Increased aortic stiffness index in patients with type 1 diabetes without cardiovascular disease compared to controls

Purpose Increased arterial stiffness is an early sign of endothelial dysfunction. Nevertheless, measures of the elastic properties of the aortic root in patients with type 1 diabetes are still lacking. The aim of this study was to compare aortic root stiffness index in type 1 diabetes and healthy co...

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Veröffentlicht in:Journal of endocrinological investigation 2019-09, Vol.42 (9), p.1109-1115
Hauptverfasser: Zoppini, G., Bergamini, C., Trombetta, M., Sabbagh, L., Dauriz, M., Mantovani, A., Targher, G., Fossà, I., Rinaldi, E., Bonora, E.
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Sprache:eng
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Zusammenfassung:Purpose Increased arterial stiffness is an early sign of endothelial dysfunction. Nevertheless, measures of the elastic properties of the aortic root in patients with type 1 diabetes are still lacking. The aim of this study was to compare aortic root stiffness index in type 1 diabetes and healthy controls. Methods Ninety-three patients with type 1 diabetes without cardiovascular diseases were recruited and compared to 33 healthy controls. Aortic root elastic properties were estimated by measuring the systolic and diastolic diameters on M-mode acquisition. Results None of the subjects showed alterations of either systolic or diastolic echocardiographic parameters. Patients with type 1 diabetes had a very low prevalence of chronic complications and their metabolic control was good. Significantly increased aortic stiffness index was found in type 1 diabetes compared to controls, and the same different pattern was found in men and women. The presence of type 1 diabetes and increased pulse pressure was significantly associated with aortic stiffness index in a multivariate linear analysis. Conclusion This study strongly suggests that patients with type 1 diabetes develop aortic root stiffness in the absence of cardiovascular diseases. This alteration may be part of a more generalized arterial dysfunction in type 1 diabetes.
ISSN:1720-8386
0391-4097
1720-8386
DOI:10.1007/s40618-019-01032-7