Why the study?
Does pharmacogenetic testing for CYP2C19 loss-of-function alleles improve outcomes in patients with CAD undergoing PCI?
Does pharmacogenetic testing for CYP2C19 loss-of-function alleles improve outcomes in patients with CAD undergoing PCI?
Answers are grounded in this paper and cite their sources.
Genotyping for CYP2C19 loss-of-function alleles is recommended for CAD patients undergoing PCI to guide and adjust antiplatelet therapy.
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.
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Yasmina et al. (2014) studied this question.
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