Childhood-onset schizophrenia and tryptophan hydroxylase gene polymorphism

Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):24-6. doi: 10.1002/ajmg.b.30009.

Abstract

We explored the relationship between the tryptophan hydroxylase gene polymorphism and susceptibility to childhood-onset schizophrenia in a Japanese sample. Subjects were 51 Japanese patients who met DSM-IV criteria for schizophrenia before age 16 and 148 Japanese healthy controls. DNA was extracted from whole blood and genotyping was performed by PCR-RFLP using Nhe I. The frequency of the A allele was relatively higher in patients with childhood-onset schizophrenia than in controls (odds ratio, OR = 1.47, 95% CI = 0.97-2.37, P = 0.097). There was a nearly doubling of the risk for childhood-onset schizophrenia associated with the AA genotype compared to other genotype groups; OR = 1.97, 95% CI = 0.91-4.22, P = 0.058.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Case-Control Studies
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Japan / epidemiology
  • Male
  • Molecular Epidemiology
  • Odds Ratio
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Risk
  • Schizophrenia / epidemiology
  • Schizophrenia / genetics*
  • Tryptophan Hydroxylase / genetics*

Substances

  • Tryptophan Hydroxylase