Evidence map›Paper›PMID 40219705›Full record

ArticleEuropean journal of neurology2025

Multivariate Pattern Analysis of fMRI Reveals Striato-Cortical Network Changes in Myoclonus-Dystonia.

Ramesh S Marapin, Bauke M de Jong, Remco J Renken, Elze R Timmers, Marina A J Tijssen, Jelle R Dalenberg

Abstract read
In one paragraph

Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic Movements.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  2. Review
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

6 authors.

Ramesh S MarapinDepartment of Neurology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0002-6344-7323
Bauke M de JongDepartment of Neurology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0002-6568-5739
Remco J RenkenDepartment of Biomedical Sciences of Cells and Systems, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Elze R TimmersDepartment of Neurology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Marina A J TijssenDepartment of Neurology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0001-5783-571X
Jelle R DalenbergDepartment of Neurology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Funding

Actelion and AOP Orphan Pharmaceuticals AGDystonia Medical Research FoundationEuropean Fund for Regional Development 01492947Fonds Psychische GezondheidPhelps StichtingStichting Wetenschapsfonds Dystoniethe province of FrieslandUniversitair Medisch Centrum GroningenZonMw 91218013
6 · The paper itself

Abstract

backgroundCurrently, the pathophysiology of myoclonus-dystonia (M-D) remains insufficiently understood. This study addresses this gap by adding innovative multivariate pattern analysis (MVPA) to traditional univariate analysis of functional magnetic resonance imaging (fMRI) data.

methodsData from 18 M-D patients and 18 age-matched healthy volunteers who performed a finger tapping fMRI task were analyzed. Whole-brain univariate and searchlight (MVPA) analysis with varying hemodynamic response function (HRF) delays were employed to examine brain responses associated with the visually guided motor task.

resultsDistinguishing response patterns between M-D patients and healthy volunteers revealed significant response reductions in the putamen, insula, and visual cortex. Compared to univariate analysis, searchlight analysis was more sensitive for brain activity patterns associated with finger tapping in both M-D patients and healthy volunteers. At short HRF delays, increased (pre)motor cortical responses were evident in M-D patients, whereas such responses emerged at a later HRF delay in healthy volunteers.

conclusionThe task-related effects observed in M-D patients support the involvement of the basal ganglia-thalamo-cortical network. Notably, cerebellar involvement was not strongly implicated in our study. We postulate that inherent deficits in the putamen trigger either premature or downstream compensatory (motor) cortical effects. The potential involvement of the visual cortex in the M-D pathophysiology is new, but its role has been suggested by a previous study investigating visual sensory processing in SGCE gene-positive M-D patients. Our findings, including the innovative searchlight method, pave the way for further studies investigating the complex interplay between brain regions and networks and their role in M-D pathogenesis.

Indexed as

Cerebral CortexCorpus StriatumDystonic DisordersMagnetic Resonance ImagingAdultBrain MappingFemaleHumansMaleMiddle AgedMultivariate AnalysisYoung Adultfinger tappingfmrimultivariate analysisMVPAmyoclonus‐dystoniasearchlight analysis

Identifiers

PMID40219705
PMCPMC11992478

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.