Evidence map›Paper›PMID 41051986›Full record

ArticleJournal of neuromuscular diseases2026

Immunohistological and electron microscopy profile of unique TIRM-MRI guided muscle biopsies of FSHD patients.

Anna Greco, Benno Kusters, Ritse Mann, Jurgen Futterer, Leon de Jong, Yordy Welling, Marieke Ploegmakers, Ger Jm Pruijn, Leo Ab Joosten, Baziel G M van Engelen

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Article in Journal of neuromuscular diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Anna GrecoDepartment of Neurology, Radboud University Medical Center, Nijmegen, The Netherlands.
Benno KustersDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Ritse MannDepartment of Radiology, Radboud University Medical Center, Nijmegen, The Netherlands.
Jurgen FuttererDepartment of Radiology, Radboud University Medical Center, Nijmegen, The Netherlands.
Leon de JongDepartment of Radiology, Radboud University Medical Center, Nijmegen, The Netherlands.
Yordy WellingDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Marieke PloegmakersDepartment of Radiology, Radboud University Medical Center, Nijmegen, The Netherlands.
Ger Jm PruijnDepartment of Biomolecular Chemistry, Institute for Molecules and Materials, Radboud University Nijmegen, Nijmegen, the Netherlands.
Leo Ab JoostenLaboratory of Experimental Internal Medicine, Department of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Baziel G M van EngelenDepartment of Neurology, Radboud University Medical Center, Nijmegen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFSHD is an inherited myopathy with complex epigenetic pathogenesis and no causal treatment. Inflammation is thought to contribute to muscle pathology, but its nature remains unclear.

objectiveTo characterize inflammatory infiltrates and morphological changes in MRI-guided FSHD muscle biopsies compared to healthy controls (HC).

methodsWe performed turbo inversion recovery magnitude (TIRM) and DIXON MRI on 43 genetically confirmed FSHD patients (50 ± 12 years, 51% men) to assess inflammation and fatty infiltration. From 24 patients with at least one TIRM + leg muscle, two MRI-guided biopsies (TIRM + and TIRM-) were obtained. Needle biopsies from 8 HC (36 ± 12 years, 62% men) served as controls. Samples underwent hematoxylin-phloxine staining and immunodetection of CD3, CD4, CD8, CD56, CD68, HLA-ABC, HLA-DR, and MAC. Electron microscopy provided ultrastructural analysis.

resultsTIRM + FSHD samples showed significantly higher histopathology and inflammation grades than paired TIRM- and HC samples. Inflammatory infiltrates, mainly CD8 + lymphocytes and CD68 + macrophages, were present in 67% of TIRM + and 20% of TIRM- muscles. Electron microscopy revealed frequent myofibrillar disorganization in TIRM + samples.

conclusionOur findings validate TIRM hyperintensity as a biomarker for active disease, correlating with histopathology and inflammation. The incidence of inflammation in FSHD appears underestimated, highlighting its role in disease pathogenesis. These results support targeting inflammation as a potential therapeutic strategy in FSHD.

Indexed as

Muscle, SkeletalMuscular Dystrophy, FacioscapulohumeralAdultFemaleHumansImage-Guided BiopsyImmunohistochemistryInflammationMagnetic Resonance ImagingMaleMicroscopy, ElectronMiddle AgedbiomarkerFSHDinflammationMRI-guided biopsies

Identifiers

PMID41051986
PMCPMC13438636

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