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血小板功能障碍会导致疑似钩端螺旋体病患者出现出血并发症。

Platelet dysfunction contributes to bleeding complications in patients with probable leptospirosis.

作者信息

Tunjungputri Rahajeng N, Gasem Muhammad Hussein, van der Does Willemijn, Sasongko Pandu H, Isbandrio Bambang, Urbanus Rolf T, de Groot Philip G, van der Ven Andre, de Mast Quirijn

机构信息

Department of Internal Medicine, Radboud university medical center, Nijmegen, The Netherlands.

Center for Tropical and Infectious Disease (CENTRID), Faculty of Medicine Diponegoro University, Dr Kariadi Hospital, Semarang, Indonesia.

出版信息

PLoS Negl Trop Dis. 2017 Sep 21;11(9):e0005915. doi: 10.1371/journal.pntd.0005915. eCollection 2017 Sep.

Abstract

BACKGROUND

Severe leptospirosis is frequently complicated by a hemorrhagic diathesis, of which the pathogenesis is still largely unknown. Thrombocytopenia is common, but often not to the degree that spontaneous bleeding is expected. We hypothesized that the hemorrhagic complications are not only related to thrombocytopenia, but also to platelet dysfunction, and that increased binding of von Willebrand factor (VWF) to platelets is involved in both platelet dysfunction and increased platelet clearance.

METHODOLOGY/PRINCIPAL FINDINGS: A prospective study was carried out in Semarang, Indonesia, enrolling 33 hospitalized patients with probable leptospirosis, of whom 15 developed clinical bleeding, and 25 healthy controls. Platelet activation and reactivity were determined using flow cytometry by measuring the expression of P-selectin and activation of the αIIbβ3 integrin by the binding of fibrinogen in unstimulated samples and after ex vivo stimulation by the platelet agonists adenosine-diphosphate (ADP) and thrombin-receptor activating peptide (TRAP). Platelet-VWF binding, before and after VWF stimulation by ristocetin, as well as plasma levels of VWF, active VWF, the VWF-inactivating enzyme ADAMTS13, thrombin-antithrombin complexes (TAT) and P-selectin were also measured. Bleeding complications were graded using the WHO bleeding scale. Our study revealed that platelet activation, with a secondary platelet dysfunction, is a feature of patients with probable leptospirosis, especially in those with bleeding manifestations. There was a significant inverse correlation of bleeding score with TRAP-stimulated P-selectin and platelet-fibrinogen binding (R = -0.72, P = 0.003 and R = -0.66, P = 0.01, respectively) but not with platelet count. Patients with bleeding also had a significantly higher platelet-VWF binding. Platelet counts were inversely correlated with platelet-VWF binding (R = -0.74; P = 0.0009. There were no correlations between platelet-VWF binding and the degree of platelet dysfunction, suggesting that increased platelet-VWF binding does not directly interfere with the platelet αIIbβ3 signaling pathway in patients with probable leptospirosis.

CONCLUSION/SIGNIFICANCE: Platelet dysfunction is common in probable leptospirosis patients with manifest bleeding. Increased VWF-platelet binding may contribute to the activation and clearance of platelets.

摘要

背景

重症钩端螺旋体病常并发出血素质,其发病机制仍大多未知。血小板减少很常见,但通常未达到预期会出现自发性出血的程度。我们推测出血并发症不仅与血小板减少有关,还与血小板功能障碍有关,并且血管性血友病因子(VWF)与血小板结合增加参与了血小板功能障碍和血小板清除增加。

方法/主要发现:在印度尼西亚三宝垄进行了一项前瞻性研究,纳入33例住院的疑似钩端螺旋体病患者,其中15例出现临床出血,以及25名健康对照者。通过流式细胞术,在未刺激样本中以及在血小板激动剂二磷酸腺苷(ADP)和凝血酶受体激活肽(TRAP)体外刺激后,通过测量P-选择素的表达和纤维蛋白原结合对αIIbβ3整合素的激活,来测定血小板活化和反应性。还测量了瑞斯托菌素刺激VWF前后的血小板-VWF结合,以及VWF、活性VWF、VWF失活酶ADAMTS13、凝血酶-抗凝血酶复合物(TAT)和P-选择素的血浆水平。使用WHO出血量表对出血并发症进行分级。我们的研究表明,血小板活化以及继发性血小板功能障碍是疑似钩端螺旋体病患者的一个特征,尤其是在有出血表现的患者中。出血评分与TRAP刺激后的P-选择素和血小板-纤维蛋白原结合呈显著负相关(R = -0.72,P = 0.003和R = -0.66,P = 0.01),但与血小板计数无关。有出血的患者血小板-VWF结合也显著更高。血小板计数与血小板-VWF结合呈负相关(R = -0.74;P = 0.0009)。血小板-VWF结合与血小板功能障碍程度之间无相关性,这表明在疑似钩端螺旋体病患者中,血小板-VWF结合增加并不直接干扰血小板αIIbβ3信号通路。

结论/意义:血小板功能障碍在有明显出血的疑似钩端螺旋体病患者中很常见。VWF-血小板结合增加可能有助于血小板的活化和清除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9988/5626517/b42f54d64951/pntd.0005915.g001.jpg

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