Literature DB >> 25300811

Towards improved diagnosis of von Willebrand disease: comparative evaluations of several automated von Willebrand factor antigen and activity assays.

Emmanuel J Favaloro1, Soma Mohammed2.   

Abstract

INTRODUCTION: 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 has important management implications and requires a wide range of tests, including VWF activity and antigen, and involves differential identification of qualitative vs quantitative defects.
METHODS: We have assessed several VWF antigen and activity assays (collagen binding [VWF:CB], ristocetin cofactor [VWF:RCo] and the new Siemens INNOVANCE assay [VWF:Ac], employing latex particles and gain of function recombinant glycoprotein Ib to facilitate VWF binding and agglutination without need for ristocetin) using different instrumentation, including the new Sysmex CS-5100, with a large sample test set (n=600). We included retrospective plus prospective study designs, and also evaluated desmopressin responsiveness plus differential sensitivity to high molecular weight VWF.
RESULTS: VWF:Ag and VWF:RCo results from different methods were respectively largely comparable, although some notable differences were evident, including one high false normal VWF:Ag value (105 U/dL) on a type 3 VWD sample, possibly due to heterophile antibody interference in the latex-based CS-5100 methodology. VWF:Ac was largely comparable to VWF:RCo, but VWF:CB showed discrepant findings to both VWF:RCo and VWF:Ac with some patients, most notably patients with type 2M VWD.
CONCLUSIONS: (a) VWF:Ag on different platforms are largely interchangeable, as are VWF:RCo on different platforms, except for occasional (some potentially important) differences, and manufacturer recommended methods may otherwise require some assay optimization; (b) VWF:RCo and VWF:Ac are largely interchangeable, except for occasional differences that may also relate to assay design (differing optimizations); (c) VWF:CB provides an additional activity to supplement VWF:RCo or VWF:Ac activity assays, and is not interchangeable with either. Crown
Copyright © 2014. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Collagen binding; INNOVANCE VWF activity; Laboratory testing; Ristocetin cofactor; von Willebrand disease; von Willebrand factor

Mesh:

Substances:

Year:  2014        PMID: 25300811     DOI: 10.1016/j.thromres.2014.09.024

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  10 in total

Review 1.  Laboratory diagnosis of von Willebrand disease.

Authors:  J C Roberts; V H Flood
Journal:  Int J Lab Hematol       Date:  2015-05       Impact factor: 2.877

2.  Establishment of an International Reference Reagent for standardization of von Willebrand factor binding to recombinant glycoprotein Ib (VWF:GPIbM and VWF:GPIbR): Official Communication of the SSC.

Authors:  Anthony R Hubbard; Sandra L Haberichter
Journal:  J Thromb Haemost       Date:  2019-05-17       Impact factor: 5.824

Review 3.  Platelet-dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH.

Authors:  I Bodó; J Eikenboom; R Montgomery; J Patzke; R Schneppenheim; J Di Paola
Journal:  J Thromb Haemost       Date:  2015-05-09       Impact factor: 5.824

4.  Comparison of von Willebrand factor platelet-binding activity assays: ELISA overreads type 2B with loss of HMW multimers.

Authors:  Attila Szederjesi; Luciano Baronciani; Ulrich Budde; Giancarlo Castaman; Paola Colpani; Andrew S Lawrie; Yuan Liu; Robert Montgomery; Flora Peyvandi; Reinhard Schneppenheim; Jürgen Patzke; Imre Bodó
Journal:  J Thromb Haemost       Date:  2020-08-27       Impact factor: 5.824

Review 5.  Towards personalised therapy for von Willebrand disease: a future role for recombinant products.

Authors:  Emmanuel J Favaloro
Journal:  Blood Transfus       Date:  2016-03-22       Impact factor: 3.443

6.  An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF study.

Authors:  A Szederjesi; L Baronciani; U Budde; G Castaman; A S Lawrie; Y Liu; R Montgomery; F Peyvandi; R Schneppenheim; A Várkonyi; J Patzke; I Bodó
Journal:  J Thromb Haemost       Date:  2018-06-13       Impact factor: 5.824

Review 7.  Rare forms of von Willebrand disease.

Authors:  Emmanuel J Favaloro
Journal:  Ann Transl Med       Date:  2018-09

8.  Role of acquired von Willebrand syndrome in the development of bleeding complications in patients treated with Impella RP devices.

Authors:  Mehmet Oezkur; Sara Reda; Heiko Rühl; Nils Theuerkauf; Stefan Kreyer; Georg Daniel Duerr; Efstratios Charitos; Miriam Silaschi; Marta Medina; Sebastian Zimmer; Christian Putensen; Hendrik Treede
Journal:  Sci Rep       Date:  2021-12-09       Impact factor: 4.379

Review 9.  Advances in laboratory assessment of thrombosis and hemostasis.

Authors:  Jaewoo Song
Journal:  Blood Res       Date:  2022-04-30

10.  Laboratory variability in the diagnosis of type 2 VWD variants.

Authors:  Stefanie DiGiandomenico; Pamela A Christopherson; Sandra L Haberichter; Thomas C Abshire; Robert R Montgomery; Veronica H Flood
Journal:  J Thromb Haemost       Date:  2020-11-10       Impact factor: 5.824

  10 in total

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