Related Experiment Video
Updated: Apr 14, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
Effect of platelet receptor gene polymorphisms on outcomes in ST-elevation myocardial infarction patients after
Jia-Hui Zhang1, Jing Wang1, Xiao-Fang Tang1
1a Department of Cardiology, State Key Laboratory of Cardiovascular Disease , Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College , Beijing , People's Republic of China.
Insights
Genetic variations in platelet receptors impact cardiovascular event risk. Specific F2R and P2RY12 gene variants predict ischemic and bleeding events, respectively, in ST-elevation myocardial infarction patients post-percutaneous coronary intervention.
Area of Science:
- Cardiovascular Genetics
- Pharmacogenomics
- Thrombosis Research
Background:
- Platelet receptor gene polymorphisms can alter platelet function.
- Understanding these genetic influences is crucial for managing patients undergoing percutaneous coronary intervention (PCI).
Purpose of the Study:
- To investigate the association between five platelet receptor gene polymorphisms and the risk of ischemic and bleeding events.
- To assess the predictive value of these polymorphisms in ST-elevation myocardial infarction (STEMI) patients treated with dual antiplatelet therapy post-PCI.
Main Methods:
- A cohort of 503 STEMI patients post-PCI were genotyped for ITGA2, GP6, F2R, and P2RY12 polymorphisms.
- Patients received standard dual antiplatelet therapy for 12 months, with follow-up for ischemic and bleeding events.
- Multivariate Cox and logistic regression analyses were used to determine independent predictors of adverse events, with validation in a second cohort of 483 patients.
Main Results:
- The F2R rs168753 minor allele was an independent predictor of composite ischemic events (HR 0.387, p=0.008).
- The P2RY12 rs6809699 minor allele independently predicted major bleedings (OR 2.71, p=0.008).
- These findings were validated in an independent cohort.
Conclusions:
- F2R rs168753 minor allele carriage is associated with a reduced risk of ischemic events.
- P2RY12 rs6809699 minor allele carriage is associated with an increased risk of bleeding events.
- Genetic testing of platelet receptors may aid in predicting adverse outcomes in STEMI patients post-PCI.
Abstract:
Polymorphisms in platelet receptor genes may influence platelet function. This study aimed to assess the impact of five polymorphisms of genes encoding platelet receptors on the risk of ischemic and bleeding events in ST-elevation myocardial infarction (STEMI) patients after percutaneous coronary intervention (PCI). 503 consecutive Chinese patients with STEMI after an uneventful PCI and exposed to standard dual antiplatelet therapy for 12 months were enrolled. Polymorphisms of platelet receptors, GPIa (ITGA2, 807C > T, rs1126643), GPVI (GP6, 13254T > C, rs1613662), PAR-1 (F2R, IVS-14A > T, rs168753) and P2Y12 (P2RY12, 34C > T, rs6785930 and H1/H2 haplotype, 52G > T, rs6809699) were detected by the ligase detection reaction. The follow-up period was 12 months. Overall, 34 (6.8%) ischemic events occurred and 46 (9.1%) major bleedings occurred. Multivariate Cox regression analysis showed the carriage of F2R rs168753 minor allele was an independent predictor of the composite ischemic events (HR 0.387, 95% CI 0.193-0.778, p = 0.008) after adjusted for established risk factors. Multivariate logistic regression model identified that carriage of P2RY12 rs6809699 minor allele (OR 2.71, 95% CI 1.298-5.659, p = 0.008) was an independent predictor of major bleedings. The associations were then validated in a second cohort of 483 STEMI patients. In STEMI patients after PCI, F2R rs168753 minor allele could significantly contribute to the risk of ischemic events, and P2RY12 rs6809699 minor allele could predict bleedings. The genetic testing of platelet receptors can be valuable in predicting adverse events in STEMI patients after PCI.
Related Concept Videos
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Pharmacogenomics: Identification of New Drug Targets
Pharmacogenetics of Drug Metabolism: Overview
Formation of the Platelet Plug
As the injured blood vessel contracts, endothelial cells undergo contraction, revealing collagen fibers in the basement membrane and underlying connective tissue. Furthermore, the plasma membrane of endothelial cells becomes adhesive, preparing the site for platelet adhesion. Platelets...

