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J Am Coll Cardiol, 2007; 49:403-414, doi:10.1016/j.jacc.2006.09.032
(Published online 11 January 2007). © 2007 by the American College of Cardiology Foundation |
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* Division of Cardiovascular Diseases, Mayo Clinic College of Medicine, Rochester, Minnesota
Department of Internal Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota
Mayo Medical Libraries, Mayo Clinic College of Medicine, Rochester, Minnesota
Division of Hypertension, Mayo Clinic College of Medicine, Rochester, Minnesota
|| Division of Endocrinology, Nutrition, and Metabolism, Mayo Clinic College of Medicine, Rochester, Minnesota
¶ Knowledge and Encounter Research Unit, Mayo Clinic College of Medicine, Rochester, Minnesota.
Manuscript received June 26, 2006; revised manuscript received September 1, 2006, accepted September 27, 2006.
* Reprint requests and correspondence: Dr. Apoor S. Gami, Division of Cardiovascular Diseases, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, Minnesota 55905. (Email: gami.apoor{at}mayo.edu).
OBJECTIVES: The purpose of this research was to assess the association between the metabolic syndrome (MetSyn) and cardiovascular events and mortality by meta-analyses of longitudinal studies.
BACKGROUND: Controversy exists regarding the cardiovascular risk associated with MetSyn.
METHODS: We searched electronic reference databases through March 2005, studies that referenced Reavens seminal article, abstracts presented at meetings in 2003 to 2004, and queried experts. Two reviewers independently assessed eligibility. Longitudinal studies reporting associations between MetSyn and cardiovascular events or mortality were eligible. Two reviewers independently used a standardized form to collect data from published reports. Authors were contacted. Study quality was assessed by the control of selection, detection, and attrition biases.
RESULTS: We found 37 eligible studies that included 43 cohorts (inception 1971 to 1997) and 172,573 individuals. Random effects meta-analyses showed MetSyn had a relative risk (RR) of cardiovascular events and death of 1.78 (95% confidence interval [CI] 1.58 to 2.00). The association was stronger in women (RR 2.63 vs. 1.98, p = 0.09), in studies enrolling lower risk (<10%) individuals (RR 1.96 vs. 1.43, p = 0.04), and in studies using factor analysis or the World Health Organization definition (RR 2.68 and 2.06 vs. 1.67 for National Cholesterol Education Program definition and 1.35 for other definitions; p = 0.005). The association remained after adjusting for traditional cardiovascular risk factors (RR 1.54, 95% CI 1.32 to 1.79).
CONCLUSIONS: The best available evidence suggests that people with MetSyn are at increased risk of cardiovascular events. These results can help clinicians counsel patients to consider lifestyle interventions, and should fuel research of other preventive interventions.
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