Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
Publication date
2022-05
Authors
WiN Study Group
Editors
Advisors
Supervisors
Document Type
Article
Metadata
Show full item recordCollections
License
cc_by
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.
Keywords
bleeding disorders, platelet activation, platelet factor 4, VWD, VWF, Hemorrhage/etiology, Phenotype, Humans, von Willebrand Factor/genetics, Platelet Factor 4, von Willebrand Diseases/genetics, Hematology, Research Support, Non-U.S. Gov't, Journal Article
Citation
WiN Study Group 2022, 'Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients', British Journal of Haematology, vol. 197, no. 4, pp. 497-501. https://doi.org/10.1111/bjh.18145