Evidence map›Paper›PMID 41295342›Full record

ReviewJournal of cardiovascular development and disease2025

The Importance of Early Diagnosis and Treatment to Limit the Impact of Dystrophic Cardiomyopathy-We've Seen This Film Before, and We Didn't Like the Ending.

DeWayne Townsend

Abstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

DeWayne TownsendDepartment of Integrative Biology and Physiology, Medical School, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0002-0246-9692

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is a rare neuromuscular disorder that is characterized by skeletal muscle wasting, loss of ambulation, and respiratory failure. In addition to these obvious external signs of disease, heart disease, the leading cause of death in DMD patients, is also progressing. Dystrophic cardiomyopathy is largely clinically silent with cardiac dysfunction masked by concurrent loss of skeletal muscle function. In older DMD patients the prevalence of heart disease is very high, offering the unique potential to predict impending heart disease from a much earlier genetic diagnosis. Randomized clinical trial data and subsequent retrospective studies in DMD demonstrate that early initiation of cardiac directed therapy results in a significant delay in the onset of cardiac dysfunction and prolonged survival. Clinical guidelines reflect this, recommending the initiation of cardiac therapy at an age of 10 years old, even in the absence of documented contractile dysfunction. Despite this data, a recent examination of registry data reveals that most DMD patients are not receiving the treatments recommended by these guidelines. While there is great excitement regarding newly developed therapies for DMD, there are so many signs that deploying the safe and effective therapies we already have can improve clinical outcomes. This review will highlight the basic science behind and clinical importance of using early cardiac directed therapy to extend the duration and quality of life of DMD patients and will offer some suggestions that may aid in achieving this goal.

Indexed as

Duchenne muscular dystrophydystrophic cardiomyopathyheart diseaseprophylactic treatment

Identifiers

PMID41295342
PMCPMC12653760

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.