Abstract

Metabolic Syndrome (MS) is recognized as a cluster of cardiovascular risk factors. All components of MS have a genetic base. Genes of the renin angiotensin system are potential candidate genes for MS. We investigated whether angiotensin converting enzyme (ACE) gene polymorphism increases susceptibility to MS as an entity in a Mexican population. In a cross-sectional study, 514 individuals were studied including 245 patients with MS and 269 subjects without MS criteria. ACE gene polymorphism was detected using PCR. MS was defined according to The National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) criteria, except that the raised fasting plasma glucose <or=100 mg/dl criterion for identification of intolerance fasting glucose was modified in accordance with the suggestion of the American Diabetes Association. Patients with MS were significantly different from subjects without MS in relation to mean body mass index (BMI), waist circumference (WC), systolic blood pressure, diastolic blood pressure, glucose, total cholesterol (C), triglycerides, HDL-C, and LDL-C (P<0.0001). The differences in the mean BMI, WC, glucose, total cholesterol, triglycerides, LDL-C, and HDL-C were maintained in patients with the MS and DD genotypes (P<0.01). The DD genotype was strongly associated with MS (adjusted OR=5.48, 95% CI 3.20-9.38, P<0.0001). We concluded that the DD genotype increases susceptibility to MS in a Mexican population. These results indicate that pharmacological and non-pharmacological treatment and a reduction in body fat will have important therapeutic implications in this disease.

Highlights

  • Metabolic Syndrome (MS) is recognized as a cluster of cardiovascular risk factors that frequently coincide with central obesity, dyslipidemia, hypertension, and hyperglycemia (Timar et al, 2000) with a frequent occurrence in various ethnic groups

  • Patients with MS were significantly different from subjects without MS in relation to the mean body mass index (BMI), waist circumference (WC), systolic blood pressure (SBP), diastolic blood pressure (DBP), glucose, total cholesterol, triglycerides, high density lipoprotein cholesterol (HDL-C), and low density lipoprotein cholesterol (LDL-C) (P

  • The results revealed a strong association of the DD genotype with MS

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Summary

Introduction

Metabolic Syndrome (MS) is recognized as a cluster of cardiovascular risk factors that frequently coincide with central obesity, dyslipidemia, hypertension, and hyperglycemia (Timar et al, 2000) with a frequent occurrence in various ethnic groups. Its presence is associated with a high risk of developing cardiovascular disease (CVD) (Isomaa et al, 2001). Recent estimates show the prevalence of MS in the adult population as 32% for Hispanic Americans, 22% for Afro-Americans, and 24% for Caucasian populations (Ford et al, 2002). This prevalence increases more than 70% in patients with type 2 diabetes (Ilanne-Parikka et al, 2004). There is an interaction or multiplying effects of polymorphism in a growing number of genes potentially involved in this disease

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