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.

Frontiers in Pharmacology
|February 7, 2022
PubMed

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.

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