Possible allelic association of a tyrosine hydroxylase polymorphism with vulnerability to alcohol-withdrawal delirium

Psychiatr Genet. 1998 Spring;8(1):13-7. doi: 10.1097/00041444-199800810-00002.

Abstract

Recently, an association has been reported between schizophrenia and a rare allele containing 10-repeats (A10) of a polymorphic tetranucleotide motif in the first intron of the tyrosine hydroxylase (TH) gene. The present association analysis tested the hypothesis that the A10 candidate allele confers vulnerability to alcohol-withdrawal delirium with visual hallucinations. The genotype of the TH tetranucleotide polymorphism was assessed in 204 German controls and 311 German alcohol-dependent subjects, including 63 alcoholics with a history of visual hallucinations during withdrawal delirium. The frequency of the A10 allele was significantly increased in the alcoholics with withdrawal delirium (3.2%) compared with that in the controls (0.5%; Fisher's exact test: P = 0.03, two-tailed; OR (A10+) = 6.85, 95% confidence interval: 1.52-30.79). The possible allelic association suggests that allelic variation at the TH locus mediates vulnerability to alcohol-withdrawal delirium in a small proportion of alcohol-dependent subjects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alcohol Withdrawal Delirium / enzymology
  • Alcohol Withdrawal Delirium / genetics*
  • Alcoholism / enzymology
  • Alcoholism / genetics*
  • Alleles
  • Ethanol / adverse effects
  • Female
  • Genetic Predisposition to Disease
  • Hallucinations / genetics
  • Humans
  • Male
  • Polymorphism, Genetic*
  • Substance Withdrawal Syndrome / genetics
  • Substance Withdrawal Syndrome / psychology
  • Tyrosine 3-Monooxygenase / genetics*

Substances

  • Ethanol
  • Tyrosine 3-Monooxygenase