首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Effects of clopidogrel and aspirin in combination versus aspirin alone on platelet activation and major receptor expression in patients after recent ischemic stroke: for the Plavix Use for Treatment of Stroke (PLUTO-Stroke) trial.
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Effects of clopidogrel and aspirin in combination versus aspirin alone on platelet activation and major receptor expression in patients after recent ischemic stroke: for the Plavix Use for Treatment of Stroke (PLUTO-Stroke) trial.

机译:氯吡格雷和阿司匹林联合使用或单独使用阿司匹林对近期缺血性卒中患者血小板活化和主要受体表达的影响:用于Plavix治疗卒中(PLUTO-Stroke)试验。

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BACKGROUND AND PURPOSE: Clopidogrel is widely used in patients after recent ischemic stroke; however, its ability to yield additional antiplatelet protection on top of aspirin has never been explored in a controlled study. To determine whether clopidogrel with aspirin (C+ASA) will produce more potent platelet inhibition than aspirin alone (ASA) in patients after ischemic stroke, we conducted the Plavix Use for Treatment of Stroke trial. METHODS: Seventy patients after ischemic stroke were randomly assigned to C+ASA or ASA groups. Platelet studies included aggregometry; cartridge-based analyzers; expression of PECAM-1, P-selectin, GP IIb/IIIa (antigen and activity), vitronectin receptor, and formation of platelet-leukocyte microparticles by flow cytometry. Platelet tests were performed at baseline and after 30 days after randomization. RESULTS: There were no deaths, hospitalizations, or serious adverse events. There were no differences in the baseline platelet characteristics between C+ASA and ASA groups, or significant changes in platelet parameters in the ASA group, except diminished collagen-induced aggregation (P=0.001). In contrast, therapy with C+ASA resulted in a significant inhibition of platelet activity assessed by ADP- (P=0.00001) and collagen-induced (P=0.02) aggregation; closure time prolongation (P=0.03), and reduction of platelet activation units with Ultegra (P=0.00001); expression of PECAM-1 (P=0.01), and GP IIb/IIIa activity with PAC-1 (P=0.02) when compared with ASA group. Therapy with C+ASA also resulted in the reduced formation of platelet-leukocyte microparticles (P=0.02). CONCLUSIONS: Treatment with C+ASA for 1 month provides significantly greater inhibition of platelet activity than ASA alone in patients after recent ischemic stroke in the frame of the small randomized trial.
机译:背景与目的:氯吡格雷在近期缺血性卒中后的患者中得到广泛应用。但是,在对照研究中从未探讨过在阿司匹林上产生额外的抗血小板保护作用的能力。为了确定在缺血性中风后使用阿司匹林(C + ASA)的氯吡格雷(C + ASA)是否比单独使用阿司匹林(ASA)产生更有效的血小板抑制作用,我们进行了Plavix Use for Treatment of Stroke试验。方法:将缺血性中风后的70例患者随机分为C + ASA或ASA组。血小板研究包括凝集法;基于盒式分析仪;流式细胞术检测PECAM-1,P-选择蛋白,GP IIb / IIIa(抗原和活性),玻连蛋白受体的表达以及血小板-白细胞微粒的形成。在基线和随机分组后30天后进行血小板测试。结果:未发生死亡,住院或严重不良事件。 C + ASA和ASA组之间的基线血小板特征无差异,或ASA组中的血小板参数无显着变化,除了胶原蛋白诱导的聚集减少(P = 0.001)。相反,用C + ASA进行治疗可显着抑制ADP-(P = 0.00001)和胶原蛋白诱导的(P = 0.02)聚集对血小板活性的抑制作用。闭合时间延长(P = 0.03),使用Ultegra降低血小板激活单位(P = 0.00001);与ASA组比较,PECAM-1的表达(P = 0.01)和PAC-1的GP IIb / IIIa活性(P = 0.02)。 C + ASA治疗还导致血小板白细胞微粒的形成减少(P = 0.02)。结论:在小型随机试验的范围内,近期缺血性卒中后,C + ASA治疗1个月对血小板活性的抑制作用比单独使用ASA显着增强。

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