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Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients

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 platelet...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314899/
https://www.ncbi.nlm.nih.gov/pubmed/36165954
http://dx.doi.org/10.1111/bjh.18145
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author 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
author_facet 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
author_sort Swinkels, Maurice
collection PubMed
description 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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spelling pubmed-93148992022-07-30 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 Br J Haematol Platelets, Thrombosis and Haemostasis 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. John Wiley and Sons Inc. 2022-03-22 2022-05 /pmc/articles/PMC9314899/ /pubmed/36165954 http://dx.doi.org/10.1111/bjh.18145 Text en © 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Platelets, Thrombosis and Haemostasis
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
Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
title Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
title_full Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
title_fullStr Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
title_full_unstemmed Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
title_short Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
title_sort platelet degranulation and bleeding phenotype in a large cohort of von willebrand disease patients
topic Platelets, Thrombosis and Haemostasis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314899/
https://www.ncbi.nlm.nih.gov/pubmed/36165954
http://dx.doi.org/10.1111/bjh.18145
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