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Effect of cytochrome P450 2C19 (CYP2C19) gene polymorphism and clopidogrel reactivity on long term prognosis of patients with coronary heart disease after PCI.
- Source :
- Journal of Geriatric Cardiology; Jan2024, Vol. 21 Issue 1, p90-103, 14p
- Publication Year :
- 2024
-
Abstract
- Objective To investigate the impact of CYP2C19 gene polymorphism on clopidogrel reactivity and its association with longterm clinical outcome in patients with coronary heart disease (CHD) undergoing percutaneous coronary intervention (PCI). Methods In total, 675 patients were enrolled. Based on the platelet inhibition rate, patients were categorized into two groups: clopidogrel low responsiveness (CLR) and normal clopidogrel responsiveness (NCR). The CLR group was divided into ticagrelor and clopidogrel group based on the antiplatelet drugs used in the follow-up treatment. Patients were classified into three groups (normal metabolizer, intermediate metabolizer, and poor metabolizer) based on the CYP2C19 genotype. We aimed to evaluate the impact of CYP2C19 gene polymorphism on clopidogrel reactivity. The cumulative rates of 12-month all-cause deaths, major adverse cardiovascular events (MACCEs), and bleeding events were calculated. Results CLR was observed in 44.4% of the overall population. Significant differences were observed in the platelet inhibition rate of clopidogrel among the three metabolic genotypes (P < 0.05). At the 12-month follow-up, 13 patients (1.9%) died and 96 patients (14.2%) experienced MACCEs. Patients with CLR (9.6% vs. 11.7% vs. 22.1%, P < 0.05) or poor metabolizer (10.7% vs. 16.4% vs. 22.6%, P = 0.026) experienced a higher rate of MACCEs. A MACCEs risk score between zero and two was calculated. The highest incidence of MACCEs significantly increased with the 2-positive results, and the area under the curve (AUC) was 0.712 (95% CI: 0.650-0.774, P < 0.05). There was no significant difference between the group with a score of one and the occurrence of MACCEs (P > 0.05). Conclusions Low response to clopidogrel in CHD patients is correlated with CYP2C19 gene polymorphism. CYP2C19 genotyping combined with platelet reactivity is an independent predictor of 12-months MACCEs in patients with clopidogrel treatment after PCI, which is better than either test alone. [ABSTRACT FROM AUTHOR]
- Subjects :
- HEMORRHAGE risk factors
BLOOD platelet aggregation
CORONARY disease
RECEIVER operating characteristic curves
T-test (Statistics)
DATA analysis
RESEARCH funding
MAJOR adverse cardiovascular events
FISHER exact test
LOGISTIC regression analysis
RETROSPECTIVE studies
DESCRIPTIVE statistics
MANN Whitney U Test
CHI-squared test
GENETIC polymorphisms
PLATELET function tests
KAPLAN-Meier estimator
LOG-rank test
PERCUTANEOUS coronary intervention
CLOPIDOGREL
DRUG efficacy
MEDICAL records
ACQUISITION of data
ONE-way analysis of variance
STATISTICS
PLATELET aggregation inhibitors
CONFIDENCE intervals
DATA analysis software
GENOTYPES
EVALUATION
Subjects
Details
- Language :
- English
- ISSN :
- 16715411
- Volume :
- 21
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Journal of Geriatric Cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 176284676
- Full Text :
- https://doi.org/10.26599/1671-5411.2024.01.004