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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...

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Autores principales: Dahal, Prawesh, Ghani, Naureen, Flinker, Adeen, Dugan, Patricia, Friedman, Daniel, Doyle, Werner, Devinsky, Orrin, Khodagholy, Dion, Gelinas, Jennifer N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
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.
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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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