al. Gemfibrozil for the secondary prevention
of coronary heart disease in men with low levels of high-density lipoprotein
cholesterol. Veterans Affairs High-Density Lipoprotein Cholesterol Intervention
Trial Study Group. N Engl J Med 1999;341(6):4108.
28. Keech A, Simes RJ, Barter P, et al. Effects of long-term fenofibrate therapy on
cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD
study): randomised controlled trial. Lancet 2005;366(9500):184961.
29. ACCORD Study Group, Ginsberg HN, Elam MB, et al. Effects of combination
lipid therapy in type 2 diabetes mellitus. N Engl J Med 2010;362(17):156374.
214 Gilbert
47. The effect of intensive treatment of diabetes on the development and progression of
long-term complications in insulin-dependent diabetes mellitus. The Diabetes Con-
trol and Complications Trial Research Group. N Engl J Med 1993;329(14):97786.
48. Effect of intensive blood-glucose control with metformin on complications in
overweight patients with type 2 diabetes (UKPDS 34). UK Prospective Diabetes
Study (UKPDS) Group. Lancet 1998;352(9131):85465.
49. ACCORD Study Group, ACCORD Eye Study Group, Chew EY, et al. Effects of
medical therapies on retinopathy progression in type 2 diabetes. N Engl J
Med 2010;363(3):23344.
50. Preliminary report on effects of photocoagulation therapy. The Diabetic Retinop-
athy Study Research Group. Am J Ophthalmol 1976;81(4):38396.
51. Bandello F, Berchicci L, La Spina C, et al. Evidence for anti-VEGF treatment of
diabetic macular edema. Ophthalmic Res 2012;48(Suppl 1):1620.
52. Nguyen QD, Brown DM, Marcus DM, et al. Ranibizumab for diabetic macular
edema: results from 2 phase III randomized trials: RISE and RIDE. Ophthal-
mology 2012;119(4):789801.
53. Chaturvedi N, Sjolie AK, Stephenson JM, et al. Effect of lisinopril on progression
of retinopathy in normotensive people with type 1 diabetes. The EUCLID Study
Group. EURODIAB Controlled Trial of Lisinopril in Insulin-Dependent Diabetes
Mellitus. Lancet 1998;351(9095):2831.
54. Beulens JW, Patel A, Vingerling JR, et al. Effects of blood pressure lowering and
intensive glucose control on the incidence and progression of retinopathy in pa-
tients with type 2 diabetes mellitus: a randomised controlled trial. Diabetologia
2009;52(10):202736.
55. Chaturvedi N, Porta M, Klein R, et al. Effect of candesartan on prevention (DIRECT-
Prevent 1) and progression (DIRECT-Protect 1) of retinopathy in type 1 diabetes:
randomised, placebo-controlled trials. Lancet 2008;372(9647):1394402.
56. Sjolie AK, Klein R, Porta M, et al. Effect of candesartan on progression and
regression of retinopathy in type 2 diabetes (DIRECT-Protect 2): a randomised
placebo-controlled trial. Lancet 2008;372(9647):138593.
57. Keech AC, Mitchell P, Summanen PA, et al. Effect of fenofibrate on the need for
laser treatment for diabetic retinopathy (FIELD study): a randomised controlled
trial. Lancet 2007;370(9600):168797.
58. Edwards JL, Vincent AM, Cheng HT, et al. Diabetic neuropathy: mechanisms to
management. Pharmacol Ther 2008;120(1):134.
59. Vinik AI, Park TS, Stansberry KB, et al. Diabetic neuropathies. Diabetologia
2000;43(8):95773.
60. Boulton AJ, Vinik AI, Arezzo JC, et al. Diabetic neuropathies: a statement by the
American Diabetes Association. Diabetes Care 2005;28(4):95662.
61. Thomas PK. Diabetic peripheral neuropathies: their cost to patient and society
and the value of knowledge of risk factors for development of interventions.
Eur Neurol 1999;41(Suppl 1):3543.
62. Genuth S. Insights from the Diabetes Control and Complications trial/Epidemi-
ology of Diabetes Interventions and Complications study on the use of intensive
glycemic treatment to reduce the risk of complications of type 1 diabetes. En-
docr Pract 2006;12(Suppl 1):3441.
63. Dyck PJ, Davies JL, Wilson DM, et al. Risk factors for severity of diabetic
polyneuropathy: intensive longitudinal assessment of the Rochester Diabetic
Neuropathy Study cohort. Diabetes Care 1999;22(9):147986.
64. Hanssen KF. Blood glucose control and microvascular and macrovascular com-
plications in diabetes. Diabetes 1997;46(Suppl 2):S1013.
216 Gilbert
65. Tesfaye S, Boulton AJ, Dyck PJ, et al. Diabetic neuropathies: update on defini-
tions, diagnostic criteria, estimation of severity, and treatments. Diabetes Care
2010;33(10):228593.
66. Davies M, Brophy S, Williams R, et al. The prevalence, severity, and impact of
painful diabetic peripheral neuropathy in type 2 diabetes. Diabetes Care
2006;29(7):151822.
67. Quattrini C, Tesfaye S. Understanding the impact of painful diabetic neuropathy.
Diabetes Metab Res Rev 2003;19(Suppl 1):S28.
68. Athans W, Stephens H. Open calcaneal fractures in diabetic patients with neu-
ropathy: a report of three cases and literature review. Foot Ankle Int 2008;29(10):
104953.
69. Veves A, Backonja M, Malik RA. Painful diabetic neuropathy: epidemiology,
natural history, early diagnosis, and treatment options. Pain Med 2008;9(6):
66074.
70. Obrosova IG. Diabetic painful and insensate neuropathy: pathogenesis and
potential treatments. Neurotherapeutics 2009;6(4):63847.
71. Gandhi RA, Marques JL, Selvarajah D, et al. Painful diabetic neuropathy is asso-
ciated with greater autonomic dysfunction than painless diabetic neuropathy.
Diabetes Care 2010;33(7):158590.
72. Singh R, Kishore L, Kaur N. Diabetic peripheral neuropathy: current perspective
and future directions. Pharmacol Res 2014;80:2135.
73. Yamakawa I, Kojima H, Terashima T, et al. Inactivation of TNF-alpha ameliorates
diabetic neuropathy in mice. Am J Physiol Endocrinol Metab 2011;301(5):
E84452.
74. Cameron NE, Cotter MA. Pro-inflammatory mechanisms in diabetic neuropathy:
focus on the nuclear factor kappa B pathway. Curr Drug Targets 2008;9(1):607.
75. Leinninger GM, Vincent AM, Feldman EL. The role of growth factors in diabetic
peripheral neuropathy. J Peripher Nerv Syst 2004;9(1):2653.
76. Deli G, Bosnyak E, Pusch G, et al. Diabetic neuropathies: diagnosis and man-
agement. Neuroendocrinology 2013;98(4):26780.
77. Hartemann A, Attal N, Bouhassira D, et al. Painful diabetic neuropathy: diag-
nosis and management. Diabetes Metab 2011;37(5):37788.
78. Martin CL, Albers J, Herman WH, et al. Neuropathy among the diabetes control
and complications trial cohort 8 years after trial completion. Diabetes Care
2006;29(2):3404.
79. Pop-Busui R, Lu J, Brooks MM, et al. Impact of glycemic control strategies on
the progression of diabetic peripheral neuropathy in the Bypass Angioplasty
Revascularization Investigation 2 Diabetes (BARI 2D) Cohort. Diabetes Care
2013;36(10):320815.
80. Herman WH, Pop-Busui R, Braffett BH, et al. Use of the Michigan Neuropathy
Screening Instrument as a measure of distal symmetrical peripheral neuropathy
in type 1 diabetes: results from the Diabetes Control and Complications Trial/
Epidemiology of Diabetes Interventions and Complications. Diabet Med 2012;
29(7):93744.
81. Graf RJ, Halter JB, Pfeifer MA, et al. Glycemic control and nerve conduction ab-
normalities in non-insulin-dependent diabetic subjects. Ann Intern Med 1981;
94(3):30711.
82. Holman RR, Dornan TL, Mayon-White V, et al. Prevention of deterioration of renal
and sensory-nerve function by more intensive management of insulin-dependent
diabetic patients. A two-year randomised prospective study. Lancet 1983;
1(8318):2048.
Common Diabetes Complications 217
83. Pietri A, Ehle AL, Raskin P. Changes in nerve conduction velocity after six weeks
of glucoregulation with portable insulin infusion pumps. Diabetes 1980;29(8):
66871.
84. Callaghan BC, Hur J, Feldman EL. Diabetic neuropathy: one disease or two?
Curr Opin Neurol 2012;25(5):53641.
85. Peltier A, Goutman SA, Callaghan BC. Painful diabetic neuropathy. BMJ 2014;
348:g1799.
