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Published on: April 1, 2019
RANTES gene G-403A polymorphism and coronary artery disease: a meta analysis of observational studies
Jun Liu1, Yan-Jun Jia, Xiao-Lin Li
1Division of Dyslipidemia, State Key Laboratory of Cardiovascular Disease, Fu Wai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
Insights
This meta-analysis found no significant link between the RANTES G-403A polymorphism and coronary artery disease (CAD) risk overall. Further research with larger sample sizes and standardized methods is needed to clarify potential ethnic differences.
Area of Science:
- Genetics and Cardiovascular Disease Research
- Molecular Biology and Disease Mechanisms
Background:
- The RANTES gene's G-403A polymorphism is hypothesized to influence coronary artery disease (CAD) development by affecting leukocyte activity.
- Previous studies on the G-403A polymorphism and CAD risk have produced conflicting results, necessitating further investigation.
Purpose of the Study:
- To conduct a meta-analysis to clarify the association between the RANTES G-403A polymorphism and CAD susceptibility.
- To resolve inconsistencies in existing research regarding this genetic variation and heart disease risk.
Main Methods:
- A comprehensive literature search was performed across PubMed and EMBASE databases up to March 2012.
- Additional studies were identified through citation reviews and author contact to ensure a thorough analysis.
- Meta-analysis was employed to synthesize data from 8 eligible studies involving 4252 CAD cases and 2150 controls.
Main Results:
- No significant association was found between the G-403A polymorphism and CAD risk across various genetic models.
- Significant heterogeneity among studies was identified, potentially explained by ethnicity and genotyping methods.
- Stratified analysis suggested a possible association with increased CAD risk in Caucasians and a protective role in Asians, though not consistently.
Conclusions:
- Current meta-analysis data do not support a direct relationship between the RANTES G-403A polymorphism and CAD development.
- Larger studies utilizing unified genotyping methods are recommended to definitively assess the influence of this polymorphism on CAD susceptibility.
Objective:
The G-403A polymorphism in RANTES gene may be involved in the development of coronary artery disease (CAD) through increasing RANTES-mediated leukocyte trafficking and activation. However, studies investigating the relationship between G-403A polymorphism and CAD yielded contradictory and inconclusive results. In order to shed some light on these inconsistent findings, a meta analysis was performed to clarify the role of G-403A polymorphism of RANTES gene in the susceptibility of CAD.
Methods:
A systemic literature search of PubMed and EMBASE was conducted from their inception to March 23, 2012, to retrieve related studies. In addition, Conference Proceedings Citation Index-Science was searched, authors of relevant studies were contacted, and reference lists of the included studies and their related citations in PubMed were reviewed for additional pertinent studies.
Results:
A total of 8 eligible studies were identified, with a total of 4252 CAD cases and 2150 controls. There was no evidence of significant association between G-403A polymorphism and CAD risk in any genetic model or pairwise comparisons (additive model: OR = 1.046, 95% CI = 0.883-1.239, I(2) = 65.9%; recessive model: OR = 1.140, 95% CI = 0.774-1.678, I(2) = 53.1%; dominant model: OR = 1.000, 95% CI = 0.820-1.21), I(2) = 62.6%; AA vs GG: OR = 1.141, 95% CI = 0.734-1.773, I(2) = 61.2%; GA vs GG: OR = 0.993, 95% CI = 0.800-1.232, I(2) = 64.6%). Subgroup analysis and meta regression indicated that ethnicity and genotyping method accounted for the significant heterogeneity among studies. In the stratified analysis by ethnic group, G-403A polymorphism was found to be associated with increased CAD risk in Caucasian population whereas its protective role was observed in Asian population in some but not all comparisons.
Conclusion:
Data from the current meta-analysis do not support the existence of a relationship between G-403A polymorphism and the development of CAD, and large sample size study employing unified genotyping method is needed to further evaluate the influence of G-403A polymorphism on susceptibility of CAD.
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