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Reduction in Left Ventricular Wall Stress and Improvement in Function in Failing Hearts using Algisyl-LVR
Published on: April 8, 2013
Randomized, double-blind, multicenter, placebo-controlled study evaluating the effect of aldosterone antagonism with
James E Udelson1, Arthur M Feldman, Barry Greenberg
1Tufts Medical Center, 750 Washington Street, Boston, MA 02111, USA. JUdelson@tuftsmedicalcenter.org
Insights
Eplerenone did not improve left ventricular remodeling in patients with mild-to-moderate heart failure (HF). This aldosterone antagonist showed no significant changes in cardiac volumes or ejection fraction over 36 weeks.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Aldosterone antagonism is established for advanced heart failure (HF).
- Limited data exist on aldosterone antagonism in mild-to-moderate HF.
- Previous studies focused on severe HF or post-myocardial infarction patients.
Purpose of the Study:
- To evaluate the efficacy of eplerenone in mild-to-moderate HF patients.
- To assess the impact of aldosterone antagonism on left ventricular (LV) remodeling.
- To investigate changes in LV volumes and ejection fraction with eplerenone treatment.
Main Methods:
- Multicenter, randomized, double-blind, placebo-controlled trial.
- 226 patients with New York Heart Association class II/III HF and LV ejection fraction (EF) ≤35%.
- Eplerenone 50 mg/day versus placebo, plus contemporary background therapy for 36 weeks.
Main Results:
- No significant difference in LV end-diastolic or end-systolic volume index changes between groups.
- Eplerenone reduced procollagen type I N-terminal propeptide and B-type natriuretic peptide.
- No improvement in HF symptoms or quality-of-life measures observed.
Conclusions:
- Eplerenone (50 mg/day) did not alter LV remodeling parameters in stable, mild-to-moderate HF patients.
- Aldosterone antagonism showed no detectable effect on LV remodeling in this population.
- Further research may be needed to clarify the role of aldosterone antagonists in less severe HF.
Background:
Aldosterone antagonism has been studied in patients with advanced heart failure (HF) and also in patients with post-myocardial infarction and left ventricular (LV) dysfunction with HF symptoms. Few data are available on effects of aldosterone antagonism in patients with mild-to-moderate HF.
Methods And Results:
In a multicenter, randomized, double-blind, placebo-controlled study in patients with mild-to-moderate HF and LV systolic dysfunction, patients with New York Heart Association class II/III HF and LV ejection fraction (EF) < or =35% were randomly assigned to receive eplerenone 50 mg/d versus placebo in addition to contemporary background therapy. Quantitative radionuclide ventriculograms to assess LV volumes and ejection fraction were performed at baseline and again after 9 months of double-blind treatment and were analyzed in a central core laboratory, blinded to treatment. The primary efficacy analysis was the between-group comparison of the change in LV end-diastolic volume index. Secondary analyses examined changes in LV end-systolic volume index and ejection fraction as well as markers of collagen turnover. Of the total 226 patients enrolled, 117 were randomly assigned to receive eplerenone and 109 to receive placebo. There was high use of contemporary background therapy at baseline, with > 90% use of angiotensin-converting enzyme inhibitors and/or angiotensin receptor blockers and > 90% use of beta-blockers. Over 36 weeks of treatment, there was no apparent between-group difference in the changes in end-diastolic volume index or end-systolic volume index. There was a reduction in the collagen turnover marker procollagen type I N-terminal propeptide and plasma B-type natriuretic peptide in the eplerenone group compared with placebo (P=0.01 and P=0.04, respectively). There was no change in symptom status or quality-of-life measures.
Conclusions:
In a clinically stable, well-treated population of patients with mild-to-moderate HF symptoms and LV dysfunction, 36 weeks of treatment of aldosterone antagonism with eplerenone at a dose of 50 mg daily had no detectable effect on parameters of LV remodeling.
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