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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Veröffentlicht in:British Journal of Haematology 2022-03, Vol.197 (4), p.497-501
Hauptverfasser: Swinkels, M., Atiq, F., Burgisser, P.E., Moort, I. van, Meijer, K., Eikenboom, J., Fijnvandraat, K., Galen, K.P.M. van, Meris, J. de, Schols, S.E.M., Bom, J.G. van der, Cnossen, M.H., Voorberg, J., Leebeek, F.W.G., Bierings, R., Jansen, A.J.G.
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Sprache:eng
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Zusammenfassung: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.
DOI:10.1111/bjh.18145