Clinical Outcomes and Sustainability of Using CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention

被引:66
作者
Lee, Craig R. [1 ,2 ,3 ]
Sriramoju, Vindhya B. [4 ]
Cervantes, Alexandra [1 ]
Howell, Lucius A. [4 ]
Varunok, Nicholas [4 ]
Madan, Shivanshu [4 ]
Hamrick, Kasey [1 ]
Polasek, Melissa J. [1 ]
Lee, John Andrew [1 ]
Clarke, Megan [5 ]
Cicci, Jonathan D. [5 ]
Weck, Karen E. [2 ,6 ]
Stouffer, George A. [3 ,4 ]
机构
[1] Univ N Carolina, UNC Eshelman Sch Pharm, Div Pharmacotherapy & Expt Therapeut, Chapel Hill, NC 27515 USA
[2] Univ N Carolina, UNC Ctr Pharmacogen & Individualized Therapy, Chapel Hill, NC 27515 USA
[3] Univ N Carolina, UNC McAllister Heart Inst, Chapel Hill, NC 27515 USA
[4] Univ N Carolina, UNC Sch Med, Div Cardiol, Chapel Hill, NC 27515 USA
[5] Univ N Carolina, Dept Pharm, UNC HealthCare Med Ctr, Chapel Hill, NC 27515 USA
[6] Univ N Carolina, UNC Sch Med, Dept Pathol & Lab Med, Chapel Hill, NC 27515 USA
来源
CIRCULATION-GENOMIC AND PRECISION MEDICINE | 2018年 / 11卷 / 04期
关键词
acute coronary syndrome; clopidogrel; cytochrome P-450 CYP2C19; genetic testing; pharmacogenetics; percutaneous coronary intervention; precision medicine; MYOCARDIAL-INFARCTION; CLOPIDOGREL THERAPY; ARTERY-DISEASE; TASK-FORCE; IMPLEMENTATION; POLYMORPHISMS; TICAGRELOR; ASSOCIATION; GUIDELINES; TRIAL;
D O I
10.1161/CIRCGEN.117.002069
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: CYP2C19 loss-of-function (LOF) alleles impair clopidogrel effectiveness after percutaneous coronary intervention. The feasibility, sustainability, and clinical impact of using CYP2C19 genotype-guided dual antiplatelet therapy (DAPT) selection in practice remains unclear. METHODS: A single-center observational study was conducted in 1193 patients who underwent percutaneous coronary intervention and received DAPT after implementation of an algorithm that recommends CYP2C19 testing in high-risk patients and alternative DAPT (prasugrel or ticagrelor) in LOF allele carriers. The frequency of genotype testing and alternative DAPT selection were the primary implementation end points. Risk of major adverse cardiovascular or cerebrovascular and clinically significant bleeding events over 12 months were compared across genotype and DAPT groups by proportional hazards regression. RESULTS: CYP2C19 genotype was obtained in 868 (72.8%) patients. Alternative DAPT was prescribed in 186 (70.7%) LOF allele carriers. CYP2C19 testing (P<0.001) and alternative DAPT use in LOF allele carriers (P=0.001) varied over time. Risk for major adverse cardiovascular or cerebrovascular was significantly higher in LOF carriers prescribed clopidogrel versus alternative DAPT (adjusted hazard ratio, 4.65; 95% confidence interval, 2.22-10.0; P<0.001), whereas no significant difference was observed in those without a LOF allele (adjusted hazard ratio, 1.37; 95% confidence interval, 0.72-2.85; P=0.347). Bleeding event rates were similar across groups (log-rank P=0.816). CONCLUSIONS: Implementing CYP2C19 genotype-guided DAPT is feasible and sustainable in a real-world setting but challenging to maintain at a consistently high level of fidelity. The higher risk of major adverse cardiovascular or cerebrovascular associated with clopidogrel use in CYP2C19 LOF allele carriers suggests that use of genotype-guided DAPT in practice may improve clinical outcomes.
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页数:12
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