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A functional micro-electrode mapping of ventral thalamus in essential tremor
Deep brain stimulation enables the delivery of therapeutic interventions to otherwise inaccessible areas of the brain while, at the same time, offering the unique opportunity to record from these same regions in awake patients. The posterior ventrolateral thalamus has become a reliable deep brain st...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113647/ https://www.ncbi.nlm.nih.gov/pubmed/30052807 http://dx.doi.org/10.1093/brain/awy192 |
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author | Pedrosa, David J Brown, Peter Cagnan, Hayriye Visser-Vandewalle, Veerle Wirths, Jochen Timmermann, Lars Brittain, John-Stuart |
author_facet | Pedrosa, David J Brown, Peter Cagnan, Hayriye Visser-Vandewalle, Veerle Wirths, Jochen Timmermann, Lars Brittain, John-Stuart |
author_sort | Pedrosa, David J |
collection | PubMed |
description | Deep brain stimulation enables the delivery of therapeutic interventions to otherwise inaccessible areas of the brain while, at the same time, offering the unique opportunity to record from these same regions in awake patients. The posterior ventrolateral thalamus has become a reliable deep brain stimulation target for medically-refractory patients suffering from essential tremor. However, the contribution of the thalamus in essential tremor, and even whether posterior ventrolateral thalamus is the optimal target, remains a matter of ongoing debate. There are several lines of evidence supporting clusters of activity within the posterior ventrolateral thalamus that are important for tremor emergence. In this study we sought to map the functional properties of these clusters through microelectrode recordings during deep brain stimulation surgery. Data were obtained from 10 severely affected patients with essential tremor (12 hemispheres) undergoing deep brain stimulation surgery. Our results demonstrate power and coherence maxima located in the inferior posterior ventrolateral thalamus and immediate ventral region. Moreover, we identified distinct yet overlapping clusters of predominantly efferent (driving) and afferent (feedback) activity, with a preference for more efferent contributors, consistent with a net role in the driving of tremor output. Finally, we demonstrate that resolvable thalamic spiking activity directly relates to background activity and that the strength of tremor may be dictated by phase relationships between efferent and afferent pockets in the posterior ventrolateral thalamus. Taken together, these results provide important evidence for the role of the inferior posterior ventrolateral thalamus and its border region in essential tremor pathophysiology. Such results progress our mechanistic understanding and promote the adoption of next-generation therapies such as high resolution segregated deep brain stimulation electrodes. |
format | Online Article Text |
id | pubmed-6113647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61136472018-09-02 A functional micro-electrode mapping of ventral thalamus in essential tremor Pedrosa, David J Brown, Peter Cagnan, Hayriye Visser-Vandewalle, Veerle Wirths, Jochen Timmermann, Lars Brittain, John-Stuart Brain Original Articles Deep brain stimulation enables the delivery of therapeutic interventions to otherwise inaccessible areas of the brain while, at the same time, offering the unique opportunity to record from these same regions in awake patients. The posterior ventrolateral thalamus has become a reliable deep brain stimulation target for medically-refractory patients suffering from essential tremor. However, the contribution of the thalamus in essential tremor, and even whether posterior ventrolateral thalamus is the optimal target, remains a matter of ongoing debate. There are several lines of evidence supporting clusters of activity within the posterior ventrolateral thalamus that are important for tremor emergence. In this study we sought to map the functional properties of these clusters through microelectrode recordings during deep brain stimulation surgery. Data were obtained from 10 severely affected patients with essential tremor (12 hemispheres) undergoing deep brain stimulation surgery. Our results demonstrate power and coherence maxima located in the inferior posterior ventrolateral thalamus and immediate ventral region. Moreover, we identified distinct yet overlapping clusters of predominantly efferent (driving) and afferent (feedback) activity, with a preference for more efferent contributors, consistent with a net role in the driving of tremor output. Finally, we demonstrate that resolvable thalamic spiking activity directly relates to background activity and that the strength of tremor may be dictated by phase relationships between efferent and afferent pockets in the posterior ventrolateral thalamus. Taken together, these results provide important evidence for the role of the inferior posterior ventrolateral thalamus and its border region in essential tremor pathophysiology. Such results progress our mechanistic understanding and promote the adoption of next-generation therapies such as high resolution segregated deep brain stimulation electrodes. Oxford University Press 2018-09 2018-07-23 /pmc/articles/PMC6113647/ /pubmed/30052807 http://dx.doi.org/10.1093/brain/awy192 Text en © The Author(s) (2018). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Pedrosa, David J Brown, Peter Cagnan, Hayriye Visser-Vandewalle, Veerle Wirths, Jochen Timmermann, Lars Brittain, John-Stuart A functional micro-electrode mapping of ventral thalamus in essential tremor |
title | A functional micro-electrode mapping of ventral thalamus in essential tremor |
title_full | A functional micro-electrode mapping of ventral thalamus in essential tremor |
title_fullStr | A functional micro-electrode mapping of ventral thalamus in essential tremor |
title_full_unstemmed | A functional micro-electrode mapping of ventral thalamus in essential tremor |
title_short | A functional micro-electrode mapping of ventral thalamus in essential tremor |
title_sort | functional micro-electrode mapping of ventral thalamus in essential tremor |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113647/ https://www.ncbi.nlm.nih.gov/pubmed/30052807 http://dx.doi.org/10.1093/brain/awy192 |
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