Literature DB >> 31741138

Evaluation of clinical severity in patients with type 2N von Willebrand disease using microchip-based flow-chamber system.

Yuto Nakajima1, Keiji Nogami2, Koji Yada1,3, Takeshi Kawamura1, Kenichi Ogiwara1, Shoko Furukawa1,4, Naruto Shimonishi1, Masahiro Takeyama1, Midori Shima1.   

Abstract

Type 2N von Willebrand disease (VWD) is characterized by impaired factor VIII (FVIII) binding to von Willebrand factor (VWF). Type 2N VWD patients generally exhibit mild bleeding tendency, but some exhibit a more severe hemorrhagic pattern. An assay for assessing hemostatic potential and predict clinical severity could significantly improve clinical management in these patients. We examined the relationship between bleeding score (BS) and the potential for thrombus formation in whole blood from type 2N VWD patients with various BS using rotational thromboelastometry (ROTEM) and microchip flow-chamber system (T-TAS®). Collagen-coated PL-chips, or thromboplastin- and collagen-coated AR-chips, were utilized in the T-TAS to assess platelet thrombus formation at high shear flow, or fibrin-rich platelet thrombus formation at low shear flow, respectively. Neither ROTEM nor the T-TAS using PL-chips reflected the BS. The AR-chip parameters in the T-TAS, however, were highly sensitive to different BS levels among these patients, despite similar FVIII/VWF-related measurements including FVIII/VWF binding. Additionally, the results with AR-chip assay were restored to normal after infusions of FVIII/VWF concentrates in the most severe patients. The data indicate that T-TAS using AR-chips may be a useful assay for predicting clinical severity and assessing therapeutic efficiency in type 2N VWD patients.

Entities:  

Keywords:  Bleeding score; Clinical severity; Microchip flow-chamber system; Type 2N von willebrand disease; Von willebrand factor

Mesh:

Year:  2019        PMID: 31741138     DOI: 10.1007/s12185-019-02782-z

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  27 in total

1.  A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD).

Authors:  A Tosetto; F Rodeghiero; G Castaman; A Goodeve; A B Federici; J Batlle; D Meyer; E Fressinaud; C Mazurier; J Goudemand; J Eikenboom; R Schneppenheim; U Budde; J Ingerslev; Z Vorlova; D Habart; L Holmberg; S Lethagen; J Pasi; F Hill; I Peake
Journal:  J Thromb Haemost       Date:  2006-04       Impact factor: 5.824

2.  Mild hemophilia A patient with novel Pro1809Leu mutation develops an anti-C2 antibody inhibiting allogeneic but not autologous factor VIII activity.

Authors:  K Yada; K Nogami; M Takeyama; K Ogiwara; H Wakabayashi; M Shima
Journal:  J Thromb Haemost       Date:  2015-09-23       Impact factor: 5.824

3.  Systematic monitoring of hemostatic management in hemophilia A patients with inhibitor in the perioperative period using rotational thromboelastometry.

Authors:  S Furukawa; K Nogami; K Ogiwara; K Yada; H Minami; M Shima
Journal:  J Thromb Haemost       Date:  2015-05-29       Impact factor: 5.824

Review 4.  Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology.

Authors:  C Mazurier; J Goudemand; L Hilbert; C Caron; E Fressinaud; D Meyer
Journal:  Best Pract Res Clin Haematol       Date:  2001-06       Impact factor: 3.020

5.  Identification of the binding site for an alloantibody to von Willebrand factor which inhibits binding to glycoprotein Ib within the amino-terminal region flanking the A1 domain.

Authors:  M Shibata; M Shima; Y Fujimura; Y Takahashi; H Nakai; Y Sakurai; M Asatani; A Nomura; H Take; J C Giddings; A Yoshioka
Journal:  Thromb Haemost       Date:  1999-05       Impact factor: 5.249

6.  A novel automated microchip flow-chamber system to quantitatively evaluate thrombus formation and antithrombotic agents under blood flow conditions.

Authors:  K Hosokawa; T Ohnishi; T Kondo; M Fukasawa; T Koide; I Maruyama; K A Tanaka
Journal:  J Thromb Haemost       Date:  2011-10       Impact factor: 5.824

7.  Monitoring of coagulation factor therapy in patients with von Willebrand disease type 3 using a microchip flow chamber system.

Authors:  Anna Ågren; Margareta Holmström; David E Schmidt; Kazuya Hosokawa; Margareta Blombäck; Paul Hjemdahl
Journal:  Thromb Haemost       Date:  2016-10-20       Impact factor: 5.249

8.  Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype.

Authors:  M E R van Meegeren; T L Mancini; S C M Schoormans; B J T van Haren; C van Duren; A Diekstra; B A P Laros-van Gorkom; P P T Brons; A Simons; L Hoefsloot; W L van Heerde
Journal:  Haemophilia       Date:  2015-07-24       Impact factor: 4.287

9.  Studies on anti-von Willebrand factor (vWF) monoclonal antibody NMC-4, which inhibits both ristocetin- and botrocetin-induced vWF binding to platelet glycoprotein Ib.

Authors:  Y Fujimura; Y Usami; K Titani; K Niinomi; K Nishio; T Takase; A Yoshioka; H Fukui
Journal:  Blood       Date:  1991-01-01       Impact factor: 22.113

Review 10.  Principles of care for the diagnosis and treatment of von Willebrand disease.

Authors:  Giancarlo Castaman; Anne Goodeve; Jeroen Eikenboom
Journal:  Haematologica       Date:  2013-05       Impact factor: 9.941

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