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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9314899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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