TIRAP C539T polymorphism contributes to tuberculosis susceptibility: evidence from a meta-analysis

Infect Genet Evol. 2014 Oct:27:32-9. doi: 10.1016/j.meegid.2014.06.025. Epub 2014 Jul 5.

Abstract

Background: Toll-interleukin 1 receptor domain containing adaptor protein (TIRAP), an important adaptor protein downstream of the Toll-like receptor (TLR) 2 and 4 pathways, is highly involved in the activation and coordination of the anti-mycobacterial immune response. We performed a meta-analysis to assess the association between TIRAP C539T polymorphism and tuberculosis (TB) risk.

Methods: A systematic literature search for relevant studies up to February 27, 2014 was conducted in PUBMED, EMBASE, Web of science, CNKI, VIP, and Wanfang database. The association between gene and disease was assessed using odds ratios (ORs) with 95% confidence intervals (95%CIs) based on five genetic models.

Results: A total of 16 qualified studies were enrolled in this meta-analysis. The results of pooling all studies detected statistically resistance of TIRAP C539T mutants to TB risk (T vs. C: OR 0.80, 95%CI 0.65-0.97; TC vs. CC: OR 0.71, 95%CI 0.55-0.92; TT+TC vs. CC: OR 0.74, 95% CI 0.58-0.94). Further subgroup analyses by ethnicity also demonstrated reduced risk of TB in European population (T vs. C: OR 0.71, 95%CI 0.52-0.95; TC vs. CC: OR 0.56, 95%CI 0.35-0.91; TT+TC vs. CC: OR 0.61, 95%CI 0.40-0.92), whereas no such effects were observed in other ethnicities.

Conclusion: This present meta-analysis suggests TIRAP C539T polymorphism is significantly correlated with reduced risk of TB infection, with stronger effect in European. Additional well-designed, larger-scale epidemiological studies among different ethnicities are needed.

Keywords: MAL; Meta-analysis; Polymorphism; TIRAP; Tuberculosis.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Case-Control Studies
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Membrane Glycoproteins / genetics*
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Publication Bias
  • Racial Groups / genetics
  • Receptors, Interleukin-1 / genetics*
  • Tuberculosis / genetics*

Substances

  • Membrane Glycoproteins
  • Receptors, Interleukin-1
  • TIRAP protein, human