Back to Search
Start Over
Multisite Investigation of Outcomes With Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention.
- Source :
-
JACC. Cardiovascular interventions [JACC Cardiovasc Interv] 2018 Jan 22; Vol. 11 (2), pp. 181-191. Date of Electronic Publication: 2017 Nov 01. - Publication Year :
- 2018
-
Abstract
- Objectives: This multicenter pragmatic investigation assessed outcomes following clinical implementation of CYP2C19 genotype-guided antiplatelet therapy after percutaneous coronary intervention (PCI).<br />Background: CYP2C19 loss-of-function alleles impair clopidogrel effectiveness after PCI.<br />Methods: After clinical genotyping, each institution recommended alternative antiplatelet therapy (prasugrel, ticagrelor) in PCI patients with a loss-of-function allele. Major adverse cardiovascular events (defined as myocardial infarction, stroke, or death) within 12 months of PCI were compared between patients with a loss-of-function allele prescribed clopidogrel versus alternative therapy. Risk was also compared between patients without a loss-of-function allele and loss-of-function allele carriers prescribed alternative therapy. Cox regression was performed, adjusting for group differences with inverse probability of treatment weights.<br />Results: Among 1,815 patients, 572 (31.5%) had a loss-of-function allele. The risk for major adverse cardiovascular events was significantly higher in patients with a loss-of-function allele prescribed clopidogrel versus alternative therapy (23.4 vs. 8.7 per 100 patient-years; adjusted hazard ratio: 2.26; 95% confidence interval: 1.18 to 4.32; p = 0.013). Similar results were observed among 1,210 patients with acute coronary syndromes at the time of PCI (adjusted hazard ratio: 2.87; 95% confidence interval: 1.35 to 6.09; p = 0.013). There was no difference in major adverse cardiovascular events between patients without a loss-of-function allele and loss-of-function allele carriers prescribed alternative therapy (adjusted hazard ratio: 1.14; 95% confidence interval: 0.69 to 1.88; p = 0.60).<br />Conclusions: These data from real-world observations demonstrate a higher risk for cardiovascular events in patients with a CYP2C19 loss-of-function allele if clopidogrel versus alternative therapy is prescribed. A future randomized study of genotype-guided antiplatelet therapy may be of value.<br /> (Copyright © 2018 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Aged
Clinical Decision-Making
Clopidogrel adverse effects
Drug Resistance genetics
Female
Humans
Male
Middle Aged
Patient Selection
Pharmacogenetics
Platelet Aggregation Inhibitors adverse effects
Prasugrel Hydrochloride adverse effects
Predictive Value of Tests
Risk Assessment
Risk Factors
Ticagrelor adverse effects
Time Factors
Treatment Outcome
United States
Clopidogrel therapeutic use
Cytochrome P-450 CYP2C19 genetics
Percutaneous Coronary Intervention adverse effects
Percutaneous Coronary Intervention mortality
Pharmacogenomic Testing
Pharmacogenomic Variants
Platelet Aggregation Inhibitors therapeutic use
Prasugrel Hydrochloride therapeutic use
Ticagrelor therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1876-7605
- Volume :
- 11
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- JACC. Cardiovascular interventions
- Publication Type :
- Academic Journal
- Accession number :
- 29102571
- Full Text :
- https://doi.org/10.1016/j.jcin.2017.07.022