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Updated: Sep 6, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
Meta-analysis of effects of ABCB1 polymorphisms on clopidogrel response among patients with coronary artery disease
Yajing Zhai1, Hairong He2, Xiancang Ma2
1Department of Pharmacy, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi, 710061, People's Republic of China.
Insights
The ABCB1 C3435T polymorphism may increase bleeding risk in Asian patients taking clopidogrel. This genetic variation
Area of Science:
- Pharmacogenetics
- Molecular Epidemiology
- Clinical Pharmacology
Background:
- Clopidogrel's antiplatelet efficacy varies significantly among patients.
- The ABCB1 C3435T polymorphism is a potential factor influencing clopidogrel response, but evidence is conflicting.
Purpose of the Study:
- To conduct a PRISMA-compliant meta-analysis.
- To precisely evaluate the association between ABCB1 C3435T polymorphism and clopidogrel's clinical efficacy.
Main Methods:
- Searched PubMed and EMBASE databases up to October 2016.
- Included 28 studies with 23,243 patients.
- Used odds ratios (OR), standard mean difference (SMD), and 95% confidence intervals (CI) for analysis.
Main Results:
- No overall association found between ABCB1 polymorphisms and the primary outcome.
- Subgroup analysis indicated C3435T mutation reduced platelet activity in dominant and heterozygous models (LTA assay), but lacked robustness.
- Significant association observed between C3435T polymorphism and increased bleeding risk in Asian patients (dominant, homozygous, heterozygous models).
Conclusions:
- ABCB1 C3435T polymorphism may elevate bleeding risk in Asian patients receiving clopidogrel.
- Further basic genetic pharmacology studies are needed to confirm this association.
Purpose:
The substantial variability in the antiplatelet efficacy of clopidogrel has raised major concerns. Molecular epidemiological research suggests that ABCB1 C3435T polymorphism may be associated with clopidogrel response, but results remain controversial. To derive a more precise evaluation of the associations between ABCB1 C3435T polymorphism and the clinical efficacy of clopidogrel, we have conducted a PRISMA-compliant meta-analysis.
Methods:
The PubMed and EMBASE databases were searched for eligible studies up to 25 October 2016. The odds ratio (OR), the standard mean difference (SMD) and 95% confidence interval (CI) were applied to assess the strength of the relationship.
Results:
Overall, 28 related studies involving 23,243 patients were analyzed. No association was found between the ABCB1 polymorphisms and the primary outcome. In the subgroup analysis, the C3435T mutation significantly reduced platelet activity as tested by the LTA assay in the dominant (SMD -0.140, 95% CI -0.272 to -0.009, P = 0.036) and heterozygous (SMD -0.154, 95% CI -0.290 to -0.017, P = 0.027) models, but the result lacked robustness in the sensitivity analysis. A significant association between the C3435T polymorphism and bleeding risk was also observed with low heterogeneity in the dominant (OR 1.805, 95% CI1.124-2.900, P =0.015, I 2 = 0%), homozygous (OR 1.952, 95% CI 1.055-3.611, P = 0.033, I 2 = 13.2%) and heterozygous (OR 1.793, 95% CI 1.091-2.946, P = 0.021, I 2 = 0%) models in Asian patients.
Conclusions:
The results of the meta-analysis suggest that ABCB1 C3435T polymorphism may increase the risk of bleeding in Asian patients treated with clopidogrel. The implied relationship needs to be verified in future basic genetic pharmacology studies.
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