PLoS ONE (Jan 2014)

MAPKAP1 rs10118570 polymorphism is associated with anti-infection and anti-hepatic fibrogenesis in schistosomiasis japonica.

  • Xiao Zhu,
  • Jinfang Zhang,
  • Wenguo Fan,
  • Yunguo Gong,
  • Jianhua Yan,
  • Zhidong Yuan,
  • Lang Wu,
  • Hongjing Cui,
  • Haiqing Luo,
  • Qingming Kong,
  • Li Tang,
  • Shuilong Leng,
  • Yufeng Liao,
  • Weiming Fu,
  • Qin Xiao,
  • Dongpei Li

DOI
https://doi.org/10.1371/journal.pone.0105995
Journal volume & issue
Vol. 9, no. 8
p. e105995

Abstract

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Chronic infection with Schistosoma japonicum is an important cause of hepatic fibrosis (HF). Human 9q33.3 is one of the most important loci for stress-related diseases. We examined the potential associations of 43 single-nucleotide polymorphisms (SNPs) with S. japonicum infection and HF in epidemic region in China. We identified a SNP (rs10118570 GG in mitogen-activated protein kinase associated protein 1, MAPKAP1) contributes to anti-infection (adjusted OR = 0.35) and anti-fibrogenesis (adjusted RR = 0.44) in the discovery study. Replicative and combined studies showed consistent protective quality for this genotype (replicative: adjusted OR = 0.37 for anti-infection, and adjusted RR = 0.40 for anti-fibrogenesis; Combined: adjusted OR = 0.45 for anti-infection, and adjusted RR = 0.42 for anti-fibrogenesis). Univariate and multivariate analysis in the discovery, replicative and combined studies, suggested that durations (years), splenomegaly, serum ALB and rs10118570 were independent predictors influencing the fibrogenesis. The analysis of gene-gene interaction showed rs10118570 functions independently. We conclude that MAPKAP1 may represent a novel anti-infection and anti-fibrogenesis genomic locus in chronic schistosomiasis japonica. And rs10118570 may be a potential biomarker and target for the treatment of this life-threatening ancient disease.