Evidence map›Paper›PMID 41307411›Full record

ArticleJournal of neuropathology and experimental neurology2026

Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA).

Angèle N Merlet, Emmanuelle Lacène, Isabelle Nelson, Guy Brochier, Clémence Labasse, Anais Chanut, Angeline Madelaine, Maud Beuvin, Gisèle Bonne, Léonard Féasson and 11 more

Abstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2026. 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

21 authors.

Angèle N MerletMyology Unit, Reference Center for Neuromuscular Diseases, Euro-NMD, Department of Clinical Physiology and Exercice, University Hospital of Saint-Etienne, Saint-Priest-en-Jarez, France.ORCID 0000-0002-7597-119X
Emmanuelle LacèneFunctional Unit of Neuromuscular Pathology, Department of Neuropathology, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
Isabelle NelsonSorbonne University, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.
Guy BrochierFunctional Unit of Neuromuscular Pathology, Department of Neuropathology, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
Clémence LabasseFunctional Unit of Neuromuscular Pathology, Department of Neuropathology, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
Anais ChanutFunctional Unit of Neuromuscular Pathology, Department of Neuropathology, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
Angeline MadelaineFunctional Unit of Neuromuscular Pathology, Department of Neuropathology, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
Maud BeuvinFunctional Unit of Neuromuscular Pathology, Department of Neuropathology, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
Gisèle BonneSorbonne University, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.ORCID 0000-0002-2516-3258
Léonard FéassonMyology Unit, Reference Center for Neuromuscular Diseases, Euro-NMD, Department of Clinical Physiology and Exercice, University Hospital of Saint-Etienne, Saint-Priest-en-Jarez, France.
Marie-Christine MinotNeuromuscular Competence Center, University Hospital of Rennes, Rennes, France.
Jean-Baptiste NouryReference Centre for Neuromuscular Diseases AOC, University Hospital of Brest, Brest, France.
Mélanie FradinDepartment of Medical Genetics, Hôpital Sud, University Hospital of Rennes, Rennes, France.ORCID 0000-0002-2535-2198
Marco SavareseFolkhälsan Research Center, Helsinki, Finland.ORCID 0000-0002-2591-244X
Gorka Fernández-EulateAP-HP, Reference Center for Neuromuscular Disorders, Institut de Myologie, Hôpital Pitié-Salpêtrière, Paris, France.
Anthony BehinAP-HP, Reference Center for Neuromuscular Disorders, Institut de Myologie, Hôpital Pitié-Salpêtrière, Paris, France.
Tanya StojkovicAP-HP, Reference Center for Neuromuscular Disorders, Institut de Myologie, Hôpital Pitié-Salpêtrière, Paris, France.ORCID 0000-0002-4054-2838
Andreas HentschelLeibniz-Institut für Analytische Wissenschaften-ISAS-e. V, Dortmund, Germany.
Pascale MarcorellesDepartment of Pathology, University Hospital of Brest, Brest, France.
Andreas RoosDepartment of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Teresinha EvangelistaFunctional Unit of Neuromuscular Pathology, Department of Neuropathology, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.ORCID 0000-0002-1329-9131

Funding

Der Regierende Bürgermeister von Berlin, Senatskanzlei Wissenschaft und ForschungDeutsche Gesellschaft für MuskelkrankeDeutsche Gesellschaft für Muskelkranke (DGM)ERDFEuropean Regional Development FundEuropean Regional Development Fund (ERDF; project NME-GPS and B2B-RARE)European Union's Horizon 2020 research and innovation programme 779257Ministerium für Kultur und Wissenschaft des Landes Nordrhein-Westfalen
6 · The paper itself

Abstract

X-linked myopathy with excessive autophagy (XMEA) is a slowly progressive disease affecting male patients, caused by hemizygous mutations in the VMA21 gene. We studied nine patients from six unrelated French families clinically suspected of having XMEA. Clinical charts were reviewed, and muscle biopsies underwent histological, immunohistochemical, and electron microscopy analysis. Sanger sequencing and next generation VMA21 gene panels were performed, and proteomic profiling was done on muscle extracts from two patients. Clinical onset ranged from childhood to adulthood with most showing proximal lower limb weakness and mild creatine kinase elevation. Three patients had cardiac and respiratory involvement. Muscle biopsies revealed cytoplasmic vacuoles, split fibers, internalized nuclei and variable fiber sizes. Vacuoles stained positively for sarcolemmal and autophagic proteins, as well as for complement C5b-9. Ultrastructural analysis showed basal lamina duplication, subsarcolemmal vacuoles, and extensive autophagosome extrusion. Proteomic analysis revealed complement activation, impaired proteolysis, and mitochondrial/cytoskeletal vulnerabilities. Biglycan and thrombospondin-4 were identified as potential novel diagnostic markers. Molecular studies found two known pathogenic variants (c.164-7T>G and c.163 + 4A>G) and a novel 3'UTR variant (c.*124A>G) in VMA21. This study expands the clinical spectrum of XMEA by reporting adult-onset cases, a novel mutation, and highlights the value of proteomics in understanding the pathophysiology of XMEA.

Indexed as

AutophagyGenetic Diseases, X-LinkedMuscular DiseasesAdolescentAdultChildFemaleHumansMaleMiddle AgedMuscle, SkeletalMutationVacuolar Proton-Translocating ATPasesYoung AdultVacuolar Proton-Translocating ATPasesVMA21 protein, humanautophagic vacuolar myopathyproteomicskeletal muscleultrastructureVMA21X-linked myopathy with excessive autophagyXMEA

Identifiers

PMID41307411
PMCPMC13017771

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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.