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Slowing less than 1 Hz is decreased near the seizure onset zone
Focal slowing (<4 Hz) of brain waves is often associated with focal cerebral dysfunction and is assumed to be increased closest to the location of dysfunction. Prior work suggests that slowing may be comprised of at least two distinct neural mechanisms: slow oscillation activity (<1 Hz) may re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470162/ https://www.ncbi.nlm.nih.gov/pubmed/30996228 http://dx.doi.org/10.1038/s41598-019-42347-y |
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author | Lundstrom, Brian Nils Boly, Melanie Duckrow, Robert Zaveri, Hitten P. Blumenfeld, Hal |
author_facet | Lundstrom, Brian Nils Boly, Melanie Duckrow, Robert Zaveri, Hitten P. Blumenfeld, Hal |
author_sort | Lundstrom, Brian Nils |
collection | PubMed |
description | Focal slowing (<4 Hz) of brain waves is often associated with focal cerebral dysfunction and is assumed to be increased closest to the location of dysfunction. Prior work suggests that slowing may be comprised of at least two distinct neural mechanisms: slow oscillation activity (<1 Hz) may reflect primarily inhibitory cortical mechanisms while power in the delta frequency (1–4 Hz) may correlate with local synaptic strength. In focal epilepsy patients, we examined slow wave activity near and far from the seizure onset zone (SOZ) during wake, sleep, and postictal states using intracranial electroencephalography. We found that slow oscillation (0.3–1 Hz) activity was decreased near the SOZ, while delta activity (2–4 Hz) activity was increased. This finding was most prominent during sleep, and accompanied by a loss of long-range intra-hemispheric synchrony. In contrast to sleep, postictal slowing was characterized by a broadband increase of spectral power, and showed a reduced modulatory effect of slow oscillations on higher frequencies. These results suggest slow oscillation focal slowing is reduced near the seizure onset zone, perhaps reflecting reduced inhibitory activity. Dissociation between slow oscillation and delta slowing could help localize the seizure onset zone from interictal intracranial recordings. |
format | Online Article Text |
id | pubmed-6470162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64701622019-04-23 Slowing less than 1 Hz is decreased near the seizure onset zone Lundstrom, Brian Nils Boly, Melanie Duckrow, Robert Zaveri, Hitten P. Blumenfeld, Hal Sci Rep Article Focal slowing (<4 Hz) of brain waves is often associated with focal cerebral dysfunction and is assumed to be increased closest to the location of dysfunction. Prior work suggests that slowing may be comprised of at least two distinct neural mechanisms: slow oscillation activity (<1 Hz) may reflect primarily inhibitory cortical mechanisms while power in the delta frequency (1–4 Hz) may correlate with local synaptic strength. In focal epilepsy patients, we examined slow wave activity near and far from the seizure onset zone (SOZ) during wake, sleep, and postictal states using intracranial electroencephalography. We found that slow oscillation (0.3–1 Hz) activity was decreased near the SOZ, while delta activity (2–4 Hz) activity was increased. This finding was most prominent during sleep, and accompanied by a loss of long-range intra-hemispheric synchrony. In contrast to sleep, postictal slowing was characterized by a broadband increase of spectral power, and showed a reduced modulatory effect of slow oscillations on higher frequencies. These results suggest slow oscillation focal slowing is reduced near the seizure onset zone, perhaps reflecting reduced inhibitory activity. Dissociation between slow oscillation and delta slowing could help localize the seizure onset zone from interictal intracranial recordings. Nature Publishing Group UK 2019-04-17 /pmc/articles/PMC6470162/ /pubmed/30996228 http://dx.doi.org/10.1038/s41598-019-42347-y Text en © The Author(s) 2019 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 Lundstrom, Brian Nils Boly, Melanie Duckrow, Robert Zaveri, Hitten P. Blumenfeld, Hal Slowing less than 1 Hz is decreased near the seizure onset zone |
title | Slowing less than 1 Hz is decreased near the seizure onset zone |
title_full | Slowing less than 1 Hz is decreased near the seizure onset zone |
title_fullStr | Slowing less than 1 Hz is decreased near the seizure onset zone |
title_full_unstemmed | Slowing less than 1 Hz is decreased near the seizure onset zone |
title_short | Slowing less than 1 Hz is decreased near the seizure onset zone |
title_sort | slowing less than 1 hz is decreased near the seizure onset zone |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470162/ https://www.ncbi.nlm.nih.gov/pubmed/30996228 http://dx.doi.org/10.1038/s41598-019-42347-y |
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