86. Max MB, Culnane M, Schafer SC, et al. Amitriptyline relieves diabetic neuropathy
pain in patients with normal or depressed mood. Neurology 1987;37(4):58996.
87. Max MB, Lynch SA, Muir J, et al. Effects of desipramine, amitriptyline, and fluox-
etine on pain in diabetic neuropathy. N Engl J Med 1992;326(19):12506.
88. Kvinesdal B, Molin J, Froland A, et al. Imipramine treatment of painful diabetic
neuropathy. JAMA 1984;251(13):172730.
89. Vrethem M, Boivie J, Arnqvist H, et al. A comparison a amitriptyline and maproti-
line in the treatment of painful polyneuropathy in diabetics and nondiabetics.
Clin J Pain 1997;13(4):31323.
90. Simpson DA. Gabapentin and venlafaxine for the treatment of painful diabetic
neuropathy. J Clin Neuromuscul Dis 2001;3(2):5362.
91. Goldstein DJ, Lu Y, Detke MJ, et al. Duloxetine vs. placebo in patients with pain-
ful diabetic neuropathy. Pain 2005;116(1-2):10918.
92. Raskin J, Pritchett YL, Wang F, et al. A double-blind, randomized multicenter trial
comparing duloxetine with placebo in the management of diabetic peripheral
neuropathic pain. Pain Med 2005;6(5):34656.
93. Wernicke JF, Pritchett YL, DSouza DN, et al. A randomized controlled trial of du-
loxetine in diabetic peripheral neuropathic pain. Neurology 2006;67(8):141120.
94. Backonja M, Beydoun A, Edwards KR, et al. Gabapentin for the symptomatic
treatment of painful neuropathy in patients with diabetes mellitus: a randomized
controlled trial. JAMA 1998;280(21):18316.
95. Vinik AI, Casellini CM. Guidelines in the management of diabetic nerve pain:
clinical utility of pregabalin. Diabetes Metab Syndr Obes 2013;6:5778.
96. Dworkin RH, Backonja M, Rowbotham MC, et al. Advances in neuropathic pain:
diagnosis, mechanisms, and treatment recommendations. Arch Neurol 2003;
60(11):152434.
97. Lesser H, Sharma U, LaMoreaux L, et al. Pregabalin relieves symptoms of pain-
ful diabetic neuropathy: a randomized controlled trial. Neurology 2004;63(11):
210410.
98. Richter RW, Portenoy R, Sharma U, et al. Relief of painful diabetic peripheral
neuropathy with pregabalin: a randomized, placebo-controlled trial. J Pain
2005;6(4):25360.
99. Rosenstock J, Tuchman M, LaMoreaux L, et al. Pregabalin for the treatment of
painful diabetic peripheral neuropathy: a double-blind, placebo-controlled trial.
Pain 2004;110(3):62838.
100. Freynhagen R, Strojek K, Griesing T, et al. Efficacy of pregabalin in neuropathic
pain evaluated in a 12-week, randomised, double-blind, multicentre, placebo-
controlled trial of flexible- and fixed-dose regimens. Pain 2005;115(3):25463.
101. Freeman R, Durso-Decruz E, Emir B. Efficacy, safety, and tolerability of pregabalin
treatment for painful diabetic peripheral neuropathy: findings from seven random-
ized, controlled trials across a range of doses. Diabetes Care 2008;31(7):144854.
102. Zaccara G, Gangemi P, Perucca P, et al. The adverse event profile of pre-
gabalin: a systematic review and meta-analysis of randomized controlled trials.
Epilepsia 2011;52(4):82636.
218 Gilbert
103. Derry S, Lloyd R, Moore RA, et al. Topical capsaicin for chronic neuropathic pain
in adults. Cochrane Database Syst Rev 2009;(4):CD007393.
104. Mason L, Moore RA, Derry S, et al. Systematic review of topical capsaicin for the
treatment of chronic pain. BMJ 2004;328(7446):991.
105. Baron R, Mayoral V, Leijon G, et al. Efficacy and safety of combination therapy
with 5% lidocaine medicated plaster and pregabalin in post-herpetic neuralgia
and diabetic polyneuropathy. Curr Med Res Opin 2009;25(7):167787.
106. Ziegler D, Ametov A, Barinov A, et al. Oral treatment with alpha-lipoic acid im-
proves symptomatic diabetic polyneuropathy: the SYDNEY 2 trial. Diabetes
Care 2006;29(11):236570.
107. Ziegler D, Nowak H, Kempler P, et al. Treatment of symptomatic diabetic poly-
neuropathy with the antioxidant alpha-lipoic acid: a meta-analysis. Diabet
Med 2004;21(2):11421.
108. Abuaisha BB, Costanzi JB, Boulton AJ. Acupuncture for the treatment of chronic
painful peripheral diabetic neuropathy: a long-term study. Diabetes Res Clin
Pract 1998;39(2):11521.
109. Watson CP, Moulin D, Watt-Watson J, et al. Controlled-release oxycodone re-
lieves neuropathic pain: a randomized controlled trial in painful diabetic neurop-
athy. Pain 2003;105(12):718.
110. Gilron I, Bailey JM, Tu D, et al. Morphine, gabapentin, or their combination for
neuropathic pain. N Engl J Med 2005;352(13):132434.
111. Steinke JM, Mauer M, International Diabetic Nephropathy Study Group. Lessons
learned from studies of the natural history of diabetic nephropathy in young type
1 diabetic patients. Pediatr Endocrinol Rev 2008;5(Suppl 4):95863.
112. Bogdanovic R. Diabetic nephropathy in children and adolescents. Pediatr
Nephrol 2008;23(4):50725.
113. Koro CE, Lee BH, Bowlin SJ. Antidiabetic medication use and prevalence of
chronic kidney disease among patients with type 2 diabetes mellitus in the
United States. Clin Ther 2009;31(11):260817.
114. Adler AI, Stevens RJ, Manley SE, et al. Development and progression of ne-
phropathy in type 2 diabetes: the United Kingdom Prospective Diabetes Study
(UKPDS 64). Kidney Int 2003;63(1):22532.
115. Atkins RC, Zimmet P, International Society of Nephrology/International Federa-
tion of Kidney Foundations World Kidney Day Steering Committee, et al. Dia-
betic kidney disease: act now or pay later. Am J Med Sci 2010;339(2):1024.
116. Mauer SM, Steffes MW, Ellis EN, et al. Structural-functional relationships in dia-
betic nephropathy. J Clin Invest 1984;74(4):114355.
117. Dalla Vestra M, Saller A, Bortoloso E, et al. Structural involvement in type 1 and
type 2 diabetic nephropathy. Diabetes Metab 2000;26(Suppl 4):814.
118. Mason RM, Wahab NA. Extracellular matrix metabolism in diabetic nephropathy.
J Am Soc Nephrol 2003;14(5):135873.
119. Ziyadeh FN. The extracellular matrix in diabetic nephropathy. Am J Kidney Dis
1993;22(5):73644.
120. Go AS, Chertow GM, Fan D, et al. Chronic kidney disease and the risks of death,
cardiovascular events, and hospitalization. N Engl J Med 2004;351(13):
1296305.
121. Wu AY, Kong NC, de Leon FA, et al. An alarmingly high prevalence of diabetic
nephropathy in Asian type 2 diabetic patients: the MicroAlbuminuria Prevalence
(MAP) Study. Diabetologia 2005;48(1):1726.
122. National Kidney Foundation. KDOQI clinical practice guideline for diabetes and
CKD: 2012 update. Am J Kidney Dis 2012;60(5):85086.
Common Diabetes Complications 219
123. Levinsky NG. Specialist evaluation in chronic kidney disease: too little, too late.
Ann Intern Med 2002;137(6):5423.
124. Steffes MW. Affecting the decline of renal function in diabetes mellitus. Kidney
Int 2001;60(1):3789.
125. Lewis EJ, Hunsicker LG, Bain RP, et al. The effect of angiotensin-converting-
enzyme inhibition on diabetic nephropathy. The Collaborative Study Group.
N Engl J Med 1993;329(20):145662.
126. Laffel LM, McGill JB, Gans DJ. The beneficial effect of angiotensin-converting
enzyme inhibition with captopril on diabetic nephropathy in normotensive
IDDM patients with microalbuminuria. North American Microalbuminuria Study
Group. Am J Med 1995;99(5):497504.
127. Mogensen CE. Microalbuminuria and hypertension with focus on type 1 and
type 2 diabetes. J Intern Med 2003;254(1):4566.
128. Viberti G, Wheeldon NM. MicroAlbuminuria Reduction With VSI. Microalbuminu-
ria reduction with valsartan in patients with type 2 diabetes mellitus: a blood
pressure-independent effect. Circulation 2002;106(6):6728.
