C4 null genes in American whites and blacks with myositis

J Rheumatol. 1990 Mar;17(3):331-4.

Abstract

The frequencies of C4A and C4B alleles were determined in 66 adults with myositis in relation to HLA class I and II. In whites with myositis, the C4A*Q0 allele occurred in 13/31 (47%) as compared to 25/101 (25%) normal controls (p = 0.08, relative risk = 2.7). Only 11/35 (31%) of black patients with myositis had a C4A*Q0 allele compared to 11/55 (20%) of controls (p = NS, RR = 1.8). Thus, the MHC class III genes do not appear to be the primary genetic risk factors for myositis in adults.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles*
  • Black People / genetics*
  • Chromosome Deletion
  • Complement C4 / genetics*
  • Dermatomyositis / ethnology
  • Dermatomyositis / genetics
  • Dermatomyositis / immunology
  • Genes*
  • HLA Antigens / analysis
  • HLA Antigens / genetics
  • Humans
  • Myositis / ethnology
  • Myositis / genetics*
  • Myositis / immunology
  • Phenotype
  • United States
  • White People / genetics*

Substances

  • Complement C4
  • HLA Antigens