ADP p2y12抑制剂治疗后血小板高反应性的鉴定:血管扩张剂刺激磷酸化蛋白测定和可变PFA-P2Y曲线形状的两种人群

Cyril Mariethoz, Emmanuelle Scala, Elena Matthey-Guirao, Jean-Benoît Rossel, Francisco Javier Gomez, Francesco Grandoni, Carlo Marcucci, Lorenzo Alberio
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引用次数: 0

摘要

氯吡格雷对ADP p2y12受体抑制的反应可通过多种技术进行评估。在这里,我们比较了功能性快速护理技术(PFA-P2Y)与VASP/ p2y12测定法评估的生化抑制程度。方法观察173例选择性脑内支架植入术患者的血小板对氯吡格雷的反应(衍生队列n = 117;验证队列n = 56)。高血小板反应性(HPR)定义为PFA-P2Y阻断时间12血小板反应性指数(PRI) >50%。结果在衍生队列中,对PFA-P2Y检测生化HPR能力的受体操作者特征分析显示,PFA-P2Y检测生化HPR的特异性高(98.4%),但灵敏度较低(20.0%),曲线下面积很低(0.59)。VASP/ p2y12检测显示两种共存的血小板群体具有不同水平的血管扩张剂刺激磷酸化(VASP):一部分高度磷酸化,抑制血小板和另一部分低磷酸化,反应性血小板。PFA-P2Y曲线形状分析显示不同类型,按闭塞时间(300秒)和模式(规则、不规则和非典型)分类。值得注意的是,晚期闭塞曲线和不规则或非典型模式的可渗透曲线与VASP-PRI >50%和较小的抑制血小板亚群相关。考虑PFA-P2Y曲线的形状,检测HPR提高了灵敏度(72.7%),保留了特异性(91.9%),AUC较高(0.823)。验证队列证实了VASP/ p2y12测定数据以及考虑PFA-P2Y曲线形状的有效性。结论在接受乙酰水杨酸和氯吡格雷治疗7-10天的患者中,VASP/P2Y 12检测显示两个共存的差异抑制血小板亚群,其相对大小预测了总体PRI和不同的PFA-P2Y曲线模式,表明氯吡格雷疗效不完全。详细分析VASP/ p2y12和PFA-P2Y是优化HPR检测的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Identification of High Platelet Reactivity Despite ADP P2Y 12 Inhibitor Treatment: Two Populations in the Vasodilator-Stimulated Phosphoprotein Assay and Variable PFA-P2Y Shapes of Curve.

Introduction  Response to ADP P2Y 12 receptor inhibition by clopidogrel can be evaluated by various techniques. Here, we compared a functional rapid point-of-care technique (PFA-P2Y) with the degree of biochemical inhibition assessed by the VASP/P2Y 12 assay. Methods  Platelet response to clopidogrel was investigated in 173 patients undergoing elective intracerebral stenting (derivation cohort n  = 117; validation cohort n  = 56). High platelet reactivity (HPR) was defined as PFA-P2Y occlusion time <106 seconds or VASP/P2Y 12 platelet reactivity index (PRI) >50%. Results  In the derivation cohort, receiver operator characteristics analysis for the ability of PFA-P2Y to detect biochemical HPR showed high specificity (98.4%) but poor sensitivity (20.0%) and a very low area under the curve (0.59). The VASP/P2Y 12 assay revealed two coexisting platelet populations with different levels of vasodilator-stimulated phosphoprotein (VASP) phosphorylation: a fraction of highly phosphorylated, inhibited platelets and another of poorly phosphorylated, reactive platelets. Analysis of the PFA-P2Y curve shape revealed different types, categorized by time of occlusion (<106 seconds, 106 to 300 seconds, >300 seconds), and pattern (regular, irregular, and atypical). Noteworthy, curves with late occlusion and permeable curves with an irregular or atypical pattern correlated with VASP-PRI >50% and smaller sizes of the inhibited platelet subpopulation. Considering the PFA-P2Y shape of the curve for the detection of HPR improved sensitivity (72.7%) and preserved specificity (91.9%), with a rather high AUC (0.823). The validation cohort confirmed the VASP/P2Y 12 assay data and the usefulness of considering the PFA-P2Y curve shape. Conclusion  In patients treated with acetylsalicylic acid and clopidogrel for 7-10 days, the VASP/P2Y 12 assay reveals two coexisting subpopulations of differentially inhibited platelets, whose relative sizes predict global PRI and distinct PFA-P2Y curve patterns, indicating incomplete clopidogrel efficacy. The detailed analysis of both VASP/P2Y 12 and PFA-P2Y is necessary for optimal detection of HPR.

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