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平均血小板体积的可重复性及其与血小板活性和抗血小板治疗的关系。

Mean platelet volume reproducibility and association with platelet activity and anti-platelet therapy.

机构信息

Department of Internal Medicine, Division of Cardiology .

出版信息

Platelets. 2014;25(3):188-92. doi: 10.3109/09537104.2013.793794. Epub 2013 Jun 20.

Abstract

Some studies suggest that mean platelet volume (MPV) correlates with increased risk for cardiovascular morbidity and mortality. In this study, we aim to assess reproducibility, need for standardized measurements, effect of aspirin, and association with other established markers of platelet activity. Following an overnight fast, 48 healthy volunteers had weekly assessment of platelet activity and were administered aspirin 81 mg daily for 7 d between weeks 3 and 4. We investigated the influence of time between phlebotomy and MPV measurement (n=10). Reproducibility was assessed by coefficient of variation (CV) and intraclass correlation coefficient (ICC). MPV measurements were reproducible (Week 1: 10.6 fL [9.9-11], Week 2: 10.6 fL [10.0-10.9], Week 3: 10.6 fL [9.8-11]). CV was ≤ 4% and ICC>0.85 (p<0.001) for each comparison, indicating excellent reproducibility. There was no effect of aspirin on MPV (10.6 fL [9.8-11] versus 10.5 fL [9.9-11]; p=0.81). MPV significantly increased as time between phlebotomy and MPV measurement increased (Spearman's rho=0.94, p=0.001). Increasing MPV tertiles was associated with collagen- and thrombin receptor-activated peptide-induced platelet aggregation but not with ADP- or arachidonic acid-induced or spontaneous platelet aggregation. In conclusion, when standardized, MPV is a reproducible marker of platelet size and not affected by low-dose aspirin. MPV is modestly associated with some, but not all, markers of platelet activity.

摘要

一些研究表明平均血小板体积(MPV)与心血管发病率和死亡率增加相关。在这项研究中,我们旨在评估重复性、标准化测量的需求、阿司匹林的影响以及与其他已建立的血小板活性标志物的相关性。在禁食过夜后,48 名健康志愿者每周评估血小板活性,并在第 3 周到第 4 周之间每周服用 81 毫克阿司匹林 7 天。我们研究了采血与 MPV 测量之间的时间间隔的影响(n=10)。通过变异系数(CV)和组内相关系数(ICC)评估重复性。MPV 测量具有可重复性(第 1 周:10.6fL[9.9-11],第 2 周:10.6fL[10.0-10.9],第 3 周:10.6fL[9.8-11])。每次比较的 CV 均≤4%,ICC>0.85(p<0.001),表明具有极好的可重复性。阿司匹林对 MPV 没有影响(10.6fL[9.8-11]与 10.5fL[9.9-11];p=0.81)。采血与 MPV 测量之间的时间间隔增加时,MPV 显著增加(Spearman's rho=0.94,p=0.001)。MPV 三分位值增加与胶原和血栓素受体激活肽诱导的血小板聚集相关,但与 ADP 或花生四烯酸诱导的或自发性血小板聚集不相关。总之,标准化时,MPV 是血小板大小的可重复标志物,不受低剂量阿司匹林的影响。MPV 与一些但不是所有的血小板活性标志物适度相关。

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