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Published on: August 14, 2017
Endothelial Function in Patients With Von Willebrand Disease
Stephanie Noone1, Ralf Schubert2, Stephan Fichtlscherer3
1Haemostaseology, Department of Internal Medicine II, Institute of Transfusion Medicine, University Hospital, Goethe University Frankfurt am Main, Frankfurt, Germany.
Patients with von Willebrand disease (vWD) do not show significantly different endothelial function compared to healthy individuals. This study investigated endothelial dysfunction markers and reactive hyperemia index in vWD patients, finding no significant variations from controls.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Vascular Biology
Background:
- Increased life expectancy in von Willebrand disease (vWD) patients necessitates understanding age-related comorbidities.
- Endothelial function is crucial for vascular health and may be affected in chronic conditions.
Purpose of the Study:
- To investigate whether patients with von Willebrand disease exhibit altered endothelial function compared to the general population.
- To compare endothelial dysfunction markers and reactive hyperemia index (RHI) between vWD patients, healthy controls, and coronary artery disease (CAD) patients.
Main Methods:
- Inclusion of 37 vWD patients (types 1, 2, 3), 14 controls, and 38 CAD patients.
- Determination of five markers of endothelial dysfunction (MOED).
- Assessment of endothelial function using Itamar Endo-PAT to calculate the reactive hyperemia index (RHI).
Main Results:
- Higher levels of soluble intercellular adhesion molecule-1, P-Selectin, interleukin-6, and monocyte chemoattractant protein-1 were observed in vWD patients but were not statistically significant compared to controls.
- Reactive hyperemia index (RHI) was impaired in CAD patients (1.855) but not significantly different between vWD patients (1.870) and controls (2.112).
Conclusions:
- Endothelial function in patients with von Willebrand disease is not significantly different from that of healthy controls.
- Further research may be needed to explore subtle endothelial changes or long-term vascular implications in vWD.
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