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
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

e0210544

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Igor Govorov (I)

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

Katarina Bremme (K)

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

Anders Larsson (A)

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

Margareta Holmström (M)

Department of Medicine, Karolinska University Hospital Solna, Stockholm, Sweden.

Eduard Komlichenko (E)

Institution of Pediatrics and Perinatology, Almazov National Medical Research Centre, Saint-Petersburg, Russia.

Roza Chaireti (R)

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Department of Hematology, Karolinska University Hospital, Stockholm, Sweden.

Miriam Mints (M)

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

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Classifications MeSH