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Published on: May 26, 2022
Aliskiren improves blood pressure control and prevents cardiac damage in high-risk hypertensive subjects
A Mazza1, D Montemurro, M Zuin
1Department of Internal Medicine, Santa Maria della Misericordia Hospital Rovigo, Italy - domenico.rubello@libero.it.
Insights
Aliskiren effectively lowered blood pressure (BP) and reduced cardiac damage in high-risk patients with impaired renal function. This antihypertensive treatment was safe and reduced the need for other BP medications.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Hypertension is a major risk factor for cardiovascular and renal diseases.
- Many patients require multiple antihypertensive medications to achieve blood pressure control.
- Patients with mild renal impairment and uncontrolled hypertension present a significant clinical challenge.
Purpose of the Study:
- To evaluate the efficacy and safety of Aliskiren in high-risk hypertensive patients with mild renal impairment.
- To assess Aliskiren's effect on cardiac damage, specifically left ventricular mass index (LVMI).
- To determine changes in blood pressure (BP) and renal function (eGFR) during treatment.
Main Methods:
- A 12-month longitudinal study involving 106 high-risk hypertensive patients with mild renal impairment.
- Patients received Aliskiren 150-300 mg once-daily, with BP monitored clinically and via 24-hour ambulatory BP monitoring (ABPM).
- Echocardiography for LVMI and biochemical tests for eGFR were performed at baseline and end-of-study.
Main Results:
- Significant reductions in both clinic and ABPM systolic and diastolic BP values were observed (P<0.0001).
- Left ventricular mass index (LVMI) significantly decreased (P<0.0001), indicating reduced cardiac damage.
- Estimated glomerular filtration rate (eGFR) remained stable, and Aliskiren was well-tolerated, with few adverse events.
Conclusions:
- Aliskiren effectively lowers BP and reduces LVMI in hypertensive patients with mild renal impairment.
- The drug demonstrated a favorable safety profile, even when used with ACE inhibitors or ARBs.
- Aliskiren treatment led to a significant reduction in the number of concomitant antihypertensive drugs needed.
Aim:
Longitudinal study aimed to evaluate the antihypertensive efficacy, safety and the effect on cardiac damage of Aliskiren, administered to a group of high-risk hypertensive patients with mild impairment of renal function and uncontrolled blood pressure (BP) despite a two-drug antihypertensive treatment.
Methods:
One hundred and six patients (56 men and 50 females) aged 61.9±12.7 years, were assigned to receive Aliskiren 150-300 mg once-daily for 12 months. Clinic BP measurements were taken at every follow-up visit (1st, 6th and 12th month), while biochemical tests, estimated glomerular filtration rate (eGFR), 24-hours ambulatory BP measurements (ABMP) and echocardiography were evaluated at baseline and at the end of follow-up. Analysis of variance for repeated measures compared BP, left ventricular mass index (LVMI) and eGFR values changes.
Results:
A significant reduction (all P<0.0001) of clinic systolic (-28.6 mmHg) and diastolic (-12.8 mmHg) BP values, mean 24h-systolic (-12.3 mmHg) and 24h-diastolic (-6.5 mmHg), day-time systolic (-11.5 mmHg) and diastolic (-6.4 mmHg), night-time systolic (-11.9 mmHg) and diastolic (-7 mmHg) ABPM values and in the use of antihypertensive drugs was observed (3.0±0.9 vs. 2.0±0.7, p=0.01). LVMI was significantly reduced (130.2±36.1 vs. 115.9±33.4 g/m2, P<0.0001); eGFR was steady (75.3±17.3 vs. 73.1±21.5 ml/min/1.73m2, P>0.05). Putative adverse events caused withdrawal of 7 subjects (6 for gastrointestinal disturbances, 1 for alopecia).
Conclusion:
Aliskiren was effective in decreasing both clinical and ABPM values and in reducing LVMI in both genders without any influence on eGFR. The treatment resulted safe, even in combination with ACE-inhibitors and angiotensin II receptor blockers. A significant reduction in the use of concomitant antihypertensive drugs was observed.
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