Journal
CLINICAL PHARMACOLOGY & THERAPEUTICS
Volume 90, Issue 2, Pages 328-332Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/clpt.2011.132
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Funding
- National Institutes of Health (NIH) [KL2 RR029885, U01 JL65962, U01 GM074492, U19 HL065962-10, R24 GM61374, U01 HL105198]
- Fondation de France
- INSERM
- Federation Francaise de Cardiologie
- Biotronik
- Medco Research Institute
- Medco Health Solutions
- Daiichi Sankyo
- Eli Lilly
- Bristol-Myers Squibb
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CYP2C19 is one of the principal enzymes involved in the bioactivation of the antiplatelet prodrug clopidogrel. A common loss-of-function allele, CYP2C19(star)2 (c. 681G>A; rs4244285), is associated with increased risk for serious adverse cardiovascular events in both heterozygous and homozygous patients (similar to 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).
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