Pharmacogenomics of oral antiplatelet drugs

Pharmacogenomics. 2014 Mar;15(4):509-28. doi: 10.2217/pgs.14.16.

Abstract

Pharmacogenomics has been implicated in the response variability of antiplatelet drugs in coronary artery disease (CAD), particularly for aspirin and clopidogrel. A large number of studies and several meta-analyses have been published on this topic, but until recently, there have been no clear conclusions and no definite guidelines on the clinical use of pharmacogenetic testing before prescribing antiplatelet drugs for CAD. In this review, the available evidence is summarized. The most consistent results are on clopidogrel, where CYP2C19 loss-of-function alleles are associated with stent thrombosis events. We recommend to genotype for CYP2C19 loss-of-function alleles in patients with CAD who are to undergo percutaneous coronary intervention and stenting, and to adjust the antiplatelet treatment based on the genotyping results.

Publication types

  • Review

MeSH terms

  • Aspirin / therapeutic use
  • Clopidogrel
  • Coronary Artery Disease / drug therapy*
  • Coronary Artery Disease / genetics*
  • Cytochrome P-450 CYP2C19 / genetics
  • Humans
  • Meta-Analysis as Topic
  • Pharmacogenetics / methods
  • Platelet Aggregation Inhibitors / therapeutic use*
  • Ticlopidine / analogs & derivatives
  • Ticlopidine / therapeutic use

Substances

  • Platelet Aggregation Inhibitors
  • Clopidogrel
  • CYP2C19 protein, human
  • Cytochrome P-450 CYP2C19
  • Ticlopidine
  • Aspirin