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Comparative efficacy of nifedipine-retard and atenolol in correction of target organ damage in patients with essential hypertension

https://doi.org/10.18705/1607-419X-2006-12-3-194-199

Abstract

The aim of the study was to assess the relationship between antihypertensive effect of nifedipine-retard and atenolol long-term therapy and changes of target organ damage (heart, carotid arteries, endothelial function) in patients with essential hypertension (HT) 2 stage. 45 patients with AH were included in the open prospective randomized study: 24 received nifedipine-retard 40 mg per day, 21 received atenolol 50 - 100 mg per day. There were no clinical and haemodynamic discrepanses between the groups at basline. Ambulatory blood pressure monitoring (ABPM), echocardiography (EchoCG), assess of endothelium-dependent and endothelium-independent vasodilatation were performed at basal state (after 14 days wash-out period) and after 6-month therapy. Both nifedipine-retard and atenolol had comparable and apparent hypotensive effect. The regression of left ventricular hypertrophy and the improvement of left ventricle diastolic function became evident during nifedipine-retard therapy in contrast to atenolol treatment. Long-term nifedipine-retard therapy is accompanied by an increase of volume flow velocity in arteria radialis and leads to correction of endothelium dysfunction in patients with HT.

About the Authors

I. V. Emelyanov
Research Institute of Cardiology
Russian Federation


S. V. Villevalde
Research Institute of Cardiology
Russian Federation


E. A. Lyasnikova
Research Institute of Cardiology
Russian Federation


O. M. Moiseeva
Research Institute of Cardiology
Russian Federation


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Review

For citations:


Emelyanov I.V., Villevalde S.V., Lyasnikova E.A., Moiseeva O.M. Comparative efficacy of nifedipine-retard and atenolol in correction of target organ damage in patients with essential hypertension. "Arterial’naya Gipertenziya" ("Arterial Hypertension"). 2006;12(3):194-199. (In Russ.) https://doi.org/10.18705/1607-419X-2006-12-3-194-199

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