BACKGROUND: The results of a number of studies in pigs and mice suggest that absence of von Willebrand factor (vWF) protects against the development of atherosclerosis. We studied whether patients with a complete deficiency of vWF (type 3 von Willebrand disease [vWD]) develop fewer atherosclerotic vessel wall changes than healthy controls. METHODS AND RESULTS: This study included 47 individuals with type 3 vWD and 84 healthy controls. Early atherosclerotic changes were assessed by measuring the thickness of the intima-media in the carotid and femoral arteries by B-mode ultrasonography. Advanced atherosclerotic changes were quantified by summing the maximal thickness of atherosclerotic plaques in the carotid and femoral arteries and were expressed as a plaque score. Established risk factors were determined to adjust for possible differences between the groups. We found no substantial difference in intima-media thickness between vWD patients and controls (adjusted difference for carotid artery 0.007 mm, 95% CI -0.022 to 0.036 mm; femoral artery 0.069 mm, 95% CI -0.056 to 0.19 mm). Similar proportions of patients and controls had atherosclerotic plaques (19% and 17%, respectively). No difference was found in the plaque score between groups (adjusted difference -0.22 mm, 95% CI -0.69 to 0.26). Among vWD patients, we found no effect of treatment with vWF concentrates on intima-media thickness or plaque score. CONCLUSIONS: The results of this study indicate that vWF does not play a substantial role in human atherogenesis.

Patients with type 3 severe von Willebrand Disease are not protected against atherosclerosis. Results from a multicenter study group / Sramek, A; Bucciarelli, P; Federici, Ab; Mannucci, Pm; DE ROSA, V; Castaman, G; Morfini, M; Mazzucconi, Maria Gabriella; Rocino, A; Schiavoni, M; Scaraggi, Fa; Reiber, Jhc; Rosendaal, F. R.. - In: CIRCULATION. - ISSN 0009-7322. - 109:(2004), pp. 740-744. [10.1161/01.CIR.0000112567.53841.10]

Patients with type 3 severe von Willebrand Disease are not protected against atherosclerosis. Results from a multicenter study group.

MAZZUCCONI, Maria Gabriella;
2004

Abstract

BACKGROUND: The results of a number of studies in pigs and mice suggest that absence of von Willebrand factor (vWF) protects against the development of atherosclerosis. We studied whether patients with a complete deficiency of vWF (type 3 von Willebrand disease [vWD]) develop fewer atherosclerotic vessel wall changes than healthy controls. METHODS AND RESULTS: This study included 47 individuals with type 3 vWD and 84 healthy controls. Early atherosclerotic changes were assessed by measuring the thickness of the intima-media in the carotid and femoral arteries by B-mode ultrasonography. Advanced atherosclerotic changes were quantified by summing the maximal thickness of atherosclerotic plaques in the carotid and femoral arteries and were expressed as a plaque score. Established risk factors were determined to adjust for possible differences between the groups. We found no substantial difference in intima-media thickness between vWD patients and controls (adjusted difference for carotid artery 0.007 mm, 95% CI -0.022 to 0.036 mm; femoral artery 0.069 mm, 95% CI -0.056 to 0.19 mm). Similar proportions of patients and controls had atherosclerotic plaques (19% and 17%, respectively). No difference was found in the plaque score between groups (adjusted difference -0.22 mm, 95% CI -0.69 to 0.26). Among vWD patients, we found no effect of treatment with vWF concentrates on intima-media thickness or plaque score. CONCLUSIONS: The results of this study indicate that vWF does not play a substantial role in human atherogenesis.
2004
atherosclerosiscoagulationvon Willebrand factorcardiovascular diseasecarotid arteries
01 Pubblicazione su rivista::01a Articolo in rivista
Patients with type 3 severe von Willebrand Disease are not protected against atherosclerosis. Results from a multicenter study group / Sramek, A; Bucciarelli, P; Federici, Ab; Mannucci, Pm; DE ROSA, V; Castaman, G; Morfini, M; Mazzucconi, Maria Gabriella; Rocino, A; Schiavoni, M; Scaraggi, Fa; Reiber, Jhc; Rosendaal, F. R.. - In: CIRCULATION. - ISSN 0009-7322. - 109:(2004), pp. 740-744. [10.1161/01.CIR.0000112567.53841.10]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/89706
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