Evidence map›Paper›PMID 40381228›Full record

ArticleRedox biology2025

Repurposed Nrf2 activator dimethyl fumarate rescues muscle inflammation and fibrosis in an aggravated mdx mouse model of Duchenne muscular dystrophy.

Stephanie Kourakis, Cara A Timpani, Ryan M Bagaric, Bo Qi, Benazir A Ali, Rebecca Boyer, Guinevere Spiesberger, Nitika Kandhari, Xu Yan, Jujiao Kuang and 6 more

Abstract read
In one paragraph

Article in Redox biology, 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. Review
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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

16 authors.

Stephanie KourakisInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia.
Cara A TimpaniInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia; Department of Medicine - Western Health, Melbourne Medical School, The University of Melbourne, St Albans, Victoria, Australia.
Ryan M BagaricInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia.
Bo QiInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia.
Benazir A AliInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia.
Rebecca BoyerInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia.
Guinevere SpiesbergerInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia.
Nitika KandhariMonash Genomics and Bioinformatics Platform, Biomedical Discovery Institute, Monash University, Clayton, Victoria, Australia.
Xu YanInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Sarcopenia Research Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia.
Jujiao KuangInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia.
Ankita TulangekarInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia.
Judy B de HaanBasic Science Domain, Oxidative Stress Laboratory, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Baker Department of Cardiometabolic Health, University of Melbourne, Parkville, Victoria, Australia.
Deanna Deveson-LucasMonash Genomics and Bioinformatics Platform, Biomedical Discovery Institute, Monash University, Clayton, Victoria, Australia.
Nicole StupkaInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Department of Medicine - Western Health, Melbourne Medical School, The University of Melbourne, St Albans, Victoria, Australia.
Dirk FischerDivision of Neuropediatric and Developmental Medicine, University Children's Hospital of Basel (UKBB), Basel, Switzerland.
Emma RybalkaInstitute for Health and Sport (IHeS), Victoria University, Melbourne, Victoria, Australia; Inherited and Acquired Myopathies Program, Australian Institute for Musculoskeletal Science (AIMSS), St Albans, Victoria, Australia. Electronic address: emma.rybalka@vu.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In inherited neuromuscular disease, Duchenne muscular dystrophy (DMD), glucocorticoids significantly slow disease progression yet impart side effects severe enough to preclude use in a significant proportion of patients. Extending our findings that acute treatment with FDA approved multiple sclerosis drug, dimethyl fumarate (DMF), rescues muscle pathology in juvenile mdx mice, we aimed to conduct tiered pre-clinical testing toward translation. To aggravate disease phenotype in adult mdx muscles that usually lack human equivalent muscle pathology, we used bi-weekly treadmill running for 4 weeks which increased plasma DMD biomarker, creatine kinase, by 2-fold and quadriceps fibrosis by ∼30 %. Using this model, we screened DMF for 5 weeks in a head-to-head comparison, and in combination, with standard-of-care prednisone (PRED), to model the most likely clinical trial scenario. We show comparable efficacy between DMF and PRED at reducing inflammation via NF-κB suppression and CD68

Indexed as

Dimethyl FumarateMuscular Dystrophy, DuchenneNF-E2-Related Factor 2AnimalsDisease Models, AnimalFibrosisHumansInflammationMaleMiceMice, Inbred mdxMuscle, SkeletalDimethyl FumarateNfe2l2 protein, mouseNF-E2-Related Factor 2Dimethyl fumarateDuchenne muscular dystrophyMuscle pathologyTherapeutics

Identifiers

PMID40381228
PMCPMC12143770

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.