129. Lewis EJ, Hunsicker LG, Clarke WR, et al. Renoprotective effect of the
angiotensin-receptor antagonist irbesartan in patients with nephropathy due
to type 2 diabetes. N Engl J Med 2001;345(12):85160.
130. Atkins RC, Briganti EM, Lewis JB, et al. Proteinuria reduction and progression to
renal failure in patients with type 2 diabetes mellitus and overt nephropathy. Am
J Kidney Dis 2005;45(2):2817.
131. Brenner BM, Cooper ME, de Zeeuw D, et al. Effects of losartan on renal and car-
diovascular outcomes in patients with type 2 diabetes and nephropathy. N Engl
J Med 2001;345(12):8619.
132. Parving HH, Lehnert H, Brochner-Mortensen J, et al. The effect of irbesartan on
the development of diabetic nephropathy in patients with type 2 diabetes.
N Engl J Med 2001;345(12):8708.
133. Mogensen CE, Neldam S, Tikkanen I, et al. Randomised controlled trial of dual
blockade of renin-angiotensin system in patients with hypertension, microalbu-
minuria, and non-insulin dependent diabetes: the Candesartan and Lisinopril
Microalbuminuria (CALM) study. BMJ 2000;321(7274):14404.
134. Schjoedt KJ, Jacobsen P, Rossing K, et al. Dual blockade of the renin-
angiotensin-aldosterone system in diabetic nephropathy: the role of aldoste-
rone. Horm Metab Res 2005;37(Suppl 1):48.
135. Schjoedt KJ, Rossing K, Juhl TR, et al. Beneficial impact of spironolactone in
diabetic nephropathy. Kidney Int 2005;68(6):282936.
136. Parving HH, Persson F, Lewis JB, et al. Aliskiren combined with losartan in type
2 diabetes and nephropathy. N Engl J Med 2008;358(23):243346.
137. Bilous R. Microvascular disease: what does the UKPDS tell us about diabetic
nephropathy? Diabet Med 2008;25(Suppl 2):259.
Polycystic Ovarian
S y n d ro m e
Subbulaxmi Trikudanathan, MD, MRCP, MMSc
KEYWORDS
Polycystic ovarian syndrome Anovulation Hyperandrogenism Insulin resistance
Infertility Type 2 diabetes
KEY POINTS
Polycystic ovarian syndrome (PCOS) is a heterogeneous endocrine disorder character-
ized by anovulation, hyperandrogenism, infertility, and metabolic dysfunction.
Diagnosis of PCOS is made based on the presence of 2 of 3 criteria: chronic anovulation,
clinical or biochemical evidence of hyperandrogenism, and polycystic ovaries on
morphology.
Management of PCOS should be tailored according to the patients clinical presentation
and desire for pregnancy.
Long-term health implications for metabolic and cardiovascular health need to be ad-
dressed throughout the lifespan with an emphasis on prevention of cardiometabolic risks.
INTRODUCTION
CLINICAL PRESENTATION
Disclosures: None.
Division of Metabolism, Endocrinology and Nutrition, Department of Medicine, University of
Washington Medical Center, 4245 Roosevelt Way Northeast, Seattle, WA 98105, USA
E-mail address: [email protected]
Endometrial
hyperplasia PCOS Dyslipidemia
Depression
Infertility and anxiety NAFLD Sleep apnea
disorder
Fig. 1. Clinical components of PCOS. This figure illustrates the clinical features of PCOS that
needs to be carefully assessed and addressed. NAFLD, non alcoholic fatty liver disease.
Menstrual Abnormalities
Oligoanovulation typically presents as oligomenorrhea (<9 cycles per year) or amen-
orrhea. Dysfunctional uterine bleeding is occasionally encountered from unopposed
estrogen stimulation with lack of progesterone from anovulation. These menstrual ir-
regularities develop peripubertally and are often noted after periods of weight gain. It is
reported that women with PCOS may ovulate spontaneously, although the frequency
of this is unknown.1 Menstrual cycles in women with PCOS tend to become more
regular as the women approach menopause.
Infertility
Women with PCOS have a higher risk for infertility from oligoanovulation. Additional
mechanisms leading to infertility include diminished oocyte competence,2 unfavorable
endometrial changes, and obesity.
Hyperandrogenism
Hyperandrogenism is clinically manifested by hirsutism, acne, and androgenic alope-
cia. Hirsutism is defined as increased terminal (coarse, pigmented) hair in a male
pattern distribution around the upper lip, chin, shoulders, chest, periareolar areas,
along the linea alba of the abdomen, inner aspects of the thighs, and midline lower
back area. The degree of hirsutism can be gauged by the Ferriman-Gallwey score,3
a semiobjective quantitative method for recording the distribution and severity of
excess body hair in 9 skin areas. Documenting these scores objectively helps in eval-
uating the response of hirsutism to treatment interventions (Fig. 2). Photographs
before the patient shaves could help document hirsutism precisely.
Other hyperandrogenic signs in women with alopecia include acne and androgenic
alopecia. Signs of virilization such as deepening of the voice, clitoromegaly, decreased
breast size, and increased muscle mass should alert the clinician to more severe forms
of androgen excess (discussed later, with examples).
Polycystic Ovarian Syndrome 223
Fig. 2. Ferriman-Gallwey score. Each of the 9 areas receive a score from 0 (no hair) to 4 (frankly
virile). These scores are finally added to obtain a total hormonal score. Total score greater
than or equal to 8 indicates hirsutism. (From Hatch R, Rosenfield RL, Kim MH, et al. Hirsutism:
implications, etiology, and management. Am J Obstet Gynecol 1981;140(7):81530.)
Metabolic Components
Women with PCOS are frequently overweight or obese, particularly with visceral
adiposity.4 It has also been well recognized that most women with PCOS have hyper-
insulinemia and insulin resistance, irrespective of obesity.5,6 Women with PCOS
should be examined for clinical signs of insulin resistance such as acanthosis nigri-
cans, multiple skin tags,7 and keratosis pilaris.8 A 2-fold increase in the prevalence
of metabolic syndrome has been noted in women with PCOS from retrospective
studies.9,10 Women with PCOS have a significantly increased risk for impaired glucose
tolerance and type 2 diabetes. Large cross-sectional studies have found 23% to 35%
prevalence for impaired glucose tolerance and 4% to 10% for diabetes. This finding
accounts for a 3-fold higher prevalence rate of impaired glucose tolerance in women
with PCOS compared with age-matched women from the National Health and Nutri-
tion Survey (NHANES) II.11,12 Approximately a 7.5-fold to 10-fold higher prevalence
rate was noted for undiagnosed type 2 diabetes in women with PCOS compared
with NHANES II women of similar age.11,12 The risk of type 2 diabetes increased in
women with PCOS in the presence of family history of diabetes.13
Women with PCOS are predisposed to hypertension and vascular endothelial
dysfunction,14 putting them at a higher risk for macrovascular diseases. Several
studies have shown dyslipidemia, especially increases in small dense low-density
lipoprotein cholesterol particles and triglyceride levels with decreased high-density li-
poprotein cholesterol.15 Although precise cardiovascular morbidity and mortality have
not been established in long-term studies, the clustering of cardiometabolic risk fac-
tors predisposes women with PCOS to coronary heart disease.
224 Trikudanathan
Other Components
Sleep apnea is common in women with PCOS. Insulin resistance seems to be a more
important predictor of the severity of obstructive sleep apnea16,17 than obesity. The
prevalence of nonalcoholic fatty liver disease has also been increased in women
with PCOS with increased serum alanine aminotransferase concentrations in up to
30% of women with PCOS.18 Women with PCOS are at higher risk to develop
mood disorders, particularly depression and anxiety.19
PATHOPHYSIOLOGY
Multiple causal factors have emerged in the pathophysiology of PCOS (Fig. 3). It is un-
clear which of these abnormalities triggers the vicious cycle of anovulation, androgen
excess, and hyperinsulinemia seen in PCOS. One of the primary neuroendocrine de-
fects described is alterations in gonadotropin secretion. There is an underlying insen-
sitivity of the hypothalamic gonadotropin-releasing hormone (GnRH) secretion to
ovarian steroids leading to increased luteinizing hormone (LH) pulse amplitude and
frequency.20 Low progesterone levels have also been postulated to enhance the pul-
satility of GnRH, leading to increased LH/follicle-stimulating hormone (FSH) ratio. The
relative increase in LH stimulates the ovarian theca cells to secrete more androgenic
precursors and androgens. The FSH regulates the aromatase activity of the ovarian
granulosa cells. Impaired FSH synthesis and secretion leads to inadequate follicle
development and reduced aromatase levels. Hence there is a relative inability to
GnRH
Insulin Liver
Free testosterone
SHBG
Familial clustering of PCOS suggests a genetic basis for this disorder. Several sus-
ceptibility genes have been implicated, particularly in the region of the insulin recep-
tor gene, insulin gene, follistatin, fibrillin-3, and other members of the transforming
growth factor beta signaling family.23 Reproductive phenotype of hyperandrogen-
ism and metabolic abnormalities aggregates in families with PCOS. Some sisters
have hyperandrogenism with regular menses and insulin resistance, whereas others
have menstrual irregularities. Mothers of women with PCOS who had menstrual ab-
normalities had higher testosterone levels, dyslipidemia, and markers of insulin
resistance.24 Brothers of women with PCOS had increased dehydroepiandroster-
one sulfate (DHEAS), suggesting defects in androgen steroidogenesis similar to
their sisters with PCOS.25 In another study, brothers of women with PCOS
showed defects in the pancreatic beta-cell function with increased risk for type 2
diabetes.26
There has been considerable controversy over the 3 different definitions that have
been proposed by professional organizations for the diagnosis of PCOS.
