Variability of platelet response to clopidogrel is not related to adverse cardiovascular events in patients with stable coronary artery disease undergoing percutaneous coronary intervention

被引:8
|
作者
Oledzki, Szymon [1 ]
Kornacewicz-Jach, Zdzislawa [1 ]
Safranow, Krzysztof [2 ]
Kiedrowicz, Radoslaw [1 ]
Gawronska-Szklarz, Barbara [3 ]
Jastrzebska, Maria [4 ]
Goracy, Jaroslaw [1 ]
机构
[1] Pomeranian Med Univ, Dept Cardiol, 72 Powstancow Wlkp Str, PL-70111 Szczecin, Poland
[2] Pomeranian Med Univ, Dept Biochem & Med Chem, 72 Powstancow Wlkp Str, PL-70111 Szczecin, Poland
[3] Dept Pharmacokinet & Therapeut Drug Monitoring, 72 Powstancow Wlkp Str, PL-70111 Szczecin, Poland
[4] Dept Lab Diagnost & Mol Med, 72 Powstancow Wlkp Str, PL-70111 Szczecin, Poland
关键词
Clopidogrel; Stable coronary artery disease; Percutaneous coronary intervention; High on-treatment platelet reactivity; Clopidogrel response; STENT PLACEMENT; MYOCARDIAL-INFARCTION; DRUG-INTERACTIONS; TASK-FORCE; REACTIVITY; OUTCOMES; RESISTANCE; PRASUGREL; ASPIRIN; IMPACT;
D O I
10.1007/s00228-017-2271-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Antiplatelet response to clopidogrel and its influence upon the risk of cardiovascular adverse events among patients with stable coronary artery disease undergoing percutaneous coronary intervention (PCI) has not been investigated fully. Methods Two hundred eleven patients treated with aspirin and clopidogrel were included in the study. Immediately before PCI, residual platelet reactivity testing with impedance aggregometry assay and a single-nucleotide polymorphism genotyping analysis targeting variants of CYP2C19, ABCB1, and PON1 genes was performed. After the index PCI, the patients were screened for cardiovascular events 6 months following bare-metal stent implantation or 12 months following drug-eluting stent implantation. Result High on-treatment platelet reactivity (HTPR) was observed in 19.43% individuals and low-TPR (LTPR) in 26.54%. In multivariate analysis, HTPR was significantly (p < 0.05) associated with a history of diabetes, higher systolic blood pressure, and platelet count comparing to that of other patients. LTPR was significantly associated with no history of hypertension, younger age, lower platelet count, absence of the CYP2C19*2 variant, and lower CRP plasma level. Overall, cardiac adverse events were noted in 14.23% patients. Survival analysis with the Cox proportional hazard model showed no influence of residual platelet reactivity during clopidogrel therapy upon both ischemic and hemorrhagic events. However, significant predictors for composite of major adverse cardiac events and hospitalization for cardiovascular causes were identified (the higher CCS class prior to coronary intervention and the higher creatinine serum concentration). Conclusions The platelet response to clopidogrel has no impact upon post-procedural adverse events at mid-term follow-up in patients with stable CAD undergoing PCI. This finding suggests that routine platelet reactivity testing is not beneficial in this group of patients.
引用
收藏
页码:1085 / 1094
页数:10
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