3.8 Article

Genetic Variation in PEAR1 Is Associated With Platelet Aggregation and Cardiovascular Outcomes

Journal

CIRCULATION-CARDIOVASCULAR GENETICS
Volume 6, Issue 2, Pages 184-+

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGENETICS.111.964627

Keywords

CYP2C19; PEAR1; percutaneous coronary intervention; pharmacogenomics; platelets

Funding

  1. National Institutes of Health [U01 GM074518, U01 HL105198, U01 HL084756, U01 GM074492, R01074730, K23 GM102678]
  2. Mid-Atlantic Nutrition and Obesity Center [P30 DK072488]
  3. University of Maryland General Clinical Research Center [M01 RR 16500]
  4. Baltimore Veterans Administration Geriatric Research and Education Clinical Center
  5. BASF Pharmaceuticals
  6. Abbott Laboratories
  7. University of Florida Opportunity Fund
  8. Sinai Hospital of Baltimore
  9. AstraZeneca
  10. Daiichi-Sankyo
  11. Bayer Healthcare
  12. Eli Lilly
  13. Portola Pharmaceuticals
  14. Haemonetics
  15. Pozen
  16. Sanofi-Aventis
  17. National Institutes of Health

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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 therapy platelet 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=7.66x10(-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.

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