Evidence map›Paper›PMID 41213899›Full record

ArticleNature communications2025

Alterations in peroxisome-mitochondria interplay in skeletal muscle accelerate muscle dysfunction.

Marco Scalabrin, Eloisa Turco, Ilaria Davigo, Riccardo Filadi, Leonardo Nogara, Gaia Gherardi, Lucia Barazzuol, Andrea Armani, Giulia Trani, Samuele Negro and 16 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
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

26 authors.

Marco Scalabrin *Department of Biomedical Sciences, University of Padova, Padova, Italy.
Eloisa Turco *Department of Biomedical Sciences, University of Padova, Padova, Italy.
Ilaria DavigoDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Riccardo FiladiDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0002-5871-2620
Leonardo NogaraDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0002-7009-8707
Gaia GherardiDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Lucia BarazzuolDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Andrea ArmaniDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Giulia TraniDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0003-4289-1799
Samuele NegroDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Anais Franco-RomeroDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Yorrick JaspersLaboratory Genetic Metabolic Diseases, Department of Laboratory Medicine, Amsterdam University Medical Center, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-9153-5734
Elisa BaschieraClinical Genetics Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.
Rossella De CegliTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.ORCID http://orcid.org/0000-0002-8526-8692
Eugenio Del PreteTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.ORCID http://orcid.org/0000-0003-3214-9021
Tito CaliDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0002-8901-1659
Bert BlaauwDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0002-4167-5106
Leonardo SalviatiClinical Genetics Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0001-5642-9963
Michela RigoniDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Cristina MammucariDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0003-3220-9610
Sylvie Caspar-BauguilInstitute of Metabolic and Cardiovascular Diseases (I2MC), Inserm, Toulouse University, Toulouse, France.
Cedric MoroInstitute of Metabolic and Cardiovascular Diseases (I2MC), Inserm, Toulouse University, Toulouse, France.ORCID http://orcid.org/0000-0003-4294-0597
Paola PizzoDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0001-6077-3265
Marco SandriDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0001-8509-7558
Stephan KempLaboratory Genetic Metabolic Diseases, Department of Laboratory Medicine, Amsterdam University Medical Center, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0003-2023-064X
Vanina RomanelloDepartment of Biomedical Sciences, University of Padova, Padova, Italy. vanina.romanello@unipd.it.ORCID http://orcid.org/0000-0002-7712-6416

Funding

AFM-Téléthon (French Muscular Dystrophy Association) 24465Fondazione Telethon (Telethon Foundation) GMR22T1055
6 · The paper itself

Abstract

Skeletal muscles, which constitute 40-50% of body mass, regulate whole-body energy expenditure and glucose and lipid metabolism. Peroxisomes are dynamic organelles that play a crucial role in lipid metabolism and clearance of reactive oxygen species, however their role in skeletal muscle remains poorly understood. To clarify this issue, we generated a muscle-specific transgenic mouse line with peroxisome import deficiency through the deletion of peroxisomal biogenesis factor 5 (Pex5). Here, we show that Pex5 inhibition results in impaired lipid metabolism, reduced muscle force and exercise performance. Moreover, mitochondrial structure, content, and function are also altered, accelerating the onset of age-related structural defects, neuromuscular junction degeneration, and muscle atrophy. Consistent with these observations, we observe a decline in peroxisomal content in the muscles of control mice undergoing natural aging. Altogether, our findings show the importance of preserving peroxisomal function and their interplay with mitochondria to maintain muscle health during aging.

Indexed as

MitochondriaMitochondria, MuscleMuscle, SkeletalPeroxisomesAgingAnimalsLipid MetabolismMaleMiceMice, Inbred C57BLMice, TransgenicMuscular AtrophyPeroxisome-Targeting Signal 1 ReceptorPhysical Conditioning, AnimalPeroxisome-Targeting Signal 1 ReceptorPex5 protein, mouse

Identifiers

PMID41213899
PMCPMC12602707

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.