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CYP2C19和P2Y12基因多态性对急性缺血性脑血管病后使用氯吡格雷患者临床结局的影响

Effects of CYP2C19 and P2Y12 Gene Polymorphisms on Clinical Results of Patients Using Clopidogrel after Acute Ischemic Cerebrovascular Disease.

作者信息

Sen H M, Silan F, Silan C, Degirmenci Y, Ozisik Kamaran H I

机构信息

Department of Neurology, School of Medicine, Çanakkale Onsekiz Mart Üniversity, Çanakkale, Turkey.

Department of Medical Genetics, School of Medicine, Çanakkale Onsekiz Mart Üniversity, Çanakkale, Turkey.

出版信息

Balkan J Med Genet. 2015 Apr 10;17(2):37-41. doi: 10.2478/bjmg-2014-0072. eCollection 2014 Dec.

Abstract

The CY2C19 and P2Y12 gene polymorphisms are responsible for resistance to clopidogrel, known as drug unresponsiveness. In this study we researched the effect of gene polymorphism on clinical results of patients who began clopidogrel therapy after acute ischemic cerebrovascular disease. The study included 51 patients. The patient group included patients who had begun prophylactic clopidogrel due to acute ischemic cerebrovascular disease in the last 2 years. All patients were monitored by the Neurology Outpatient Clinic at Çanakkale Onsekiz Mart Üniversity Research Hospital, Çanakkale, Turkey, and only those monitored for at least 1 year were included in the study. When the *1, *2 and *3 alleles of the CYP2C19 gene polymorphism were evaluated, two patients were homozygotes for *2/*2, 13 patients were heterozygous for *1/*2 and 36 patients were homozygotes for the wild type *1/*1. No patient had the *3 allele. Three heterozygous patients, one for *2/*2 and two for *1/2, stopped clopidogrel therapy due to repeated strokes and began taking warfarin. When evaluating P2Y12 52 (G>T) and 34 (C>T) polymorphisms, all alleles were of the wild type. The CYP2C19 and P2Y12 gene polymorphisms may cause recurring strokes linked to insufficient response to treatment of ischemic cerebrovascular disease. In our patient group, three patients suffered repeated strokes and these patients had the CYP2C192 gene polymorphism. As a result, before medication use, genetic testing is important for human life, quality of life and economic burden.

摘要

细胞色素P450 2C19(CY2C19)和P2Y12基因多态性是导致对氯吡格雷耐药(即药物无反应性)的原因。在本研究中,我们探讨了基因多态性对急性缺血性脑血管病后开始氯吡格雷治疗患者临床结局的影响。该研究纳入了51例患者。患者组包括过去2年内因急性缺血性脑血管病开始预防性使用氯吡格雷的患者。所有患者均由土耳其恰纳卡莱奥塞基兹马尔特大学研究医院的神经科门诊进行监测,只有那些接受监测至少1年的患者才纳入研究。当评估CYP2C19基因多态性的1、2和3等位基因时,2例患者为2/2纯合子,13例患者为1/2杂合子,36例患者为野生型1/1纯合子。没有患者携带3等位基因。3例杂合子患者(1例*2/2和2例1/2)因反复中风停止氯吡格雷治疗,开始服用华法林。在评估P2Y12 52(G>T)和34(C>T)多态性时,所有等位基因均为野生型。CYP2C19和P2Y12基因多态性可能导致与缺血性脑血管病治疗反应不足相关的反复中风。在我们的患者组中,3例患者发生反复中风,这些患者具有CYP2C192基因多态性。因此,在用药前进行基因检测对人类生命、生活质量和经济负担都很重要。

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