Use of Tirofiban to Prevent Ischemic Events in Patients with CYP2C19 Loss-of-Function Alleles during Flow Diversion of Intracranial Aneurysm: A Multicenter Cohort Study.

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY Translational Stroke Research Pub Date : 2024-10-01 Epub Date: 2023-07-31 DOI:10.1007/s12975-023-01171-3
Yangyang Zhou, Huibin Kang, Wenqiang Li, Bin Luo, Chao Wang, Ruhang Xie, Yongnan Zhu, Qichen Peng, Yisen Zhang, Jian Liu, Ying Zhang, Shiqing Mu, Sheng Guan, Wenfeng Feng, Xinjian Yang
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Abstract

To analyze the effect of tirofiban on ischemic events in CYP2C19 loss-of-function (LOF) allele carriers during pipeline embolization device (PED) implantation. Demographic information, imaging data, ischemic complications, CYP2C19 genotyping, and platelet function test results were collected from patients with PED-treated intracranial aneurysms at three centers. Multivariate logistic regression was used to analyze risk factors for ischemic events. Patients were grouped according to LOF alleles and antiplatelet drugs, the baseline information of LOF allele carriers and non-carriers were compared, and the efficacy of tirofiban was analyzed by comparing the incidence of ischemic events in each group. In total, 278 patients were included in the study, 24 of whom had an ischemic event. 157 (56.5%) patients carried the LOF allele and were more likely to develop resistance to clopidogrel (P < 0.001) and hypertension (P = 0.010). Multivariate logistic regression analysis revealed that the independent risk factors for ischemic events were age of > 55 years (OR = 3.308, P = 0.028), LOF alleles (OR = 3.960, P = 0.036), and clopidogrel nonresponsiveness (OR = 3.301, P = 0.014). For LOF allele carriers, prophylactic use of tirofiban after PED implantation helped to reduce ischemic events (4.3% vs. 16.4%, P = 0.039). This study supports CYP2C19 genotyping before flow diversion because LOF alleles increase the risk of ischemic events. Prophylactic use of tirofiban may help reduce ischemic events in LOF allele carriers.

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使用替罗非班预防颅内动脉瘤血流分流过程中 CYP2C19 功能缺失等位基因患者的缺血事件:一项多中心队列研究。
目的分析在管道栓塞装置(PED)植入过程中替罗非班对CYP2C19功能缺失(LOF)等位基因携带者缺血事件的影响。在三个中心收集了经 PED 治疗的颅内动脉瘤患者的人口统计学信息、影像学数据、缺血性并发症、CYP2C19 基因分型和血小板功能测试结果。采用多变量逻辑回归分析缺血事件的风险因素。根据 LOF 等位基因和抗血小板药物对患者进行分组,比较 LOF 等位基因携带者和非携带者的基线信息,并通过比较各组缺血事件的发生率分析替罗非班的疗效。研究共纳入了 278 例患者,其中 24 例发生了缺血事件。157例(56.5%)患者携带LOF等位基因,更有可能对氯吡格雷产生耐药性(P 55岁,OR = 3.308,P = 0.028)、LOF等位基因(OR = 3.960,P = 0.036)和氯吡格雷无反应性(OR = 3.301,P = 0.014)。对于 LOF 等位基因携带者,在植入 PED 后预防性使用替罗非班有助于减少缺血事件(4.3% 对 16.4%,P = 0.039)。由于 LOF 等位基因会增加缺血事件的风险,因此本研究支持在血流分流前进行 CYP2C19 基因分型。预防性使用替罗非班可能有助于减少 LOF 等位基因携带者的缺血事件。
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来源期刊
Translational Stroke Research
Translational Stroke Research CLINICAL NEUROLOGY-NEUROSCIENCES
CiteScore
13.80
自引率
4.30%
发文量
130
审稿时长
6-12 weeks
期刊介绍: Translational Stroke Research covers basic, translational, and clinical studies. The Journal emphasizes novel approaches to help both to understand clinical phenomenon through basic science tools, and to translate basic science discoveries into the development of new strategies for the prevention, assessment, treatment, and enhancement of central nervous system repair after stroke and other forms of neurotrauma. Translational Stroke Research focuses on translational research and is relevant to both basic scientists and physicians, including but not restricted to neuroscientists, vascular biologists, neurologists, neuroimagers, and neurosurgeons.
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