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血小板减少症中血小板功能的评估。

Evaluation of platelet function in thrombocytopenia.

机构信息

a Centre for Haemophilia and Thrombosis , Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus , Denmark.

b Department of Haematology , Aarhus University Hospital, Aarhus University Hospital , Denmark.

出版信息

Platelets. 2018 May;29(3):270-276. doi: 10.1080/09537104.2017.1296566. Epub 2017 Apr 14.

Abstract

Whole blood aggregometry is a functional assay for determination of platelet function. Until now, whole blood aggregometry has not been considered feasible at low platelet counts. Hence, the objectives of the present study were to explore platelet function in thrombocytopenia using a novel index of impedance aggregometry adjusted for platelet count and evaluate the association to platelet function assessed by flow cytometry. Hirudin anticoagulated blood was collected from 20 healthy volunteers, 20 patients with primary immune thrombocytopenia (ITP), and 17 hematological cancer patients. Platelet function was analyzed by impedance aggregometry and by flow cytometry. Collagen, adenosine diphosphate, thrombin receptor agonist peptide-6, and ristocetin were used as agonists for both analyses. Thrombocytopenia in healthy whole blood was induced in vitro employing a recently published method. Platelet aggregation of thrombocytopenic patients was evaluated relative to the aggregation of healthy volunteers at the same platelet count. In flow cytometry, platelet function was described as expression of the platelet surface glycoproteins: bound fibrinogen, CD63, and P-selectin. Similar platelet counts were obtained in the patient groups (p = 0.69) (range: 13-129 × 10/l). Aggregation adjusted for platelet count was significantly increased in ITP patients compared to healthy platelets across all agonists. The platelet aggregation was high in the 95% prediction interval, with 18 ITP patients above the prediction interval in at least two agonists. In contrast, the platelet aggregation was low in the prediction interval in cancer patients, and three cancer patients with platelet aggregation below the prediction interval in at least one agonist. ITP patients displayed increased expression of bound fibrinogen and CD63 following activation, compared with particularly cancer patients, but also compared with healthy platelets. This study demonstrated the feasibility of a novel approach to perform platelet function analyses in thrombocytopenia using impedance aggregometry adjusted for platelet count.

摘要

全血聚集仪是一种用于测定血小板功能的功能检测方法。到目前为止,全血聚集仪在血小板计数较低时并不被认为是可行的。因此,本研究的目的是利用一种新的血小板计数校正的阻抗聚集仪指数来探讨血小板减少症中的血小板功能,并评估其与流式细胞术评估的血小板功能之间的相关性。从 20 名健康志愿者、20 名原发性免疫性血小板减少症 (ITP) 患者和 17 名血液病癌症患者中采集肝素抗凝血液。使用阻抗聚集仪和流式细胞术分析血小板功能。使用胶原、二磷酸腺苷、血栓素受体激动肽-6 和瑞斯托霉素作为两种分析的激动剂。采用最近发表的方法在体外诱导健康全血中的血小板减少症。相对于健康志愿者在相同血小板计数下的聚集,评估血小板减少症患者的血小板聚集。在流式细胞术,血小板功能描述为血小板表面糖蛋白的表达:结合纤维蛋白原、CD63 和 P-选择素。患者组的血小板计数相似 (p = 0.69)(范围:13-129×10/L)。与健康血小板相比,ITP 患者的血小板聚集在所有激动剂中经血小板计数校正后均显著增加。在至少两种激动剂中,有 18 名 ITP 患者的血小板聚集在 95%预测区间上限之上。相比之下,癌症患者的血小板聚集在预测区间内较低,有 3 名癌症患者在至少一种激动剂中的血小板聚集低于预测区间。与癌症患者相比,尤其是与健康血小板相比,激活后 ITP 患者的结合纤维蛋白原和 CD63 的表达增加。本研究证明了使用血小板计数校正的阻抗聚集仪在血小板减少症中进行血小板功能分析的新方法的可行性。

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