Evidence map›Paper›PMID 41854350›Full record

ArticleJournal of neuromuscular diseases2026

Semi-quantitative analyses of muscle magnetic resonance imaging for pattern recognition in early idiopathic inflammatory myopathies.

Yana Leven, Suam Kim, Antoine Sanner, Fatma Merzou, Sergio Groppa, Christopher Nelke, Ahmed Othman, Andreas Deistung, Benjamin Troppa, Alexander Mensch and 3 more

Abstract read
In one paragraph

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. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Yana LevenDepartment of Neurology, University Hospital Düsseldorf, Düsseldorf, Germany.ORCID 0009-0005-4143-6729
Suam KimDepartment of Neuroradiology, University Medical Center Mainz, Mainz, Germany.ORCID 0000-0001-8940-4076
Antoine SannerDepartment of Neuroradiology, University Medical Center Mainz, Mainz, Germany.ORCID 0000-0002-4917-9529
Fatma MerzouDepartment of Neurology, University Hospital of Saarland, Homburg, Germany.ORCID 0000-0001-7464-4122
Sergio GroppaDepartment of Neurology, University Hospital of Saarland, Homburg, Germany.
Christopher NelkeRuhr University Bochum, Department of Neurology, BG University Hospital Bergmannsheil, Bochum, Germany.
Ahmed OthmanDepartment of Neuroradiology, University Medical Center Mainz, Mainz, Germany.
Andreas DeistungDepartment of Radiology, University Medicine Halle, Halle (Saale), Germany.ORCID 0000-0002-2427-1302
Benjamin TroppaDepartment of Radiology, University Medicine Halle, Halle (Saale), Germany.
Alexander MenschDepartment of Neurology, University Medical Center Halle (Saale), Halle (Saale), Germany.ORCID 0000-0003-0089-4473
Sven G MeuthDepartment of Neurology, University Hospital Düsseldorf, Düsseldorf, Germany.
Tobias RuckRuhr University Bochum, Department of Neurology, BG University Hospital Bergmannsheil, Bochum, Germany.ORCID 0000-0001-6332-8650
Marc PawlitzkiDepartment of Neurology, University Hospital Düsseldorf, Düsseldorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdiopathic inflammatory myopathies (IIM) are a group of autoimmune diseases characterized by skeletal muscle inflammation. Magnetic resonance imaging (MRI) is increasingly used in IIM diagnosis, yet standardized protocols and comprehensive datasets remain limited. This study aimed to characterize MRI findings across IIM subtypes, identify muscle involvement patterns, and assess correlations between imaging abnormalities and clinical severity.

methodsIn this retrospective cohort study, 34 patients with IIM evaluated between 2012 and 2020 in Düsseldorf and Halle (Germany) were included: Inclusion Body Myositis (IBM, n = 9), Dermatomyositis (DM, n = 5), Polymyositis (PM, n = 6), Anti-Synthetase Syndrome (ASYS, n = 5), and Immune-mediated Necrotizing Myopathy (IMNM, n = 9). Clinical data (autoantibody status, creatine kinase [CK] levels, and muscle strength via Manual-Muscle-Testing-8 [MMT-8]) and muscle MRI findings were analysed. Muscle involvement patterns were characterized, and associations with clinical severity were evaluated using univariate linear regression.

resultsMRI abnormalities were evident even in early disease stages (median disease duration: 7 months [IQR: 2-18]). Patterns of muscle involvement differed markedly across IIM subtypes; notably, ASYS and IBM showed minimal involvement of upper extremities. A significant correlation was found between MRI-visible pathology and MMT-8 scores (p = 0.027) as well as CK levels (p = 0.028).

conclusionMRI reveals subclinical muscle involvement in early IIM and uncovers subtype-specific patterns. Given the heterogeneity of MRI findings, individualized imaging approaches are warranted. While MRI serves as a valuable adjunct in diagnosis and management of IIM, its utility depends on standardized protocols and integration with clinical and laboratory data to enable accurate interpretation and informed decision-making in clinical practice.

Indexed as

anti-synthetase syndromedermatomyositisidiopathic inflammatory myopathyimmune-mediated necrotizing myopathyinclusion-body-myositismagnetic resonance imaging

Identifiers

PMID41854350
PMCPMC13438526

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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.