Interpreting high levels of unfolded Von Willebrand Factor in patients with the antiphospholipid syndrome

Romy de Laat-Kremers*, Shengshi Huang, Hugo ten Cate, Marisa Ninivaggi, Bas de Laat*, Katrien Devreese

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

<bold>Introduction:</bold> Unfolded Von Willebrand Factor (VWF) is increased in thrombotic pathologies such as myocardial infarction. Unfolded VWF mediates the binding of platelets without the need for collagen. beta(2)-glycoprotein I (beta(2)-GPI) is a natural inhibitor of the platelet-VWF interaction. The antiphospholipid syndrome (APS) is associated with thrombosis, with an important pathophysiological role of auto-antibodies directed against beta(2)-GPI. <bold>Methods:</bold> (Unfolded) VWF levels were studied in normal controls (n=93), APS patients (n=64), non-APS thrombosis patients (n=39) and non-APS auto-immune disease (AID) patients (n=49. <bold>Results:</bold> Unfolded VWF levels were respectively, 53%, 50% and 36% higher in APS patients, non-APS thrombosis patients and AID patients, compared to normal controls (p<0.0001). Unfolded VWF levels above the 90(th) percentile in normal controls were associated with an odds of APS (OR: 8.51; CI:3.26 - 22.2; p<0.001), compared to ORs of non-APS thrombosis (OR:5.87; CI:2.07 - 16.7, p=0.001) and AID (OR:3.71; CI:1.40 - 9.87; p=0.009). <bold>Discussion:</bold> We found that APS patients have high levels of unfolded VWF in their circulation. In APS, auto-antibodies against-beta 2-GPI may interfere with the beta 2-GPI-mediated inhibition of VWF-platelet interaction. Therefore, the higher unfolded VWF levels in APS could in part explain the association of APS and thrombotic complications.
Original languageEnglish
Article number1514433
Number of pages8
JournalFrontiers in Immunology
Volume15
DOIs
Publication statusPublished - 12 Dec 2024

Keywords

  • Von Willbrand Factor
  • antiphospholipid syndrome
  • thrombosis
  • unfolded VWF
  • VWF pro-peptide
  • INDEPENDENT RISK-FACTOR
  • PLATELET-ADHESION
  • PLASMA-LEVELS
  • THROMBOSIS
  • HEMOSTASIS
  • UPDATE

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