The CYP3A5 non-expressor genotype was associated with a significantly higher risk of atherothrombotic events (adjusted OR 4.89) compared to the expressor genotype in patients taking clopidogrel after coronary stenting.
Cohort (n=348)
Double-blind (to genotype)
No
Does the CYP3A5 non-expressor genotype increase the risk of atherothrombotic events in patients taking clopidogrel after coronary angioplasty with bare-metal stent implantation?
Patients with the CYP3A5 non-expressor genotype have an increased risk of atherothrombotic events when taking clopidogrel after bare-metal stent implantation, likely due to greater vulnerability to CYP3A inhibition.
Effect estimate: Adjusted OR 4.89 (95% CI 1.28-18.7)
Absolute Event Rate: 7.25% vs 1.94%
p-value: p=0.023
BACKGROUND: Clopidogrel is a prodrug requiring metabolism by cytochrome P450 3A (CYP3A) isoenzymes, including CYP3A5, in order to be active. It is controversial whether clopidogrel interacts with CYP3A inhibitors. We investigated the influence of CYP3A5 polymorphism on the drug interaction of clopidogrel. METHODS: In phase 1 of the study, we administered clopidogrel to 16 healthy volunteers who had the CYP3A5 non-expressor genotype (*3 allele) and 16 who had the CYP3A5 expressor genotype (*1 allele) with and without pretreatment with itraconazole, a potent CYP3A inhibitor. A platelet aggregation test was performed at baseline, 4 hours, 24 hours and 6 days after clopidogrel administration. In phase 2, we compared clinical outcomes of 348 patients treated with clopidogrel after successful coronary angioplasty with bare-metal stent implantation according to their CYP3A5 genotype; the primary end point was a composite of atherothrombotic events (cardiovascular death, myocardial infarction and non-hemorrhagic stroke) within 1 and 6 months after stent implantation. RESULTS: In phase 1, the change in platelet aggregation after clopidogrel administration and pretreatment with itraconazole was greater among the subjects with the CYP3A5 expressor genotype than among those with the non-expressor genotype: 24.9% (standard deviation SD 13.9%) v. 6.2% (SD 13.5%) at 4 hours (p < 0.001); 27.7% (SD 16.5%) v. 2.5% (SD 8.3%) at 24 hours (p < 0.001); and 33.5% (SD 18.6%) v. 17.8% (SD 13.8%) at day 7 (p < 0.01). In phase 2, atherothrombotic events occurred more frequently within 6 months after stent implantation among the patients with the non-expressor genotype than among those with the expressor genotype (14/193 v. 3/155; p = 0.023). Multivariable analysis showed that the CYP3A5 polymorphism was a predictor of atherothrombotic events in clopidogrel users. INTERPRETATION: People with the CYP3A5 non-expressor genotype are vulnerable to drug interactions between clopidogrel and CYP3A inhibitors. This phenomenon may be associated with worse outcomes in patients with the non-expressor genotype who are given clopidogrel after coronary angioplasty and implantation of bare-metal stents.
Jung‐Won Suh (Mon,) conducted a cohort in Coronary artery disease post-angioplasty with bare-metal stent (n=348). CYP3A5 non-expressor genotype vs. CYP3A5 expressor genotype was evaluated on Composite of atherothrombotic events (cardiovascular death, myocardial infarction, and non-hemorrhagic stroke) within 6 months (Adjusted OR 4.89, 95% CI 1.28-18.7, p=0.023). The CYP3A5 non-expressor genotype was associated with a significantly higher risk of atherothrombotic events (adjusted OR 4.89) compared to the expressor genotype in patients taking clopidogrel after coronary stenting.