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Effects of nebivolol and atenolol on central aortic pressure in hypertensive patients: a multicenter, randomized,
Josep Redón1, Jose M Pascual-Izuel, Enrique Rodilla
1Hospital Clínico Universitario de Valencia, INCLIVA, University of Valencia and CIBERObn , ISC III.
Insights
Nebivolol had a lesser impact on the augmentation index compared to atenolol in hypertensive patients. This study compared the effects of these two common blood pressure medications.
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Research
Background:
- Essential hypertension affects a significant portion of the adult population.
- Augmentation index is a key indicator of arterial stiffness and cardiovascular risk.
- Nebivolol and atenolol are commonly prescribed antihypertensive medications with different mechanisms of action.
Purpose of the Study:
- To compare the mean change in augmentation index between hypertensive patients treated with nebivolol versus atenolol.
- To evaluate the impact of nebivolol and atenolol on arterial stiffness markers.
Main Methods:
- A multicenter, double-blind, randomized study involving 138 outpatients with mild to moderate essential hypertension.
- Patients received either nebivolol 5 mg or atenolol 50 mg daily, with options for dose titration and addition of hydrochlorothiazide.
- Augmentation index was measured over a 10-week follow-up period.
Main Results:
- Nebivolol demonstrated a significantly lesser modification of the mean augmentation index compared to atenolol after 10 weeks (mean difference 3.1%, p = 0.027).
- While both drugs similarly reduced central and peripheral blood pressure, a higher proportion of patients on atenolol required a diuretic.
- Baseline characteristics and response in blood pressure were comparable between the two groups.
Conclusions:
- Nebivolol exerts a less pronounced effect on the augmentation index than atenolol in patients with essential hypertension.
- These findings suggest differential effects of nebivolol and atenolol on arterial properties beyond blood pressure reduction.
Introduction:
The main objective was to compare the mean change in augmentation index of hypertensive patients treated with nebivolol or atenolol.
Methods:
Multicenter, double-blind randomized study conducted in six Spanish centers. We enrolled outpatients between the ages of 40 and 65 years with mild or moderate essential hypertension (systolic blood pressure, SBP ≥ 140 mmHg to ≤ 179 mmHg and diastolic blood pressure, DBP ≥ 90 mmHg to ≤ 109 mmHg after a 2-week run-in placebo period). Patients received nebivolol 5 mg or atenolol 50 mg once daily. At week 3, atenolol could be titrated up to 100 mg qd for non-responders. Additionally, patients not achieving normal blood pressure after 6 weeks could be treated with 25 mg hydrochlorothiazide. Follow-up visits were at 3, 6 and 10 weeks.
Results:
The final study population of 138 patients (58% men; median age 52.6 years, range 40-67 years) was randomized into two groups of 69 patients each. Baseline characteristics of the two groups were similar. At the screening visit, 69% presented with mild hypertension. Nebivolol modified the mean augmentation index to a lesser extent than atenolol after 10 weeks (mean difference 3.1%, 95% CI 0.55-5.69; p = 0.027). A higher proportion of patients in the atenolol group required a diuretic. Reductions in central aortic pressure and peripheral arterial pressure were similar for both treatment groups.
Conclusions:
The study confirms that nebivolol produces a less pronounced impact on augmentation index than atenolol.
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