The National Institutes of Health (NIH) in 1990 proposed the following diagnostic
criteria for PCOS:
Chronic anovulation
Clinical and/or biochemical signs of hyperandrogenism
Exclusion of other causes of hyperandrogenism, such as congenital adrenal hy-
perplasia, androgen-secreting tumors, and hyperprolactinemia
Rotterdam Criteria
The European Society of Human Reproduction and Embryology/American Society of
Reproductive Medicine held a consensus meeting at Rotterdam in 2003 and devel-
oped revised criteria incorporating a wider spectrum of phenotypes in PCOS.27 Two
out of 3 criteria would be needed to make the diagnosis after exclusion of the other
causes for hyperandrogenism.
226 Trikudanathan
EVALUATION
Serum total testosterone provides the best estimate of the androgen status because
direct assays for free testosterone can be inaccurate unless the equilibrium dialysis
method is used. Serum total testosterone can be measured at any point during the
menstrual cycle. Liquid chromatographytandem mass spectrometry accurately mea-
sures the testosterone levels in female patients. However, several clinical laboratories
use direct immunoassays to minimize the cost and increase throughput. Because the
direct immunoassays skip the extraction steps, there is considerable cross reactivity
from other steroids, leading to inaccuracies.28 Another factor to consider is low circu-
lating levels of testosterone in women (1520 times lower than in men). Other mea-
surements to assess androgen excess in women with PCOS include free androgen
index (FAI), androstenedione, and DHEAS.
FAI is defined as the ratio between total testosterone and SHBG and can also be
used to evaluate hyperandrogenemia. Androstenedione, an immediate precursor
of testosterone, is produced by the ovaries, adrenals, and peripheral tissues. A
recent study reported that measuring both androstenedione and total testos-
terone better predicted metabolic risks in women with PCOS.29 This study also
revealed that androstenedione levels can be increased when total testosterone
levels are normal in women with PCOS. The utility of androstenedione merits
further investigation in longitudinal studies. Levels of DHEAS primarily derived
from the adrenal glands, although not routinely measured, can also be increased
in women with PCOS.
In the past, increased LH/FSH ratio has been used for diagnosis of PCOS. However,
LH secretion is pulsatile and a single measurement of LH can miss the intrinsic vari-
ability. Hence an increased LH/FSH ratio contributes to the diagnosis of PCOS, but
the absence does not rule out the diagnosis of PCOS.
Fig. 4. Transvaginal ultrasonography of the pelvis showing the polycystic morphology of the
right ovary. There is increased central ovarian stroma with the arrangement of subcapsular
follicles in a string-of-pearls pattern. (Courtesy of Dr Diane E. Woodford, Clinical Assistant
professor, Reproductive Endocrinology and Infertility, University of Washington Medical
Center, Seattle.)
228 Trikudanathan
DIFFERENTIAL DIAGNOSIS
Hyperandrogenism
In women who do not desire pregnancy, hormonal contraceptives (estrogen/pro-
gestin combinations) remain the first line of treatment of hirsutism and acne. The
progestin component in oral contraceptives (OC) inhibits LH secretion, thereby
reducing the LH-dependent androgen production.31 The estrogen component in-
creases hepatic synthesis of SHBG, thus reducing free testosterone levels. OC pills
Box 1
Conditions to exclude before the diagnosis of PCOS
also mildly reduce adrenal androgen production (the exact mechanism is unclear)
and reduce the binding of androgen to its receptors. The progestin component of
OC pills bind with progesterone and androgen receptors. The first-generation pro-
gestins, norethindrone and norethindrone acetate, are possible options in women
with PCOS for hyperandrogenism. Levonorgestrel, a second-generation progestin,
has the most androgenic properties with adverse metabolic effects and should be
avoided. The third-generation progestins such as norgestimate, desogestrel, and
gestodene have less androgenic activity and fewer metabolic effects; however,
there are concerns about increased risk of venous thrombosis. Some progestins
like drospirenone (a derivative of spironolactone) have antiandrogenic and antimi-
neralocorticoid properties but need to be carefully prescribed in light of increased
concerns about an increased risk of venous thromboembolism.4 Note that the ab-
solute risk for venous thromboembolism is minimal but may outweigh the overall
benefits of OC pill in reducing androgen excess.
Screening for contraindications to hormonal contraceptives is similar in all users.
Available data do not confer additional risk for venous thromboembolism (VTE) in
women with PCOS. Risk factors for VTE, such as age, obesity, smoking, prior VTE,
and family history of thromboembolism, should be carefully considered. A trial of at
least 6 months of therapy should be given before changing the preparation or adding
another antiandrogen.
Spironolactone, an aldosterone antagonist, inhibits androgen receptor and
5a-reductase activity. It is usually started at 50 mg once daily and increased to
100 mg twice daily. It rarely results in hyperkalemia, although menstrual irregularities
are seen at higher doses, and it is usually used in combination with the OC pill. Potas-
sium levels are usually measured 4 to 6 weeks after initiating therapy and after dose
escalation. Spironolactone is teratogenic and causes feminization of male fetal geni-
talia. Therefore, it should be used with adequate contraceptive coverage in women
of childbearing age.
Cyproterone acetate (CPA) has antiandrogen activity at the level of androgen recep-
tor and suppresses serum gonadotropins and androgen levels. It is administered for
the first 10 days of the menstrual cycle at a dose of 50 to 100 mg/d. CPA is currently
unavailable in the United States but is widely used in Europe and Canada. Finasteride
inhibits type 2 5a-reductase enzyme, thereby reducing hirsutism. It is commonly used
at the 5-mg dose after ensuring safe contraception. Flutamide has significant antian-
drogen effects but has potential hepatotoxicity resulting in liver failure and even death.
Hence flutamide is not recommended in routine use. The addition of metformin has not
been shown to be effective for hirsutism.
Eflornithine is an irreversible inhibitor of ornithine decarboxylase, an enzyme
involved in hair follicle formation. Topical therapy with eflornithine hydrochloride
cream helps to reduce the rate of hair growth. Patients need to be advised that the
hair growth returns on discontinuing the treatment.
Some women choose temporary hair removal therapy such as plucking, waxing,
and chemical depilation. Other methods of hair reduction include electrolysis and
photoepilation therapy. Photoepilation therapy includes lasers and nonlaser light
sources such as intense pulsed light (IPL). The ideal women for laser hair removal
are light-skinned women with dark hair, whereas long-wavelength laser or IPL is
used for dark-skinned women.34 The laser energy is absorbed by melanin of the
hair follicle rather than the surrounding tissue. In the presence of androgen excess,
the remaining vellus hair follicles can be converted to terminal dark hair. Hence it
becomes important to treat underlying hyperandrogenemia to prevent hair
regrowth.
230 Trikudanathan
ENDOMETRIAL PROTECTION
Women with PCOS have an increased risk for endometrial hyperplasia and possible
endometrial cancer. OC, transdermal patches, or vaginal rings provide endometrial
protection and regulate menstrual cycles. Women who chose not to use combined es-
trogen and progesterone can use intermittent progestin therapy or a progestin-
releasing intrauterine device. Medroxyprogesterone 5 to 10 mg for 10 days every 2
to 3 months is usually a good option to shed the endometrium and protect from endo-
metrial hyperplasia.
INFERTILITY
Women with PCOS have anovulatory infertility. These women are also at a higher risk
for developing gestational diabetes, preterm delivery, and preeclampsia. Therefore,
women seeking fertility assistance should have prepregnancy evaluations of body
mass index (BMI), blood pressure, and OGTT.
