Genotype-guided prescribing predictors in CYP2C19 intermediate metabolizers receiving percutaneous coronary intervention.
Joshua J ParkGervacio Y CabelKevin K ChengJefferson DangAmer K ArdatiJin HanJames C LeePublished in: Pharmacogenomics (2024)
Background: Previous differences in guideline recommendation strength for CYP2C19 intermediate metabolizers may have limited genotype (PGx)-optimal post-percutaneous coronary intervention antiplatelet prescribing. Results: In this single-center retrospective observational cohort study of CYP2C19 intermediate metabolizers, patients prescribed PGx-optimal therapy were younger and less likely on anticoagulation (2 vs 12%; p = 0.006). More patients prescribed PGx-optimal therapy possessed commercial insurance (36 vs 7%; p < 0.001), which was a predictor for PGx-optimal selection (OR: 6.464; 95% CI: 2.386-17.516; p < 0.001). Conclusion: Anticoagulation use was significantly associated with clopidogrel use (OR: 0.138; 95% CI: 0.026 - 0.730; p = 0.020). No statistical difference in composite major adverse cardiovascular events (5 vs 14%; p = 0.173) or bleeding (8 vs 6%; Not significant) was observed between PGx-optimal and PGx-suboptimal therapy.
Keyphrases
- percutaneous coronary intervention
- end stage renal disease
- cardiovascular events
- atrial fibrillation
- coronary artery disease
- acute coronary syndrome
- ejection fraction
- newly diagnosed
- chronic kidney disease
- primary care
- st segment elevation myocardial infarction
- acute myocardial infarction
- cardiovascular disease
- antiplatelet therapy
- peritoneal dialysis
- venous thromboembolism
- stem cells
- coronary artery bypass grafting
- healthcare
- heart failure
- patient reported outcomes
- patient reported
- adverse drug
- left ventricular