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评估用于血管性血友病识别及治疗监测的血管性血友病因子三项检测组合及基于化学发光的检测系统。

Evaluation of a von Willebrand factor three test panel and chemiluminescent-based assay system for identification of, and therapy monitoring in, von Willebrand disease.

作者信息

Favaloro Emmanuel J, Mohammed Soma

机构信息

Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), Sydney Centres for Thrombosis and Haemostasis, Pathology West, NSW Health Pathology, Westmead Hospital, Westmead, NSW, Australia.

Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), Sydney Centres for Thrombosis and Haemostasis, Pathology West, NSW Health Pathology, Westmead Hospital, Westmead, NSW, Australia.

出版信息

Thromb Res. 2016 May;141:202-11. doi: 10.1016/j.thromres.2015.12.010. Epub 2015 Dec 17.

Abstract

von Willebrand disease (VWD) is reportedly the most common bleeding disorder and arises from deficiency and/or defects of von Willebrand factor (VWF). Laboratory diagnosis and typing of VWD has important management implications and requires a wide range of tests, including VWF antigen (VWF:Ag) and various activities, involving differential identification of qualitative vs quantitative VWF defects. We have assessed a new hemostasis instrument, the chemiluminescent assay based ACL AcuStar™, and an associated HemosIL AcuStar three test panel comprising VWF:Ag, VWF ristocetin cofactor (VWF:RCo) and VWF collagen binding (VWF:CB) (Instrumentation Laboratory, Bedford, Ma. USA) for ability to identify VWD, to help provisionally type VWD, and for potential use in therapy monitoring. This test system was compared to previously evaluated and validated test systems including VWF:RCo on CS-5100 and BCS analyzers, the new Siemens INNOVANCE assay (VWF Ac) on CS-5100, and VWF:Ag and VWF:CB assays performed by automated ELISA. We employed a large total sample test set (n=535) comprising plasma and platelet-lysate samples from individuals with and without VWD, some on treatment, normal plasmas, and normal and pathological controls. We also evaluated desmopressin (DDAVP) responsiveness, plus differential sensitivity to reduction in high molecular weight (HMW) VWF. The chemiluminescent test panel (VWF:Ag, VWF:RCo, VWF:CB) showed good comparability to similar assays performed by alternate methods, and broadly similar data for identification of VWD, provisional VWD type identification, DDAVP and VWD therapy, and HMW VWF sensitivity, although some notable differences were evident. The chemiluminescent system showed best low level VWF sensitivity, and lowest inter-assay variability, compared to all other systems. In conclusion, we have validated theACL AcuStar and the chemiluminescent HemosIL AcuStar VWF test panel for use in VWD diagnostics, and have identified some favorable characteristics that may improve the future diagnosis of VWD.

摘要

据报道,血管性血友病(VWD)是最常见的出血性疾病,由血管性血友病因子(VWF)缺乏和/或缺陷引起。VWD的实验室诊断和分型对治疗管理具有重要意义,需要进行广泛的检测,包括VWF抗原(VWF:Ag)和各种活性检测,涉及定性与定量VWF缺陷的鉴别。我们评估了一种新型止血仪器——基于化学发光检测的ACL AcuStar™,以及一个相关的HemosIL AcuStar三项检测组合,该组合包括VWF:Ag、VWF瑞斯托霉素辅因子(VWF:RCo)和VWF胶原结合(VWF:CB)(美国马萨诸塞州贝德福德的仪器实验室),以确定其识别VWD、初步分型VWD以及在治疗监测中潜在应用的能力。将该检测系统与先前评估和验证的检测系统进行了比较,包括CS - 5100和BCS分析仪上的VWF:RCo检测、CS - 5100上的新型西门子INNOVANCE检测(VWF Ac)以及通过自动酶联免疫吸附测定法进行的VWF:Ag和VWF:CB检测。我们使用了一个大型总样本检测集(n = 535),包括来自有或无VWD个体的血浆和血小板裂解物样本,其中一些正在接受治疗,还有正常血浆以及正常和病理对照。我们还评估了去氨加压素(DDAVP)的反应性,以及对高分子量(HMW)VWF减少的差异敏感性。化学发光检测组合(VWF:Ag、VWF:RCo、VWF:CB)与通过其他方法进行的类似检测具有良好的可比性,在VWD识别、VWD初步分型、DDAVP与VWD治疗以及HMW VWF敏感性方面的数据大致相似,尽管存在一些明显差异。与所有其他系统相比,化学发光系统显示出最佳的低水平VWF敏感性和最低的批间变异性。总之,我们已经验证了ACL AcuStar和化学发光HemosIL AcuStar VWF检测组合可用于VWD诊断,并确定了一些可能改善未来VWD诊断的有利特性。

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