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      The Metabolic Syndrome

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          Abstract

          The “metabolic syndrome” (MetS) is a clustering of components that reflect overnutrition, sedentary lifestyles, and resultant excess adiposity. The MetS includes the clustering of abdominal obesity, insulin resistance, dyslipidemia, and elevated blood pressure and is associated with other comorbidities including the prothrombotic state, proinflammatory state, nonalcoholic fatty liver disease, and reproductive disorders. Because the MetS is a cluster of different conditions, and not a single disease, the development of multiple concurrent definitions has resulted. The prevalence of the MetS is increasing to epidemic proportions not only in the United States and the remainder of the urbanized world but also in developing nations. Most studies show that the MetS is associated with an approximate doubling of cardiovascular disease risk and a 5-fold increased risk for incident type 2 diabetes mellitus. Although it is unclear whether there is a unifying pathophysiological mechanism resulting in the MetS, abdominal adiposity and insulin resistance appear to be central to the MetS and its individual components. Lifestyle modification and weight loss should, therefore, be at the core of treating or preventing the MetS and its components. In addition, there is a general consensus that other cardiac risk factors should be aggressively managed in individuals with the MetS. Finally, in 2008 the MetS is an evolving concept that continues to be data driven and evidence based with revisions forthcoming.

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          Author and article information

          Journal
          Endocr Rev
          Endocr. Rev
          edrv
          Endocrine Reviews
          Endocrine Society
          0163-769X
          1945-7189
          December 1, 2008
          : 29
          : 7
          : 777-822
          Affiliations
          University of Colorado Denver School of Medicine, Aurora, Colorado 80045
          Author notes
          Address all correspondence and requests for reprints to: Marc-Andre Cornier, M.D., University of Colorado Denver, Division of Endocrinology, Metabolism, and Diabetes, Mail Stop 8106, 12801 East 17 th Avenue, Room 7103, Aurora, Colorado 80045. E-mail: marc.cornier@ 123456ucdenver.edu .
          Article
          PMC5393149 PMC5393149 5393149 2707
          10.1210/er.2008-0024
          5393149
          18971485
          3d859692-608f-421e-a870-9d02b80c4e13
          © 2008 by The Endocrine Society
          History
          : 23 October 2008
          : 30 May 2008
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          Custom metadata
          777
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