Metabolic syndromeBMJ 2005; 331 doi: https://doi.org/10.1136/bmj.331.7526.1153 (Published 17 November 2005) Cite this as: BMJ 2005;331:1153
- Kamlesh Khunti, clinical senior lecturer (, )
- Melanie Davies, honorary senior lecturer
- Department of Health Sciences, University of Leicester, Leicester General Hospital, Leicester LE5 4PW
- University Hospitals of Leicester NHS Trust, Leicester Royal Infirmary, Leicester LE1 5WW
Metabolic syndrome is characterised by hyper-insulinaemia, low glucose tolerance, dyslipidaemia, hypertension, and obesity. This cluster of factors has been recognised for many years, but the syndrome was not formally labelled until Reaven did so in 1988 and suggested that insulin resistance was its central characteristic.1 Insulin resistance seems to be the main underlying factor leading to the increased risk of mortality from coronary heart disease among people with the syndrome.2 Strategies to combat the forecast epidemic of type 2 diabetes and its vascular complications should focus on preventing and intervening early in metabolic syndrome.
Established macrovascular pathology is common when diabetes is diagnosed,3 implying either delayed diagnosis or an atherogenic prediabetic state. The UK prospective diabetes study showed that, once diabetes is diagnosed glycaemia is only modestly related to cardiovascular disease.4 Insulin resistance may be the common antecedent of metabolic syndrome, type 2 diabetes, and cardiovascular disease. Any strategy aimed at preventing the principal cause of death in type 2 diabetes should, therefore, encompass treatment of the metabolic syndrome.
The clinical identification of metabolic syndrome is based on measures of abdominal obesity, atherogenic dyslipidaemia, hypertension, and glucose intolerance. The World Health Organization's definition of metabolic syndrome requires evidence of insulin resistance and measurement of fasting insulin or its surrogates as essential criteria.w1However, the Adult Treatment Panel III of the US National Cholesterol Education Program (NCEP) proposed a simpler definition, developed for clinical use and not including any estimation of insulin resistance.w2People meeting three of the following criteria qualify as having the metabolic syndrome: raised blood pressure (> 130/85 mm Hg), a low serum concentration of HDL cholesterol (< 1.04 mmol/l in men and < 1.29 mmol/l in women), a high serum triglyceride concentration (> 1.69 mmol/l), a high fasting plasma glucose concentration (> 6.1 mmol/l), and abdominal obesity (waist circumference > 102 cm in men and > 88 cm in women). A new definition, proposed recently by the International Diabetes Federation, has central obesity as an essential criterion, with a range of cut-offs for waist circumference for people from different ethnic groups.5
In a recent joint statement, the American Diabetes Association and European Association for the Study of Diabetes questioned the diagnosis of metabolic syndrome.w3The debate will, no doubt, continue. Yet the concept of metabolic syndrome provides a practical and useful way to identify patients with multiple factors that place them at high risk of developing diabetes and cardiovascular disease.5
The prevalence of metabolic syndrome in the adult population in developed countries is 22-39% and varies depending on the definition used and on ethnicity.2 6 7 As defined by both WHO and NCEP metabolic syndrome is associated with future coronary heart disease events and type 2 diabetes.w4Both definitions also predict cardiovascular mortality,w5although only the NCEP definition has also been shown to predict all cause mortality.w6Metabolic syndrome seems to evolve gradually. Having even one or two features of the syndrome was associated in one study with increased risk of mortality from coronary heart disease and cardiovascular disease.w7
People with metabolic syndrome and a Framingham risk score greater than 20% have an increased risk of major coronary events over the next 10 years compared with people without metabolic syndrome and with the same risk score.8 Furthermore, the Framingham risk score—based on age, serum concentrations of both LDL and HDL cholesterol, blood pressure, cigarette smoking, and diabetes mellitus—predicts full development only of cardiovascular disease whereas the presence of metabolic syndrome predicts both diabetes and cardiovascular disease.
What does the diagnosis of metabolic syndrome mean for screening for and preventing chronic disease, particularly in primary care? All components of the NCEP and the International Diabetes Federation criteria for metabolic syndrome—hypertension, dyslipidaemia, abdominal obesity, and fasting glucose concentration—can readily be measured in primary care. Unlike the WHO criteria, these criteria do not include a glucose tolerance test, which would increase workload in primary care. Patients and primary care teams should focus on preventing all components of metabolic syndrome, bearing in mind that the risk of developing the metabolic syndrome increases with weight gain9 and insulin insensitivity is improved by weight loss,10 and eating less saturated fat.11 Earlier this month in its report Preventing chronic diseases: a vital investment, WHO published its latest projections on increased premature deaths from chronic diseases, including diabetes, and called for urgent action on modifiable risk factors such as unhealthy diets and physical inactivity.w8
It is becoming increasingly clear that a proinflammatory state is a common feature of the syndrome and of atheromatous disease. A recent randomised controlled trial showed that insulin resistance and measurements of C reactive protein were significantly lower at two year follow-up in patients with metabolic syndrome who had been allocated to a Mediterranean diet than in those who continued their normal diets.12 Although large intervention studies have shown that intensive modification of lifestyle delays the onset of diabetes in patients with impaired glucose tolerance,w9no similar trials have aimed at reducing all the cardiovascular disease risk factors among people with metabolic syndrome.
Additional references w1-w9 are on bmj.com
Competing interests None declared.