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

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

Journal

International journal of hematology
ISSN: 1865-3774
Titre abrégé: Int J Hematol
Pays: Japan
ID NLM: 9111627

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 30 08 2019
accepted: 12 11 2019
revised: 08 11 2019
pubmed: 20 11 2019
medline: 28 8 2020
entrez: 20 11 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31741138
doi: 10.1007/s12185-019-02782-z
pii: 10.1007/s12185-019-02782-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

369-377

Subventions

Organisme : Ministry of Education, Culture, Sports, Science and Technology
ID : 18K07885

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Auteurs

Yuto Nakajima (Y)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.

Keiji Nogami (K)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan. roc-noga@naramed-u.ac.jp.

Koji Yada (K)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.
The Course of Hemophilia Education, Nara Medical University, Kashihara, Nara, Japan.

Takeshi Kawamura (T)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.

Kenichi Ogiwara (K)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.

Shoko Furukawa (S)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.
The Course of Thrombosis and Hemostasis Molecular Pathology, Nara Medical University, Kashihara, Nara, Japan.

Naruto Shimonishi (N)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.

Masahiro Takeyama (M)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.

Midori Shima (M)

Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, 634-8522, Nara, Japan.

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