CD14 gene-159C/T polymorphism and coronary artery disease: a meta-analysis involving 4467 subjects

Yan-Yan Li1, Xiang-Ming Wang1, Chuan-Wei Zhou1

  • 1Department of Geriatrics, First Affiliated Hospital of Nanjing Medical University Nanjing 210029, China.

Insights

The cluster of differentiation antigen 14 (CD14) gene-159C/T polymorphism is linked to coronary artery disease (CAD) susceptibility, especially in the Chinese population. The T allele may increase the risk of developing CAD.

Area of Science:

  • Genetics
  • Cardiovascular Disease Research
  • Molecular Biology

Background:

  • The cluster of differentiation antigen 14 (CD14) gene-159C/T polymorphism is a potential factor influencing coronary artery disease (CAD) susceptibility.
  • Existing studies on the association between CD14 gene-159C/T polymorphism and CAD risk have yielded conflicting results.

Purpose of the Study:

  • To conduct a comprehensive meta-analysis to clarify the relationship between the CD14 gene-159C/T polymorphism and CAD.
  • To evaluate the pooled odds ratios (ORs) and confidence intervals (CIs) using random or fixed effect models.

Main Methods:

  • Meta-analysis of 7 individual studies involving 4467 subjects.
  • Statistical analysis using random or fixed effect models to assess pooled ORs and 95% CIs.
  • Subgroup analysis was performed based on ethnicity (Chinese and Caucasian populations).

Main Results:

  • A significant association was observed between CD14 gene-159C/T polymorphism and CAD across allelic, recessive, homozygous, and additive genetic models.
  • No significant association was found under dominant and heterozygous genetic models.
  • Subgroup analysis revealed a significant association in the Chinese population but not in the Caucasian subgroup.

Conclusions:

  • The CD14 gene-159C/T polymorphism is significantly associated with CAD susceptibility, particularly in the Chinese population.
  • Individuals carrying the T allele of the CD14 gene-159C/T polymorphism may have an increased predisposition to CAD.
  • No clear association between this polymorphism and CAD was identified in the Caucasian subgroup.
Abstract

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