| Literature DB >> 27886818 |
Larisa H Cavallari1, Aniwaa Owusu Obeng2.
Abstract
There is significant interpatient variability in clopidogrel effectiveness, which is due in part to cytochrome P450 (CYP) 2C19 genotype. Approximately 30% of individuals carry CYP2C19 loss-of-function alleles, which have been consistently shown to reduce clopidogrel effectiveness after an acute coronary syndrome and percutaneous coronary intervention. Guidelines recommend consideration of prasugrel or ticagrelor in these patients. A clinical trial examining outcomes with CYP2C19 genotype-guided antiplatelet therapy is ongoing. In the meantime, based on the evidence available to date, several institutions have started clinically implementing CYP2C19 genotyping to assist with antiplatelet selection after percutaneous coronary intervention. Copyright ÂEntities:
Keywords: CYP2C19; Clopidogrel; Genotype; Pharmacogenomics; Prasugrel; Ticagrelor
Mesh:
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Year: 2017 PMID: 27886818 PMCID: PMC5134418 DOI: 10.1016/j.iccl.2016.08.010
Source DB: PubMed Journal: Interv Cardiol Clin ISSN: 2211-7458