Weight loss is the first line of treatment in overweight and obese women with PCOS
and should be initiated before fertility therapies. Even 5% to 10% weight loss can
improve menstrual irregularities, enhance the response to ovulation induction, and
reduce obstetric complications.35
Current guidelines recommend clomiphene citrate as the first line of therapy for
ovulation induction in women with PCOS.31 Clomiphene citrate is a selective estrogen
receptor modulator that binds to the estrogen receptors in the hypothalamus, thus
inhibiting the negative feedback of estrogen on the hypothalamus. There is a second-
ary increase in FSH that stimulates follicular formation and induces ovulation. Clomi-
phene citrate is typically administered at a dose of 50 mg for 5 days from days 2 to 5
after the onset of menstrual periods. A dose escalation of up to 150 mg/d can be
reached for a total of 6 cycles. In a large randomized controlled trial comparing the ef-
ficacy of clomiphene citrate versus metformin in women with PCOS, women in the
clomiphene citrate arm had significantly more live births compared with women given
metformin alone (22.5% vs 7.2%).36 The combination of clomiphene and metformin
did not show any significant increase in live birth rates.36 The rate of multiple births
was 6% in the clomiphene group compared with 0% in the metformin group.36 Met-
formin can be used to reduce multiple pregnancy rates because it has been thought
to induce monofollicular ovulation. A Finnish study recently showed that women
with BMI greater than 27 benefitted from 3 months pretreatment with metformin in
improving live birth rates.37 Metformin (up to 12 g/d in divided doses)38 is currently
used as an adjuvant therapy to prevent ovarian hyperstimulation syndrome in women
with PCOS undergoing in vitro fertilization.31
Aromatase inhibitors such as letrozole have also been used for ovulation induction.
Letrozole blocks the conversion of androgens to estrogen. Therefore, there is less
negative feedback on the hypothalamus leading to increased levels of GnRH and
thereby FSH. Letrozole is usually used in women resistant to clomiphene citrate or
who have side effects from clomiphene, such as vasomotor symptoms, headaches,
and thin endometrium. A recent NIH-sponsored clinical trial showed a significant in-
crease in live births with letrozole compared with clomiphene in women with PCOS,
adding letrozole in the treatment armentarium.39
In clomiphene-resistant patients, gonadotropin therapy with FSH administration can
be used for ovulation induction. This option has a higher risk for ovarian hyperstimu-
lation syndrome and multiple pregnancies. Another procedure considered in
clomiphene-resistant women who are not candidates for FSH therapy is laparoscopic
ovarian drilling. This surgical procedure is performed with laser or electrocautery and
Polycystic Ovarian Syndrome 231
involves perforation of 5 to 6 holes on the surface and stroma of the ovary.35 Needle
punctures induce thermal damage, thereby reducing ovarian stromal blood flow,
which in turn decreases the androgen microenvironment. This procedure does not
improve insulin sensitivity and therefore is not useful in obese patients seeking fertility.
In addition, in vitro fertilization is offered for clomiphene-resistant women or in women
with PCOS with coexisting reproductive issues such as tubal damage, endometriosis,
or male factor infertility.40
Weight loss from dietary interventions and exercise forms the first line of management in
obese women with PCOS. Several studies have attempted to use variations of the Dia-
betes Prevention Program41 (DPP) to tailor lifestyle therapy in PCOS. One-hundred and
fifty minutes per week in divided sessions of moderate to vigorous exercise along with a
500-calorie deficit per day promotes 450 g (1 pound) of weight loss per week. About 5%
to 10% weight loss has a beneficial influence on metabolic risk factors and improved
ovulation. Although there is a paucity of large randomized trials showing exercise ben-
efits in PCOS populations, there is overall evidence of the benefits of exercise in
reducing the risk of metabolic disease. In the DPP study, lifestyle modifications with ex-
ercise and diet reduced the progression of impaired glucose tolerance to T2 diabetes by
58% versus a 31% decrease with metformin. Current guidelines recommend metformin
in women with PCOS who have impaired glucose tolerance and to prevent diabetes,
especially in women who fail lifestyle modifications.31 The unfavorable side effects of
thiazolidinediones have discouraged their use in women with PCOS, especially in the
childbearing age group. Other insulin-sensitizing agents that promote weight loss,
such as glucagon like peptide -1 (GLP-1) analogues, have not been widely studied in
women with PCOS. Newer weight loss medications, such as phenteramine/topiramate
and locarserin, have shown promise in sustained weight loss and metabolic benefits in
obese adults42 but have not been studied in women with PCOS. Bariatric surgery has
been used to treat morbid obesity with PCOS and some small studies have shown res-
olution of metabolic abnormalities43 and improved fertility.44
Other cardiometabolic risks, such as dyslipidemia and obstructive sleep apnea,
need appropriate treatment according to the standard of care.
Oligomenorrhea with anovulatory cycles are common during the first 2 years after the
onset of menarche. Persistence of menstrual irregularities beyond this period is indi-
cates PCOS. Current guidelines31 suggest that the diagnosis of PCOS in adolescents
should be made based predominantly on hyperandrogenism (clinical or biochemical)
in the presence of oligomenorrhea. However, there is a lack of normative cutoff values
for androgen levels during puberty. The Rotterdam ultrasonography criteria for PCO
morphology have not been validated for adolescents because multifollicular ovaries
are seen in normal puberty.31 Because transvaginal ultrasonography raises a practical
concern in this age group, transabdominal ultrasonography is preferred, but may not
be sensitive in evaluating ovarian follicles. OC pills are the first-line therapy for hirsut-
ism and anovulatory symptoms. Although there is a lack of large randomized
controlled trials, a few smaller studies have suggested the benefits of exercise in
women with PCOS.45 Lifestyle modifications with a calorie-restricted diet along with
exercise are advocated for overweight and obese adolescents to improve their meta-
bolic profile and regulate ovulation. Metformin can be used in the presence of meta-
bolic syndrome or impaired glucose tolerance.
232 Trikudanathan
It is unusual to develop PCOS for the first time during menopause; usually these
women have symptoms of PCOS much earlier during adult life. There is paucity of
data tracking the natural history of PCOS through menopause. Ovarian follicular
count, AMH, and androgen levels decline with age46 in women with and without
PCOS. In the presence of very high androgen levels and rapid onset of virilization, it
is pertinent to rule out androgen-secreting tumors.
Large longitudinal studies are needed to determine whether increased cardiovascu-
lar risks in women with PCOS persist after menopause.47 There is an increased risk for
endometrial cancer in women with PCOS. Assessment of the endometrial thickness
by ultrasonography and prevention of endometrial hyperplasia with progesterone
withdrawal bleed may reduce the risk for endometrial cancer. Despite the increased
risk of endometrial cancer and PCOS, current guidelines do not recommend routine
ultrasonography screening for endometrial thickness.31,42 There is also a suggestion
of increased risk for breast and ovarian cancer in women with PCOS.
SUMMARY
Women with PCOS present with signs of chronic anovulation, hyperandrogenism, and
metabolic abnormalities. The NIH recently embraced the Rotterdam criteria to broadly
identify all the phenotypes of PCOS. Women with PCOS are often obese with insulin
resistance and hence have an increased susceptibility to glucose intolerance and type
2 diabetes. Future research should focus on the genetic, epigenetic, and environ-
mental determinants of PCOS to develop new therapies to address the prevention
of this disorder and its long-term complications.
ACKNOWLEDGMENTS
The ultrasonography image (see Fig. 3) was kindly provided by Dr Diane E. Wood-
ford, Clinical Assistant professor, Reproductive Endocrinology and Infertility, Univer-
sity of Washington Medical Center, Seattle, Washington.
REFERENCES
8. Plascencia Gomez A, Vega Memije ME, Torres Tamayo M, et al. Skin disorders in
overweight and obese patients and their relationship with insulin. Actas Dermosi-
filiogr 2014;105(2):17885. http://dx.doi.org/10.1016/j.ad.2013.09.1008.
9. Apridonidze T, Essah PA, Iuorno MJ, et al. Prevalence and characteristics of the
metabolic syndrome in women with polycystic ovary syndrome. J Clin Endocrinol
Metab 2005;90(4):192935.
10. Dokras A, Bochner M, Hollinrake E, et al. Screening women with polycystic ovary
syndrome for metabolic syndrome. Obstet Gynecol 2005;106(1):1317.
11. Legro RS, Kunselman AR, Dodson WC, et al. Prevalence and predictors of risk for
type 2 diabetes mellitus and impaired glucose tolerance in polycystic ovary syn-
drome: a prospective, controlled study in 254 affected women. J Clin Endocrinol
Metab 1999;84(1):1659.
12. Ehrmann DA, Barnes RB, Rosenfield RL, et al. Prevalence of impaired glucose
tolerance and diabetes in women with polycystic ovary syndrome. Diabetes
Care 1999;22(1):1416.
13. Ehrmann DA, Kasza K, Azziz R, et al. Effects of race and family history of type 2
diabetes on metabolic status of women with polycystic ovary syndrome. J Clin
Endocrinol Metab 2005;90(1):6671.
14. Kelly CJ, Speirs A, Gould GW, et al. Altered vascular function in young women
with polycystic ovary syndrome. J Clin Endocrinol Metab 2002;87(2):7426.
