Association of genetic variations in the STAT4 and IRF7/KIAA1542 regions with systemic lupus erythematosus in a Northern Han Chinese population

Hum Immunol. 2011 Mar;72(3):249-55. doi: 10.1016/j.humimm.2010.12.011. Epub 2010 Dec 15.

Abstract

Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease with complex genetic inheritance. Genome-wide association studies have identified SLE susceptibility variations at the IRF7/KIAA1542 locus and with STAT4 gene in European populations. We decided to investigate the association of single-nucleotide polymorphisms (SNPs) in the IRF7/KIAA1542 region (rs4963128, rs2246614, and rs702966) and in STAT4 (rs7574865 and rs7582694) with SLE disease in a Northern Han Chinese population of 748 patients and 750 healthy controls. Our study indicated a strong association between rs7574865 (odds ratio = 0.68; 95% confidence interval 0.59-0.79; p = 1.57 × 10(-6)) and SLE and between rs7574865 and the production of anti-Sm antibodies. Additionally, rs4963128 and rs2246614 were correlated with a variety of clinical subphenotypes, such as lupus nephritis, arthritis, and the production of anti-SSA/B autoantibodies, despite a lack of significant association between these two SNPs and SLE disease susceptibility in general.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Arthritis / genetics
  • Autoantibodies
  • China
  • Female
  • Genetic Predisposition to Disease*
  • Genetic Variation
  • Genome-Wide Association Study
  • Genotype
  • Humans
  • Interferon Regulatory Factor-7 / genetics*
  • Lupus Erythematosus, Systemic / genetics*
  • Lupus Nephritis / genetics
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • STAT4 Transcription Factor / genetics*
  • Signal Transduction

Substances

  • Autoantibodies
  • IRF7 protein, human
  • Interferon Regulatory Factor-7
  • STAT4 Transcription Factor
  • STAT4 protein, human