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Saturday, 17 May, 2008



Metabolic Syndrome—A Common and Dangerous Health Problem

Francisco Lopez-Jimenez Division of Cardiovascular Diseases, Department of Medicine, Mayo Clinic College of Medicine

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For many years, scientists and clinicians have recognized the association between several relatively common conditions such as hypertension, abnormal glucose metabolism (diabetes and other milder forms of glucose intolerance), and obesity. The observed association has also included other factors such as abnormal lipids (cholesterol and triglycerides), elevated uric acid, and microscopic amounts of protein in the urine. This association has received many names, including insulin resistance syndrome, syndrome X, and the deadly quartet, and is now widely known as metabolic syndrome (MetSx).

The relevance of MetSx relies on its high prevalence in both developed and less developed countries and on its association with a high risk for developing cardiovascular disease and type 2 diabetes mellitus. This review will summarize the current data regarding the diagnosis and prevalence of MetSx worldwide, its risk factors, clinical relevance, and treatment. This review will also discuss some of the ongoing controversies related to MetSx that major medical organizations and recognized authorities have spurred, and how the lack of a global agreement can distract attention from an epidemic that affects all ages.

Diagnosis

Although there is full agreement that several factors such as hypertension, abnormal glucose metabolism, abnormal lipids, and obesity are strongly associated and may indeed share one or more physiopathological pathways, there is significant variability in the way in which MetSx is defined. To illustrate this lack of consensus, Table 1 displays the three most commonly used definitions of MetSx, revealing major differences in the diagnostic criteria. For example, the World Health Organization (WHO) requires a measure of insulin resistance to make the diagnosis of MetSx and includes microalbuminuria as a possible criterion, while the International Diabetes Federation (IDF) requires the presence of central obesity but does not require the documentation of glucose intolerance or insulin resistance to determine the presence of MetSx. A more clinically oriented definition is provided by the National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III) by using measurements that are commonly used in clinical practice. This lack of a standard way to define the diagnosis of MetSx has caused some skepticism in the scientific community and even some quarrels among major medical organizations, as documented in the position statement of the American Diabetes Association (ADA), which minimizes the importance of diagnosing patients with this ‘new’ nomenclature. This lack of a unified diagnostic method also makes it difficult to compare or combine results of studies assessing the incidence and prevalence of MetSx and the effect of therapeutic interventions on MetSx.

Prevalence

The prevalence of MetSx has been estimated in multiple studies, showing that about one-quarter of the US population meet diagnostic criteria for MetSx. National surveys performed with similar methodology prove that the prevalence of MetSx has increased by 25% in only 10 years, parallel to the increase in the prevalence of obesity and diabetes.

The prevalence of MetSx is higher in Native Americans and Mexican- Americans than in Non-Hispanic Whites or African-Americans. Gender appears to affect the prevalence of MetSx depending on the country or ethnic group. For example, in France and the US, the prevalence of MetSx is lower in women than in men, while the opposite occurs among Native Americans and in Turkey, India, and other parts of the world. It is not clear why these country- or race-related differences exist, but they may be related to some genetic traits and to different levels of physical activity between men and women depending on the country of origin. The prevalence of MetSx also increases with age, as suggested by prevalence studies showing that MetSx is six times more common in people older than 50 years compared with young adults aged between 20 and 29 years. This increased prevalence with older age may reflect a more sedentary lifestyle in elderly groups, which is a major risk factor for MetSx, but also reflects the higher prevalence of several of the MetSx criteria—such as hypertension, diabetes, and obesity—compared with younger people.
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Author(s) Biography
Francisco Lopez-Jimenez, MD, MSc, is Director of the Cardiometabolic Program at the Mayo Clinic and Co-Director of Cardiovision 2020, a community-based program for heart disease prevention in Olmsted County, Minnesota. His previous positions at the Mayo Clinic include Associate Director for Research in the Cardiovascular Health Clinic, Assistant Professor of Medicine, and Staff Physician. His research interests include: translational research assessing the effect of obesity, metabolic syndrome, and sleep apnea on cardiovascular health; measurements of body fatness; and the implementation of effective weight-loss techniques in clinical practice. He holds several grants supporting research on bariatric surgery and cardiovascular disease mechanisms and others supporting research on dietary interventions in metabolic syndrome. Dr Lopez-Jimenenz has written several books and book chapters on preventive cardiology and evidence-based medicine and has published more than 45 scientific reports in peer-reviewed journals. He has also been a featured speaker at many international meetings in America and Europe. Dr Lopez-Jimenez received his medical degree with honors from the Leon School of Medicine, Guanajuato University, Leon, Mexico. He then carried out his clinical training in internal medicine at the Instituto Nacional de la Nutricion, Medicina e Investigacion ‘Salvador Zubiran,’ Mexico City, Mexico. He continued his training in cardiology at the Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts and at the Mount Sinai Medical Center, Miami Beach, Florida, and completed an MSc in Clinical Epidemiology at Harvard School of Public Health, Harvard University.

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