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Clinical Pharmacogenetics Implementation Consortium Guidelines for Cytochrome P450-2C19 (CYP2C19) Genotype and Clopidogrel Therapy

Clinical Pharmacology & Therapeutics · 2011 · Vol. 90(2) · pp. 328–332
Stuart A. ScottKatrin SangkuhlE E GardnerCatherine M. SteinJean‐Sébastien HulotJ. A. JohnsonD M RodenTeri E. KleinAlan R. Shuldiner

Abstract

CYP2C19 is one of the principal enzymes involved in the bioactivation of the antiplatelet prodrug clopidogrel. A common loss-of-function allele, CYP2C19*2 (c.681G>A; rs4244285), is associated with increased risk for serious adverse cardiovascular events in both heterozygous and homozygous patients (~25–50% of the population) with acute coronary syndromes (ACSs) who are receiving clopidogrel, particularly among those undergoing percutaneous coronary intervention (PCI). We provide evidence from published literature and guidelines for CYPC19 genotype–directed antiplatelet therapy (periodically updated at http://www.pharmgkb.org). Clinical Pharmacology & Therapeutics (2011) 90 2, 328–332. doi:10.1038/clpt.2011.132

Antiplatelet Therapy and Cardiovascular DiseasesInflammatory mediators and NSAID effectsDiabetes Treatment and ManagementCYP2C19ClopidogrelMedicinePercutaneous coronary interventionPharmacogeneticsProdrugClinical pharmacologyConventional PCIPharmacologyInternal medicine

MeSH terms

ClopidogrelAllelesAryl Hydrocarbon HydroxylasesGenotypeHumansPharmacogeneticsPlatelet Aggregation InhibitorsTiclopidineAngioplasty, Balloon, CoronaryAcute Coronary SyndromeCytochrome P-450 CYP2C19
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References
Ticagrelor versus Clopidogrel in Patients with Acute Coronary Syndromes
New England Journal of Medicine · 2009 · 7,018 citations
Prasugrel versus Clopidogrel in Patients with Acute Coronary Syndromes
New England Journal of Medicine · 2007 · 6,705 citations
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