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Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder

High-frequency deep brain stimulation of the subthalamic nucleus can be used to treat severe obsessive-compulsive disorders that are refractory to conventional treatments. The mechanisms of action of this approach possibly rely on the modulation of associative-limbic subcortical–cortical loops, but...

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Autores principales: Kibleur, A, Gras-Combe, G, Benis, D, Bastin, J, Bougerol, T, Chabardès, S, Polosan, M, David, O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315551/
https://www.ncbi.nlm.nih.gov/pubmed/27754484
http://dx.doi.org/10.1038/tp.2016.192
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author Kibleur, A
Gras-Combe, G
Benis, D
Bastin, J
Bougerol, T
Chabardès, S
Polosan, M
David, O
author_facet Kibleur, A
Gras-Combe, G
Benis, D
Bastin, J
Bougerol, T
Chabardès, S
Polosan, M
David, O
author_sort Kibleur, A
collection PubMed
description High-frequency deep brain stimulation of the subthalamic nucleus can be used to treat severe obsessive-compulsive disorders that are refractory to conventional treatments. The mechanisms of action of this approach possibly rely on the modulation of associative-limbic subcortical–cortical loops, but remain to be fully elucidated. Here in 12 patients, we report the effects of high-frequency stimulation of the subthalamic nucleus on behavior, and on electroencephalographic responses and inferred effective connectivity during motor inhibition processes involved in the stop signal task. First, we found that patients were faster to respond and had slower motor inhibition processes when stimulated. Second, the subthalamic stimulation modulated the amplitude and delayed inhibition-related electroencephalographic responses. The power of reconstructed cortical current densities decreased in the stimulation condition in a parietal–frontal network including cortical regions of the inhibition network such as the superior parts of the inferior frontal gyri and the dorsolateral prefrontal cortex. Finally, dynamic causal modeling revealed that the subthalamic stimulation was more likely to modulate efferent connections from the basal ganglia, modeled as a hidden source, to the cortex. The connection from the basal ganglia to the right inferior frontal gyrus was significantly decreased by subthalamic stimulation. Beyond motor inhibition, our study thus strongly suggests that the mechanisms of action of high-frequency subthalamic stimulation are not restricted to the subthalamic nucleus, but also involve the modulation of distributed subcortical–cortical networks.
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spelling pubmed-53155512017-02-27 Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder Kibleur, A Gras-Combe, G Benis, D Bastin, J Bougerol, T Chabardès, S Polosan, M David, O Transl Psychiatry Original Article High-frequency deep brain stimulation of the subthalamic nucleus can be used to treat severe obsessive-compulsive disorders that are refractory to conventional treatments. The mechanisms of action of this approach possibly rely on the modulation of associative-limbic subcortical–cortical loops, but remain to be fully elucidated. Here in 12 patients, we report the effects of high-frequency stimulation of the subthalamic nucleus on behavior, and on electroencephalographic responses and inferred effective connectivity during motor inhibition processes involved in the stop signal task. First, we found that patients were faster to respond and had slower motor inhibition processes when stimulated. Second, the subthalamic stimulation modulated the amplitude and delayed inhibition-related electroencephalographic responses. The power of reconstructed cortical current densities decreased in the stimulation condition in a parietal–frontal network including cortical regions of the inhibition network such as the superior parts of the inferior frontal gyri and the dorsolateral prefrontal cortex. Finally, dynamic causal modeling revealed that the subthalamic stimulation was more likely to modulate efferent connections from the basal ganglia, modeled as a hidden source, to the cortex. The connection from the basal ganglia to the right inferior frontal gyrus was significantly decreased by subthalamic stimulation. Beyond motor inhibition, our study thus strongly suggests that the mechanisms of action of high-frequency subthalamic stimulation are not restricted to the subthalamic nucleus, but also involve the modulation of distributed subcortical–cortical networks. Nature Publishing Group 2016-10 2016-10-18 /pmc/articles/PMC5315551/ /pubmed/27754484 http://dx.doi.org/10.1038/tp.2016.192 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Kibleur, A
Gras-Combe, G
Benis, D
Bastin, J
Bougerol, T
Chabardès, S
Polosan, M
David, O
Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder
title Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder
title_full Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder
title_fullStr Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder
title_full_unstemmed Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder
title_short Modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder
title_sort modulation of motor inhibition by subthalamic stimulation in obsessive-compulsive disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315551/
https://www.ncbi.nlm.nih.gov/pubmed/27754484
http://dx.doi.org/10.1038/tp.2016.192
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