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Anti-Remodeling Cardiac Therapy in Patients With Duchenne Muscular Dystrophy, Meta-Analysis Study
Bruria Hirsh Raccah1,2, Bar Biton1, Offer Amir2,3
1Division of Clinical Pharmacy, Faculty of Medicine, School of Pharmacy, Institute for Drug Research, the Hebrew University of Jerusalem, Jerusalem, Israel.
Insights
Anti-remodeling cardiac therapy for Duchenne muscular dystrophy cardiomyopathy (DMDCM) shows promise. This meta-analysis found that treatments decreased heart rate and improved left ventricular ejection fraction in DMDCM patients.
Area of Science:
- Cardiology
- Genetics
- Pharmacology
Background:
- Duchenne muscular dystrophy (DMD) frequently leads to cardiomyopathy (DMDCM) in adult patients.
- Current treatment efficacy for DMDCM is not well-established, leading to under-treatment.
- There is a need to evaluate anti-remodeling cardiac therapies for DMDCM.
Purpose of the Study:
- To assess the efficacy of anti-remodeling cardiac therapy in Duchenne muscular dystrophy cardiomyopathy (DMDCM).
- To evaluate the impact of these therapies on mortality, left ventricular ejection fraction (LVEF), natriuretic peptide levels (BNP), and heart rate (HR).
Main Methods:
- A systematic meta-analysis of randomized control trials, case-control studies, and observational studies.
- Searched databases: PubMed (MEDLINE), Embase, and Cochrane Library up to January 2021.
- Included studies assessing cardiovascular outcomes and mortality in patients using specific cardiac medications (ACE inhibitors, ARBs, beta-blockers, MRAs, Ivabradine).
Main Results:
- Twelve studies with 439 patients were analyzed.
- Pharmacologic therapy significantly reduced heart rate (HR) by -17 bpm (p < 0.01).
- Left ventricular ejection fraction (LVEF) improved by 3.77% (p < 0.03), with trends towards reduced mortality and BNP levels.
Conclusions:
- Pharmacologic treatment in DMDCM patients is linked to decreased heart rate and improved LVEF.
- Guideline-directed heart failure therapy may benefit patients with DMDCM.
- Further research is warranted to confirm mortality benefits.
Abstract:
Background: Almost all Duchenne muscular dystrophy (DMD) patients that reach their 30s present cardiomyopathy. As a result, this population remains under-treated. There is no sufficient proof of the efficacy of anti-remodeling cardiac therapy for DMD cardiomyopathy (DMDCM). We aim to assess the efficacy of anti-remodeling cardiac therapy for DMDCM by using meta-analysis. Methods: PubMed (MEDLINE), Embase, and Cochrane library were searched through January 2021. Randomized control trials, case-control studies, and observational studies that reported assessments of cardiovascular outcomes and death of participants using angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, beta-blockers, mineralocorticoid-receptor antagonists and Ivabradine, were included. The primary outcome was total mortality. Secondary outcomes included changes in left ventricular ejection fraction (LVEF), serum natriuretic peptide levels (BNP), and heart rate (HR). Data were extracted for eligibility by two independent reviewers. Random-effects meta-analysis was used to pool results. Results: Twelve studies with 439 patients were included in our meta-analysis. Treated patients have lower HR, mean difference of -17 beats per minute (CI [-25]-[-9], p < 0.01). The LVEF was improved in treated patients, with a mean difference of LVEF of 3.77% (CI 0.44-7.12, p < 0.03). Although mortality rates did not reach statistical significance there was a trend for total mortality reduction (hazard ratio 0.36, CI (0.1-1.25), p = 0.107) and for BNP reduction (SSMD: 0.141, CI ([-0.19]-[0.47]), p = 0.3). Conclusion: Pharmacologic treatment for DMDCM patients is associated with decreased HR and improved LVEF. Therefore, DMDCM patients may benefit from implementing guideline therapy for HF.
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