15. Talbott E, Guzick D, Clerici A, et al. Coronary heart disease risk factors in
women with polycystic ovary syndrome. Arterioscler Thromb Vasc Biol 1995;
15(7):8216.
16. Vgontzas AN, Legro RS, Bixler EO, et al. Polycystic ovary syndrome is associated
with obstructive sleep apnea and daytime sleepiness: role of insulin resistance.
J Clin Endocrinol Metab 2001;86(2):51720.
17. Tasali E, Van Cauter E, Ehrmann DA. Relationships between sleep disordered
breathing and glucose metabolism in polycystic ovary syndrome. J Clin Endocri-
nol Metab 2006;91(1):3642.
18. Schwimmer JB, Khorram O, Chiu V, et al. Abnormal aminotransferase activity in
women with polycystic ovary syndrome. Fertil Steril 2005;83(2):4947.
19. Barry JA, Kuczmierczyk AR, Hardiman PJ. Anxiety and depression in polycystic
ovary syndrome: a systematic review and meta-analysis. Hum Reprod 2011;
26(9):244251. http://dx.doi.org/10.1093/humrep/der197.
20. McCartney CR, Eagleson CA, Marshall JC. Regulation of gonadotropin secretion:
implications for polycystic ovary syndrome. Semin Reprod Med 2002;20(4):
31726.
21. Ehrmann DA. Polycystic ovary syndrome. N Engl J Med 2005;352(12):122336.
22. Tsilchorozidou T, Overton C, Conway GS. The pathophysiology of polycystic
ovary syndrome. Clin Endocrinol (Oxf) 2004;60(1):117.
23. Diamanti-Kandarakis E, Dunaif A. Insulin resistance and the polycystic ovary syn-
drome revisited: an update on mechanisms and implications. Endocr Rev 2012;
33(6):9811030. http://dx.doi.org/10.1210/er.2011-1034.
24. Sam S, Legro RS, Essah PA, et al. Evidence for metabolic and reproductive phe-
notypes in mothers of women with polycystic ovary syndrome. Proc Natl Acad Sci
U S A 2006;103(18):70305.
25. Legro RS, Kunselman AR, Demers L, et al. Elevated dehydroepiandrosterone sul-
fate levels as the reproductive phenotype in the brothers of women with polycy-
stic ovary syndrome. J Clin Endocrinol Metab 2002;87(5):21348.
26. Sam S, Sung YA, Legro RS, et al. Evidence for pancreatic beta-cell dysfunction in
brothers of women with polycystic ovary syndrome. Metabolism 2008;57(1):849.
234 Trikudanathan
27. Fauser BC, Tarlatzis BC, Rebar RW, et al. Consensus on womens health aspects
of polycystic ovary syndrome (PCOS): the Amsterdam ESHRE/ASRM-Sponsored
3rd PCOS Consensus Workshop Group. Fertil Steril 2012;97(1):2838.e25. http://
dx.doi.org/10.1016/j.fertnstert.2011.1009.1024.
28. Keevil BG. How do we measure hyperandrogenemia in patients with PCOS? J Clin
Endocrinol Metab 2014;99(3):7779. http://dx.doi.org/10.1210/jc.2014-1307.
29. OReilly MW, Taylor AE, Crabtree NJ, et al. Hyperandrogenemia predicts meta-
bolic phenotype in polycystic ovary syndrome: the utility of serum androstenedi-
one. J Clin Endocrinol Metab 2014;99(3):102736. http://dx.doi.org/10.1210/jc.
2013-3399.
30. Eilertsen TB, Vanky E, Carlsen SM. Anti-Mullerian hormone in the diagnosis of
polycystic ovary syndrome: can morphologic description be replaced? Hum Re-
prod 2012;27(8):2494502. http://dx.doi.org/10.1093/humrep/des213.
31. Legro RS, Arslanian SA, Ehrmann DA, et al. Diagnosis and treatment of polycystic
ovary syndrome: an Endocrine Society clinical practice guideline. J Clin Endocri-
nol Metab 2013;98(12):456592. http://dx.doi.org/10.1210/jc.2013-2350.
32. Johnstone EB, Rosen MP, Neril R, et al. The polycystic ovary post-Rotterdam: a
common, age-dependent finding in ovulatory women without metabolic signifi-
cance. J Clin Endocrinol Metab 2010;95(11):496572. http://dx.doi.org/10.1210/
jc.2010-0202.
33. Dewailly D, Lujan ME, Carmina E, et al. Definition and significance of polycystic
ovarian morphology: a task force report from the Androgen Excess and Polycy-
stic Ovary Syndrome Society. Hum Reprod Update 2014;20(3):33452. http://
dx.doi.org/10.1093/humupd/dmt061.
34. Martin KA, Chang RJ, Ehrmann DA, et al. Evaluation and treatment of hirsutism in
premenopausal women: an endocrine society clinical practice guideline. J Clin
Endocrinol Metab 2008;93(4):110520. http://dx.doi.org/10.1210/jc.2007-2437.
35. Usadi RS, Legro RS. Reproductive impact of polycystic ovary syndrome. Curr
Opin Endocrinol Diabetes Obes 2012;19(6):50511. http://dx.doi.org/10.1097/
MED.0b013e328359ff92.
36. Legro RS, Barnhart HX, Schlaff WD, et al. Clomiphene, metformin, or both for
infertility in the polycystic ovary syndrome. N Engl J Med 2007;356(6):
55166.
37. Morin-Papunen L, Rantala AS, Unkila-Kallio L, et al. Metformin improves preg-
nancy and live-birth rates in women with polycystic ovary syndrome (PCOS): a
multicenter, double-blind, placebo-controlled randomized trial. J Clin Endocrinol
Metab 2012;97(5):1492500. http://dx.doi.org/10.1210/jc.2011-3061.
38. Palomba S, Falbo A, Carrillo L, et al. Metformin reduces risk of ovarian hyperstim-
ulation syndrome in patients with polycystic ovary syndrome during gonadotropin-
stimulated in vitro fertilization cycles: a randomized, controlled trial. Fertil Steril
2011;96(6):138490.e4.
39. Legro RS, Brzyski RG, Diamond MP, et al. The pregnancy in polycystic ovary syn-
drome II study: baseline characteristics and effects of obesity from a multicenter
randomized clinical trial. Fertil Steril 2014;101(1):25869.e8. http://dx.doi.org/10.
1016/j.fertnstert.2013.08.056.
40. Perales-Puchalt A, Legro RS. Ovulation induction in women with polycystic ovary
syndrome. Steroids 2013;78(8):76772. http://dx.doi.org/10.1016/j.steroids.2013.
05.005.
41. Knowler WC, Barrett-Connor E, Fowler SE, et al. Reduction in the incidence of
type 2 diabetes with lifestyle intervention or metformin. N Engl J Med 2002;
346(6):393403.
Polycystic Ovarian Syndrome 235
42. Bates GW, Legro RS. Longterm management of polycystic ovarian syndrome
(PCOS). Mol Cell Endocrinol 2013;373(12):917. http://dx.doi.org/10.1016/j.
mce.2012.1010.1029.
43. Escobar-Morreale HF, Botella-Carretero JI, Alvarez-Blasco F, et al. The polycystic
ovary syndrome associated with morbid obesity may resolve after weight loss
induced by bariatric surgery. J Clin Endocrinol Metab 2005;90(12):63649.
44. Eid GM, Cottam DR, Velcu LM, et al. Effective treatment of polycystic ovarian syn-
drome with Roux-en-Y gastric bypass. Surg Obes Relat Dis 2005;1(2):7780.
45. Harrison CL, Lombard CB, Moran LJ, et al. Exercise therapy in polycystic ovary
syndrome: a systematic review. Hum Reprod Update 2011;17(2):17183.
46. Winters SJ, Talbott E, Guzick DS, et al. Serum testosterone levels decrease in
middle age in women with the polycystic ovary syndrome. Fertil Steril 2000;
73(4):7249.
47. Welt CK, Carmina E. Clinical review: lifecycle of polycystic ovary syndrome
(PCOS): from in utero to menopause. J Clin Endocrinol Metab 2013;98(12):
462938.
I ndex
Note: Page numbers of article titles are in boldface type.
