Platelet-activating factor receptor gene polymorphism in Japanese patients with multiple sclerosis

J Neuroimmunol. 2005 Apr;161(1-2):195-8. doi: 10.1016/j.jneuroim.2004.12.014.

Abstract

We evaluated the association of the platelet-activating factor receptor (PAFR) gene polymorphism (A224D) with the susceptibility and severity of multiple sclerosis (MS) in a Japanese population. DNA was collected from 162 Japanese patients with clinically definite 'conventional' MS (MS) and 245 healthy controls. The missense mutation A224D that impairs PAF-PAFR signaling was determined by polymerase chain reaction restriction fragment length polymorphism. The frequency of the AD/DD genotypes was significantly higher in MS patients (21.0%) than in healthy controls (13.5%) (p=0.045; odds ratio (OR), 1.71; 95% confidence interval (CI), 1.01-2.89). Moreover, the frequency of D allele in MS patients (11.7%) was also significantly higher than those in healthy controls (6.9%) (p=0.019; OR, 1.78; 95% CI, 1.10-2.89). These findings suggest that the PAFR gene missense mutation has a relation to the susceptibility for MS.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chi-Square Distribution
  • Confidence Intervals
  • Disease Susceptibility*
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Multiple Sclerosis / genetics*
  • Mutation, Missense
  • Odds Ratio
  • Platelet Membrane Glycoproteins / genetics*
  • Polymorphism, Genetic*
  • RNA, Messenger / biosynthesis
  • Receptors, G-Protein-Coupled / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Statistics, Nonparametric

Substances

  • Platelet Membrane Glycoproteins
  • RNA, Messenger
  • Receptors, G-Protein-Coupled
  • platelet activating factor receptor