Evidence map›Paper›PMID 39333780›Full record

ArticleScientific reports2024

Psychiatric phenotype in neurodevelopmental myoclonus-dystonia is underpinned by abnormality of cerebellar modulation on the cerebral cortex.

Clément Tarrano, Cécile Galléa, Cécile Delorme, Eavan M McGovern, Cyril Atkinson-Clement, Vanessa Brochard, Stéphane Thobois, Christine Tranchant, David Grabli, Bertrand Degos and 12 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 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. Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia.Annals of clinical and translational neurology · 2026
    Article
  3. Review
  4. Sex-specific alterations of Purkinje cell firing inDystonia (Lausanne, Switzerland) · 2025
    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

22 authors.

Clément TarranoParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Cécile GalléaParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Cécile DelormeParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Eavan M McGovernDepartment of Neurology, St Vincent's University Hospital Dublin, Dublin, Ireland.
Cyril Atkinson-ClementParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Vanessa BrochardDepartment of Neurology, Clinical Investigation Center for Neurosciences, Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Paris, France.
Stéphane ThoboisDepartment of Neurology, Hospices Civils de Lyon, Pierre Wertheimer Neurological Hospital, Expert Parkinson Center NS-PARK/FCRIN, Bron, France.
Christine TranchantDépartement of Neurology, Universitary Hospital of Strasbourg, Strasbourg, France.
David GrabliDepartment of Neurology, Clinical Investigation Center for Neurosciences, Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Paris, France.
Bertrand DegosDepartment of Neurology, Avicenne Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne Paris Nord, Bobigny, France.
Jean Christophe CorvolParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Jean-Michel PedespanDepartment of Neuropediatry, Universitary Hospital of Pellegrin, Bordeaux, France.
Pierre Krystkowiak, Abu Dhabi Stem Cells Centre, Abu Dhabi, United Arab Emirates.
Jean-Luc HouetoDepartment of Neurology CHU Limoges, EpiMaCT - Epidemiology of chronic diseases in tropical zone, Institute of Epidemiology and Tropical Neurology, Inserm U1094, IRD U270, Univ. Limoges, OmegaHealth, Limoges, France.
Adrian DegardinDepartment of Neurology, Tourcoing Hospital, Tourcoing, France.
Luc Defebvre, Troubles cognitifs dégénératifs et vasculaires, Lille, F-59000, France.
Benoit BerangerParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Davide MartinoDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Emmanuelle ApartisParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Marie VidailhetParis Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Emmanuel Roze *Paris Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France.
Yulia Worbe *Paris Brain Institute, Sorbonne University - ICM, Inserm CNRS, Paris, F-75013, France. yulia.worbe@aphp.fr.

Funding

AMADYS Fonds de Dotation Brou de LaurièreEuropean Commission EJP RD COFUND-EJP N° 825575 - EurDyscover
6 · The paper itself

Abstract

Psychiatric symptoms are common in neurodevelopmental movement disorders, including some types of dystonia. However, research has mainly focused on motor manifestations and underlying circuits. Myoclonus-dystonia is a rare and homogeneous neurodevelopmental condition serving as an illustrative paradigm of childhood-onset dystonias, associated with psychiatric symptoms. Here, we assessed the prevalence of psychiatric disorders and the severity of depressive symptoms in patients with myoclonus-dystonia and healthy volunteers (HV). Using resting-state functional neuroimaging, we compared the effective connectivity within and among non-motor and motor brain networks between patients and HV. We further explored the hierarchical organization of these networks and examined the relationship between their connectivity and the depressive symptoms. Comparing 19 patients to 25 HV, we found a higher prevalence of anxiety disorders and more depressive symptoms in the patient group. Patients exhibited abnormal modulation of the cerebellum on the cerebral cortex in the sensorimotor, dorsal attention, salience, and default mode networks. Moreover, the salience network activity was directed by the cerebellum in patients and was related to depressive symptoms. Altogether, our findings highlight the role of the cerebellar drive on both motor and non-motor cortical areas in this disorder, suggesting cerebellar involvement in the complex phenotype of such neurodevelopmental movement disorders.

Indexed as

CerebellumCerebral CortexDystonic DisordersAdolescentAdultDepressionFemaleHumansMagnetic Resonance ImagingMaleNeurodevelopmental DisordersPhenotypeYoung AdultCerebellumDystoniaMRIMyoclonusNetwork

Identifiers

PMID39333780
PMCPMC11437022

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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.