MEFV mutations in Japanese rheumatoid arthritis patients

Clin Exp Rheumatol. 2008 Nov-Dec;26(6):1091-4.

Abstract

Objective: Familiar Mediterranean Fever (FMF) is common among Mediterranean populations, while other populations are rarely affected. The aim of this study was to assess the involvement of MEFV gene mutations among Japanese rheumatoid arthritis patients with or without amyloid A (AA) amyloidosis.

Methods: The frequency of the MEFV mutations, which were identified in Japanese FMF patients, was determined in 126 Japanese RA patients and 76 Japanese healthy subjects.

Results: The M694I mutation was not observed among RA patients and healthy subjects. Allele frequency of R408Q, P369S, E148Q, L110P mutations account respectively for 3.3%, 3.9%, 23.7%, 9.2% in healthy subjects and 5.6%, 6.7%, 24.2%, 9.5% in RA patients. The overall mutation rate was comparable between the RA patients and healthy subjects, as well as between the RA patients with and without amyloidosis.

Conclusion: This study shows the high prevalence of mutations of the MEFV genes in Japanese RA patients. However, our data suggest that the MEFV gene mutations may not be a genetic factor affecting the susceptibility of RA or the development of amyloidosis in a Japanese population.

MeSH terms

  • Aged
  • Amyloidosis / ethnology
  • Amyloidosis / genetics
  • Arthritis, Rheumatoid / ethnology*
  • Arthritis, Rheumatoid / genetics*
  • Asian People / statistics & numerical data*
  • Cytoskeletal Proteins / genetics*
  • Familial Mediterranean Fever / ethnology
  • Familial Mediterranean Fever / genetics
  • Female
  • Genetic Predisposition to Disease / ethnology
  • Humans
  • Japan / epidemiology
  • Male
  • Middle Aged
  • Point Mutation
  • Prevalence
  • Pyrin

Substances

  • Cytoskeletal Proteins
  • MEFV protein, human
  • Pyrin