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.

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