Genetic studies of IgA nephropathy: what have we learned from genome-wide association studies

Contrib Nephrol. 2013:181:52-64. doi: 10.1159/000348652. Epub 2013 May 8.

Abstract

Primary IgA nephropathy (IgAN) is the most common glomerulonephritis in the world. It is most common in Asian populations, followed by Caucasians, yet relatively infrequent amongst African populations. The striking difference in the prevalence of IgAN between world populations, together with the known familial aggregation of disease, suggests an inherited mechanism. Recently three genome-wide association studies (GWAS) of IgAN have identified seven susceptibility loci, providing initial insight into the genetic architecture of this trait. While genetic studies of complex traits are challenging, applying new techniques and methods of analysis, especially Next-Generation Sequencing, will push the genetic studies of IgAN forward.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Complement Factor H / genetics
  • Genome-Wide Association Study*
  • Glomerulonephritis, IGA / etiology
  • Glomerulonephritis, IGA / genetics*
  • HLA-DP beta-Chains / genetics
  • HLA-DRB1 Chains / genetics
  • Humans
  • Protein Tyrosine Phosphatases, Non-Receptor / genetics
  • Tumor Necrosis Factor Ligand Superfamily Member 13 / genetics
  • alpha-Defensins / genetics

Substances

  • HLA-DP beta-Chains
  • HLA-DPB1 antigen
  • HLA-DRB1 Chains
  • TNFSF13 protein, human
  • Tumor Necrosis Factor Ligand Superfamily Member 13
  • alpha-Defensins
  • Complement Factor H
  • MTMR3 protein, human
  • Protein Tyrosine Phosphatases, Non-Receptor