Alcohol dehydrogenase 2 variant is associated with cerebral infarction and lacunae

Neurology. 2004 Nov 9;63(9):1711-3. doi: 10.1212/01.wnl.0000142971.08275.db.

Abstract

The authors examined the association of the alcohol dehydrogenase 2 (ADH2) genotype with vascular events in community-dwelling Japanese (1,102 men/1,093 women). The allele ADH2*2 encodes an isozyme with a higher level of activity than ADH2*1. Here, the authors show that the ADH2*1 carriage is associated with high prevalence of cerebral infarction and lacunae in men. Multiple regression analyses confirmed that the risk of lacunae and cerebral infarction was increased by the ADH2*1 allele.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alcohol Dehydrogenase / genetics*
  • Alleles*
  • Asian People / genetics
  • Cerebral Infarction / ethnology
  • Cerebral Infarction / genetics*
  • Cerebral Infarction / pathology
  • Female
  • Genetic Predisposition to Disease*
  • Genetic Variation
  • Humans
  • Japan
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged

Substances

  • ADH1B protein, human
  • Alcohol Dehydrogenase