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椎动脉支架治疗患者中CYP2C19基因分型与支架内再狭窄的关联。

The association between CYP2C19 genotype and of in-stent restenosis among patients with vertebral artery stent treatment.

作者信息

Lin Yong-Juan, Li Jing-Wei, Zhang Mei-Juan, Qian Lai, Yang Wen-Jie, Zhang Chun-Lei, Shao Yuan, Zhang Yang, Huang Yu-Jie, Xu Yun

机构信息

Department of Neurology, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China; Stroke Center for Diagnosis and Therapy in Jiangsu province, Nanjing, China.

出版信息

CNS Neurosci Ther. 2014 Feb;20(2):125-30. doi: 10.1111/cns.12173. Epub 2013 Dec 12.

Abstract

AIMS

Preventing stroke through endovascular treatment with vertebral artery stent remains a great challenge due to the occurrence of an in-stent restenosis.

MATERIALS & METHODS: In this study, a retrospective analysis was conducted in 90 patients who had been treated with VAS between 2004 and 2011 in Nanjing Drum Tower Hospital. Patients were followed up at 3 months, 6 months,and 1 year after VAS treatment and annually thereafter. For each time point, neurological function tests, vessel ultrasound and computer tomography angiography were performed to preliminarily screen the vessel stenosis. Digital subtraction angiography was used to verify the narrow sign on CTA or ultrasound. Clinical features of each patient including clopidogrel metabolization genes (CYP2C19, CYP3A4, and P2Y12) were recorded with purpose to investigate the possible risk factors for the development of ISR.

RESULTS

Single factor analysis dem-onstrated that hyperlipidemia (P < 0.05) and CYP2C19 (P < 0.01) loss-of-function geno-type increased the likelihood of ISR. A multiple logistic cox regression analysis also showed that stroke patients with hyperlipidemia (HR 3.719, 95% CI: 1.094-12.637, P = 0.035), and CYP2C19 loss-of-function genotype (HR 2.959, 95% CI: 1.325-6.610, P = 0.008) were more likely to suffer from ISR. Furthermore, CYP2C19 alleles were mainly divided into three groups: wt/wt (CYP2C19 *1/*1), wt/m (CYP2C19 *1/*2 and *1/*3), and m/m (CYP2C19 *2/*2,*2/3 and3/*3). Recurrent rate of ischemic stroke in m/m and wt/m groups was higher than the wt/wt group (OR: 0.141, 95% CI: 0.016-1.221, P = 0.042).

CONCLUSION

The study leads to the conclusion that hyperlipidemia and CYP2C19 impotency are possible risk factors for the development of ISR in VAS-treated patients with ischemic. Moreover, VAS-treated patients with CYP2C19 impotency were susceptible to recurrent stroke during our 54-month follow-up.

摘要

目的

由于支架内再狭窄的发生,通过椎动脉支架进行血管内治疗预防中风仍然是一个巨大的挑战。

材料与方法

本研究对2004年至2011年在南京鼓楼医院接受椎动脉支架治疗的90例患者进行了回顾性分析。在椎动脉支架治疗后3个月、6个月和1年进行随访,此后每年随访一次。对于每个时间点,进行神经功能测试、血管超声和计算机断层血管造影以初步筛查血管狭窄。使用数字减影血管造影来验证CTA或超声上的狭窄迹象。记录每位患者的临床特征,包括氯吡格雷代谢基因(CYP2C19、CYP3A4和P2Y12),以调查支架内再狭窄发生的可能危险因素。

结果

单因素分析表明,高脂血症(P < 0.05)和CYP2C19(P < 0.01)功能丧失基因型增加了支架内再狭窄的可能性。多元逻辑Cox回归分析还表明,患有高脂血症的中风患者(HR 3.719,95% CI:1.094 - 12.637,P = 0.035)和CYP2C19功能丧失基因型(HR 2.959,95% CI:1.325 - 6.610,P = 0.008)更容易发生支架内再狭窄。此外,CYP2C19等位基因主要分为三组:wt/wt(CYP2C19 *1/*1)、wt/m(CYP2C19 *1/2和1/*3)和m/m(CYP2C19 *2/*2、*2/3和3/*3)。m/m组和wt/m组缺血性中风的复发率高于wt/wt组(OR:0.141,95% CI:0.016 - 1.221,P =

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