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Benefits of pallidal stimulation in dystonia are linked to cerebellar volume and cortical inhibition
A. Fečíková, R. Jech, V. Čejka, V. Čapek, D. Šťastná, I. Štětkářová, K. Mueller, ML. Schroeter, F. Růžička, D. Urgošík,
Language English Country Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
GAČR 16-13323S
Grantová Agentura České Republiky (Grant Agency of the Czech Republic) - International
Progres Q27/LF1
Univerzita Karlova v Praze (Charles University) - International
MJFF-11362
Michael J. Fox Foundation for Parkinson's Research (Michael J. Fox Foundation) - International
MJFF-11362
Michael J. Fox Foundation for Parkinson's Research (Michael J. Fox Foundation) - International
MJFF-11362
Michael J. Fox Foundation for Parkinson's Research (Michael J. Fox Foundation) - International
PDF-IRG-1307
Parkinson's Disease Foundation (Parkinson's Disease Foundation, Inc.) - International
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- MeSH
- Adult MeSH
- Dystonia therapy MeSH
- Globus Pallidus physiology MeSH
- Deep Brain Stimulation methods MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Motor Cortex physiology MeSH
- Cerebellum physiology MeSH
- Neural Inhibition * MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Clinical benefits of pallidal deep brain stimulation (GPi DBS) in dystonia increase relatively slowly suggesting slow plastic processes in the motor network. Twenty-two patients with dystonia of various distribution and etiology treated by chronic GPi DBS and 22 healthy subjects were examined for short-latency intracortical inhibition of the motor cortex elicited by paired transcranial magnetic stimulation. The relationships between grey matter volume and intracortical inhibition considering the long-term clinical outcome and states of the GPi DBS were analysed. The acute effects of GPi DBS were associated with a shortening of the motor response whereas the grey matter of chronically treated patients with a better clinical outcome showed hypertrophy of the supplementary motor area and cerebellar vermis. In addition, the volume of the cerebellar hemispheres of patients correlated with the improvement of intracortical inhibition which was generally less effective in patients than in controls regardless of the DBS states. Importantly, good responders to GPi DBS showed a similar level of short-latency intracortical inhibition in the motor cortex as healthy controls whereas non-responders were unable to increase it. All these results support the multilevel impact of effective DBS on the motor networks in dystonia and suggest potential biomarkers of responsiveness to this treatment.
Department of Neurosurgery Na Homolce Hospital Prague Czech Republic
Department of Stereotactic and Radiation Neurosurgery Na Homolce Hospital Prague Czech Republic
Max Planck Institute for Human Cognitive and Brain Sciences Leipzig Germany
References provided by Crossref.org
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- $a Clinical benefits of pallidal deep brain stimulation (GPi DBS) in dystonia increase relatively slowly suggesting slow plastic processes in the motor network. Twenty-two patients with dystonia of various distribution and etiology treated by chronic GPi DBS and 22 healthy subjects were examined for short-latency intracortical inhibition of the motor cortex elicited by paired transcranial magnetic stimulation. The relationships between grey matter volume and intracortical inhibition considering the long-term clinical outcome and states of the GPi DBS were analysed. The acute effects of GPi DBS were associated with a shortening of the motor response whereas the grey matter of chronically treated patients with a better clinical outcome showed hypertrophy of the supplementary motor area and cerebellar vermis. In addition, the volume of the cerebellar hemispheres of patients correlated with the improvement of intracortical inhibition which was generally less effective in patients than in controls regardless of the DBS states. Importantly, good responders to GPi DBS showed a similar level of short-latency intracortical inhibition in the motor cortex as healthy controls whereas non-responders were unable to increase it. All these results support the multilevel impact of effective DBS on the motor networks in dystonia and suggest potential biomarkers of responsiveness to this treatment.
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