Association of alcohol dehydrogenase 2*1 allele with liver damage and insulin concentration in the Japanese

J Hum Genet. 2006;51(1):31-37. doi: 10.1007/s10038-005-0318-9. Epub 2005 Nov 24.

Abstract

The Japanese have a polymorphism in the alcohol dehydrogenase 2 gene (ADH2). The alleles of ADH2 (ADH2*1 and ADH2*2) encode more active and less active forms for ethanol metabolism, respectively. We examined whether liver damage and the insulin-glucose axis vary according to ADH2 genotype in the Japanese. The 2,232 subjects (1,126 men and 1,106 women) were recruited from a population-based prospective cohort study. Clinical evaluations including alcohol consumption, percentage of alcohol drinkers, plasma glucose, HbA1c, insulin, AST, ALT, gamma-GTP, and prevalence of diabetes were compared among the ADH2 genotypes. The percentage of drinkers, alcohol consumption, AST, ALT, and gamma-GTP were higher in group ADH2*1/1 than in group ADH2*1/2 or ADH2*2/2 (all P < 0.05). Hence, ADH2*1/1 is associated with excess alcohol intake and liver disorders. However, the prevalence of diabetes did not differ among the three groups. For the glucose-insulin axis, we examined subjects who did not receive insulin therapy or oral anti-diabetes medication. While amounts of alcohol consumed and glucose levels were nearly the same between ADH*1/2 and ADH2*2/2, insulin concentrations were lower in ADH2*2/1 than in ADH2*2/2 (P < 0.05 in men). This finding suggests that the ADH2*1 allele is associated with a lower insulin concentration when alcohol intake is light or moderate. It also suggests that the genetic effect of ADH2*1 plays an important role in alcohol drinking behavior and in the occurrence of liver injury, but the effect is so mild that it does not influence the glucose-insulin axis or prevalence of diabetes.

MeSH terms

  • Alcohol Dehydrogenase / genetics*
  • Alleles*
  • Base Sequence
  • DNA Primers
  • Genotype
  • Humans
  • Insulin / blood*
  • Japan
  • Liver Diseases, Alcoholic / enzymology
  • Liver Diseases, Alcoholic / genetics*
  • Polymerase Chain Reaction

Substances

  • DNA Primers
  • Insulin
  • ADH1B protein, human
  • Alcohol Dehydrogenase