Evidence map›Paper›PMID 41330974›Full record

ArticleScientific reports2025

Characterizing white matter hyperintensities in myotonic dystrophy type 1 through IVIM derived metrics.

Marina Di Stefano, Nivedita Agarwal, Giulia Canella, Eleonora Diella, Morena Delle Fave, Giovanni Meola, Maria Grazia D'Angelo, Denis Peruzzo

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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

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

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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

8 authors.

Marina Di StefanoNeuroImaging Laboratory, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.
Nivedita AgarwalDiagnostic Imaging and Neuroradiology Unit, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy. nivedita.agarwal@lanostrafamiglia.it.
Giulia CanellaUnit of Rehabilitation of Rare Diseases of the Central and Peripheral Nervous System, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.
Eleonora DiellaUnit of Rehabilitation of Rare Diseases of the Central and Peripheral Nervous System, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.
Morena Delle FaveUnit of Rehabilitation of Rare Diseases of the Central and Peripheral Nervous System, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.
Giovanni MeolaDepartment of Biomedical Sciences for Health, Department of Neurorehabilitation Sciences Casa di Cura IGEA Spa, University of Milan, Fondazione Malattie Miotoniche ETS, Milan, Italy.
Maria Grazia D'AngeloUnit of Rehabilitation of Rare Diseases of the Central and Peripheral Nervous System, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.
Denis PeruzzoNeuroImaging Laboratory, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myotonic dystrophy type 1 (DM1) is a genetic disease which affects multiple systems including the central nervous system. One of its key neuroimaging biomarkers are white matter hyperintensities (WMHs). The clinical relevance of WMHs remains unclear, and treating them as a uniform entity may overlook their heterogeneous composition and spatial distribution. To assess WMHs heterogeneity we applied intra-voxel incoherent motion (IVIM) modelling, an advanced magnetic resonance imaging technique, to a cohort of 23 patients with DM1 (age [mean ± std]: 44.1 ± 11.9 years; M/F = 8/15). WMHs were distinguished into periventricular (PWMHs) and deep (DWMHs) subtypes using criteria based on continuity and distance rules. A quantitative evaluation of their distribution among white matter tracts was conducted, together with correlation analysis between WMHs and clinical scales. Our research reveals that PWMHs have higher parenchymal diffusivity than DWMHs, consistently with their closeness to the ventricles. Significant positive correlation is identified between PWMH volumes and age, while DWMHs seem to be more strongly associated with an impairment of cognitive functions. Overall, these findings could have possible implications in clinics, highlighting the importance of considering WMHs heterogeneity and opening the door to a better comprehension of their role in the disease.

Indexed as

Magnetic Resonance ImagingMyotonic DystrophyWhite MatterAdultFemaleHumansMaleMiddle AgedCognitive impairmentMR diffusionMyotonic dystrophy type 1White matter hyperintensities

Identifiers

PMID41330974
PMCPMC12673117

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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.