Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics

Neurosci Lett. 1998 Feb 27;243(1-3):109-12. doi: 10.1016/s0304-3940(98)00100-1.

Abstract

Catechol-O-methyltransferase (COMT) is an enzyme which inactivates catecholamine neurotransmitters by methylation, and is considered a candidate for involvement in schizophrenia. A functional COMT gene polymorphism influencing the enzyme activities, the high activity (val-108) and the low activity allele (met-108), was recently confirmed. We investigated a genetic association between schizophrenia and the COMT gene polymorphism in 150 Japanese schizophrenics and controls. We detected the low activity met-108 allele more frequently in schizophrenics than in the controls, and found that subjects sharing the met-108 allele (val/met and met/met) are significantly more common in the patients than in the controls. The results suggest that the low activity met-108 allele may be involved in susceptibility for schizophrenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Catechol O-Methyltransferase / genetics*
  • Chromosomes, Human, Pair 22*
  • Dopamine / physiology
  • Female
  • Genetic Linkage*
  • Genotype
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Schizophrenia / enzymology
  • Schizophrenia / genetics*

Substances

  • Catechol O-Methyltransferase
  • Dopamine