The CD14--159C/T polymorphisms and the risks of tuberculosis: a meta-analysis

Infect Genet Evol. 2013 Aug:18:277-83. doi: 10.1016/j.meegid.2013.06.001. Epub 2013 Jun 12.

Abstract

Previous studies about the association between CD14--159C/T polymorphisms and the risks of tuberculosis (TB) have yielded conflicting results, and thus a meta-analysis was performed in order to provide a more accurate estimation. A computerized literature search with additional manual search was conducted for the relevant available studies. Pooled odds ratio (ORs) and 95% confidence intervals (95%CIs) were calculated by either fixed-effects model or random-effects model based on heterogeneity test. A total of 8 eligible studies (1729 cases and 1803 controls) were included in the meta-analyses. Overall, a significant association between CD14--59C/T polymorphism and TB risks was detected in the recessive model (TT vs. TC/CC, OR=1.48, 95%CI 1.06-2.07). Significant associations were also detected in Asians (T vs. C, OR=1.49, 95%CI 1.33-1.67; TT vs. CC, OR=1.94, 95%CI 1.54-2.45; TT vs.

Tc/cc: OR=1.86, 95%CI 1.57-2.20). In contrast, no significant association was detected in Caucasians in each genetic model. The subgroup analysis stratified by TB types showed a significant association between CD14--159C/T polymorphism and pulmonary TB risks (T vs. C, OR=1.51, 95%CI 1.01-2.26; TT vs. TC/CC, OR=1.84, 95%CI 1.03-3.29), which did not reach statistically significance when the P values were Bonferroni adjusted to 0.025. No publication bias was detected in any comparisons. Collectively, the results of this meta-analysis suggest a possible association between CD14--59C/T polymorphism and TB risks in Asians, but not in Caucasians. Well-designed case-control studies with larger sample size are needed to confirm these results.

Keywords: CD14; Gene polymorphism; Meta-analysis; Tuberculosis.

Publication types

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

MeSH terms

  • Adult
  • Asian People / genetics
  • Case-Control Studies
  • Chi-Square Distribution
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Lipopolysaccharide Receptors / genetics*
  • Male
  • Middle Aged
  • Odds Ratio
  • Polymorphism, Single Nucleotide
  • Tuberculosis / genetics*
  • White People / genetics

Substances

  • Lipopolysaccharide Receptors