Association between IL-6-174G/C polymorphism and the risk of sepsis and mortality: a systematic review and meta-analysis

PLoS One. 2015 Mar 3;10(3):e0118843. doi: 10.1371/journal.pone.0118843. eCollection 2015.

Abstract

Background: Recent studies have reported the association between IL-6-174G/C polymorphism and sepsis. However, the results are inconclusive and conflicting. To better understand the role of IL-6-174G/C polymorphism in sepsis, we conducted a comprehensive meta-analysis.

Methodology: Literature search was conducted through PubMed, Embase, Web of Knowledge databases until July 29, 2013. The pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using fixed- or random-effect model based on heterogeneity test in total and subgroup analyses.

Results: Twenty studies on the risk of sepsis and seven studies on sepsis mortality were included. None of the results showed evidence of a significant association between IL-6-174G/C polymorphism and sepsis risk in overall analysis or subgroup analyses based on sepsis type, ethnicity, source of control and age under any genetic model (the allele comparison, the codominant, the recessive or the dominant model). Although there was a statistically significant association between IL-6-174 G/C polymorphism and sepsis-related mortality under the recessive model, the significance did not exist after Bonferroni's correction.

Conclusions: Current evidence does not support a direct effect of IL-6-174 G/C polymorphism on the risk of sepsis. In addition, there was no association between IL-6-174 G/C polymorphism and sepsis mortality after Bonferroni's correction. Further analyses of gene-environment interactions and more studies based on larger sample size and homogeneous sepsis patients are required.

Publication types

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

MeSH terms

  • Adult
  • Alleles
  • Child
  • Gene Expression
  • Genetic Association Studies
  • Humans
  • Infant
  • Interleukin-6 / genetics*
  • Models, Genetic
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Racial Groups
  • Risk
  • Sepsis / ethnology
  • Sepsis / genetics*
  • Sepsis / mortality*
  • Sepsis / pathology
  • Survival Analysis

Substances

  • IL6 protein, human
  • Interleukin-6

Grants and funding

This work is supported by National Key Technology R&D Program (2012BAI11B01), the Major State Basic Research Development Program of China (2012CB518104), National Natural Science Funds for Distinguished Young Scholar (81201462), and Open fund of State Key Laboratory of Trauma, Burns and Combined Injury, Third Military Medical University (SKLZZ201104). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.