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Interictal epileptiform discharges shape large-scale intercortical communication
Dynamic interactions between remote but functionally specialized brain regions enable complex information processing. This intercortical communication is disrupted in the neural networks of patients with focal epilepsy, and epileptic activity can exert widespread effects within the brain. Using larg...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821283/ https://www.ncbi.nlm.nih.gov/pubmed/31501850 http://dx.doi.org/10.1093/brain/awz269 |
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author | Dahal, Prawesh Ghani, Naureen Flinker, Adeen Dugan, Patricia Friedman, Daniel Doyle, Werner Devinsky, Orrin Khodagholy, Dion Gelinas, Jennifer N |
author_facet | Dahal, Prawesh Ghani, Naureen Flinker, Adeen Dugan, Patricia Friedman, Daniel Doyle, Werner Devinsky, Orrin Khodagholy, Dion Gelinas, Jennifer N |
author_sort | Dahal, Prawesh |
collection | PubMed |
description | Dynamic interactions between remote but functionally specialized brain regions enable complex information processing. This intercortical communication is disrupted in the neural networks of patients with focal epilepsy, and epileptic activity can exert widespread effects within the brain. Using large-scale human intracranial electroencephalography recordings, we show that interictal epileptiform discharges (IEDs) are significantly coupled with spindles in discrete, individualized brain regions outside of the epileptic network. We found that a substantial proportion of these localized spindles travel across the cortical surface. Brain regions that participate in this IED-driven oscillatory coupling express spindles that have a broader spatial extent and higher tendency to propagate than spindles occurring in uncoupled regions. These altered spatiotemporal oscillatory properties identify areas that are shaped by epileptic activity independent of IED or seizure detection. Our findings suggest that IED-spindle coupling may be an important mechanism of interictal global network dysfunction that could be targeted to prevent disruption of normal neural activity. |
format | Online Article Text |
id | pubmed-6821283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68212832019-11-04 Interictal epileptiform discharges shape large-scale intercortical communication Dahal, Prawesh Ghani, Naureen Flinker, Adeen Dugan, Patricia Friedman, Daniel Doyle, Werner Devinsky, Orrin Khodagholy, Dion Gelinas, Jennifer N Brain Original Articles Dynamic interactions between remote but functionally specialized brain regions enable complex information processing. This intercortical communication is disrupted in the neural networks of patients with focal epilepsy, and epileptic activity can exert widespread effects within the brain. Using large-scale human intracranial electroencephalography recordings, we show that interictal epileptiform discharges (IEDs) are significantly coupled with spindles in discrete, individualized brain regions outside of the epileptic network. We found that a substantial proportion of these localized spindles travel across the cortical surface. Brain regions that participate in this IED-driven oscillatory coupling express spindles that have a broader spatial extent and higher tendency to propagate than spindles occurring in uncoupled regions. These altered spatiotemporal oscillatory properties identify areas that are shaped by epileptic activity independent of IED or seizure detection. Our findings suggest that IED-spindle coupling may be an important mechanism of interictal global network dysfunction that could be targeted to prevent disruption of normal neural activity. Oxford University Press 2019-11 2019-09-09 /pmc/articles/PMC6821283/ /pubmed/31501850 http://dx.doi.org/10.1093/brain/awz269 Text en © The Author(s) (2019). 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 (http://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 Dahal, Prawesh Ghani, Naureen Flinker, Adeen Dugan, Patricia Friedman, Daniel Doyle, Werner Devinsky, Orrin Khodagholy, Dion Gelinas, Jennifer N Interictal epileptiform discharges shape large-scale intercortical communication |
title | Interictal epileptiform discharges shape large-scale intercortical communication |
title_full | Interictal epileptiform discharges shape large-scale intercortical communication |
title_fullStr | Interictal epileptiform discharges shape large-scale intercortical communication |
title_full_unstemmed | Interictal epileptiform discharges shape large-scale intercortical communication |
title_short | Interictal epileptiform discharges shape large-scale intercortical communication |
title_sort | interictal epileptiform discharges shape large-scale intercortical communication |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821283/ https://www.ncbi.nlm.nih.gov/pubmed/31501850 http://dx.doi.org/10.1093/brain/awz269 |
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