Blood inflammatory and endothelial markers in women with von Willebrand disease.
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2019
2019
Historique:
received:
30
09
2018
accepted:
27
12
2018
entrez:
11
1
2019
pubmed:
11
1
2019
medline:
23
10
2019
Statut:
epublish
Résumé
VWD-affected females often experience menorrhagia. Periodical fluctuations of the sex steroids during the menstrual cycle cause changes both in the coagulation and immune system. The aim of the current study was to assess the changes in selected inflammatory and endothelial markers in women with VWD during two phases of the menstrual cycle (follicular and luteal) and to compare it with corresponding data from healthy controls. The study group included 12 VWD-affected females with regular menstrual cycle, with none of them being prescribed hormone treatment. They were not pregnant or breastfeeding. The control group consisted of 102 healthy females, matched for age and BMI. Within the VWD group, endostatin was higher during the follicular phase, compared to the luteal phase, although the difference was not significant (p = 0.062). sICAM-1 and IL-6 were higher in VWD-affected females, compared to the controls, sVCAM-1, cathepsin S and sP-selectin were lower (p<0.003 for all cases). The pattern was constant throughout the menstrual cycle. Higher levels of endostatin during early follicular phase could potentially predispose women with VWD to the development of heavy menstrual bleeding, due to antiangiogenic properties and ability to suppress several coagulation factors. Lower p-selectin levels in VWD group, compared to controls, may also contribute to the bleeding tendency. Changes in other proteins, involved in angiogenesis are hypothetically related to the formation of angiodysplasia-common complication of VWF deficiency. The latter statement requires confirmation in larger studies.
Identifiants
pubmed: 30629692
doi: 10.1371/journal.pone.0210544
pii: PONE-D-18-28460
pmc: PMC6328189
doi:
Substances chimiques
Biomarkers
0
ICAM1 protein, human
0
Interleukin-6
0
P-Selectin
0
Intercellular Adhesion Molecule-1
126547-89-5
Cathepsins
EC 3.4.-
cathepsin S
EC 3.4.22.27
Banques de données
figshare
['10.6084/m9.figshare.7422620.v1']
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0210544Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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