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Ticagrelor versus Clopidogrel in CYP2C19 Loss-of-Function Carriers with Stroke or TIA

医学 氯吡格雷 替卡格雷 危险系数 阿司匹林 内科学 CYP2C19型 安慰剂 置信区间 冲程(发动机) 新陈代谢 机械工程 工程类 病理 替代医学 细胞色素P450
作者
Yongjun Wang,Xia Meng,Anxin Wang,Xuewei Xie,Yuesong Pan,S. Claiborne Johnston,Hao Li,Philip M.W. Bath,Qiang Dong,Anding Xu,Jing Jing,Jinxi Lin,Siying Niu,Yilong Wang,Wenjuan Wang,Zixiao Li,Yong Jiang,Wei Li,Liping Liu,Jie Xu,Liguo Chang,Lihua Wang,Xun Zhuang,Jinhui Zhao,Yan Ting Feng,Honghao Man,Guozhong Li,Wei Wang,Chance Investigators
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:385 (27): 2520-2530 被引量:163
标识
DOI:10.1056/nejmoa2111749
摘要

Comparisons between ticagrelor and clopidogrel for the secondary prevention of stroke in CYP2C19 loss-of-function carriers have not been extensively performed.We conducted a randomized, double-blind, placebo-controlled trial at 202 centers in China involving patients with a minor ischemic stroke or transient ischemic attack (TIA) who carried CYP2C19 loss-of-function alleles. Patients were assigned within 24 hours after symptom onset, in a 1:1 ratio, to receive ticagrelor (180 mg on day 1 followed by 90 mg twice daily on days 2 through 90) and placebo clopidogrel or to receive clopidogrel (300 mg on day 1 followed by 75 mg once daily on days 2 through 90) and placebo ticagrelor; both groups received aspirin for 21 days. The primary efficacy outcome was new stroke, and the primary safety outcome was severe or moderate bleeding, both within 90 days.A total of 11,255 patients were screened and 6412 patients were enrolled, with 3205 assigned to the ticagrelor group and 3207 to the clopidogrel group. The median age of the patients was 64.8 years, and 33.8% were women; 98.0% belonged to the Han Chinese ethnic group. Stroke occurred within 90 days in 191 patients (6.0%) in the ticagrelor group and 243 patients (7.6%) in the clopidogrel group (hazard ratio, 0.77; 95% confidence interval, 0.64 to 0.94; P = 0.008). Secondary outcomes were generally in the same direction as the primary outcome. Severe or moderate bleeding occurred in 9 patients (0.3%) in the ticagrelor group and in 11 patients (0.3%) in the clopidogrel group; any bleeding occurred in 170 patients (5.3%) and 80 patients (2.5%), respectively.Among Chinese patients with minor ischemic stroke or TIA who were carriers of CYP2C19 loss-of-function alleles, the risk of stroke at 90 days was modestly lower with ticagrelor than with clopidogrel. The risk of severe or moderate bleeding did not differ between the two treatment groups, but ticagrelor was associated with more total bleeding events than clopidogrel. (Funded by the Ministry of Science and Technology of the People's Republic of China and others; CHANCE-2 ClinicalTrials.gov number, NCT04078737.).
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