Association of STAT4 polymorphisms with susceptibility to type-1 autoimmune hepatitis in the Japanese population

PLoS One. 2013 Aug 22;8(8):e71382. doi: 10.1371/journal.pone.0071382. eCollection 2013.

Abstract

Background/aims: Recent studies demonstrated an association of STAT4 polymorphisms with autoimmune diseases including systemic lupus erythematosus and rheumatoid arthritis, indicating multiple autoimmune diseases share common susceptibility genes. We therefore investigated the influence of STAT4 polymorphisms on the susceptibility and phenotype of type-1 autoimmune hepatitis in a Japanese National Hospital Organization (NHO) AIH multicenter cohort study.

Methodology/principal findings: Genomic DNA from 460 individuals of Japanese origin including 230 patients with type-1 autoimmune hepatitis and 230 healthy controls was analyzed for two single nucleotide polymorphisms in the STAT4 gene (rs7574865, rs7582694). The STAT4 rs7574865T allele conferred risk for type-1 autoimmune hepatitis (OR = 1.61, 95% CI = 1.23-2.11; P = 0.001), and patients without accompanying autoimmune diseases exhibited an association with the rs7574865T allele (OR = 1.50, 95%CI = 1.13-1.99; P = 0.005). Detailed genotype-phenotype analysis of type-1 autoimmune hepatitis patients with (n = 44) or without liver cirrhosis (n = 186) demonstrated that rs7574865 was not associated with the development of liver cirrhosis and phenotype (biochemical data and the presence of auto-antibodies).

Conclusions/significance: This is the first study to show a positive association between a STAT4 polymorphism and type-1 autoimmune hepatitis, suggesting that autoimmune hepatitis shares a gene commonly associated with risk for other autoimmune diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Asian People / genetics
  • Cohort Studies
  • Female
  • Genetic Predisposition to Disease*
  • Genetic Variation
  • Genotype
  • Hepatitis, Autoimmune / genetics*
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Phenotype
  • Polymorphism, Genetic*
  • Polymorphism, Single Nucleotide
  • STAT4 Transcription Factor / genetics*
  • Sequence Analysis, DNA

Substances

  • STAT4 Transcription Factor
  • STAT4 protein, human

Grants and funding

This study was supported by the research grant for National Hospital Organization (NHO) network study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.