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Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex

Objectives: Hemispheric disconnection has been used as a treatment of medically refractory epilepsy and evolved from anatomic hemispherectomy to functional hemispherectomies to hemispherotomies. The hemispherotomy procedure involves disconnection of an entire hemisphere with limited tissue resection...

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Autores principales: Hawasli, Ammar H., Chacko, Ravi, Szrama, Nicholas P., Bundy, David T., Pahwa, Mrinal, Yarbrough, Chester K., Dlouhy, Brian J., Limbrick, David D., Barbour, Dennis L., Smyth, Matthew D., Leuthardt, Eric C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371676/
https://www.ncbi.nlm.nih.gov/pubmed/28424599
http://dx.doi.org/10.3389/fnhum.2017.00149
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author Hawasli, Ammar H.
Chacko, Ravi
Szrama, Nicholas P.
Bundy, David T.
Pahwa, Mrinal
Yarbrough, Chester K.
Dlouhy, Brian J.
Limbrick, David D.
Barbour, Dennis L.
Smyth, Matthew D.
Leuthardt, Eric C.
author_facet Hawasli, Ammar H.
Chacko, Ravi
Szrama, Nicholas P.
Bundy, David T.
Pahwa, Mrinal
Yarbrough, Chester K.
Dlouhy, Brian J.
Limbrick, David D.
Barbour, Dennis L.
Smyth, Matthew D.
Leuthardt, Eric C.
author_sort Hawasli, Ammar H.
collection PubMed
description Objectives: Hemispheric disconnection has been used as a treatment of medically refractory epilepsy and evolved from anatomic hemispherectomy to functional hemispherectomies to hemispherotomies. The hemispherotomy procedure involves disconnection of an entire hemisphere with limited tissue resection and is reserved for medically-refractory epilepsy due to diffuse hemispheric disease. Although it is thought to be effective by preventing seizures from spreading to the contralateral hemisphere, the electrophysiological effects of a hemispherotomy on the ipsilateral hemisphere remain poorly defined. The objective of this study was to evaluate the effects of hemispherotomy on the electrophysiologic dynamics in peri-stroke and dysplastic cortex. Methods: Intraoperative electrocorticography (ECoG) was recorded from ipsilateral cortex in 5 human subjects with refractory epilepsy before and after hemispherotomy. Power spectral density, mutual information, and phase-amplitude coupling were measured from the ECoG signals. Results: Epilepsy was a result of remote perinatal stroke in three of the subjects. In two of the subjects, seizures were a consequence of dysplastic tissue: one with hemimegalencephaly and the second with Rasmussen's encephalitis. Hemispherotomy reduced broad-band power spectral density in peri-stroke cortex. Meanwhile, hemispherotomy increased power in the low and high frequency bands for dysplastic cortex. Functional connectivity was increased in lower frequency bands in peri-stroke tissue but not affected in dysplastic tissue after hemispherotomy. Finally, hemispherotomy reduced band-specific phase-amplitude coupling in peristroke cortex but not dysplastic cortex. Significance: Disconnecting deep subcortical connections to peri-stroke cortex via a hemispherotomy attenuates power of oscillations and impairs the transfer of information from large-scale distributed brain networks to the local cortex. Hence, hemispherotomy reduces heterogeneity between neighboring cortex while impairing phase-amplitude coupling. In contrast, dysfunctional networks in dysplastic cortex lack the normal connectivity with distant networks. Therefore hemispherotomy does not produce the same effects.
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spelling pubmed-53716762017-04-19 Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex Hawasli, Ammar H. Chacko, Ravi Szrama, Nicholas P. Bundy, David T. Pahwa, Mrinal Yarbrough, Chester K. Dlouhy, Brian J. Limbrick, David D. Barbour, Dennis L. Smyth, Matthew D. Leuthardt, Eric C. Front Hum Neurosci Neuroscience Objectives: Hemispheric disconnection has been used as a treatment of medically refractory epilepsy and evolved from anatomic hemispherectomy to functional hemispherectomies to hemispherotomies. The hemispherotomy procedure involves disconnection of an entire hemisphere with limited tissue resection and is reserved for medically-refractory epilepsy due to diffuse hemispheric disease. Although it is thought to be effective by preventing seizures from spreading to the contralateral hemisphere, the electrophysiological effects of a hemispherotomy on the ipsilateral hemisphere remain poorly defined. The objective of this study was to evaluate the effects of hemispherotomy on the electrophysiologic dynamics in peri-stroke and dysplastic cortex. Methods: Intraoperative electrocorticography (ECoG) was recorded from ipsilateral cortex in 5 human subjects with refractory epilepsy before and after hemispherotomy. Power spectral density, mutual information, and phase-amplitude coupling were measured from the ECoG signals. Results: Epilepsy was a result of remote perinatal stroke in three of the subjects. In two of the subjects, seizures were a consequence of dysplastic tissue: one with hemimegalencephaly and the second with Rasmussen's encephalitis. Hemispherotomy reduced broad-band power spectral density in peri-stroke cortex. Meanwhile, hemispherotomy increased power in the low and high frequency bands for dysplastic cortex. Functional connectivity was increased in lower frequency bands in peri-stroke tissue but not affected in dysplastic tissue after hemispherotomy. Finally, hemispherotomy reduced band-specific phase-amplitude coupling in peristroke cortex but not dysplastic cortex. Significance: Disconnecting deep subcortical connections to peri-stroke cortex via a hemispherotomy attenuates power of oscillations and impairs the transfer of information from large-scale distributed brain networks to the local cortex. Hence, hemispherotomy reduces heterogeneity between neighboring cortex while impairing phase-amplitude coupling. In contrast, dysfunctional networks in dysplastic cortex lack the normal connectivity with distant networks. Therefore hemispherotomy does not produce the same effects. Frontiers Media S.A. 2017-03-30 /pmc/articles/PMC5371676/ /pubmed/28424599 http://dx.doi.org/10.3389/fnhum.2017.00149 Text en Copyright © 2017 Hawasli, Chacko, Szrama, Bundy, Pahwa, Yarbrough, Dlouhy, Limbrick, Barbour, Smyth and Leuthardt. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Hawasli, Ammar H.
Chacko, Ravi
Szrama, Nicholas P.
Bundy, David T.
Pahwa, Mrinal
Yarbrough, Chester K.
Dlouhy, Brian J.
Limbrick, David D.
Barbour, Dennis L.
Smyth, Matthew D.
Leuthardt, Eric C.
Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex
title Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex
title_full Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex
title_fullStr Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex
title_full_unstemmed Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex
title_short Electrophysiological Sequelae of Hemispherotomy in Ipsilateral Human Cortex
title_sort electrophysiological sequelae of hemispherotomy in ipsilateral human cortex
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371676/
https://www.ncbi.nlm.nih.gov/pubmed/28424599
http://dx.doi.org/10.3389/fnhum.2017.00149
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