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采用自动化方法测定的未成熟血小板分数(IPF)可预测氯吡格雷低反应性。

Immature platelet fraction (IPF) determined with an automated method predicts clopidogrel hyporesponsiveness.

机构信息

Methodist DeBakey Heart and Vascular Center, 6565 Fannin MS F-1035, Houston, TX 77030, USA.

出版信息

J Thromb Thrombolysis. 2012 Feb;33(2):137-42. doi: 10.1007/s11239-011-0665-7.

Abstract

The mechanisms for the variability in antiplatelet effects of clopidogrel are not elucidated entirely. Immature (reticulated) platelets may modulate the antiplatelet effects of clopidogrel but must be measured using flow cytometry. Whether new automated detection techniques yield similar results is not known. The objectives of the study to evaluate the role of immature platelets assessed by an automated method in response to the antiplatelet effects of clopidogrel. Twenty-nine healthy volunteers had platelet studies performed before and 1 week after 75 mg daily dosing of clopidogrel. Immature platelet fraction (IPF) was determined using an automated particle counter. Subjects were stratified into tertiles based on the IPF. Platelet studies included light transmission aggregometry (LTA), and vasodilator stimulated phosphoprotein phosphorylation (VASP-P) determined by platelet reactivity index (PRI). Baseline platelet aggregation responses to 2, 5 and 20 μM ADP, were similar in all three tertiles, however they were greater in the upper than in the lower tertile of immature platelets after clopidogrel in response to 5 μM ADP (54% vs. 23%, P = 0.02), with concordant trends for the other two concentrations. PRI was also greater in the upper tertile after clopidogrel (71.2% vs. 57.8%, P = 0.04). The frequency of clopidogrel hyporesponsiveness (aggregation >50% in response to 5 μM of ADP) was also higher in the upper tertile when compared to lower tertile, (60%) versus (10%) respectively (P = 0.02). [corrected]. Immature platelets measured using an automated method, are associated with impaired response to antiplatelet effects of clopidogrel.

摘要

尚未完全阐明氯吡格雷抗血小板作用变异性的机制。未成熟(网织)血小板可能调节氯吡格雷的抗血小板作用,但必须使用流式细胞术进行测量。新的自动化检测技术是否产生类似结果尚不清楚。本研究旨在评估通过自动化方法评估未成熟血小板在氯吡格雷抗血小板作用中的作用。29 名健康志愿者在每日 75mg 氯吡格雷治疗前和 1 周后进行血小板研究。使用自动颗粒计数器测定未成熟血小板分数(IPF)。根据 IPF 将受试者分为三分位。血小板研究包括透光比浊聚集测定法(LTA)和通过血小板反应指数(PRI)测定的血管扩张刺激磷酸蛋白磷酸化(VASP-P)。在所有三分位中,ADP 浓度为 2、5 和 20 μM 时,基线血小板聚集反应相似,但在氯吡格雷治疗后,在较高三分位时,ADP 浓度为 5 μM 时的血小板聚集反应更高(54%比 23%,P=0.02),对于另外两个浓度也有相似的趋势。氯吡格雷治疗后,PRI 在较高三分位也更高(71.2%比 57.8%,P=0.04)。与下三分位相比,氯吡格雷低反应(ADP 浓度为 5 μM 时聚集反应>50%)的频率在上三分位也更高(分别为 60%和 10%,P=0.02)。[校正后]使用自动方法测量的未成熟血小板与氯吡格雷抗血小板作用的反应受损相关。

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