A
A Diabetes Outcome Progression Trial (ADOPT), 91, 94, 163
ABCC8 gene mutations, 67
Acarbose, 97, 99, 181
ACCORD (Action to Control Cardiovascular Risk in Diabetes) trial, 5761, 202203, 206
Acidosis, lactic, metformin-induced, 8990
Acne, in polycystic ovarian syndrome, 222
Action in Diabetes and Vascular Disease Controlled Evaluation Renal Measurement
(ADREM), 206
Action in Diabetes and Vascular disease: Preterax and Diamicron Modified Release
Controlled Evaluation (ADVANCE) trial, 5761, 202, 206, 211
Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial, 5761, 202203, 206
Acute Insulin Response to Glucose, 160
ADOPT (A Diabetes Outcome Progression Trial), 91, 94, 163
ADREM (Action in Diabetes and Vascular Disease Controlled Evaluation Renal
Measurement), 206
ADVANCE (Action in Diabetes and Vascular disease: Preterax and Diamicron Modified
Release Controlled Evaluation) trial, 5761, 202, 206, 211
A3434G gene mutations, 7
Albiglutide, 110111, 116117
Albumin/creatinine ratio, 209
Alogliptin, 118, 122, 181
Alopecia, in polycystic ovarian syndrome, 222
Alpha-glucosidase inhibitors, 97, 99, 181
American Association of Clinical Endocrinologists, insulin therapy guidelines of, 161164
American College of Sports Medicine, physical activity guidelines of, 73
American Diabetes Association, insulin therapy guidelines of, 161163
American Diabetes Association-European Association for the Study of Diabetes position
statement, 62
Amitriptyline, 208
Amylinomimetics, 181
Analog preparations, insulin, 170
Androgen Excess Society criteria, 226
Angiotensin receptor blockers, 189190, 211
Angiotensin-converting enzyme inhibitors, 189190, 211
1,5-Anhydroglucitrol measurement, 140
Anovulation, in polycystic ovarian syndrome, 221235
Antidepressants, 208
Antihypoglycemics, oral. See Oral antihypoglycemics.
Antimullerian hormone, in polycystic ovarian syndrome, 226
Antipsychotics, atypical, diabetes mellitus due to, 9
Antiretroviral drugs, diabetes mellitus due to, 10
Anxiety, 193
Aripiprazole, diabetes mellitus due to, 9
Artificial sweeteners, 7778
Aspirin, 203204
Atherosclerosis, prevention of, 191192
Autoimmune diabetes mellitus. See Diabetes mellitus, type 1.
Autonomic neuropathy, 207
B
Baltimore Longitudinal Study of Aging, 5
Basal insulin therapy, 147148, 171, 173
Bile acid sequestrants, 9799, 181
Blindness, 4850, 54, 204206
Blood glucose, hemoglobin A1c correlation with, 36
Blood glucose monitoring
accuracy of, 38
continuous, 3942, 152
decision support in, 39
implementation of, 3839
in type 1 diabetes mellitus, 152
in type 2 diabetes mellitus, 164165
internet systems for, 1733
methods for, 3545
Bolus calculator, 39
Bolus insulin therapy, 148, 173178
Bromocriptine mesylate, 9899, 181
C
Calcineurin inhibitors, diabetes mellitus due to, 9
Canagliflozin, 96, 99, 135140, 181
Canagliflozin Cardiovascular Assessment Study (CANVAS), 140
CANagliflozin treatment and trial analysis-sulfonylurea (CANTATA-SU) trial, 96
Cancer
endometrial, in polycystic ovarian syndrome, 222, 230
pancreatic, 8
risk of, metformin effects on, 89
CANTATA-SU (CANagliflozin treatment and trial analysis-sulfonylurea) trial, 96
CANVAS (Canagliflozin Cardiovascular Assessment Study), 140
Capsaicin, 208209
Carbohydrate counting, 149, 174177
Carbohydrate ratio, 149
Cardiovascular disease, 5052
in polycystic ovarian syndrome, 223, 227, 231
incretin-induced, 122123
internet blood glucose monitoring systems effects on, 26
prevention of, 191192
sodium glucose cotransporter 2 inhibitor effects on, 139140
Cardiovascular Outcomes Event Trial in Type 2 Diabetes Mellitus Patients, 140
CFTR gene mutations, 8
Index 239
Chlorpropamide, 91
Clomiphene citrate, for polycystic ovarian syndrome, 230
Closed-loop insulin delivery, 42
Clozapine, diabetes mellitus due to, 9
Colesevelam, 9799, 181
Complications and targets for damage, 4767, 187200
cardiovascular disease. See Cardiovascular disease.
clinical trials involving, 5263
driving ability, 196
glucose hypothesis and, 47
hypertension, 188191, 202204
lipid, 191192, 203204
macrovascular disease, 5052
mental health, 193
meta-analysis of, 60
microvascular disease, 4850
nephropathy, 4850, 54, 188191, 209212
peripheral neuropathy, 4850, 79, 206209
retinopathy, 4850, 54, 204206
summary of, 195
weight control, 193194
Congenital diabetes, 67
Continuous blood glucose monitoring, 3942
Coronary heart disease, 5052
Corticosteroids, diabetes mellitus due to, 9
Cost-effectiveness, of internet blood glucose monitoring system, 27
Cyclosporine, diabetes mellitus due to, 9
Cyproterone acetate, for polycystic ovarian syndrome, 229
Cystic fibrosis, 78
D
Dapagliflozin, 96, 99, 135, 137140, 181
DCCT (Diabetes Control and Complications Trial), 36, 5254, 58, 146, 202, 207
Decision support, for blood glucose monitoring, 39
DECLARE-TIMI58 study, 140
Dehydroepiandrosterone sulfate, in polycystic ovarian syndrome, 226
Depression, 193
Desipramine, 208
Diabetes Control and Complications Trial (DCCT), 36, 5254, 58, 146, 202, 207
Diabetes mellitus
classification of, 116
complications of. See Complications and targets for damage.
diagnosis of, 12
gestational, 56
latent autoimmune, 34
mitochondrial, 7
monitoring of. See Blood glucose monitoring.
monogenic, 67
nonautoimmune, 711. See also Diabetes mellitus, type 2.
polycystic ovarian syndrome and, 221235
240 Index
Diabetes (continued )
secondary, 711
treatment of
glycemic targets in, 4767
ncretin-based, 107129
insulin for. See Insulin.
lifestyle interventions for. See Lifestyle interventions.
nonglycemic targets in, 187200
oral antihyperglycemics for. See Oral antihypoglycemics.
primary care provider role in, 201219
sodium glucose cotransporter 2 inhibitors for, 131143
syndromes associated with, 11
type 1
description of, 24
incidence of, 145
insulin therapy for, 145156
internet blood glucose monitoring systems for, 1719, 2225, 28
self-monitoring in, 37
type 2
description of, 45
insulin therapy for, 157186
internet blood glucose monitoring systems for, 1722, 2425, 28
oral antihypoglycemics for, 87106
self-monitored blood glucose monitoring in, 38
Diabetes Reduction Assessment with Ramipril and Rosiglitazone Medication (DREAM), 94
Diabetes self-management program, 7180
Diabetic Retinopathy Candesartan Trials (DIRECT), 206
Diabetic Retinopathy Study, 206
Diet therapy, 7180
Digital retinal photography, 205
Dipeptidyl peptidase, therapy based on, 109, 117122, 181
DIRECT (Diabetic Retinopathy Candesartan Trials), 206
Doleur neuropathique 4 questions, 207
DREAM (Diabetes Reduction Assessment with Ramipril and Rosiglitazone Medication), 94
Driving ability, evaluation of, 196
Duloxetine, 208
Dyslipidemias, 191192, 203204
E
EDIC (Epidemiology of Diabetes Interventions and Complications) study, 5354, 146, 207
Eflornitine, for polycystic ovarian syndrome, 229
Emotional distress, 193
Empaglifozin, 137139
Endocrine Society, blood glucose monitoring guidelines of, 40
Endometrial cancer, in polycystic ovarian syndrome, 222
Epidemiology of Diabetes Interventions and Complications (EDIC) study, 146, 207, 230
Ertugliflozin, 140
Estimated Average Glucose, 165
EUCLID study, 206
EURODIAS study, 206
Index 241
F
Fenofibrate, 203
Ferriman-Gallowey score, in polycystic ovarian syndrome, 222
Fibrocalculous pancreatic diabetes, 8
FIELD study, 206
Follicle-stimulating hormone, in polycystic ovarian syndrome, 224225, 230
Free androgen index, in polycystic ovarian syndrome, 226
G
Gabapentin, 208209
Gastric inhibitory peptide, therapy based on, 107108
Gemfibrozil, 203
Generalized Anxiety Disorder questionnaire, 193
Genetics, of polycystic ovarian syndrome, 221224
Gestational diabetes mellitus, 56
Glimepiride, 9092, 99, 181
Glinides, 9293, 99, 181
Glipizide, 9092, 99
Glomerular filtration rate, 210211
GLOWS (Glucose Lowering effect of WelChol study), 97
Glucagon-like peptide, therapy based on, 107117
Glucokinase defects, 7
Gluconeogenesis, in kidney, 132
Glucose. See also Blood glucose; Glycemia; Glycemic control; Glycemic targets.
