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冠心病患者中凝血酶诱导的血小板-纤维蛋白凝块强度与血小板体积指数及炎症标志物的关系

Thrombin induced platelet-fibrin clot strength in relation to platelet volume indices and inflammatory markers in patients with coronary artery disease.

作者信息

Lv Hai-Chen, Wu Hong-Yi, Yin Jia-Sheng, Ge Jun-Bo

机构信息

Department of Cardiology, First Affiliated Hospital of Dalian Medical University, Dalian, China.

Shanghai Institute of Cardiovascular Diseases, Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Oncotarget. 2017 Jul 22;8(38):64217-64223. doi: 10.18632/oncotarget.19450. eCollection 2017 Sep 8.

Abstract

Platelet aggregation and inflammation are both implicated in coronary artery disease (CAD). Thrombin induced platelet-fibrin clot strength (MA) measured by thrombelastography (TEG) has been proved to be a novel marker of platelet aggregation. The aim of this study was to investigate the correlation of MA to platelet volume indices (PVIs) or to inflammatory markers in different types of CAD. 206 patients with different types of CAD were enrolled. MA, PVIs, including mean platelet volume (MPV), platelet distribution width (PDW), and platelet-large cell ratio (P-LCR) as well as inflammatory markers, including high-sensitivity C-reactive protein (hs-CRP) and fibrinogen (Fbg) were measured. Multiple linear regression models were used to analyze the association between MA, PVIs, and inflammatory markers. MA and inflammatory markers both varied with CAD types (P<0.001). MA was correlated to PVIs in NSTEMI individuals (MPV, r=0.393, P=0.007; PDW, r=0.334, P=0.023; P-LCR, r=0.382, P=0.008), but had inner-link with inflammatory markers in STEMI cases (hs-CRP, r=0.499, P<0.001; Fbg, r=0.500, P<0.001). These findings may suggest different mechanisms of platelet aggregation in different types of CAD. Moreover, MA may be used as a potential parameter to evaluate platelet aggregation and inflammation together.

摘要

血小板聚集和炎症均与冠状动脉疾病(CAD)有关。通过血栓弹力图(TEG)测量的凝血酶诱导的血小板 - 纤维蛋白凝块强度(MA)已被证明是血小板聚集的一种新标志物。本研究的目的是探讨MA与不同类型CAD中血小板体积指数(PVI)或炎症标志物之间的相关性。纳入了206例不同类型CAD患者。测量了MA、PVI,包括平均血小板体积(MPV)、血小板分布宽度(PDW)和血小板大细胞比率(P-LCR),以及炎症标志物,包括高敏C反应蛋白(hs-CRP)和纤维蛋白原(Fbg)。使用多元线性回归模型分析MA、PVI和炎症标志物之间的关联。MA和炎症标志物均随CAD类型而变化(P<0.001)。MA与非ST段抬高型心肌梗死(NSTEMI)患者的PVI相关(MPV,r = 0.393,P = 0.007;PDW,r = 0.334,P = 0.023;P-LCR,r = 0.382,P = 0.008),但在ST段抬高型心肌梗死(STEMI)病例中与炎症标志物有内在联系(hs-CRP,r = 0.499,P<0.001;Fbg,r = 0.500,P<0.001)。这些发现可能提示不同类型CAD中血小板聚集的不同机制。此外,MA可能作为一个潜在参数来同时评估血小板聚集和炎症。

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