Evidence map›Paper›PMID 41415511›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Mapping the Neuroanatomy of Dystonia Using Causal Brain Lesions.

Daniel T Corp, Jaakko Kungshamn, Elizabeth G Ellis, Maximilian U Friedrich, Kalle J Niemi, Christopher J Greenwood, Jordan Morrison-Ham, Shiro Horisawa, Martin M Reich, Hyder A Jinnah and 3 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

13 authors.

Daniel T CorpCognitive Neuroscience Unit, School of Psychology, Deakin University, Burwood, Australia.
Jaakko KungshamnTurku Brain and Mind Center, Clinical Neurosciences, University of Turku, Turku, Finland.
Elizabeth G EllisCognitive Neuroscience Unit, School of Psychology, Deakin University, Burwood, Australia.
Maximilian U FriedrichCenter for Brain Circuit Therapeutics, Departments of Neurology, Psychiatry, and Radiology, Brigham & Women's Hospital, Boston.
Kalle J NiemiTurku Brain and Mind Center, Clinical Neurosciences, University of Turku, Turku, Finland.
Christopher J GreenwoodDeakin University, SEED Lifespan Strategic Research Centre, School of Psychology, Faculty of Health, Geelong, Australia.ORCID 0000-0002-9211-6312
Jordan Morrison-HamCognitive Neuroscience Unit, School of Psychology, Deakin University, Burwood, Australia.
Shiro HorisawaDepartment of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan.
Martin M ReichDepartment of Neurology, University Hospital of Würzburg, Josef-Schneider-Straße 11, 97080 Würzburg, Germany.
Hyder A JinnahDepartments of Neurology, Human Genetics, and Pediatrics, Emory University, Atlanta, GA, United States.
Andreas HornCenter for Brain Circuit Therapeutics, Departments of Neurology, Psychiatry, and Radiology, Brigham & Women's Hospital, Boston.
Michael D FoxCenter for Brain Circuit Therapeutics, Departments of Neurology, Psychiatry, and Radiology, Brigham & Women's Hospital, Boston.
Juho JoutsaTurku Brain and Mind Center, Clinical Neurosciences, University of Turku, Turku, Finland.ORCID 0000-0002-3457-9415

Funding

BRAIN CONNECTS: The center for Large-scale Imaging of Neural Circuits (LINC)UM1NS132358 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI Suzanne N Haber, Elizabeth M. C. Hillman · 2023 to 2026
$17.5M
Dystonia Coalition- Pilot ProjectU54NS116025 · NINDS · EMORY UNIVERSITY · PI JINNAH, HYDER A · 2019 to 2023
$7.1M
Dystonia CoalitionU54NS065701 · NINDS · EMORY UNIVERSITY · PI JINNAH, HYDER A · 2009 to 2014
$7.0M
Using human brain connectivity to identify the causal neuroanatomical substrate of depression symptomsR01MH113929 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHAEL D FOX · 2017 to 2026
$6.9M
Toward Connectomic Deep Brain Stimulation in Obsessive Compulsive DisorderR01MH130666 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHAEL D FOX · 2022 to 2026
$3.9M
Using Brain Lesions and Deep Brain Stimulation to Identify an Epilepsy CircuitR01NS127892 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHAEL D FOX · 2022 to 2026
$3.4M
Dystonia CoalitionU54TR001456 · NCATS · EMORY UNIVERSITY · PI JINNAH, HYDER A · 2015 to 2016
$2.5M
Transdiagnostic memory, mood and motor circuits in Alzheimer's and neurodegenerative diseaseR56AG069086 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI FOX, MICHAEL D · 2021 to 2021
$873k
Identifying neuromodulation targets for pain in the human brainR21NS123813 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI FOX, MICHAEL D · 2022 to 2023
$492k
Targeted modulation of symptom-specific brain circuits with transcranial magnetic stimulationR21MH126271 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI FOX, MICHAEL D · 2021 to 2022
$492k
NCATS NIH HHS U54 TR001456NIA NIH HHS R56 AG069086NIMH NIH HHS R01 MH113929NIMH NIH HHS R01 MH130666NIMH NIH HHS R21 MH126271NINDS NIH HHS R01 NS127892NINDS NIH HHS R21 NS123813NINDS NIH HHS U54 NS065701NINDS NIH HHS U54 NS116025NINDS NIH HHS UM1 NS132358
6 · The paper itself

Abstract

Dystonia is one of the most prevalent movement disorders, but its neural substrates have remained enigmatic despite decades of research. Brain lesions leading to dystonia offer unique causal inference that could lend insight into the neural networks driving the disorder. Here, we studied the published cases of lesions causing dystonia to a variety of different body parts (n=179) and used lesion network mapping to test whether lesion locations mapped to a common brain network. Specificity was investigated by comparing the findings to 216 lesions causing other movement disorders, and 499 lesions causing non-specific neurological symptoms. While lesions causing dystonia occurred in heterogeneous locations, they localised to a common and specific cortico-basal ganglia-cerebellar network. Stronger connectivity to this dystonia network from a causal brain lesion was associated with a greater extent of dystonia throughout the body. Further, there were significant differences in the brain networks depending on the body parts affected by dystonia, which also demonstrated different somatotopic representations in the cerebellum. Our results suggest that dystonia stems from a cortico-basal ganglia-cerebellar network, with the manifestation in the body depending on the preferential involvement of the hubs of the network, and its somatotopy.

Identifiers

PMID41415511
PMCPMC12709489

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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.