Implementation and evaluation of a CYP2C19 genotype-guided antiplatelet therapy algorithm in high-risk coronary artery disease patients

Author:

Lee John Andrew1,Lee Craig R123,Reed Brent N4,Plitt David C5,Polasek Melissa J1,Howell Lucius A5,Cicci Jonathan D6,Tasca Kristen E6,Weck Karen E27,Rossi Joseph S8,Stouffer George A35

Affiliation:

1. Division of Pharmacotherapy & Experimental Therapeutics, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

2. UNC Center for Pharmacogenomics & Individualized Therapy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

3. UNC McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

4. Department of Pharmacy Practice & Science, University of Maryland School of Pharmacy, Baltimore, MD 21201, USA

5. Division of Cardiology, UNC School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

6. Department of Pharmacy, UNC Hospitals & Clinics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA

7. Department of Pathology & Laboratory Medicine, UNC School of Medicine, University of North Carolina at Chapel Hill, NC 27599, USA

8. St Vincent Medical Group, Indianapolis, IN 46290, USA

Abstract

Aim: An algorithm that uses clinical factors and CYP2C19 genotype to guide P2Y12 inhibitor selection in high-risk patients undergoing percutaneous coronary intervention was implemented at our institution. We sought to evaluate use of this algorithm and identify which factors influenced P2Y12 inhibitor selection. Patients & methods: This retrospective cohort study included 264 patients receiving percutaneous coronary intervention from July–December 2012. Results: CYP2C19 genotype was obtained in 229 patients; of these, 30% were intermediate or poor metabolizers. CYP2C19 intermediate or poor metabolizer phenotype was among the strongest predictors for selecting prasugrel or ticagrelor as maintenance therapy (p < 0.001), and was the only significant predictor of a change in therapy (p < 0.001). Conclusion: These findings suggest that using CYP2C19 genotype to guide P2Y12 inhibitor selection is feasible. Original submitted 27 October 2014; revision submitted 19 December 2014

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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