Abstract
UNLABELLED: The ratios between von Willebrand factor propeptide (VWFpp) or factor VIII activity (
FVIII: C) and VWF antigen (VWF:Ag) reflect synthesis, secretion, and clearance of VWF. We aimed to define the pathophysiology of 658 patients with type 1, 2, or 3 von Willebrand disease (VWD) with VWF levels ≤30 U/dL from the Willebrand in The Netherlands (WiN) study using the VWFpp/VWF:Ag and
FVIII: C/VWF:Ag ratios. We evaluated the use of VWFpp in the classification and diagnosis of VWD. On the basis of the ratios, reduced VWF synthesis was observed in 18% of type 1 and only 2% of type 2 patients. A significant proportion of type 3 patients had detectable VWFpp (41%). These patients had a lower bleeding score than type 3 patients who had a complete absence of VWF:Ag and VWFpp (14.0 vs 19.5; P = .025). The majority of these patients had missense mutations with rapid VWF clearance, whereas type 3 patients with no VWFpp were homozygous for null alleles. In conclusion, VWFpp identified severe type 1 VWD with very low VWF levels in patients who had previously been classified as type 3 VWD. This study underlines the clinical significance of the VWFpp assay in the diagnosis and classification of VWD.
Original language | English |
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Pages (from-to) | 3006-3013 |
Number of pages | 8 |
Journal | Blood |
Volume | 125 |
Issue number | 19 |
DOIs | |
Publication status | Published - 2015 |
Keywords
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Child
- Child, Preschool
- Cross-Sectional Studies
- Female
- Follow-Up Studies
- Hemorrhage
- Humans
- Infant
- Male
- Middle Aged
- Mutation
- Netherlands
- Phenotype
- Prognosis
- Protein Precursors
- Young Adult
- von Willebrand Diseases
- von Willebrand Factor