Evidence map›Paper›PMID 41659033›Full record

ArticleBrain communications2026

Quantitative susceptibility mapping in myotonic dystrophy: clinical relevance of subcortical iron accumulation.

Cristiana Fiscone, Magali J Rochat, Silvia De Pasqua, Micaela Mitolo, Gianfranco Vornetti, Fiorina Bartiromo, Lorenzo Cirignotta, Fabio Pizza, Marianna Nardozza, Greta Venturi and 5 more

Abstract read
In one paragraph

Article in Brain communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

15 authors.

Cristiana FisconeDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40126, Italy.
Magali J RochatFunctional and Molecular Neuroimaging Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Silvia De PasquaUOC Clinica Neurologica, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Micaela MitoloFunctional and Molecular Neuroimaging Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Gianfranco VornettiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40126, Italy.
Fiorina BartiromoFunctional and Molecular Neuroimaging Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Lorenzo CirignottaDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna 40138, Italy.
Fabio PizzaDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40126, Italy.
Marianna NardozzaCardiology Department, Bellaria Hospital, Bologna 40139, Italy.
Greta VenturiFunctional and Molecular Neuroimaging Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
David Neil MannersFunctional and Molecular Neuroimaging Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna 40139, Italy.
Patrizia AvoniDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40126, Italy.
Rocco LiguoriDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40126, Italy.
Caterina TononDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40126, Italy.
Raffaele LodiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40126, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myotonic dystrophy type 1 is a dominantly inherited disorder, affecting musculoskeletal and central nervous systems and mainly characterized by progressive muscular atrophy and multisystemic damages including cardiac, respiratory and sleep dysfunctions. Neuroimaging studies conducted in myotonic dystrophy type 1 patients have documented widespread cerebral alterations encompassing structural, microstructural, functional and metabolic aspects of the brain, while comparatively few studies have investigated the role of iron concentration in the pathophysiology of central nervous system impairment. We report here the use of quantitative susceptibility (χ) mapping to explore iron content of both cortical and subcortical structures in myotonic dystrophy type 1 patients and to assess its possible clinical relevance, combining imaging and clinical data. Thirty-four myotonic dystrophy type 1 participants (20 females, 46.8 ± 12.0 years old) and 35 age- and sex- matched healthy controls (20 females, 50.5 ± 17.3 years old) were included in the study. All participants underwent MRI examinations in the same 3-Tesla scanner. The MRI protocol included 3D morphological T

Indexed as

biomarkerdisease progressionmyotonic dystrophy type 1quantitative susceptibility mappingsubcortical structures

Identifiers

PMID41659033
PMCPMC12875119

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.