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Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients.
Swinkels, Maurice; Atiq, Ferdows; Bürgisser, Petra E; van Moort, Iris; Meijer, Karina; Eikenboom, Jeroen; Fijnvandraat, Karin; van Galen, Karin P M; de Meris, Joke; Schols, Saskia E M; van der Bom, Johanna G; Cnossen, Marjon H; Voorberg, Jan; Leebeek, Frank W G; Bierings, Ruben; Jansen, A J Gerard.
Afiliación
  • Swinkels M; Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Atiq F; Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Bürgisser PE; Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • van Moort I; Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Meijer K; Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Eikenboom J; Department of Internal Medicine, Division of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands.
  • Fijnvandraat K; Einthoven Laboratory for Vascular and Regenerative Medicine, Leiden University Medical Center, Leiden, The Netherlands.
  • van Galen KPM; Department of Pediatric Hematology, Emma Children's Hospital-Academic Medical Centre, Amsterdam, The Netherlands.
  • de Meris J; Van Creveldkliniek, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Schols SEM; Netherlands Hemophilia Society, Leiden, The Netherlands.
  • van der Bom JG; Department of Hematology, Radboud University Medical Center and Hemophilia Treatment Center Nijmegen-Eindhoven-Maastricht, Nijmegen, The Netherlands.
  • Cnossen MH; Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
  • Voorberg J; Department of Pediatric Hematology, Erasmus University Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Leebeek FWG; Department of Molecular Hematology, Sanquin Research and Landsteiner Laboratory, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Bierings R; Department of Experimental Vascular Medicine, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Jansen AJG; Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Br J Haematol ; 197(4): 497-501, 2022 05.
Article en En | MEDLINE | ID: mdl-36165954
ABSTRACT
Von Willebrand disease (VWD) is a bleeding disorder caused by quantitative (type 1 or 3) or qualitative (type 2A/2B/2M/2N) defects of circulating von Willebrand factor (VWF). Circulating VWF levels not always fully explain bleeding phenotypes, suggesting a role for alternative factors, like platelets. Here, we investigated platelet factor 4 (PF4) in a large cohort of patients with VWD. PF4 levels were lower in type 2B and current bleeding phenotype was significantly associated with higher PF4 levels, particularly in type 1 VWD. Based on our findings we speculate that platelet degranulation and cargo release may play a role across VWD subtypes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de von Willebrand Tipo de estudio: Etiology_studies / Qualitative_research / Risk_factors_studies Límite: Humans Idioma: En Revista: Br J Haematol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de von Willebrand Tipo de estudio: Etiology_studies / Qualitative_research / Risk_factors_studies Límite: Humans Idioma: En Revista: Br J Haematol Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos