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Updated: Jun 8, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
The GPIIIA PlA2 polymorphism is associated with an increased risk of cardiovascular adverse events
Gennaro Galasso1, Gaetano Santulli, Federico Piscione
1Department of Clinical Medicine, Cardiovascular and Immunologic Sciences, Federico II University School of Medicine, Naples, Italy.
Insights
The PlA2 polymorphism is linked to increased risks of cardiac death, myocardial infarction, and stroke in patients with atherosclerosis. This genetic factor independently predicts major adverse cardiac events and cerebrovascular events.
Area of Science:
- Genetics
- Cardiology
- Neurology
Background:
- The role of PlA2 polymorphism in thrombotic cardiovascular complications remains unclear.
- Previous studies have yielded conflicting results regarding its clinical impact.
Purpose of the Study:
- To investigate the effect of PlA2 polymorphism on outcomes in patients with atherosclerosis.
- To determine if PlA2 allele presence is associated with thrombotic cardiovascular events.
Main Methods:
- A study of 400 coronary artery disease patients undergoing percutaneous coronary intervention.
- A replication study in 74 hypertensive patients with cerebrovascular events and 100 healthy controls.
- PlA genotype determined by PCR-RFLP; major adverse cardiac events (MACE) recorded over a mean follow-up of 24 months.
Main Results:
- PlA2 allele presence associated with higher cardiac death (13.1% vs 1.5%), myocardial infarction (10.7% vs 2.6%), and revascularization needs (34.8% vs 17.7%) in CAD patients.
- Kaplan-Meier analysis showed worse long-term outcome for patients with PlA2 allele (p=0.015).
- PlA2 independently predicted cardiac death (OR: 9.594) and MACE (OR: 1.829); increased stroke risk (OR: 4.1) in replication study.
Conclusions:
- The PlA2 allele is associated with an increased risk of thrombotic cardiovascular complications in patients with severe atherosclerosis.
- PlA2 polymorphism serves as an independent predictor for adverse cardiovascular and cerebrovascular events.
Background:
The clinical impact of PlA2 polymorphism has been investigated in several diseases, but the definition of its specific role on thrombotic cardiovascular complications has been challenging. We aimed to explore the effect of PlA2 polymorphism on outcome in patients with atherosclerosis.
Methods:
We studied 400 consecutive patients with coronary artery disease (CAD) undergoing percutaneous coronary intervention. A replication study was conducted in 74 hypertensive patients with cerebrovascular events while a group of 100 healthy subjects was included as control population. PlA genotype was determined by PCR-RFLP on genomic DNA from peripheral blood cells. Major adverse cardiac events (MACE), were considered as end points, and recorded at a mean follow up of 24 ± 4.3 months.
Results:
The frequencies of PlA2 polymorphism was similar between groups and genotype distribution was in Hardy-Weinberg equilibrium. In patients with CAD, the presence of PlA2 allele was associated with higher incidence of cardiac death (13.1% vs. 1.5%, p = 0.0001), myocardial infarction (10.7% vs. 2.6%, p = 0.004) and needs of new revascularization (34.8% vs. 17.7%, p = 0.010). Accordingly, the Kaplan-Meier analysis for event free survival in patients harboring the PlA2 allele showed worse long-term outcome for these patients (p = 0.015). Cox regression analysis identified the presence of PlA2 as an independent predictor of cardiac death (OR: 9.594, 95% CI: 2.6 to 35.3, p = 0.002) and overall MACE (OR: 1.829, 95% CI: 1.054 to 3.176, p = 0.032). In the replication study, the PlA2 polymorphism increased the risk of stroke (OR: 4.1, 95% CI: 1.63-12.4, p = 0.02) over TIA and was identified as an independent risk factor for stroke (B:-1.39; Wald: 7.15; p = 0.001).
Conclusions:
Our study demonstrates that in patients with severe atherosclerosis the presence of PlA2 allele is associated with thrombotic cardiovascular complications.
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