Promoter Polymorphism (-174, G/C) of Interleukin-6 and Arterial Thromboembolic Events: A Meta-Analysis

Su Kang Kim1, Joo-Ho Chung1, Oh Young Kwon2

  • 1Kohwang Medical Research Institute, School of Medicine, Kyung Hee University, Seoul, South Korea.

Insights

This meta-analysis found no significant link between the IL-6 gene

Area of Science:

  • Cardiovascular Genetics
  • Molecular Epidemiology
  • Thrombosis Research

Background:

  • Ischemic stroke and myocardial infarction are leading causes of death globally.
  • Interleukin-6 (IL-6) plays a role in arterial thromboembolic events, but its genetic associations are debated.
  • The single-nucleotide polymorphism (SNP) rs1800795 in the IL-6 gene promoter has been investigated for its role in these conditions.

Purpose of the Study:

  • To conduct a meta-analysis to clarify the association between the IL-6 gene promoter SNP (rs1800795) and arterial thromboembolic event susceptibility.
  • To evaluate the relationship between this specific IL-6 polymorphism and the risk of ischemic stroke and myocardial infarction.

Main Methods:

  • A systematic literature search was performed across PubMed, Embase, Google Scholar, and KISS databases.
  • Meta-analysis was conducted using Comprehensive Meta-analysis software, calculating odds ratios (OR) and 95% confidence intervals (CI).
  • Data from 13 eligible studies were analyzed to assess the association between the IL-6 rs1800795 SNP and arterial thromboembolic events.

Main Results:

  • The meta-analysis revealed no statistically significant association between the IL-6 rs1800795 SNP and susceptibility to arterial thromboembolic events.
  • Specific genetic models (C vs. G allele, CC vs. GG, CC+CG vs. GG) showed no significant risk increase or decrease.
  • No significant association was found between the IL-6 SNP and the risk of ischemic stroke or myocardial infarction.

Conclusions:

  • The IL-6 gene rs1800795 SNP is not significantly related to the risk of arterial thromboembolic events.
  • Current evidence suggests this specific genetic variation does not contribute to the susceptibility of ischemic stroke or myocardial infarction.
  • Further research is warranted to definitively confirm these findings and explore other genetic factors.

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