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Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis
In focal ictogenesis, gamma oscillations (30–70 Hz) recorded by electroencephalography (EEG) are related to the epileptiform synchronization of interneurons that links the seizure onset zone (SOZ) to the surrounding epileptogenic zone. We hypothesized that the synchronization of interneurons could b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570997/ https://www.ncbi.nlm.nih.gov/pubmed/28839247 http://dx.doi.org/10.1038/s41598-017-09931-6 |
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author | Sato, Yosuke Wong, Simeon M. Iimura, Yasushi Ochi, Ayako Doesburg, Sam M. Otsubo, Hiroshi |
author_facet | Sato, Yosuke Wong, Simeon M. Iimura, Yasushi Ochi, Ayako Doesburg, Sam M. Otsubo, Hiroshi |
author_sort | Sato, Yosuke |
collection | PubMed |
description | In focal ictogenesis, gamma oscillations (30–70 Hz) recorded by electroencephalography (EEG) are related to the epileptiform synchronization of interneurons that links the seizure onset zone (SOZ) to the surrounding epileptogenic zone. We hypothesized that the synchronization of interneurons could be detected as changes in the regularity of gamma oscillation rhythmicity. We used multiscale entropy (MSE) analysis, which can quantify the regularity of EEG rhythmicity, to investigate how the regularity of gamma oscillations changes over the course of a seizure event. We analyzed intracranial EEG data from 13 pediatric patients with focal cortical dysplasia. The MSE analysis revealed the following characteristic changes of MSE score (gamma oscillations): (1) during the interictal periods, the lowest MSE score (the most regular gamma oscillations) was always found in the SOZ; (2) during the preictal periods, the SOZ became more similar to the epileptogenic zone as the MSE score increased in the SOZ (gamma oscillations became less regular in the SOZ); and (3) during the ictal periods, a decreasing MSE score (highly regular gamma oscillations) propagated over the epileptogenic zone. These spatiotemporal changes in regularity of gamma oscillations constitute an important demonstration that focal ictogenesis is caused by dynamic changes in interneuron synchronization. |
format | Online Article Text |
id | pubmed-5570997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55709972017-09-01 Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis Sato, Yosuke Wong, Simeon M. Iimura, Yasushi Ochi, Ayako Doesburg, Sam M. Otsubo, Hiroshi Sci Rep Article In focal ictogenesis, gamma oscillations (30–70 Hz) recorded by electroencephalography (EEG) are related to the epileptiform synchronization of interneurons that links the seizure onset zone (SOZ) to the surrounding epileptogenic zone. We hypothesized that the synchronization of interneurons could be detected as changes in the regularity of gamma oscillation rhythmicity. We used multiscale entropy (MSE) analysis, which can quantify the regularity of EEG rhythmicity, to investigate how the regularity of gamma oscillations changes over the course of a seizure event. We analyzed intracranial EEG data from 13 pediatric patients with focal cortical dysplasia. The MSE analysis revealed the following characteristic changes of MSE score (gamma oscillations): (1) during the interictal periods, the lowest MSE score (the most regular gamma oscillations) was always found in the SOZ; (2) during the preictal periods, the SOZ became more similar to the epileptogenic zone as the MSE score increased in the SOZ (gamma oscillations became less regular in the SOZ); and (3) during the ictal periods, a decreasing MSE score (highly regular gamma oscillations) propagated over the epileptogenic zone. These spatiotemporal changes in regularity of gamma oscillations constitute an important demonstration that focal ictogenesis is caused by dynamic changes in interneuron synchronization. Nature Publishing Group UK 2017-08-24 /pmc/articles/PMC5570997/ /pubmed/28839247 http://dx.doi.org/10.1038/s41598-017-09931-6 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sato, Yosuke Wong, Simeon M. Iimura, Yasushi Ochi, Ayako Doesburg, Sam M. Otsubo, Hiroshi Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis |
title | Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis |
title_full | Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis |
title_fullStr | Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis |
title_full_unstemmed | Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis |
title_short | Spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis |
title_sort | spatiotemporal changes in regularity of gamma oscillations contribute to focal ictogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570997/ https://www.ncbi.nlm.nih.gov/pubmed/28839247 http://dx.doi.org/10.1038/s41598-017-09931-6 |
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