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

Br J Haematol. 2022 May;197(4):497-501. doi: 10.1111/bjh.18145. Epub 2022 Mar 22.

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: VWD; VWF; bleeding disorders; platelet activation; platelet factor 4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Hemorrhage / etiology
  • Humans
  • Phenotype
  • Platelet Factor 4
  • von Willebrand Diseases* / genetics
  • von Willebrand Factor / genetics

Substances

  • von Willebrand Factor
  • Platelet Factor 4