Impact of obesity on factor VIII and von Willebrand factor levels in patients with Type 1 von Willebrand disease and low von Willebrand factor: An analysis of the ATHNdataset.


Journal

Haemophilia : the official journal of the World Federation of Hemophilia
ISSN: 1365-2516
Titre abrégé: Haemophilia
Pays: England
ID NLM: 9442916

Informations de publication

Date de publication:
Jan 2022
Historique:
revised: 26 10 2021
received: 16 06 2021
accepted: 14 11 2021
pubmed: 8 12 2021
medline: 14 1 2022
entrez: 7 12 2021
Statut: ppublish

Résumé

Obesity is associated with endothelial dysfunction, haemostatic and fibrinolytic disturbances, however the impact of obesity on von Willebrand factor (VWF) is unclear. The aim of this study was to test our hypothesis that the prevalence of obesity is higher among participants with low VWF (LVWF) compared to type 1 von Willebrand disease (T1VWD). A retrospective review of the ATHNdataset as of March 2018 was performed. Participants were categorized as T1VWD if their VWF ristocetin cofactor activity was 30 IU/dL and LVWF if the values were 30-50 IU/dL, and by the NIH definitions for body mass index (BMI) for adult participants (≥ 18 years of age) or BMI z-score for paediatric participants (< 18 years). The prevalence of obesity was not significantly different between adults with T1VWD (n = 186) and LVWF (n = 362) (32% vs 36%; p = .345). The mean factor VIII (FVIII) increased with increasing BMIs in both groups. In the paediatric cohort (T1VWD, n = 583; LVWF, n = 1702), there was no difference in the prevalence of obesity, but BMI was positively correlated with mean FVIII (p < .001). Children < 10 years were 27.6% more likely to be diagnosed with T1VWD compared to > 10 years. Among participants in the ATHNdataset, the prevalence of obesity was similar among those with LVWF and T1VWD. However, higher BMI levels were associated with elevated FVIII. Further research is needed to evaluate the impact of obesity on bleeding phenotype and treatment practices.

Identifiants

pubmed: 34874087
doi: 10.1111/hae.14467
doi:

Substances chimiques

Hemostatics 0
von Willebrand Factor 0
Factor VIII 9001-27-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109-116

Subventions

Organisme : 2018 HTRS/ATHN DREAM Award from the Hemostasis and Thrombosis Research Society (HTRS) and the American Thrombosis and Hemostasis Network (ATHN), which was supported by Hemophilia of Georgia.

Informations de copyright

© 2021 John Wiley & Sons Ltd.

Références

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Auteurs

Beverly A Schaefer (BA)

University at Buffalo, Roswell Park Oishei Children's Cancer and Blood Disorders Program, Buffalo, NY, USA.
Western New York BloodCare, Buffalo, New York, USA.

Dunlei Cheng (D)

American Thrombosis and Hemostasis Network, Rochester, New York, USA.

Peter Kouides (P)

University of Rochester School of Medicine, Mary M. Gooley Hemophilia Treatment Center, Rochester, New York, USA.

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