Evidence map›Paper›PMID 42168111›Full record

ArticleMuscle & nerve2026

MRI-Determined Muscle Fat Fractions and Contractile Volumes in Myotonic Dystrophy Type 2.

Lauren M Hinkley, Kathryn R Wagner, Michael A Jacobs, Doris G Leung

Abstract read
In one paragraph

Article in Muscle & nerve, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Lauren M HinkleyThe Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0003-1338-0383
Kathryn R WagnerThe Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Michael A JacobsThe Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Doris G LeungThe Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-2558-7798

Funding

Sleep and Circadian Dysfunction, Brain and Neurobehavioral Development in AutismP50HD103538 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI S. Ali Fatemi, Bradley L Schlaggar · 2020 to 2026
$9.9M
Magnetic resonance imaging and spectroscopy biomarkers for facioscapulohumeral muscular dystrophyK23NS091379 · NINDS · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI LEUNG, DORIS G · 2015 to 2019
$885k
National Cancer Institute, Core-Imaging Radiological Assessment Team (IRAT) P30CA006973NICHD NIH HHS P50 HD103538NINDS NIH HHS 5K23NS091379NINDS NIH HHS K23 NS091379
6 · The paper itself

Abstract

introductionAlthough magnetic resonance imaging (MRI) has been used to selectively characterize patterns of muscle involvement in myotonic dystrophy type 2 (DM2), the relationship between quantitative MRI-derived muscle composition and functional performance remains incompletely defined. This study aimed to characterize the imaging phenotype in DM2 using whole-body MRI scans and to evaluate the association between MRI-based muscle measurements and clinical endpoints.

methodsClinical endpoints collected included strength, physical function, and patient-reported outcomes. AI-based algorithms were utilized to segment 38 muscles bilaterally from Dixon MRI scans collected in a prospective, cross-sectional study. The segmentations were used to calculate muscle fat fraction (MFF) and contractile volume (CV) for each muscle. Associations between MRI measurements and clinical outcomes were examined using Spearman correlations.

resultsAdult patients (6 females, 6 males) with DM2 and no contraindications to MRI were enrolled at a single center. The mean age was 52.5 ± 15.4 years and mean disease duration was 12.5 ± 7.8 years. The gluteus maximus and erector spinae muscles had the highest average MFF. Mean MFF in fully captured muscles ranged from 7.4% to 36.5%. Higher MFFs were moderately associated with shorter 6-min walk distances (ρ = -0.62, p = 0.03) and slower 10-m walk/run times (ρ = 0.61, p = 0.04). Higher CVs were moderately associated with longer 6-min walk distance (ρ = 0.67, p = 0.02) and faster 10-m walk/run (ρ = -0.67, p = 0.02). DISCUSSION: These results identify a pattern of proximal muscle involvement and moderate associations between MFFs and CVs with physical function. Larger longitudinal studies are needed to validate the utility of imaging biomarkers in DM2.

Indexed as

Adipose TissueMagnetic Resonance ImagingMuscle ContractionMuscle, SkeletalMyotonic DystrophyAdultAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedMuscle StrengthProspective Studiesimaging biomarkersMRImuscular dystrophymyotonic dystrophymyotonic dystrophy type 2

Identifiers

PMID42168111
PMCPMC13322453

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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.