Diabetes complications increase with disease duration. No study was performed on the relationship between aortic stiffness and diabetes duration, taking into account the respective influence of such factors on macro- and microcirculation. In total, 618 subjects with type 2 diabetes (259 men) attending the Department of Internal Medicine of Tizi Ouzou Hospital (Algeria) were studied in collaboration with Hotel-Dieu Hospital (Paris, France). Brachial blood pressure (BP), anthropometric, clinical and biological data were evaluated. Aortic stiffness was estimated by carotid-femoral pulse wave velocity (PWV). From lower to higher tertile of diabetes duration, age, BP and PWV (10.1±2.7 to 12.3±2.8 m s-1) increased, while diabetes control and renal function worsened (all P<0.01). Diabetes duration was independently associated with PWV (R2 =0.035, P<0.0001), even after adjustment for age, BP, heart rate, cardiovascular events and metabolic syndrome. Diabetes duration was significantly correlated to the prevalence of microalbuminuria (OR (95% CL) 1.3 (1.06-1.63), P=0.01), independently of age, sex, BP and renal function. Increased aortic stiffness was independently associated with the prevalence of cardiovascular events (P<0.001), reaching its maximal value above the first 2 years of diabetes duration. In conclusion, diabetes duration is an independent determinant of aortic stiffness in subjects with type 2 diabetes, representing about 4% of PWV variability. Diabetes duration is associated with microvascular complications independently of renal function, and with macrovascular complications through the presence of increased aortic stiffness.

Clinical interaction between diabetes duration and aortic stiffness in type 2 diabetes mellitus / Agnoletti D.; Mansour A.S.; Zhang Y.; Protogerou A.D.; Ouerdane S.; Blacher J.; Safar M.E.. - In: JOURNAL OF HUMAN HYPERTENSION. - ISSN 0950-9240. - ELETTRONICO. - 31:3(2017), pp. 189-194. [10.1038/jhh.2016.58]

Clinical interaction between diabetes duration and aortic stiffness in type 2 diabetes mellitus

Agnoletti D.
Primo
;
2017

Abstract

Diabetes complications increase with disease duration. No study was performed on the relationship between aortic stiffness and diabetes duration, taking into account the respective influence of such factors on macro- and microcirculation. In total, 618 subjects with type 2 diabetes (259 men) attending the Department of Internal Medicine of Tizi Ouzou Hospital (Algeria) were studied in collaboration with Hotel-Dieu Hospital (Paris, France). Brachial blood pressure (BP), anthropometric, clinical and biological data were evaluated. Aortic stiffness was estimated by carotid-femoral pulse wave velocity (PWV). From lower to higher tertile of diabetes duration, age, BP and PWV (10.1±2.7 to 12.3±2.8 m s-1) increased, while diabetes control and renal function worsened (all P<0.01). Diabetes duration was independently associated with PWV (R2 =0.035, P<0.0001), even after adjustment for age, BP, heart rate, cardiovascular events and metabolic syndrome. Diabetes duration was significantly correlated to the prevalence of microalbuminuria (OR (95% CL) 1.3 (1.06-1.63), P=0.01), independently of age, sex, BP and renal function. Increased aortic stiffness was independently associated with the prevalence of cardiovascular events (P<0.001), reaching its maximal value above the first 2 years of diabetes duration. In conclusion, diabetes duration is an independent determinant of aortic stiffness in subjects with type 2 diabetes, representing about 4% of PWV variability. Diabetes duration is associated with microvascular complications independently of renal function, and with macrovascular complications through the presence of increased aortic stiffness.
2017
Clinical interaction between diabetes duration and aortic stiffness in type 2 diabetes mellitus / Agnoletti D.; Mansour A.S.; Zhang Y.; Protogerou A.D.; Ouerdane S.; Blacher J.; Safar M.E.. - In: JOURNAL OF HUMAN HYPERTENSION. - ISSN 0950-9240. - ELETTRONICO. - 31:3(2017), pp. 189-194. [10.1038/jhh.2016.58]
Agnoletti D.; Mansour A.S.; Zhang Y.; Protogerou A.D.; Ouerdane S.; Blacher J.; Safar M.E.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/862854
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