Rare variant of complement C4 is seen in high frequency in patients with primary glomerulonephritis

Lancet. 1984 Apr 21;1(8382):872-4. doi: 10.1016/s0140-6736(84)91339-4.

Abstract

59 unselected patients with primary glomerulonephritis were phenotyped for alleles of the MHC-linked complement genes, C4A, C4B, and BF. A rare variant of the C4B locus, C4B*2.9, was found in 25% of these patients compared with only 2% of the normal population--a relative risk of 22.1 for glomerulonephritis in individuals with this variant. Subdivision of patients by histological classification of glomerulonephritis revealed a significant association of C4B*2.9 with the membranoproliferative form. There were no significant associations between primary glomerulonephritis or its subtypes and the other HLA markers tested.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Biopsy
  • Complement C4 / analysis
  • Complement C4 / genetics*
  • Complement C4a
  • Complement C4b
  • Genetic Variation
  • Glomerulonephritis / genetics*
  • Glomerulonephritis / immunology
  • Glomerulonephritis / pathology
  • HLA Antigens / analysis
  • HLA Antigens / genetics
  • Humans
  • Kidney Glomerulus / pathology
  • Nephrosis, Lipoid / genetics
  • Nephrosis, Lipoid / immunology
  • Nephrosis, Lipoid / pathology
  • Phenotype
  • Polymorphism, Genetic

Substances

  • Complement C4
  • HLA Antigens
  • Complement C4a
  • Complement C4b