Key result
Aliskiren improved flow-mediated dilatation (P<0.001) and increased endothelial progenitor cells (P<0.001) in patients with type 2 diabetes and hypertension, effects abolished by HCTZ substitution.
Why the study?
Does aliskiren improve vascular function and endothelial progenitor cell numbers compared to hydrochlorothiazide in patients with type 2 diabetes and essential hypertension?
Does aliskiren improve vascular function and endothelial progenitor cell numbers compared to hydrochlorothiazide in patients with type 2 diabetes and essential hypertension?
Aliskiren improves endothelial function, arterial stiffness, and EPC numbers independently of its blood pressure-lowering effects in patients with type 2 diabetes and hypertension.
Aliskiren-associated endothelial improvements in diabetic hypertension should not yet change practice; hypothesis-generating and requires randomized outcome trials.
BACKGROUND: The aim of this study was to investigate the effects of aliskiren on vascular function and endothelial progenitor cells (EPCs) in patients with type 2 diabetes and essential hypertension. METHODS: The study enrolled type 2 diabetic patients aged >50 years under stable glycemic control and first diagnosed mild essential hypertension. In phase A (n = 20), patients received aliskiren 150-300 mg daily for 3 months. In phase B (n = 12), hydrochlorothiazide (HCTZ) 12.5-25mg daily substituted for aliskiren for 3 more months. At baseline and at the end of each phase, we assessed (i) brachial blood pressure (BBP); (ii) central aortic systolic pressure (CSP), aortic augmentation index (Aix), and pulse wave velocity (PWV) as markers of arterial stiffness; (iii) brachial artery flow-mediated dilatation (FMD) as a marker of endothelial function; (iv) left ventricular (LV) twisting and untwisting as markers of LV function and (v) EPC numbers in culture of peripheral blood mononuclear cells. RESULTS: Aliskiren similarly reduced BBP and CSP, increased FMD (P < 0.001) and EPC numbers (P < 0.001), decreased PWV and Aix (P < 0.05), and improved LV twisting and untwisting (P < 0.05). Although substitution of HCTZ sustained BBP at similar levels, CSP and echocardiographic indices nearly returned at baseline levels, and the improvement of FMD, PWV, Aix, and EPC numbers was abolished. CONCLUSIONS: Aliskiren had a favorable effect on endothelial function and EPCs, reduced arterial stiffness, and improved LV twisting and untwisting. These effects were independent of BBP lowering, as they were not observed after the achievement of similar values of BBP with HCTZ.
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Raptis et al. (2014) studied Type 2 diabetes and essential hypertension (n=20). Aliskiren vs. Hydrochlorothiazide (HCTZ) 12.5-25mg daily was evaluated on Vascular function (FMD, PWV, Aix), left ventricular function, and endothelial progenitor cell (EPC) numbers (p=<0.001). Aliskiren improved flow-mediated dilatation (P<0.001) and increased endothelial progenitor cells (P<0.001) in patients with type 2 diabetes and hypertension, effects abolished by HCTZ substitution.
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