Relationship of Von Willebrand Factor with carotid artery and aortic arch calcification in ischemic stroke patients

Abstract Background Large population studies have revealed that increased von Willebrand Factor (VWF) levels are associated with an increased risk of ischemic stroke. In previous studies VWF was associated with atherosclerosis in healthy individuals. However, it is yet unknown what the association i...

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Veröffentlicht in:Atherosclerosis 2013-10, Vol.230 (2), p.210-215
Hauptverfasser: Sonneveld, Michelle A.H, van Dijk, Anouk C, van den Herik, Evita G, van Loon, Janine E, de Lau, Lonneke M.L, van der Lugt, Aad, Koudstaal, Peter J, de Maat, Moniek P.M, Leebeek, Frank W.G
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Sprache:eng
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Zusammenfassung:Abstract Background Large population studies have revealed that increased von Willebrand Factor (VWF) levels are associated with an increased risk of ischemic stroke. In previous studies VWF was associated with atherosclerosis in healthy individuals. However, it is yet unknown what the association is between atherosclerosis and VWF levels in patients with ischemic stroke. Objectives The aim of our study was to determine the association of atherosclerosis, measured with recent developed techniques, and VWF levels in a large, well characterized, cohort of ischemic stroke patients and to determine the prognostic value. Methods We included 925 consecutive patients with transient ischemic attack (TIA) or ischemic stroke. Calcification volumes (mm3 ) were scored in the aortic arch and both carotid arteries using multidetector computed tomography (CT) angiography. VWF antigen (VWF:Ag) levels were measured using ELISA. Results Mean VWF:Ag levels were significantly higher in the presence of calcification in either the aortic arch (1.47 vs. 1.37 IU/ml [ P  = 0.039]) or the carotid arteries (1.49 vs. 1.34 IU/ml [ P  = 0.001]). Patients with a large artery atherosclerosis ischemic stroke had significantly higher VWF:Ag levels then the other TOAST subtypes ( P  2 vs. ≤2; 1.64 vs. 1.41 IU/ml, [ P  
ISSN:0021-9150
1879-1484
DOI:10.1016/j.atherosclerosis.2013.07.046