Evidence map›Paper›PMID 42538854›Full record

ArticleEuropean journal of neurology2026

3D Radiomic Texture Analysis of Quantitative Muscle MRI Enhances the Distinction Between Myotonic Dystrophy Type 1 and Charcot-Marie-Tooth Neuropathy Type 1A: A Proof-of-Concept Study.

Louise Iterbeke, Lotte Huysmans, Kobe Bamps, Ronald Peeters, Veerle Goosens, Frederik Maes, Patrick Dupont, Kristl G Claeys

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Article in European journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Louise IterbekeLaboratory for Muscle Diseases and Neuropathies, Department of Neurosciences, KU Leuven, and Leuven Brain Institute (LBI) and Leuven Institute for Rare Diseases (Leuven.IRD), Leuven, Belgium.ORCID https://orcid.org/0000-0002-4676-5119
Lotte HuysmansDepartment ESAT/PSI, KU Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0003-1726-0880
Kobe BampsDepartment of Cardiology, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0002-3248-2142
Ronald PeetersDepartment of Radiology, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0002-7055-4039
Veerle GoosensDepartment of Radiology, University Hospitals Leuven, Leuven, Belgium.
Frederik MaesDepartment ESAT/PSI, KU Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0003-0027-1479
Patrick DupontLaboratory for Cognitive Neurology, Department of Neurosciences, KU Leuven, and Leuven Brain Institute (LBI), Leuven, Belgium.ORCID https://orcid.org/0000-0003-1980-2540
Kristl G ClaeysLaboratory for Muscle Diseases and Neuropathies, Department of Neurosciences, KU Leuven, and Leuven Brain Institute (LBI) and Leuven Institute for Rare Diseases (Leuven.IRD), Leuven, Belgium.ORCID https://orcid.org/0000-0001-9937-443X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDifferentiating myogenic from neurogenic neuromuscular diseases (NMDs) can be clinically challenging. While quantitative muscle MRI (qMRI) with proton density fat fraction (PDFF,%) quantifies fat replacement, it misses micro-spatial patterns linked to underlying pathology. This study investigates whether qMRI with 3D radiomic texture analysis (TA) might improve differentiation between myogenic and neurogenic diseases, using myotonic dystrophy type 1 (DM1) and Charcot-Marie-Tooth neuropathy type 1A (CMT1A) as proof-of-concept models.

methodsThirty-three adults with DM1, 33 with CMT1A, and 33 matched healthy controls were included. qMRI on a 3T Philips Achieva system using a 6-point Dixon sequence generated PDFF(%) maps of the lower limbs, and a convolutional neural network performed 3D segmentation of 28 lower limb muscles. We extracted macroscopic features, including muscle volume, asymmetry, and disto-proximal gradients, alongside micro-spatial radiomic features (entropy, contrast, homogeneity) to quantify tissue heterogeneity.

resultsBoth patient cohorts exhibited higher PDFF(%) in all lower limb muscles compared to controls (p < 0.001). DM1 predominantly involved the posterior compartment, while CMT1A targeted the anterolateral compartment with significantly steeper disto-proximal fat gradients (p < 0.05). TA revealed higher entropy and contrast, and lower homogeneity in CMT1A compared to DM1, reflecting a more reticular pattern of fat infiltration vs. the confluent pattern in DM1.

conclusionIn this proof-of-concept study, 3D radiomic texture analysis of PDFF(%) maps revealed distinct spatial patterns of fat replacement in DM1 and CMT1A. Integrating radiomic and conventional qMRI features may enhance the non-invasive distinction between DM1 and CMT1A and warrants further investigation in a broader range of NMDs.

Indexed as

Charcot-Marie-Tooth DiseaseImaging, Three-DimensionalMagnetic Resonance ImagingMuscle, SkeletalMyotonic DystrophyAdultDiagnosis, DifferentialFemaleHumansMaleMiddle AgedProof of Concept StudyRadiomics3D muscle segmentationCharcot–Marie‐tooth type 1Amyotonic dystrophy type 1Radiomicstexture analysis

Identifiers

PMID42538854
PMCPMC13428258

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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.