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Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease

The disruption of pathologically enhanced beta oscillations is considered one of the key mechanisms mediating the clinical effects of deep brain stimulation on motor symptoms in Parkinson’s disease. However, a specific modulation of other distinct physiological or pathological oscillatory activities...

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Autores principales: Muthuraman, Muthuraman, Bange, Manuel, Koirala, Nabin, Ciolac, Dumitru, Pintea, Bogdan, Glaser, Martin, Tinkhauser, Gerd, Brown, Peter, Deuschl, Günther, Groppa, Sergiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116448/
https://www.ncbi.nlm.nih.gov/pubmed/33150359
http://dx.doi.org/10.1093/brain/awaa297
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author Muthuraman, Muthuraman
Bange, Manuel
Koirala, Nabin
Ciolac, Dumitru
Pintea, Bogdan
Glaser, Martin
Tinkhauser, Gerd
Brown, Peter
Deuschl, Günther
Groppa, Sergiu
author_facet Muthuraman, Muthuraman
Bange, Manuel
Koirala, Nabin
Ciolac, Dumitru
Pintea, Bogdan
Glaser, Martin
Tinkhauser, Gerd
Brown, Peter
Deuschl, Günther
Groppa, Sergiu
author_sort Muthuraman, Muthuraman
collection PubMed
description The disruption of pathologically enhanced beta oscillations is considered one of the key mechanisms mediating the clinical effects of deep brain stimulation on motor symptoms in Parkinson’s disease. However, a specific modulation of other distinct physiological or pathological oscillatory activities could also play an important role in symptom control and motor function recovery during deep brain stimulation. Finely tuned gamma oscillations have been suggested to be prokinetic in nature, facilitating the preferential processing of physiological neural activity. In this study, we postulate that clinically effective high-frequency stimulation of the subthalamic nucleus imposes cross-frequency interactions with gamma oscillations in a cortico-subcortical network of interconnected regions and normalizes the balance between beta and gamma oscillations. To this end we acquired resting state high-density (256 channels) EEG from 31 patients with Parkinson’s disease who underwent deep brain stimulation to compare spectral power and power-to-power cross-frequency coupling using a beamformer algorithm for coherent sources. To show that modulations exclusively relate to stimulation frequencies that alleviate motor symptoms, two clinically ineffective frequencies were tested as control conditions. We observed a robust reduction of beta and increase of gamma power, attested in the regions of a cortical (motor cortex, supplementary motor area, premotor cortex) and subcortical network (subthalamic nucleus and cerebellum). Additionally, we found a clear cross-frequency coupling of narrowband gamma frequencies to the stimulation frequency in all of these nodes, which negatively correlated with motor impairment. No such dynamics were revealed within the control posterior parietal cortex region. Furthermore, deep brain stimulation at clinically ineffective frequencies did not alter the source power spectra or cross-frequency coupling in any region. These findings demonstrate that clinically effective deep brain stimulation of the subthalamic nucleus differentially modifies different oscillatory activities in a widespread network of cortical and subcortical regions. Particularly the cross-frequency interactions between finely tuned gamma oscillations and the stimulation frequency may suggest an entrainment mechanism that could promote dynamic neural processing underlying motor symptom alleviation.
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spelling pubmed-71164482020-12-09 Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease Muthuraman, Muthuraman Bange, Manuel Koirala, Nabin Ciolac, Dumitru Pintea, Bogdan Glaser, Martin Tinkhauser, Gerd Brown, Peter Deuschl, Günther Groppa, Sergiu Brain Original Articles The disruption of pathologically enhanced beta oscillations is considered one of the key mechanisms mediating the clinical effects of deep brain stimulation on motor symptoms in Parkinson’s disease. However, a specific modulation of other distinct physiological or pathological oscillatory activities could also play an important role in symptom control and motor function recovery during deep brain stimulation. Finely tuned gamma oscillations have been suggested to be prokinetic in nature, facilitating the preferential processing of physiological neural activity. In this study, we postulate that clinically effective high-frequency stimulation of the subthalamic nucleus imposes cross-frequency interactions with gamma oscillations in a cortico-subcortical network of interconnected regions and normalizes the balance between beta and gamma oscillations. To this end we acquired resting state high-density (256 channels) EEG from 31 patients with Parkinson’s disease who underwent deep brain stimulation to compare spectral power and power-to-power cross-frequency coupling using a beamformer algorithm for coherent sources. To show that modulations exclusively relate to stimulation frequencies that alleviate motor symptoms, two clinically ineffective frequencies were tested as control conditions. We observed a robust reduction of beta and increase of gamma power, attested in the regions of a cortical (motor cortex, supplementary motor area, premotor cortex) and subcortical network (subthalamic nucleus and cerebellum). Additionally, we found a clear cross-frequency coupling of narrowband gamma frequencies to the stimulation frequency in all of these nodes, which negatively correlated with motor impairment. No such dynamics were revealed within the control posterior parietal cortex region. Furthermore, deep brain stimulation at clinically ineffective frequencies did not alter the source power spectra or cross-frequency coupling in any region. These findings demonstrate that clinically effective deep brain stimulation of the subthalamic nucleus differentially modifies different oscillatory activities in a widespread network of cortical and subcortical regions. Particularly the cross-frequency interactions between finely tuned gamma oscillations and the stimulation frequency may suggest an entrainment mechanism that could promote dynamic neural processing underlying motor symptom alleviation. Oxford University Press 2020-11-05 /pmc/articles/PMC7116448/ /pubmed/33150359 http://dx.doi.org/10.1093/brain/awaa297 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (ttp://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Muthuraman, Muthuraman
Bange, Manuel
Koirala, Nabin
Ciolac, Dumitru
Pintea, Bogdan
Glaser, Martin
Tinkhauser, Gerd
Brown, Peter
Deuschl, Günther
Groppa, Sergiu
Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease
title Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease
title_full Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease
title_fullStr Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease
title_full_unstemmed Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease
title_short Cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in Parkinson’s disease
title_sort cross-frequency coupling between gamma oscillations and deep brain stimulation frequency in parkinson’s disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116448/
https://www.ncbi.nlm.nih.gov/pubmed/33150359
http://dx.doi.org/10.1093/brain/awaa297
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