Evidence map›Paper›PMID 39113268›Full record

ArticleJournal of cachexia, sarcopenia and muscle2024

Different outcomes of endurance and resistance exercise in skeletal muscles of Oculopharyngeal muscular dystrophy.

Alexis Boulinguiez, Jamila Dhiab, Barbara Crisol, Laura Muraine, Ludovic Gaut, Corentin Rouxel, Justine Flaire, Hadidja-Rose Mouigni, Mégane Lemaitre, Benoit Giroux and 8 more

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

18 authors.

Alexis BoulinguiezDepartment of Biological Sciences, School of Life Sciences and the Environment, Royal Holloway University of London, London, UK.ORCID 0000-0001-6886-6140
Jamila DhiabCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.ORCID 0000-0002-2684-0097
Barbara CrisolCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.ORCID 0000-0003-2026-2844
Laura MuraineCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.
Ludovic GautCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.
Corentin RouxelCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.
Justine FlaireCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.
Hadidja-Rose MouigniCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.
Mégane LemaitreSorbonne Université, INSERM, UMS28 - Phénotypage du petit animal, Paris, France.
Benoit GirouxSorbonne Université, INSERM, UMS28 - Phénotypage du petit animal, Paris, France.
Lucie AudouxUniversité Paris Cité, CNRS, INSERM, Institut Cochin, Paris, France.
Benjamin SaintPierreUniversité Paris Cité, CNRS, INSERM, Institut Cochin, Paris, France.
Arnaud FerryCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.ORCID 0000-0002-6050-4556
Vincent MoulyCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.ORCID 0000-0003-3809-4033
Gillian Butler-BrowneCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.ORCID 0000-0002-3431-242X
Elisa NegroniCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.ORCID 0000-0001-8302-2544
Alberto MalerbaDepartment of Biological Sciences, School of Life Sciences and the Environment, Royal Holloway University of London, London, UK.ORCID 0000-0002-0536-5231
Capucine TrolletCentre de Recherche en Myologie, Sorbonne Université, INSERM, Institut de Myologie, Paris, France.ORCID 0000-0002-4838-3712

Funding

Agence Nationale pour la recherche ANR-18-HDHL-0002-05Association Institut de MyologieFondation Recherche Médicale EQUIPE FRM EQU201903007784INSERMSorbonne Université
6 · The paper itself

Abstract

backgroundExercise is widely considered to have beneficial impact on skeletal muscle aging. In addition, there are also several studies demonstrating a positive effect of exercise on muscular dystrophies. Oculopharyngeal muscular dystrophy (OPMD) is a late-onset autosomal dominant inherited neuromuscular disorder caused by mutations in the PAPBN1 gene. These mutations consist in short (1-8) and meiotically stable GCN trinucleotide repeat expansions in its coding region responsible for the formation of PAPBN1 intranuclear aggregates. This study aims to characterize the effects of two types of chronic exercise, resistance and endurance, on the OPMD skeletal muscle phenotype using a relevant murine model of OPMD.

methodsIn this study, we tested two protocols of exercise. In the first, based on endurance exercise, FvB (wild-type) and A17 (OPMD) mice underwent a 6-week-long motorized treadmill protocol consisting in three sessions per week of running 20 cm/s for 20 min. In the second protocol, based on resistance exercise generated by chronic mechanical overload (OVL), surgical removal of gastrocnemius and soleus muscles was performed, inducing hypertrophy of the plantaris muscle. In both types of exercise, muscles of A17 and FvB mice were compared with those of respective sedentary mice. For all the groups, force measurement, muscle histology, and molecular analyses were conducted.

resultsFollowing the endurance exercise protocol, we did not observe any major changes in the muscle physiological parameters, but an increase in the number of PABPN1 intranuclear aggregates in both tibialis anterior (+24%, **P = 0.0026) and gastrocnemius (+18%, ****P < 0.0001) as well as enhanced collagen deposition (+20%, **P = 0.0064 in the tibialis anterior; +35%, **P = 0.0042 in the gastrocnemius) in the exercised A17 OPMD mice. In the supraphysiological resistance overload protocol, we also observed an increased collagen deposition (×2, ****P < 0.0001) in the plantaris muscle of A17 OPMD mice which was associated with larger muscle mass (×2, ****P < 0.0001) and fibre cross sectional area (×2, ***P = 0.0007) and increased absolute maximal force (×2, ****P < 0.0001) as well as a reduction in PABPN1 aggregate number (-16%, ****P < 0.0001).

conclusionsRunning exercise and mechanical overload led to very different outcome in skeletal muscles of A17 mice. Both types of exercise enhanced collagen deposition but while the running protocol increased aggregates, the OVL reduced them. More importantly OVL reversed muscle atrophy and maximal force in the A17 mice. Our study performed in a relevant model gives an indication of the effect of different types of exercise on OPMD muscle which should be further evaluated in humans for future recommendations as a part of the lifestyle of individuals with OPMD.

Indexed as

Disease Models, AnimalMuscle, SkeletalMuscular Dystrophy, OculopharyngealPhysical Conditioning, AnimalResistance TrainingAnimalsMaleMicePhysical EnduranceAtrophyExerciseFibrosisOPMDPAPBN1Skeletal muscle

Identifiers

PMID39113268
PMCPMC11446690

What Socratic 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 Socratic graph.