| Literature DB >> 24956245 |
Joseph S Rossi1, Michael Cammarata, Jayalalitha Dharmavaram, Karen Weck, Christine Walko, Don Gabriel, Jack Kuritzky, Kenneth Muldrew, George A Stouffer.
Abstract
This pilot study examined the feasibility of outpatient screening and clopidogrel dose adjustment for patients with previous percutaneous coronary intervention and at least one CYP2C19 loss-of-function allele. After screening a total of 211 outpatients, 50 patients were enrolled in a crossover study comparing 30 days of standard dose (75 mg) to 30 days of high-dose clopidogrel (150 mg). Platelet function was assessed with the VerifyNow P2Y12 assay. In patients with CYP2C19*2, 150 mg daily of clopidogrel was associated with improved ADP-specific platelet inhibition (217 vs 258 P2Y12 reaction units, p = 0.01). Outpatient screening for CYP2C19 loss-of-function polymorphisms is feasible, and a strategy of clopidogrel dose escalation may improve platelet inhibition in appropriately selected patients.Entities:
Keywords: clopidogrel; genetic testing; platelet function; polymorphism
Mesh:
Substances:
Year: 2014 PMID: 24956245 DOI: 10.2217/pgs.14.17
Source DB: PubMed Journal: Pharmacogenomics ISSN: 1462-2416 Impact factor: 2.533