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Clinical Pharmacogenetics Implementation Consortium Guideline for <i>CYP2C19</i> Genotype and Clopidogrel Therapy: 2022 Update

Craig R. Lee, Jasmine A. Luzum, Katrin Sangkuhl, Roseann S. Gammal, Marc S. Sabatine, Charles Michael Stein, David F. Kisor, Nita A. Limdi, Yee Ming Lee, Stuart A. Scott, Jean‐Sébastien Hulot, Dan M. Roden, Andrea Gaedigk, Kelly E. Caudle, Teri E. Klein, Julie A. Johnson, Alan R. Shuldiner

2022Clinical Pharmacology & Therapeutics461 citationsDOIOpen Access PDF

Abstract

CYP2C19 catalyzes the bioactivation of the antiplatelet prodrug clopidogrel, and CYP2C19 genotype impacts clopidogrel active metabolite formation. CYP2C19 intermediate and poor metabolizers who receive clopidogrel experience reduced platelet inhibition and increased risk for major adverse cardiovascular and cerebrovascular events. This guideline is an update to the 2013 Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for the use of clopidogrel based on CYP2C19 genotype and includes expanded indications for CYP2C19 genotype-guided antiplatelet therapy, increased strength of recommendation for CYP2C19 intermediate metabolizers, updated CYP2C19 genotype to phenotype translation, and evidence from an expanded literature review (updates at www.cpicpgx.org).

Topics & Concepts

ClopidogrelCYP2C19MedicineGuidelinePharmacogeneticsProdrugGenotypeInternal medicinePharmacologyActive metaboliteAdverse effectPlatelet aggregation inhibitorDosingPharmacogenomicsClinical PracticePharmacokineticsTiclopidineCYP2C9Intensive care medicineAntiplatelet drugClinical significanceThienopyridinePharmacotherapyAntiplatelet Therapy and Cardiovascular DiseasesPlatelet Disorders and TreatmentsPharmacogenetics and Drug Metabolism
Clinical Pharmacogenetics Implementation Consortium Guideline for <i>CYP2C19</i> Genotype and Clopidogrel Therapy: 2022 Update | Litcius