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Metabolic Syndrome Diagnosis
Metabolic Syndrome Diagnosis
A joint interim statement of the International Diabetes Federation Task Force on Epidemiology
and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World
Heart Federation; International Atherosclerosis Society; and International Association for the
Study of Obesity published a guideline to harmonize the definition of the metabolic syndrome.[39]
This definition recognizes that the risk associated with a particular waist measurement will differ
in different populations. Whether it is better at this time to set the level at which risk starts to
increase or at which there is already substantially increased risk will be up to local decisionmaking groups. However, for international comparisons and to facilitate the etiology, it is critical
that a commonly agreed-upon set of criteria be used worldwide, with agreed-upon cut points for
different ethnic groups and sexes. There are many people in the world of mixed ethnicity, and in
those cases, pragmatic decisions will have to be made.
The previous definitions of the metabolic syndrome by the International Diabetes Federation[40]
and the revised National Cholesterol Education Program are very similar and they identify
individuals with a given set of symptoms as having metabolic syndrome. There are two
differences, however: the IDF definition states that if body mass index (BMI) is greater than
30 kg/m2, central obesity can be assumed, and waist circumference does not need to be
measured. However, this potentially excludes any subject without increased waist circumference
if BMI is less than 30. Conversely, the NCEP definition indicates that metabolic syndrome can
be diagnosed based on other criteria. Also, the IDF uses geography-specific cut points for waist
circumference, while NCEP uses only one set of cut points for waist circumference regardless of
geography. These two definitions are much more similar than the original NCEP and WHO
definitions.
IDF
The International Diabetes Federation[40] consensus worldwide definition of the metabolic
syndrome (2006) is: Central obesity (defined as waist circumference# with ethnicity-specific
values) AND any two of the following:
Raised triglycerides: > 150 mg/dL (1.7 mmol/L), or specific treatment for this lipid
abnormality
Reduced HDL cholesterol: < 40 mg/dL (1.03 mmol/L) in males, < 50 mg/dL
(1.29 mmol/L) in females, or specific treatment for this lipid abnormality
Raised blood pressure (BP): systolic BP > 130 or diastolic BP >85 mm Hg, or treatment
of previously diagnosed hypertension
Raised fasting plasma glucose (FPG): >100 mg/dL (5.6 mmol/L), or previously
diagnosed type 2 diabetes
If FPG is >5.6 mmol/L or 100 mg/dL, an oral glucose tolerance test is strongly recommended,
but is not necessary to define presence of the syndrome.
#
If BMI is >30 kg/m, central obesity can be assumed and waist circumference does not need to
be measured
WHO
The World Health Organization 1999 criteria[41] require the presence of any one of diabetes
mellitus, impaired glucose tolerance, impaired fasting glucose or insulin resistance, AND two of
the following:
Central obesity: waist:hip ratio > 0.90 (male); > 0.85 (female), or body mass index >
30 kg/m2
EGIR
The European Group for the Study of Insulin Resistance (1999) requires insulin resistance
defined as the top 25% of the fasting insulin values among nondiabetic individuals AND two or
more of the following:
Dyslipidemia: TG 2.0 mmol/L and/or HDL-C < 1.0 mmol/L or treated for dyslipidemia
NCEP
The US National Cholesterol Education Program Adult Treatment Panel III (2001) requires at
least three of the following:[42]
Elevated blood pressure: Equal to or greater than 130/85 mm Hg or use of medication for
hypertension
Elevated fasting glucose: Equal to or greater than 100 mg/dL (5.6 mmol/L) or use of
medication for hyperglycemia
Other
High-sensitivity C-reactive protein has been developed and used as a marker to predict coronary
vascular diseases in metabolic syndrome, and it was recently used as a predictor for nonalcoholic
fatty liver disease (steatohepatitis) in correlation with serum markers that indicated lipid and
glucose metabolism.[45] Fatty liver disease and steatohepatitis can be considered as manifestations
of metabolic syndrome, indicative of abnormal energy storage as fat in ectopic distribution.
Reproductive disorders (such as polycystic ovary syndrome in women of reproductive age), and
erectile dysfunction or decreased total testosterone (low testosterone-binding globulin) in men
can be attributed to metabolic syndrome.[46]
Rheumatic diseases
There are new findings regarding the comorbidity associated with rheumatic diseases. Both
psoriasis and psoriatic arthritis have been found to be associated with metabolic syndrome.[47]