Evidence map›Paper›PMID 40672936›Full record

ArticleBrain communications2025

Motor network organization in healthy development and chronic tic disorders.

Theresa V Heinen, Julia Schmidgen, Theresa Paul, Lukas Hensel, Gereon R Fink, Lukas J Volz, Christian Grefkes, Stephan Bender, Kerstin Konrad

Abstract read
In one paragraph

Article in Brain communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

9 authors.

Theresa V HeinenChild Neuropsychology Section, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Medical Faculty, RWTH Aachen University, Aachen 52074, Germany.ORCID https://orcid.org/0009-0009-6145-0586
Julia SchmidgenDepartment of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne 50931, Germany.
Theresa PaulMedical Faculty, University of Cologne, and Department of Neurology, University Hospital Cologne, Cologne 50937, Germany.
Lukas HenselMedical Faculty, University of Cologne, and Department of Neurology, University Hospital Cologne, Cologne 50937, Germany.
Gereon R FinkMedical Faculty, University of Cologne, and Department of Neurology, University Hospital Cologne, Cologne 50937, Germany.
Lukas J VolzMedical Faculty, University of Cologne, and Department of Neurology, University Hospital Cologne, Cologne 50937, Germany.ORCID https://orcid.org/0000-0002-0161-654X
Christian GrefkesDepartment of Neurology, Goethe University Frankfurt and University Hospital, Frankfurt 60528, Germany.
Stephan BenderDepartment of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne 50931, Germany.
Kerstin KonradChild Neuropsychology Section, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Medical Faculty, RWTH Aachen University, Aachen 52074, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tic disorders (TD) are childhood-onset neurodevelopmental disorders characterized by sudden, repetitive motor and vocal tics, often with partial or complete remission by the time young adulthood is reached. We here investigated motor control and compensatory neural processes in drug-naïve children and adolescents with chronic Motor Tic Disorder or Tourette Syndrome (TD) by examining motor network activity and connectivity compared to healthy controls. Using a reaction time (RT) task under varying cueing conditions, combined with functional magnetic resonance imaging (fMRI) and dynamic causal modelling (DCM), we explored how TD-related motor networks adapt to support volitional movement control. Participants with TD demonstrated enhanced task accuracy across internally and externally cued conditions despite deficits in sustained motor inhibition (blink suppression). Relative to controls, individuals with TD exhibited increased task-related activation in ipsilateral motor regions, particularly in the primary motor cortex, and somatosensory cortex, and enhanced interhemispheric connectivity between parietal sensory-motor hubs. Notably, while in typically developing participants, age-related increases in parietal lobe activation and modulatory connectivity between primary motor and premotor regions were linked to improved task accuracy, working memory and visuomotor coordination, TD patients deviated from this normative developmental trajectory with distinct, atypical but neither delayed nor accelerated neural activation and connectivity patterns. Our data suggest that TD involves compensatory neuroplastic adaptations that leverage additional sensorimotor resources to improve motor control but do not extend to motor inhibition processes. Moreover, the findings emphasize the intricate interplay between motor control and neural plasticity in TD, highlighting how compensatory mechanisms may serve as adaptive responses to motor challenges. These findings open avenues for therapeutic strategies that harness the brain's compensatory capacities to enhance motor control and facilitate TD management.

Indexed as

brain motor network organizationchronic motor ticsdynamic causal modelling (DCM)typical and atypical development

Identifiers

PMID40672936
PMCPMC12264489

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Registered trials

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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.