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有症状颅内动脉粥样硬化患者中CYP2C19基因多态性的患病率

The Prevalence of CYP2C19 Polymorphism in Patients with Symptomatic Intracranial Atherosclerosis.

作者信息

Kittipanprayoon Songchai, Vorasayan Pongpat, Chutinet Aurauma, Chariyavilaskul Pajaree, Suwanwela Nijasri C

机构信息

Department of Medicine, Hatyai Hospital, Songkhla, Thailand.

Chulalongkorn Stroke Center, King Chulalongkorn Memorial Hospital, Bangkok, Thailand,

出版信息

Cerebrovasc Dis Extra. 2025;15(1):68-72. doi: 10.1159/000543331. Epub 2025 Jan 2.

Abstract

INTRODUCTION

Clopidogrel and aspirin were proved to have benefit in symptomatic intracranial stenosis. CYP2C19 polymorphism (CYP2C191, CYP2C192, CYP2C193, and CYP2C1917 alleles) affects efficacy of clopidogrel. Epidemiologic study of CYP2C19 polymorphism has been conducted in Thai population. There was no data showed the frequency of allelic variants of CYP2C19 in Thai symptomatic intracranial stenosis patients. The aim of this study was to determine the prevalence of CYP2C19 polymorphism in symptomatic intracranial stenosis patients.

METHODS

The study group included 100 Thai symptomatic intracranial stenosis patients. Genotyping of CYP2C19 alleles (CYP2C191, CYP2C192, CYP2C193, and CYP2C1917 alleles) was carried out by real-time polymerase chain reaction (rt-PCR) technique.

RESULTS

The allele frequency of CYP2C191, CYP2C192, CYP2C193, and CYP2C1917 were 70.5%, 26%, 2.5%, and 1%, respectively. The result showed that 53% of symptomatic intracranial stenosis patients are normal metabolizers, while intermediate and poor metabolizer were 36 and 10 percent, respectively.

CONCLUSION

Almost one-half of Thai symptomatic intracranial stenosis patients were intermediate or poor metabolizers. Usage of combination of aspirin and clopidogrel might not be effective in this group of patients.

摘要

引言

氯吡格雷和阿司匹林已被证明对有症状的颅内狭窄有益。细胞色素P450 2C19基因多态性(CYP2C191、CYP2C192、CYP2C193和CYP2C1917等位基因)会影响氯吡格雷的疗效。已在泰国人群中开展了关于CYP2C19基因多态性的流行病学研究。尚无数据显示泰国有症状颅内狭窄患者中CYP2C19等位基因变异的频率。本研究的目的是确定有症状颅内狭窄患者中CYP2C19基因多态性的患病率。

方法

研究组包括100例泰国有症状颅内狭窄患者。采用实时聚合酶链反应(rt-PCR)技术对CYP2C19等位基因(CYP2C191、CYP2C192、CYP2C193和CYP2C1917等位基因)进行基因分型。

结果

CYP2C191、CYP2C192、CYP2C193和CYP2C1917的等位基因频率分别为70.5%、26%、2.5%和1%。结果显示,53%的有症状颅内狭窄患者为正常代谢者,而中间代谢者和慢代谢者分别为36%和10%。

结论

近一半的泰国有症状颅内狭窄患者为中间代谢者或慢代谢者。阿司匹林和氯吡格雷联合使用对该组患者可能无效。

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