Hobl Eva-Luise, Jilma Bernd, Derhaschnig Ulla, Schoergenhofer Christian, Schwameis Michael, Jilma-Stohlawetz Petra
Departments of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Cytometry B Clin Cytom. 2013 Jul 29. doi: 10.1002/cytob.21119.
Ticagrelor is a P2Y receptor antagonist, with superior effects but also ensuing enhanced bleeding risk as compared to clopidogrel. Determination of platelet inhibition may be useful to confirm efficient platelet inhibition on an individual patient level and to identify patients at risk for bleeding. The vasodilator-associated stimulated phosphoprotein (VASP) phosphorylation assay specifically measures platelet P2Y inhibition, but has so far required individual sample processing. A new ELISA-based VASP assay has been developed which allows batch analysis after initial platelet activation. Due to the reversible binding of ticagrelor it is unclear if the ELISA and flow cytometric assays provide comparable results; several washing steps of the ELISA may potentially result in false low results through dilution.
We hypothesized that the conventional and new methods may be comparable when ticagrelor is used. We pair-wise compared the platelet reactivity index (PRI) between assays in a prospective clinical trial. Six healthy volunteers received a single 180 mg loading dose of ticagrelor.
PRI-values of the two methods correlated well (r=0.97, p<0.001). Ticagrelor rapidly decreased PRI values on average after 50 minutes, but nadir levels 2-6 hours after ticagrelor intake were 15% higher when PRI% was measured with the flow cytometric method. Bland-Altman analysis showed that the flow cytometric assay measured markedly higher PRI levels than the new ELISA-based technique (mean difference 13%).
The new ELISA-based VASP assay offers an alternative to the currently used flow cytometric method, but measures lower PRI levels, particularly when PRI falls below 20% after ticagrelor intake. © 2013 Clinical Cytometry Society.
替格瑞洛是一种P2Y受体拮抗剂,与氯吡格雷相比,其效果更佳,但出血风险也随之增加。测定血小板抑制作用对于在个体患者层面确认有效的血小板抑制以及识别出血风险患者可能有用。血管扩张剂相关刺激磷蛋白(VASP)磷酸化检测可特异性测量血小板P2Y抑制作用,但迄今为止需要对单个样本进行处理。已开发出一种基于酶联免疫吸附测定(ELISA)的新型VASP检测方法,该方法在血小板初始激活后可进行批量分析。由于替格瑞洛的可逆结合,尚不清楚ELISA和流式细胞术检测结果是否具有可比性;ELISA的几个洗涤步骤可能会因稀释而导致结果假性偏低。
我们假设使用替格瑞洛时传统方法和新方法可能具有可比性。在一项前瞻性临床试验中,我们对不同检测方法之间的血小板反应性指数(PRI)进行了两两比较。六名健康志愿者接受了单次180 mg的替格瑞洛负荷剂量。
两种方法的PRI值相关性良好(r = 0.97,p < 0.001)。替格瑞洛给药后平均50分钟PRI值迅速下降,但采用流式细胞术测量PRI%时,替格瑞洛摄入后2 - 6小时的最低点水平高15%。布兰德-奥特曼分析表明,流式细胞术检测的PRI水平明显高于基于ELISA的新技术(平均差异13%)。
基于ELISA的新型VASP检测方法为目前使用的流式细胞术方法提供了一种替代方案,但测量的PRI水平较低,尤其是在替格瑞洛摄入后PRI降至20%以下时。© 2013临床细胞计量学会。