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dc.contributor.authorWang, Yuchao
dc.contributor.authorHuynh, Baothy
dc.contributor.authorRen, Jianxun
dc.contributor.authorChen, Mo
dc.contributor.authorZhang, Wei
dc.contributor.authorHu, Dan
dc.contributor.authorLi, Shasha
dc.contributor.authorLiu, Hesheng
dc.contributor.authorKimberley, Teresa J.
dc.date.accessioned2025-11-07T16:39:57Z
dc.date.available2025-11-07T16:39:57Z
dc.date.issued2025-08-28
dc.identifier.issn0885-3185
dc.identifier.issn1531-8257
dc.identifier.urihttps://hdl.handle.net/1721.1/163601
dc.description.abstractBackground The central pathology causing idiopathic focal dystonia remains unclear. The recently identified somato-cognitive action network (SCAN) has been implicated. Objective We tested whether the effector-agnostic SCAN may constitute a central pathology shared across dystonia subtypes, whereas the effector-specific regions in the primary sensorimotor cortex may show distinct functional changes specific to the dystonic body part. Methods We collected functional magnetic resonance imaging (MRI) from patients with focal dystonia (laryngeal dystonia [LD], N = 24; focal hand dystonia [FHD], N = 18) and healthy control participants (N = 21). Regions of interest were selected a priori within the basal ganglia-thalamo-cortical and cerebello-thalamo-cortical sensorimotor pathways. We investigated dystonia-dependent resting-state connectivity changes: between SCAN and related cortical regions, between cortical and noncortical regions, and among noncortical regions. Cortical network boundaries were individualized based on resting-state data. Separately, individualized hand and mouth/larynx regions were also generated from task-based MRI (finger-tapping and phonation, respectively) for comparison. Results Both focal dystonia subtypes showed significant functional changes (P = 0.048 for LD, P = 0.017 for FHD) compared to controls, driven by SCAN's higher functional connectivity to task-based mouth/larynx region and concomitantly lower connectivity to the cingulo-opercular network. No significant subcortical or cerebellar changes were observed when LD and FHD were modeled as independent groups. However, exploratory analysis combining LD and FHD suggested a dystonia-dependent asynchronization between SCAN and sensorimotor cerebellum (P = 0.010) that may indicate a pathological rather than compensatory process. Conclusions We demonstrate that SCAN is uniquely associated with focal dystonia dysfunction beyond the dystonic effector regions, offering insights into pathophysiology and treatments. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.en_US
dc.publisherWileyen_US
dc.relation.isversionofhttps://doi.org/10.1002/mds.70021en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceWileyen_US
dc.titleSomato‐Cognitive Action Network in Focal Dystoniaen_US
dc.typeArticleen_US
dc.identifier.citationWang, Y., Huynh, B., Ren, J., Chen, M., Zhang, W., Hu, D., Li, S., Liu, H. and Kimberley, T.J. (2025), Somato-Cognitive Action Network in Focal Dystonia. Mov Disord.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.relation.journalMovement Disordersen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.identifier.doihttps://doi.org/10.1002/mds.70021
dspace.date.submission2025-11-07T16:13:17Z
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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