Evidence map›Paper›PMID 41475892›Full record

ArticleAnnals of clinical and translational neurology2026

Whole-Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies.

Laura Costa-Comellas, Mauro Monforte, Angel Sanchez-Montañez, Penélope Romero-Duque, Elena Pegoraro, Jordi Díaz-Manera, Dmitry Vlodavets, Lorenzo Maggi, Marco Moscatelli, Adele D'Amico and 30 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of clinical and translational neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Whole-Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies.Annals of clinical and translational neurology · 2026
    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

40 authors.

Laura Costa-ComellasPediatric Neuromuscular Disorders Unit, Pediatric Neurology Department, Vall D'hebron Barcelona Hospital Campus, Barcelona, Spain.ORCID 0000-0002-1180-8772
Mauro MonforteUnità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-4327-6969
Angel Sanchez-MontañezPediatric Neuroradiology Unit, Radiology Department, Vall D'hebron University Hospital, Barcelona, Spain.
Penélope Romero-DuquePediatric Neurology Research Group, Vall D'hebron Research Institute (VHIR), Barcelona, Spain.
Elena PegoraroDepartment of Neurological and Psychiatric Sciences, University of Padova, Padova, Italy.ORCID 0000-0002-7740-4156
Jordi Díaz-ManeraJohn Walton Muscular Dystrophy Research Centre, NIHR Newcastle Biomedical Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Dmitry VlodavetsRussian Children Neuromuscular Center, Veltischev Clinical Pediatrics and Pediatric Surgery, Research Institute of Pirogov Russian National Research Medical University, Moscow, Russia.
Lorenzo MaggiNeuroimmunology and Neuromuscular Disease Unit, Fondazione IRCCS Istituto Carlo Besta, Milano, Italy.
Marco MoscatelliNeuroradiology Unit, Fondazione IRCCS Istituto Carlo Besta, Milano, Italy.ORCID 0000-0002-6745-474X
Adele D'AmicoNeuromuscular and Neurodegenerative Disorders Unit, Department of Neurosciences, Bambino Gesu' Children's Hospital IRCCS, Roma, Italy.ORCID 0000-0003-2438-2624
Montse OlivéNeuromuscular Diseases Unit, Foundation of the Hospital de la Santa Creu i Sant Pau Research Institute, Barcelona, Spain.
Jorge Alonso-PérezNeuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Giacomo ComiNeurology Unit, Fondazione IRCCS ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
José Miguel Escudero-FernándezPediatric Neuroradiology Unit, Radiology Department, Vall D'hebron University Hospital, Barcelona, Spain.
Gabriela S UrcuyoPediatric Neurology Research Group, Vall D'hebron Research Institute (VHIR), Barcelona, Spain.
Anna PichiecchioDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Angela BerardinelliChild Neurology and Psychiatry Unit, RCCS Mondino Foundation, Pavia, Italy.
Kristl G ClaeysDepartment of Neurology, University Hospitals Leuven and Laboratory for Muscle Diseases and Neuropathies, Department of Neurosciences, KU Leuven, Leuven, Belgium.
Claudio BrunoCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0002-3426-2901
Chiara PanicucciCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genova, Italy.ORCID 0000-0003-4571-611X
Sara BortolaniUnità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-6472-0563
Eleonora TorchiaUnità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Enzo RicciUnità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Soledad MongesDepartment of Neurology, "Prof. Dr. Juan P. Garrahan" Pediatric Hospital, Combate de los Pozos, Buenos Aires, Argentina.
Jorge A BevilacquaNeuromuscular Unit, Neurology and Neurosurgery Department, University of Chile Clinical Hospital, Santiago de Chile, Chile.
Jorge Diaz-JaraRadiology Department, University of Chile Clinical Hospital, Santiago de Chile, Chile.
Maggie C WalterDepartment of Neurology, Friedrich-Baur-Institut, LMU Hospital, Ludwig-Maximilians-University, Munich, Germany.
Simone ThieleDepartment of Neurology, Friedrich-Baur-Institut, LMU Hospital, Ludwig-Maximilians-University, Munich, Germany.
Nicoline LøkkenCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
John VissingCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0001-6144-8544
Susana Quijano-RoyNeuromuscular Unit, Child Neurology and ICU Department, University Hospital Raymond-Poincaré APHP, GH Université Paris-Saclay, Garches, France.
Robert Y CarlierDMU Smart Imaging, Medical Imaging Department, University Hospital Raymond-Poincaré APHP, GH Université Paris-Saclay, Garches, France.
Nicol C VoermansDepartment of Neurology, Radboud University, Nijmegen, the Netherlands.
Chiara Marini-BettoloJohn Walton Muscular Dystrophy Research Centre, NIHR Newcastle Biomedical Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Michela GuglieriJohn Walton Muscular Dystrophy Research Centre, NIHR Newcastle Biomedical Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Volker StraubJohn Walton Muscular Dystrophy Research Centre, NIHR Newcastle Biomedical Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Lea LeonardisInstitute of Clinical Neurophysiology, University Medical Centre Ljubljana, Ljubljana, Slovenia.ORCID 0000-0002-7522-5293
Francina MunellPediatric Neuromuscular Disorders Unit, Pediatric Neurology Department, Vall D'hebron Barcelona Hospital Campus, Barcelona, Spain.
David Gómez-AndrésPediatric Neuromuscular Disorders Unit, Pediatric Neurology Department, Vall D'hebron Barcelona Hospital Campus, Barcelona, Spain.
Giorgio TascaUnità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID 0000-0003-0849-9144

