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Published on: April 8, 2013
Impact of mineralocorticoid receptor antagonists on changes in cardiac structure and function of left ventricular
Xiaobo Li1, Yue Qi, Yuqiong Li
1State Key Laboratory of Medical Genomics, Ruijin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Background:
A comprehensive evaluation of the benefits of mineralocorticoid receptor antagonists on cardiac remodeling is lacking. We aimed to evaluate the impact of mineralocorticoid receptor antagonists on changes in cardiac structure and function of left ventricular dysfunction.
Methods And Results:
Articles were identified by online searches in PubMed, EMBASE, Cochrane, and ClinicalTrials.gov databases before June 2012, by hand searches of reviews and relevant journals, and by contact with the authors. Qualified articles were restricted to randomized controlled trials. There were, respectively, 12, 4, and 3 qualified trials that randomized 572, 647, and 407 patients to spironolactone, canrenoate, and eplerenone, and 531, 655, and 395 patients to placebo or active treatment, respectively. Overall, under mineralocorticoid receptor antagonist treatment there was improvement in left ventricular ejection fraction (weighted mean difference, 2.97; 95% confidence interval [95% CI], 2.26-3.67; P<0.0005), left ventricular end-systolic and end-diastolic volume index (weighted mean difference, -5.64; 95% CI, -7.94 to -3.34; P<0.0005 and weighted mean difference, -7.46; 95% CI, -11.63 to -3.3; P<0.0005), serum amino-terminal peptide of procollagen type-III (weighted mean difference, -1.12; 95% CI, -1.49 to -0.74; P<0.0005), B-type natriuretic peptide (weighted mean difference, -67.06; 95% CI, -91.24 to -42.88; P<0.0005), peak velocities of early mitral inflow (E; weighted mean difference, -9.57; 95% CI, -12.98 to -6.17; P<0.0005), and E wave deceleration time (weighted mean difference, 7.08; 95% CI, 4.07-10.09; P<0.0005). There was low probability of heterogeneity and publication bias.
Conclusions:
Our findings demonstrate that mineralocorticoid receptor antagonist treatment may exert beneficial effects on the reversal of cardiac remodeling and improvement of left ventricular function.
Insights
Mineralocorticoid receptor antagonists improve cardiac structure and function in patients with left ventricular dysfunction. This meta-analysis of randomized controlled trials shows significant benefits in ejection fraction and reduced cardiac volumes.
Area of Science:
- Cardiology
- Pharmacology
- Medical Research
Background:
- Limited comprehensive evaluations exist for mineralocorticoid receptor antagonists (MRAs) in cardiac remodeling.
- Left ventricular dysfunction necessitates understanding treatments that improve cardiac structure and function.
Purpose of the Study:
- To evaluate the impact of MRAs on cardiac remodeling in patients with left ventricular dysfunction.
- To synthesize evidence from randomized controlled trials on MRA efficacy.
Main Methods:
- Systematic search of PubMed, EMBASE, Cochrane, and ClinicalTrials.gov databases.
- Inclusion of randomized controlled trials (RCTs) investigating spironolactone, canrenoate, and eplerenone.
- Meta-analysis of data from 12, 4, and 3 RCTs, respectively.
Main Results:
- MRAs significantly improved left ventricular ejection fraction (WMD, 2.97; P<0.0005).
- Treatment led to reductions in left ventricular end-systolic and end-diastolic volumes (WMD, -5.64 and -7.46; P<0.0005).
- Biomarkers of cardiac remodeling and dysfunction, including NT-pro-III-P and BNP, were significantly reduced.
Conclusions:
- Mineralocorticoid receptor antagonist treatment demonstrates beneficial effects on reversing cardiac remodeling.
- MRAs contribute to the improvement of left ventricular function in relevant patient populations.
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