CYP2C19型
氯吡格雷
经皮冠状动脉介入治疗
医学
传统PCI
内科学
心脏病学
血栓形成
药理学
心肌梗塞
细胞色素P450
新陈代谢
作者
Dirk Sibbing,Julia Stegherr,Wolfgang Latz,Werner Koch,Julinda Mehilli,K. Dörrler,Tanja Morath,Albert Schömig,Adnan Kastrati,N. von Beckerath
标识
DOI:10.1093/eurheartj/ehp041
摘要
AimsSeveral studies have demonstrated that the mutant *2 allele of the CYP2C19 681G>A loss-of-function polymorphism is associated with diminished metabolization of clopidogrel into its active thiol metabolite and an attenuated platelet response to clopidogrel treatment. It is not known whether patients carrying the mutant CYP2C19*2 allele have a higher risk of stent thrombosis (ST) compared with homozygous CYP2C19*1 wild-type allele carriers following percutaneous coronary intervention (PCI). The aim of this study was to assess the impact of the CYP2C19 681G>A loss-of-function polymorphism on ST following PCI performed after pre-treatment with clopidogrel.
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