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Clinical Outcomes and Sustainability of Using CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention.
- Source :
-
Circulation. Genomic and precision medicine [Circ Genom Precis Med] 2018 Apr; Vol. 11 (4), pp. e002069. - Publication Year :
- 2018
-
Abstract
- 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.<br />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.<br />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).<br />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.<br /> (© 2018 American Heart Association, Inc.)
- Subjects :
- Aged
Clinical Decision-Making
Clopidogrel adverse effects
Clopidogrel metabolism
Coronary Disease blood
Coronary Disease diagnosis
Cytochrome P-450 CYP2C19 metabolism
Feasibility Studies
Female
Humans
Male
Middle Aged
North Carolina
Patient Selection
Platelet Aggregation Inhibitors adverse effects
Platelet Aggregation Inhibitors metabolism
Prasugrel Hydrochloride adverse effects
Prasugrel Hydrochloride metabolism
Predictive Value of Tests
Reproducibility of Results
Retrospective Studies
Risk Factors
Stents
Ticagrelor adverse effects
Ticagrelor metabolism
Treatment Outcome
Clopidogrel administration & dosage
Coronary Disease surgery
Cytochrome P-450 CYP2C19 genetics
Percutaneous Coronary Intervention instrumentation
Pharmacogenomic Testing methods
Pharmacogenomic Variants
Platelet Aggregation Inhibitors administration & dosage
Prasugrel Hydrochloride administration & dosage
Ticagrelor administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 2574-8300
- Volume :
- 11
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Circulation. Genomic and precision medicine
- Publication Type :
- Academic Journal
- Accession number :
- 29615454
- Full Text :
- https://doi.org/10.1161/CIRCGEN.117.002069