Funding

Academy of Medical SciencesComisión Nacional de Investigación Científica y Tecnológica FONDECYT 1151383NIHR Newcastle Biomedical Research Centre
6 · The paper itself

Abstract

objectiveTo characterize whole-body intramuscular fat distribution pattern in patients with sarcoglycanopathies and explore correlations with disease severity, duration and age at onset.

methodsRetrospective, cross-sectional, multicentric study enrolling patients with variants in one of the four sarcoglycan genes who underwent whole-body muscle MRI. Intramuscular fatty replacement was evaluated on T1-weighted images and represented by heatmaps. Dimensionality reduction and linear spline models examined relationships between patterns of intramuscular fat replacement and clinical findings.

resultsMRI scans from 64 patients (age range 4-67 years) covering 4160 muscles were analyzed. Disease severity ranged from asymptomatic (9%) to non-ambulant (39%) patients. Sarcoglycanopathies showed consistent, selective patterns of muscle involvement across genotypes. Latissimus dorsi and subscapularis were the earliest affected muscles in the upper body, whereas head, neck and forearm muscles remained largely preserved. Distinct gradients characterized the topography of degeneration both within individual muscles and along body and limb axes. Disease severity correlated with MRI changes in both upper and lower body muscles, and with one of the dimensions identified by the multi-correspondence analysis. Patients with onset in the first decade showed a steeper cross-sectional association between disease duration and MRI abnormalities, while later-onset patients displayed a more gradual, linear relationship.

interpretationSarcoglycanopathies display selective muscle vulnerability with characteristic gradients of fat replacement. Scapular girdle muscles are affected early in the disease course. Intramuscular fat correlates with functional impairment and disease duration, supporting its use as a surrogate endpoint in clinical trials. Age at onset emerges as a critical prognostic factor.

Indexed as

Adipose TissueMuscle, SkeletalSarcoglycanopathiesAdolescentAdultAgedChildChild, PreschoolCross-Sectional StudiesDisease ProgressionFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedRetrospective StudiesSarcoglycansdisease progressionlimb girdle muscular dystrophymuscle MRIsarcoglycanopathywhole‐body pattern

Identifiers

PMID41475892
PMCPMC13251455

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