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Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy
Chronic brain recordings suggest that seizure risk is not uniform, but rather varies systematically relative to daily (circadian) and multiday (multidien) cycles. Here, one human and seven dogs with naturally occurring epilepsy had continuous intracranial EEG (median 298 days) using novel implantabl...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688461/ https://www.ncbi.nlm.nih.gov/pubmed/34930926 http://dx.doi.org/10.1038/s41598-021-03555-7 |
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author | Gregg, Nicholas M. Sladky, Vladimir Nejedly, Petr Mivalt, Filip Kim, Inyong Balzekas, Irena Sturges, Beverly K. Crowe, Chelsea Patterson, Edward E. Van Gompel, Jamie J. Lundstrom, Brian N. Leyde, Kent Denison, Timothy J. Brinkmann, Benjamin H. Kremen, Vaclav Worrell, Gregory A. |
author_facet | Gregg, Nicholas M. Sladky, Vladimir Nejedly, Petr Mivalt, Filip Kim, Inyong Balzekas, Irena Sturges, Beverly K. Crowe, Chelsea Patterson, Edward E. Van Gompel, Jamie J. Lundstrom, Brian N. Leyde, Kent Denison, Timothy J. Brinkmann, Benjamin H. Kremen, Vaclav Worrell, Gregory A. |
author_sort | Gregg, Nicholas M. |
collection | PubMed |
description | Chronic brain recordings suggest that seizure risk is not uniform, but rather varies systematically relative to daily (circadian) and multiday (multidien) cycles. Here, one human and seven dogs with naturally occurring epilepsy had continuous intracranial EEG (median 298 days) using novel implantable sensing and stimulation devices. Two pet dogs and the human subject received concurrent thalamic deep brain stimulation (DBS) over multiple months. All subjects had circadian and multiday cycles in the rate of interictal epileptiform spikes (IES). There was seizure phase locking to circadian and multiday IES cycles in five and seven out of eight subjects, respectively. Thalamic DBS modified circadian (all 3 subjects) and multiday (analysis limited to the human participant) IES cycles. DBS modified seizure clustering and circadian phase locking in the human subject. Multiscale cycles in brain excitability and seizure risk are features of human and canine epilepsy and are modifiable by thalamic DBS. |
format | Online Article Text |
id | pubmed-8688461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86884612021-12-22 Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy Gregg, Nicholas M. Sladky, Vladimir Nejedly, Petr Mivalt, Filip Kim, Inyong Balzekas, Irena Sturges, Beverly K. Crowe, Chelsea Patterson, Edward E. Van Gompel, Jamie J. Lundstrom, Brian N. Leyde, Kent Denison, Timothy J. Brinkmann, Benjamin H. Kremen, Vaclav Worrell, Gregory A. Sci Rep Article Chronic brain recordings suggest that seizure risk is not uniform, but rather varies systematically relative to daily (circadian) and multiday (multidien) cycles. Here, one human and seven dogs with naturally occurring epilepsy had continuous intracranial EEG (median 298 days) using novel implantable sensing and stimulation devices. Two pet dogs and the human subject received concurrent thalamic deep brain stimulation (DBS) over multiple months. All subjects had circadian and multiday cycles in the rate of interictal epileptiform spikes (IES). There was seizure phase locking to circadian and multiday IES cycles in five and seven out of eight subjects, respectively. Thalamic DBS modified circadian (all 3 subjects) and multiday (analysis limited to the human participant) IES cycles. DBS modified seizure clustering and circadian phase locking in the human subject. Multiscale cycles in brain excitability and seizure risk are features of human and canine epilepsy and are modifiable by thalamic DBS. Nature Publishing Group UK 2021-12-20 /pmc/articles/PMC8688461/ /pubmed/34930926 http://dx.doi.org/10.1038/s41598-021-03555-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gregg, Nicholas M. Sladky, Vladimir Nejedly, Petr Mivalt, Filip Kim, Inyong Balzekas, Irena Sturges, Beverly K. Crowe, Chelsea Patterson, Edward E. Van Gompel, Jamie J. Lundstrom, Brian N. Leyde, Kent Denison, Timothy J. Brinkmann, Benjamin H. Kremen, Vaclav Worrell, Gregory A. Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy |
title | Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy |
title_full | Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy |
title_fullStr | Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy |
title_full_unstemmed | Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy |
title_short | Thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy |
title_sort | thalamic deep brain stimulation modulates cycles of seizure risk in epilepsy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688461/ https://www.ncbi.nlm.nih.gov/pubmed/34930926 http://dx.doi.org/10.1038/s41598-021-03555-7 |
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