Evidence map›Paper›PMID 41821399›Full record

ArticleJournal of cachexia, sarcopenia and muscle2026

Evaluation of Dysphagia in Myositis and Muscular Dystrophy Using Real-Time MRI and Quantitative Muscle Ultrasound.

Rachel Zeng, Anke Rietveld, Omar Al-Bourini, Rosemarie H M J M Kroon, Arno Olthoff, Matthias Weidenmüller, Per-Ole Carstens, Isabel Kommerell, Saskia G Schütz, Corinne G C Horlings and 9 more

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 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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0cells of the map it votes in
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

19 authors.

Rachel ZengDepartment of Neurology, Neuromuscular Center, University Medical Center Göttingen, Göttingen, Germany.ORCID https://orcid.org/0009-0003-0988-4762
Anke RietveldDepartment of Neurology, Radboudumc Research Institute for Medical Innovation, Nijmegen, the Netherlands.
Omar Al-BouriniDepartment of Clinical and Interventional Radiology, University Medical Center Göttingen, Göttingen, Germany.
Rosemarie H M J M KroonDepartment of Rehabilitation, Radboudumc Research Institute for Medical Innovation, Nijmegen, the Netherlands.
Arno OlthoffDepartment of Otorhinolaryngology, Phoniatrics and Pedaudiology, University Medical Center Göttingen, Göttingen, Germany.
Matthias WeidenmüllerDepartment of Otorhinolaryngology, Phoniatrics and Pedaudiology, University Medical Center Göttingen, Göttingen, Germany.
Per-Ole CarstensDepartment of Neurology, Neuromuscular Center, University Medical Center Göttingen, Göttingen, Germany.
Isabel KommerellDepartment of Neurology, Neuromuscular Center, University Medical Center Göttingen, Göttingen, Germany.
Saskia G SchützDepartment of Neurology, Neuromuscular Center, University Medical Center Göttingen, Göttingen, Germany.
Corinne G C HorlingsDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.
Johanna G KalfDepartment of Rehabilitation, Radboudumc Research Institute for Medical Innovation, Nijmegen, the Netherlands.
Bert J M de SwartDepartment of Rehabilitation, Radboudumc Research Institute for Medical Innovation, Nijmegen, the Netherlands.
Baziel G M van EngelenDepartment of Neurology, Radboudumc Research Institute for Medical Innovation, Nijmegen, the Netherlands.
Tim FriedeDepartment of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany.ORCID https://orcid.org/0000-0001-5347-7441
Sabine HoferDepartment of Neurology, University Medical Center Göttingen, Göttingen, Germany.
Jens FrahmBiomedical NMR, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
Ali Seif Amir HosseiniDepartment of Clinical and Interventional Radiology, University Medical Center Göttingen, Göttingen, Germany.
Jens SchmidtDepartment of Neurology, Neuromuscular Center, University Medical Center Göttingen, Göttingen, Germany.ORCID https://orcid.org/0000-0002-5589-2371
Christiaan G J SarisDepartment of Neurology, Radboudumc Research Institute for Medical Innovation, Nijmegen, the Netherlands.ORCID https://orcid.org/0000-0003-2633-0588

Funding

Association Française contre les Myopathies (AFM-Téléthon) 20301Deutsche Gesellschaft für Muskelkranke (DGM) Sc21/1
6 · The paper itself

Abstract

backgroundSwallowing dysfunction-dysphagia-is a frequent and debilitating symptom in neuromuscular disorders, leading to malnutrition, cachexia, aspiration pneumonia, and death. Identification of the underlying pathophysiological mechanisms is important for diagnosis and treatment. As standard assessments have limitations, novel imaging techniques are needed. We here studied the utility of real-time MRI and quantitative muscle ultrasound for characterizing dysphagia in two different neuromuscular disorders.

methodsThis prospective cohort study included 18 patients with inclusion body myositis (IBM, 33% female, age 68.9 ± 7.7 years) and 13 with oculopharyngeal muscular dystrophy (OPMD, 62% female, age 55.9 ± 7.0 years) from two European Neuromuscular research centers (Nijmegen, NL; Göttingen, DE). Swallowing function was studied using real-time MRI (RT-MRI), FEES (flexible endoscopic evaluation of swallowing), and clinical assessments. T1-mapping and quantitative muscle ultrasound (QMUS) were used to analyse tissue properties in swallowing muscles. Outcomes were compared between the two muscle diseases. RT-MRI values were also compared with 22 age- and sex-matched non-myopathic controls.

resultsRT-MRI revealed significantly prolonged oral transit times in OPMD vs. controls (difference between means = 581.2 ms, 95% CI 225.9-936.4, p = 0.002). Pharyngeal transit time was significantly prolonged in IBM vs. controls (difference between means = 1132.8 ms, 95% CI 482.2-1783, p = 0.001). A cricopharyngeal bar as a well-established morphological indicator of dysphagia was identified in 80% of patients with IBM compared with 53% in OPMD. Fatty degeneration of the tongue in OPMD significantly correlated between MRI-T1 values and ultrasound echogenicity (Spearman's ρ = -0.52, p = 0.005). ROC revealed excellent discrimination between diseases by combining RT-MRI, T1-mapping and QMUS (AUC = 0.95, 95% CI 0.86-1.00), while FEES and clinical assessments failed to differentiate specific patterns of dysphagia.

conclusionsThis study supports the value of novel MRI and ultrasound techniques for clinical use by identifying the pathophysiology and severity of impaired swallowing. Differentiating the phenotypes of dysphagia can aid in the diagnosis and treatment of affected patients. RT-MRI and QMUS may serve as outcome measures for swallowing in clinical trials.

Indexed as

Deglutition DisordersMagnetic Resonance ImagingMuscle, SkeletalMuscular DystrophiesMyositisAgedFemaleHumansMaleMiddle AgedMuscular Dystrophy, OculopharyngealProspective StudiesUltrasonographycricopharyngeal barimagingneuromuscular disordersquantitative MRIswallowing muscles

Identifiers

PMID41821399
PMCPMC13140979

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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.