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首页> 外文期刊>Experimental and therapeutic medicine >Influence of CYP2C19 genotype on antiplatelet treatment outcomes after percutaneous coronary intervention in patients with coronary heart disease
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Influence of CYP2C19 genotype on antiplatelet treatment outcomes after percutaneous coronary intervention in patients with coronary heart disease

机译:CYP2C19基因型对冠心病患者经皮冠状动脉介入后抗血小板治疗结果的影响

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The aim of the study was to compare the clinical efficacy and safety of ticagrelor and clopidogrel in patients with coronary heart disease one year after percutaneous coronary intervention (PCI), and to explore their association with the CYP2C19 gene polymorphism. A total of 971 patients with coronary heart disease who were hospitalized and underwent PCI from April 2016 to May 2017 were studied. All 971 patients were divided into three subgroups according to CYP2C19 gene types as fast metabolizing, slow metabolizing and very slow metabolizing type. Patients were also classified according to the oral antiplatelet aggregation drugs they received: clopidogrel group and ticagrelor group. The incidence of major adverse cardiac events (MACE) and bleeding events in the clopidogrel-treated and ticagrelor-treated groups and in patients with fast, slow, and very slow CYP2C19 metabolisms were compared. Binary logistic regression analysis was carried out to analyze the risk factors associated with MACEs and hemorrhagic events. Patients on ticagrelor had a greater number of bleeding complications compared to those on clopidogrel (P<0.001), with no difference in MACE between the two groups (P=0.399). The incidence of MACE was significantly higher in very slow metabolizing patients receiving clopidogrel (P<0.001) while the incidence of bleeding complications was significantly higher in fast metabolizing patients receiving ticagrelor (P<0.001). The regression analysis revealed that the CYP2C19 gene mutation, a dual-antiplatelet therapy, and a stroke history were all significantly associated with MACE. By contrast, a dual-antiplatelet therapy and a stroke history were significantly associated with bleeding events. Findings of the present study indicated that clopidogrel and ticagrelor were equally efficacious post-PCI. Efficacy of clopidogrel was reduced in patients with very slow CYP2C19 genotype while bleeding complications were higher in patients with fast CYP2C19 genotype receiving ticagrelor. CYP2C19 genotyping may be used to provide guidance to optimize individual antiplatelet treatment.
机译:该研究的目的是比较经皮冠状动脉介入(PCI)后一年冠心病患者TiCagreloLoL和Clopidogrel的临床疗效和安全性,并探讨其与CYP2C19基因多态性的关系。从2016年4月到2017年4月,共有971例患有冠心病的冠心病患者入住并接受了PCI。所有971名患者根据CYP2C19基因类型分为三个亚组,作为快速代谢,缓慢代谢和代谢类型非常缓慢。患者还根据他们所接受的口服抗血小板聚集药物分类:氯吡格雷基团和TicagreloR组。比较了主要不良心脏事件(MACE)和氯吡格雷治疗组和快速,缓慢和非常缓慢的CYP2C19代谢患者中的主要不良心脏事件(MACE)和出血事件的发生率。进行二元逻辑回归分析,以分析与甘露甘露出血事件相关的危险因素。与氯吡格雷(P <0.001)相比,TiCagreloLoR的患者具有更多的出血并发症,两组之间的芯片没有差异(p = 0.399)。在接受氯吡格雷的非常缓慢的代谢患者中,智慧的发病率显着高(P <0.001),而在接受TiCagreler的快速代谢患者的出血并发症的发病率显着较高(P <0.001)。回归分析显示,CYP2C19基因突变,双抗血小板治疗和中风历史都与MACE显着相关。相比之下,双抗血小板治疗和行程历史与出血事件显着相关。本研究的结果表明,氯吡格雷和钛戈氏蛋白在PCI后同样有效。 CYP2C19基因型患者的患者减少了氯吡格雷的疗效,同时快速CYP2C19基因型接受TICAGRELER的患者出血并发症。 CYP2C19基因分型可用于提供优化个体抗血小板治疗的指导。

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