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VerifyNow P2Y12 检测和 CYP2C19*2 检测对心血管疾病患者临床结局的影响:系统评价和荟萃分析。

Effects of VerifyNow P2Y12 test and CYP2C19*2 testing on clinical outcomes of patients with cardiovascular disease: a systematic review and meta-analysis.

机构信息

Department of Laboratory Medicine, Keio University School of Medicine, Tokyo, Japan.

出版信息

Platelets. 2013;24(5):352-61. doi: 10.3109/09537104.2012.700969. Epub 2012 Jul 3.

Abstract

The VerifyNow P2Y12 test is a whole-blood, light transmission-based optical detection assay that measures adenosine diphosphate-induced platelet aggregation in a cartridge containing fibrinogen-coated beads. The usefulness of this device to assess the effect of clopidogrel on platelet function was recently highlighted for predicting cardiovascular (CV) events. We therefore performed a meta-analysis to analyze whether adverse clinical outcomes of patients with CV disease increase in association with high on-treatment platelet reactivity (HPR) using the VerifyNow P2Y12 test. We also investigated the effect of the CYP2C192 polymorphism on the occurrence of CV events among clopidogrel-treated patients. Relevant studies were searched for in the PubMed database and Cochrane Central Register of Controlled Trials database, and selected if they included data about platelet function assessed using the VerifyNow P2Y12 test or CYP2C192 polymorphism in clopidogrel-treated patients with CV disease, and the occurrence of CV events within 6-12 months. In our meta-analysis, 4817 subjects from eight studies and 5307 subjects from seven studies were included for review of platelet function and CYP2C192 polymorphism, respectively. Overall, 2237 (46.4%) patients had HPR and these patients had significantly higher odds of CV events compared to patients without HPR (odds ratio(OR) = 3.05, 95% confidence interval: 2.33-3.98, p < 0.001). Heterogeneity among studies was not significant (Cochran's Q-test, p = 0.80 and I(2) = 0%). In the secondary investigation, 1926 (36.3%) patients had at least one CYP2C192 allele. Heterogeneity in the OR of the CV events between the CYP2C19*2 allele carriers and non-carriers was observed among the seven studies (Cochran's Q-test, p = 0.01 and I(2) = 56.5%), and the range of the ORs among the seven studies was 0.58-16.6. In conclusion, HPR assessed by VerifyNow P2Y12 test was associated with increased adverse clinical outcomes of clopidogrel-treated patients with CV disease.

摘要

VerifyNow P2Y12 检测是一种全血、光传输基础的光学检测分析方法,用于测量在含有纤维蛋白原包被珠的检测管中,ADP 诱导的血小板聚集。该设备用于评估氯吡格雷对血小板功能的影响,以预测心血管(CV)事件,最近已引起关注。因此,我们进行了一项荟萃分析,以分析使用 VerifyNow P2Y12 检测评估的高治疗血小板反应性(HPR)与 CV 疾病患者的不良临床结局之间的关系。我们还研究了 CYP2C192 多态性对氯吡格雷治疗的 CV 疾病患者 CV 事件发生的影响。在 PubMed 数据库和 Cochrane 对照试验中心注册数据库中搜索了相关研究,并选择了包括使用 VerifyNow P2Y12 检测评估血小板功能和 CYP2C192 多态性的数据,以及在 6-12 个月内发生 CV 事件的研究。在我们的荟萃分析中,共有来自八项研究的 4817 名患者和来自七项研究的 5307 名患者纳入了血小板功能和 CYP2C192 多态性的回顾性分析。总体而言,2237 名(46.4%)患者存在 HPR,这些患者发生 CV 事件的可能性明显高于无 HPR 患者(比值比(OR)=3.05,95%置信区间:2.33-3.98,p<0.001)。研究之间的异质性不显著(Cochran's Q 检验,p=0.80 和 I(2)=0%)。在次要调查中,1926 名(36.3%)患者至少携带一个 CYP2C192 等位基因。在七项研究中,CYP2C19*2 等位基因携带者与非携带者之间的 CV 事件 OR 存在异质性(Cochran's Q 检验,p=0.01 和 I(2)=56.5%),并且这七项研究的 OR 范围为 0.58-16.6。总之,VerifyNow P2Y12 检测评估的 HPR 与 CV 疾病氯吡格雷治疗患者的不良临床结局增加相关。

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