Why the study?
Does nifedipine-retard improve target organ damage compared to atenolol in patients with essential hypertension stage 2?
Does nifedipine-retard improve target organ damage compared to atenolol in patients with essential hypertension stage 2?
Nifedipine-retard provides superior regression of left ventricular hypertrophy and improvement in endothelial function compared to atenolol in patients with stage 2 essential hypertension, despite comparable blood pressure lowering.
Supports preferring nifedipine-retard over atenolol for LVH regression in stage 2 hypertension; extends RCT evidence for target-organ benefits beyond equivalent BP reduction.
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.
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Emelyanov et al. (2006) studied this question.
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