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Published on: April 6, 2017
Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes
Joshua P Lewis1, Kathleen Ryan, Jeffrey R O'Connell
1Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Insights
Genetic variations in the PEAR1 gene influence how patients respond to aspirin and clopidogrel therapy. This genetic factor is linked to increased cardiovascular events in patients undergoing antiplatelet treatment.
Area of Science:
- Cardiovascular Medicine
- Pharmacogenomics
- Genetics
Background:
- Aspirin and clopidogrel are standard antiplatelet therapies for patients at high cardiovascular risk.
- Genetic factors influencing patient response to these therapies are largely unknown.
Purpose of the Study:
- To identify genetic determinants of variable response to aspirin and dual antiplatelet therapy (aspirin plus clopidogrel).
- To investigate the association between genetic variations and cardiovascular outcomes in patients receiving antiplatelet therapy.
Main Methods:
- Genome-wide association study (GWAS) of ex vivo platelet aggregation in 565 patients from the Pharmacogenomics of Anti-Platelet Intervention (PAPI) Study.
- Genotyping of single-nucleotide polymorphisms (SNPs) and association analysis with dual antiplatelet therapy response.
- Validation in two independent aspirin-treated cohorts (percutaneous coronary intervention patients and INVEST-GENES substudy).
Main Results:
- A strong association was found between SNPs on chromosome 1q23 and post-therapy platelet aggregation.
- The rs12041331 SNP in the PEAR1 gene showed the strongest association with dual antiplatelet therapy response (P=7.66×10(-9)).
- Carriers of the rs12041331 A-allele had increased risk of cardiovascular events or death in PCI patients and increased risk of myocardial infarction in aspirin-treated patients.
Conclusions:
- Common genetic variations in the PEAR1 gene may determine platelet response to aspirin and clopidogrel.
- PEAR1 genotype may influence cardiovascular event risk in patients on antiplatelet therapy.
- These findings suggest potential for genotype-guided antiplatelet therapy selection.
Abstract:
BACKGROUND- Aspirin or dual antiplatelet therapy with aspirin and clopidogrel is a standard therapy for patients who are at increased risk for cardiovascular events. However, the genetic determinants of variable response to aspirin (alone and in combination with clopidogrel) are not known. METHODS AND RESULTS- We measured ex vivo platelet aggregation before and after dual antiplatelet therapy in individuals (n=565) from the Pharmacogenomics of Anti-Platelet Intervention (PAPI) Study and conducted a genome-wide association study of drug response. Significant findings were extended by examining genotype and cardiovascular outcomes in 2 independent aspirin-treated cohorts: 227 percutaneous coronary intervention patients and 1000 patients of the International Verapamil SR/Trandolapril Study (INVEST) Genetic Substudy (INVEST-GENES). Results from the genome-wide association study revealed a strong association between single-nucleotide polymorphisms on chromosome 1q23 and post-dual antiplatelet therapyplatelet aggregation. Further genotyping revealed rs12041331 in the platelet endothelial aggregation receptor-1 (PEAR1) gene to be most strongly associated with dual antiplatelet therapy response (P=7.66×10(-9)). In white and black patients undergoing percutaneous coronary intervention, A-allele carriers of rs12041331 were more likely to experience a cardiovascular event or death compared with GG homozygotes (hazard ratio, 2.62; 95% confidence interval, 0.96-7.10; P=0.059; and hazard ratio, 3.97; 95% confidence interval, 1.10-14.31; P=0.035, respectively). In aspirin-treated INVEST-GENES patients, rs12041331 A-allele carriers had significantly increased risk of myocardial infarction compared with GG homozygotes (odds ratio, 2.03; 95% confidence interval, 1.01-4.09; P=0.048). CONCLUSION- Common genetic variation in PEAR1 may be a determinant of platelet response and cardiovascular events in patients on aspirin alone or in combination with clopidogrel. Clinical Trial Registration- URL: http://www.clinicaltrials.gov. Unique identifiers: NCT00799396 and NCT00370045.
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