Evidence map›Paper›PMID 39973402›Full record

ReviewJournal of neuromuscular diseases2025

Taking ACTION to detect myocarditis related to recombinant gene transfer therapy for Duchenne Muscular Dystrophy; Consensus recommendations for cardiac surveillance.

Beth D Kaufman, Aravindhan Veerapandiyan, Jonathan H Soslow, Carol Wittlieb-Weber, Paul Esteso, Aaron K Olson, Renata Shih, Neha Bansal, Ashwin Lal, Katheryn Gambetta and 4 more

Abstract readReviewConsensus Statement
In one paragraph

Review in Journal of neuromuscular diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Real-world outcomes of delandistrogene moxeparvovec gene therapy: Motor outcomes and emerging safety concerns.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  5. Article
  6. Article
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

14 authors.

Beth D KaufmanLucile Packard Children's Hospital, USA.ORCID 0000-0003-0484-5281
Aravindhan VeerapandiyanUniversity of Arkansas for Medical Sciences, Arkansas Children's Hospital, USA.ORCID 0000-0002-3065-3956
Jonathan H SoslowMonroe Carell Jr. Children's Hospital at Vanderbilt, USA.
Carol Wittlieb-WeberThe Children's Hospital of Philadelphia, USA.ORCID 0000-0001-8841-4926
Paul EstesoBoston Children's Hospital, USA.ORCID 0000-0003-3697-6972
Aaron K OlsonSeattle Children's Hospital, USA.
Renata ShihChild Health Research Institute at University of Florida, USA.ORCID 0000-0001-5213-9301
Neha BansalMount Sinai Kravis Children's Hospital, USA.ORCID 0000-0001-7026-3058
Ashwin LalPrimary Children's Hospital, USA.
Katheryn GambettaLurie Chiildren's Hospital, USA.
Daphne HsuChildren's Hospital at Montefiore, USA.
Linda CripeNationwide Children's Hospital, USA.
Chet VillaCincinnati Children's Hospital, USA.
Deipanjan NandiNationwide Children's Hospital, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA viral vector recombinant gene transfer therapy (GTT) has recently been approved by the FDA for males of all ages with Duchenne Muscular Dystrophy (DMD) without limitations regarding preexisting cardiac impairment. Acute myocarditis is a potential life-threatening short-term complication that has been reported following GTT. This immune mediated response can range from troponin elevation to rapid cardiovascular compromise and death, particularly in those with abnormal cardiac status at baseline. Early detection of cardiac compromise is essential to optimize outcomes.

objectivesThe primary objective of this consensus statement is to advocate for caution with DMD GTT patient selection and to initiate preemptive monitoring for those who may be at increased risk for cardiac adverse events. Secondary objective is to deepen our understanding of short and long-term impact of DMD gene therapies on the heart.

methodsA national learning network of pediatric cardiologists with expertise in DMD developed recommendations for cardiac surveillance of DMD males receiving GTT based on available evidence and expert consensus opinion. A monitoring and treatment plan for standard and high cardiac risk patients was developed.

conclusionPartnership of cardiologists with GTT prescribers is essential to identify patient-specific considerations that might influence risk for adverse cardiac events and alter post infusion monitoring and management plans. Consistency in cardiac surveillance practices across centers will expedite our knowledge regarding potential short- and long-term cardiac effects of GTT for DMD.

Indexed as

Genetic TherapyGene Transfer TechniquesMuscular Dystrophy, DuchenneMyocarditisHumansMalecardiac adverse eventduchenne muscular dystrophyexpert consensusgenetic therapymyocarditis

Identifiers

PMID39973402
PMCPMC13142859

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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.