3.8 Article

Alcohol Intake, Myocardial Infarction, Biochemical Risk Factors, and Alcohol Dehydrogenase Genotypes

Journal

CIRCULATION-CARDIOVASCULAR GENETICS
Volume 2, Issue 5, Pages 507-514

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGENETICS.109.873604

Keywords

genetics; cardiovascular diseases; myocardial infarction; epidemiology; alcohol; cardiovascular risk factors; alcohol dehydrogenase genes

Funding

  1. Danish Graduate School of Public Health
  2. Danish Heart Foundation
  3. Chief Physician Johan Boserup and Lise Boserup Foundation
  4. Health Insurance Foundation
  5. Ministry of the Interior and Health
  6. Danish Cancer Society, and the Danish National Board of Health

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Background-The risk of myocardial infarction is lower among light-to-moderate alcohol drinkers compared with abstainers. We tested associations between alcohol intake and risk of myocardial infarction and risk factors and whether these associations are modified by variations in alcohol dehydrogenases. Methods and Results-We used information on 9584 men and women from the Danish general population in the Copenhagen City Heart Study. During follow-up, from 1991 to 2007, 663 incident cases of myocardial infarction occurred. We observed that increasing alcohol intake was associated with decreasing risk of myocardial infarction, decreasing low-density lipoprotein cholesterol and fibrinogen, increasing diastolic and systolic blood pressure and high-density lipoprotein cholesterol, and with U-shaped nonfasting triglycerides. In contrast, ADH1B and ADH1C genotypes were not associated with risk of myocardial infarction or with any of the cardiovascular biochemical risk factors, and there was no indication that associations between alcohol intake and myocardial infarction and between alcohol intake and risk factors were modified by genotypes. Conclusions-Increasing alcohol intake is associated with decreasing risk of myocardial infarction, decreasing low-density lipoprotein cholesterol and fibrinogen, increasing diastolic and systolic blood pressure and high-density lipoprotein cholesterol, and U-shaped nonfasting triglycerides. These associations were not modified by ADH1B and ADH1C are genotypes. (Circ Cardiovasc Genet. 2009;2:507-514.)

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