Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. Short communication

J Neural Transm (Vienna). 1997;104(11-12):1313-7. doi: 10.1007/BF01294732.

Abstract

We report -108Met/Val polymorphism of the COMT gene in Japanese patients with Parkinson's disease (PD). The allele frequency for -108Val was higher in PD patients compared with controls, although the differences did not reach the statistical significance. However, the frequency of -108Val homozygotes was significantly higher in PD patients (56.8%) than in control subjects (44.2%), and heterozygotes of -108Met/Val were less in PD. COMT gene polymorphism may constitute a genetic risk factor for PD among Japanese.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Alleles
  • Catechol O-Methyltransferase / genetics*
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Parkinson Disease / enzymology
  • Parkinson Disease / genetics*
  • Polymorphism, Genetic

Substances

  • Catechol O-Methyltransferase