Evidence map›Paper›PMID 40562489›Full record

ArticleJACC. Basic to translational science2025

Long-Term Dystrophin Replacement Therapy in Duchenne Muscular Dystrophy Causes Cardiac Inflammation.

Anne Forand, Sophie Moog, Nathalie Mougenot, Mégane Lemaitre, Caroline Sevoz-Couche, Zoheir Guesmia, Laura Virtanen, Lorenzo Giordani, Antoine Muchir, France Pietri-Rouxel

Abstract read
In one paragraph

Article in JACC. Basic to translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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
  6. Review
  7. Review
  8. Review
  9. 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

10 authors.

Anne ForandInovarion, Paris, France; Centre de Recherche en Myologie-Sorbonne Université-UMRS974-Inserm-Institut de Myologie-Faculté de Médecine de la Pitié Salpêtrière, Paris, France. Electronic address: anne.forand@inovarion.com.
Sophie MoogInovarion, Paris, France; Centre de Recherche en Myologie-Sorbonne Université-UMRS974-Inserm-Institut de Myologie-Faculté de Médecine de la Pitié Salpêtrière, Paris, France.
Nathalie MougenotSorbonne Université-UPMC Paris 06-INSERM UMS28-Phénotypage du petit animal-Faculté de Médecine Pierre et Marie Curie, Paris, France.
Mégane LemaitreSorbonne Université-UPMC Paris 06-INSERM UMS28-Phénotypage du petit animal-Faculté de Médecine Pierre et Marie Curie, Paris, France.
Caroline Sevoz-CoucheSorbonne Université-UPMC Université Paris 06-INSERM UMRS1158-Neurophysiologie Respiratoire Expérimentale et Clinique-Faculté de Médecine Pierre et Marie Curie, Paris, France; Université Paris 12 Saclay, UVSQ-UMR 1018-CESP-Inserm-Faculté de Médecine Bicêtre, Le Kremlin-Bicêtre, France.
Zoheir GuesmiaCentre de Recherche en Myologie-Sorbonne Université-UMRS974-Inserm-Institut de Myologie-Faculté de Médecine de la Pitié Salpêtrière, Paris, France.
Laura VirtanenCentre de Recherche en Myologie-Sorbonne Université-UMRS974-Inserm-Institut de Myologie-Faculté de Médecine de la Pitié Salpêtrière, Paris, France.
Lorenzo GiordaniCentre de Recherche en Myologie-Sorbonne Université-UMRS974-Inserm-Institut de Myologie-Faculté de Médecine de la Pitié Salpêtrière, Paris, France.
Antoine MuchirCentre de Recherche en Myologie-Sorbonne Université-UMRS974-Inserm-Institut de Myologie-Faculté de Médecine de la Pitié Salpêtrière, Paris, France.
France Pietri-RouxelCentre de Recherche en Myologie-Sorbonne Université-UMRS974-Inserm-Institut de Myologie-Faculté de Médecine de la Pitié Salpêtrière, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Micro-dystrophin replacement gene therapy is currently under clinical trials in Duchenne muscular dystrophy (DMD) patients. However, recent adverse cardiac events has led to serious concerns about this therapeutic intervention. We studied the long-term effect of dystrophin replacement strategies in a severe model of DMD (mdx; utrophin

Indexed as

Duchenne muscular dystrophygene therapyheartinflammationmicro-dystrophin

Identifiers

PMID40562489
PMCPMC12230499

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.