kidney handling of, 132134
toxicity of, 180
Glucose Buddy app, 27
Glucose hypothesis, 47
Glucose Lowering effect of WelChol study (GLOWS), 97
Glyburide, 9092, 181
Glycemia. See also Hyperglycemia; Hypoglycemia.
control of. See Glycemic control.
monitoring of
internet systems for, 1733
methods for, 3545
Glycemic control
for cardiovascular disease prevention, 202
for peripheral neuropathy, 207
internet blood glucose monitoring systems effects on, 2526
markers for, 3537
monitoring for
internet systems for, 1733
methods for, 3545
self-monitored
242 Index
Glycemic (continued )
internet system for, 1733
methods for, 3739
Glycemic targets, 4767
clinical trials involving, 5263
glucose hypothesis and, 47
macrovascular disease, 5052
meta-analysis of, 60
microvascular disease, 4850
Gonadotropin secretion, in polycystic ovarian syndrome, 224225
H
Haloperidol, diabetes mellitus due to, 9
Health, Aging, and Body Composition observational study, 94
Hemochromatosis, hereditary, 8
Hemoglobin A1c
as guide to therapy, 161164
canagliflozin and, 136137
dapagliflozin and, 137
for monitoring, 3537
metformin and, 8889
Hereditary hemochromatosis, 8
Highly concentrated insulin, 171, 178179
Hirsutism, in polycystic ovarian syndrome, 222, 229
HIV infections, diabetes mellitus due to, 1011
HNF gene mutations, 67
Human insulin, 165, 168170
Hyperandrogenism, in polycystic ovarian syndrome, 221235
Hyperglycemia
idiopathic. See Diabetes mellitus, type 2.
toxicity of, 45
Hyperglycemia and Adverse Pregnancy Outcome study, 56
Hyperkalemia, 190
Hypertension, 188191, 202204
Hypertension in the Very Elderly trial, 190
Hypoglycemia
in insulin therapy, 147152, 179180
internet blood glucose monitoring systems effects on, 25
I
Idiopathic hyperglycemia. See Diabetes mellitus, type 2.
Imipramine, 208
Immunology of Diabetes Society, 4
Incretin-based therapy, 107129
cardiovascular safety of, 122123
incretin effect in, 108
options for, 108121
Infertility, in polycystic ovarian syndrome, 222
Insulin. See also Insulin therapy.
Index 243
Internet (continued )
clinical studies of, 1726
cost-effectiveness of, 27
hypoglycemia and, 25
implementation statistics for, 28
mechanisms for, 2526
practical tips for, 29
quality of life with, 2627
Iprafliflozin, 140
ISIS 388626, 140
J
Joint National Committee guidelines, for hypertension, 189190
Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study, 40, 153
K
KCNJ11 gene mutations, 67
KDIGO (Kidney Disease Improving Global Outcomes), 189190
Ketosis, in diabetes mellitus type 2, 5
Kidney
dysfunction of, 4850, 54, 188191, 209212
glucose regulation in, 132134
Kidney Disease Improving Global Outcomes (KDIGO), 189190
Kumamoto study, 5658, 60
L
Lactic acidosis, metformin-induced, 8990
Latent autoimmune diabetes of adults, 34
Letrozole, for polycystic ovarian syndrome, 230
Lidocaine, 208209
Lifestyle interventions, 6985, 204
nutrition therapy, 7180, 203
outcome of, 76
physical activity, 7280, 204
priorities in, 7680
resistance to, 74
Linagliptin, 118, 120122, 181
Lipid targets, 191192, 203204
Lipotoxicity, in diabetes mellitus, 45
Liraglutide, 110111, 113114, 122, 181
Long-acting insulin, 168, 170
Look AHEAD trial, 193
Luteinizing hormone, in polycystic ovarian syndrome, 224225
LX 4211, 140
M
Macrovascular disease, 5052
Index 245
N
Nateglinide, 9293, 99, 181
National Glycohemoglobin Standardization Program, 36
NAVIGATOR trial, 192
Neonatal diabetes mellitus, 67
Nephropathy, 4850, 54, 188191, 209212
Neuropathy, peripheral, 4840, 79, 206209
Neutral protamine Hagedorn insulin, 147148, 166170
Nortriptyline, 208
Nutrition therapy, 7180, 203
O
Obesity, 193196
in polycystic ovarian syndrome, 223, 230
weight loss for, 7180, 193196, 231
Olanzapine, diabetes mellitus due to, 9
Oligomenorrhea, in polycystic ovarian syndrome, 222
Ophthalmoscopy, for retinopathy, 205
Oral antihypoglycemics, 87106
alpha-glucosidase inhibitors, 97, 99, 181
bromocriptine mesylate, 9899, 181
colesevelam, 9798, 181
glinides, 9293, 99, 181
metformin, 8890, 99, 161162, 181
sodium-glucose transporter type 2 inhibitors, 9596, 131143
sulfonylureas, 9092
thiazolidinediones, 9395
Oral contraceptives, for polycystic ovarian syndrome, 228229
Ovarian theca cell abnormalities, in polycystic ovarian syndrome, 225
Ovary, polycystic disease of, 221235
Ovulation, induction of, for polycystic ovarian syndrome, 230
Oxycodone, 208
246 Index
P
Pain, in peripheral neuropathy, 206209
Pancreas, disorders of, 78
Pancreatectomy, 8
Pancreatitis, 8
Patch, insulin, 172
Patient Health Questionnaire, 193
Pens, for insulin delivery, 172
Peripheral neuropathy, 4850, 79, 206209
Personal continuous glucose monitoring, 4041
Photography, digital retinal, 205
Physical activity, 7280, 204
Pioglitazone, 9395, 99, 181
Polycystic ovarian syndrome, 221235
cardiovascular risks in, 231
clinical presentation of, 221224
diagnosis of, 225226
differential diagnosis of, 228
endometrial protection in, 230
evaluation of, 226227
genetics of, 225
in adolescents, 231
in menopause, 232
infertility management in, 230231
pathophysiology of, 224225
treatment of, 228229
Pramlintide, 181
Pregabalin, 208209
Pregnancy
diabetes mellitus in, 56
in polycystic ovarian syndrome, 230231
retinopathy in, 205
Premixed insulin, 167, 170, 178
Problem Areas in Diabetes Questionnaire, 193
Professional continuous glucose monitoring, 40
Prospective Pioglitazone Clinical Trial in the Macrovascular Events, 60, 94
Proteinuria, 190
Pumps, for insulin delivery, 150151, 172, 179
Q
Quality of life, internet blood glucose monitoring systems effects on, 2627
Quetiapine, diabetes mellitus due to, 9
R
Rapid-acting insulin, 168
Real-time continuous glucose monitoring, 4142
RECORD (Rosiglitazone Evaluated for Cardiovascular Outcomes in Oral Agent
Combination Therapy for Type 2 Diabetes) trial, 94
Registered dietitians, in nutrition therapy, 7080
Repaglinide, 9293, 99, 181
Index 247
S
Saxagliptin, 118120, 122, 181
Self-monitored glycemic control
in type 2 diabetes mellitus, 164165
internet system for, 1733
methods for, 3739
Short-acting insulin, 168169
Sirolimus, diabetes mellitus due to, 9
Sitagliptin, 118119, 122, 181
Sleep apnea, in polycystic ovarian syndrome, 224
Sodium glucose cotransporter 2 inhibitors, 9596, 99, 131143
adverse events due to, 135
1,5-anhydroglucitrol measurement interference from, 140
cardiovascular outcomes of, 139140
drug interactions with, 139
in development stage, 140
in kidney disease, 138
kidney function and, 132134
mechanism of action of, 134135
options for, 135138
Spironolactone, for polycystic ovarian syndrome, 229
STAR3 study, 4041
Statins, 10, 192, 203
Sulfonylureas, 9092, 99, 181
Syringes, for insulin delivery, 172
T
Tacrolimus, diabetes mellitus due to, 9
T1D Exchange Registry, 151
Team approach, to insulin therapy, 152153
Thiazides, diabetes mellitus due to, 10
Thiazolidinediones, 9395, 99, 181
Tolbutamide, 91
Tramadol, 208
Transcutaneous electrical nerve stimulation, 209
Triglyceride reduction, 203
Tumors, pancreatic, 8
U
UKPDS (United Kingdom Prospective Diabetes Study), 35, 36, 5356, 5860, 89, 202,
205206, 209
248 Index
V
VADT (Veterans Affairs Diabetes Trial), 5761
Vascular endothelial growth factors, in retinopathy, 206
Venlafaxine, 208
Veterans Affairs Diabetes Trial (VADT), 5761
Vidagliptin, 181
Virilization, in polycystic ovarian syndrome, 222
W
Weight loss, 7180, 193196, 231
Well-Being Index, 193
Wisconsin Epidemiologic Study of Diabetic Retinopathy, 48, 204
Wolfram syndrome, 7
Z
Ziprasidone, diabetes mellitus due to, 9