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Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics

Single‐photon emission computed tomography (SPECT) during seizures and magnetoencephalography (MEG) during the interictal state are noninvasive modalities employed in the localization of the epileptogenic zone in patients with drug‐resistant focal epilepsy (DRFE). The present study aims to investiga...

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Autores principales: Krishnan, Balu, Tousseyn, Simon, Wang, Zhong Irene, Murakami, Hiroatsu, Wu, Guiyun, Burgess, Richard, Iasemidis, Leonidas, Najm, Imad, Alexopoulos, Andreas V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9921232/
https://www.ncbi.nlm.nih.gov/pubmed/36480260
http://dx.doi.org/10.1002/hbm.26168
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author Krishnan, Balu
Tousseyn, Simon
Wang, Zhong Irene
Murakami, Hiroatsu
Wu, Guiyun
Burgess, Richard
Iasemidis, Leonidas
Najm, Imad
Alexopoulos, Andreas V.
author_facet Krishnan, Balu
Tousseyn, Simon
Wang, Zhong Irene
Murakami, Hiroatsu
Wu, Guiyun
Burgess, Richard
Iasemidis, Leonidas
Najm, Imad
Alexopoulos, Andreas V.
author_sort Krishnan, Balu
collection PubMed
description Single‐photon emission computed tomography (SPECT) during seizures and magnetoencephalography (MEG) during the interictal state are noninvasive modalities employed in the localization of the epileptogenic zone in patients with drug‐resistant focal epilepsy (DRFE). The present study aims to investigate whether there exists a preferentially high MEG functional connectivity (FC) among those regions of the brain that exhibit hyperperfusion or hypoperfusion during seizures. We studied MEG and SPECT data in 30 consecutive DRFE patients who had resective epilepsy surgery. We parcellated each ictal perfusion map into 200 regions of interest (ROIs) and generated ROI time series using source modeling of MEG data. FC between ROIs was quantified using coherence and phase‐locking value. We defined a generalized linear model to relate the connectivity of each ROI, ictal perfusion z score, and distance between ROIs. We compared the coefficients relating perfusion z score to FC of each ROI and estimated the connectivity within and between resected and unresected ROIs. We found that perfusion z scores were strongly correlated with the FC of hyper‐, and separately, hypoperfused ROIs across patients. High interictal connectivity was observed between hyperperfused brain regions inside and outside the resected area. High connectivity was also observed between regions of ictal hypoperfusion. Importantly, the ictally hypoperfused regions had a low interictal connectivity to regions that became hyperperfused during seizures. We conclude that brain regions exhibiting hyperperfusion during seizures highlight a preferentially connected interictal network, whereas regions of ictal hypoperfusion highlight a separate, discrete and interconnected, interictal network.
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spelling pubmed-99212322023-02-13 Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics Krishnan, Balu Tousseyn, Simon Wang, Zhong Irene Murakami, Hiroatsu Wu, Guiyun Burgess, Richard Iasemidis, Leonidas Najm, Imad Alexopoulos, Andreas V. Hum Brain Mapp Research Articles Single‐photon emission computed tomography (SPECT) during seizures and magnetoencephalography (MEG) during the interictal state are noninvasive modalities employed in the localization of the epileptogenic zone in patients with drug‐resistant focal epilepsy (DRFE). The present study aims to investigate whether there exists a preferentially high MEG functional connectivity (FC) among those regions of the brain that exhibit hyperperfusion or hypoperfusion during seizures. We studied MEG and SPECT data in 30 consecutive DRFE patients who had resective epilepsy surgery. We parcellated each ictal perfusion map into 200 regions of interest (ROIs) and generated ROI time series using source modeling of MEG data. FC between ROIs was quantified using coherence and phase‐locking value. We defined a generalized linear model to relate the connectivity of each ROI, ictal perfusion z score, and distance between ROIs. We compared the coefficients relating perfusion z score to FC of each ROI and estimated the connectivity within and between resected and unresected ROIs. We found that perfusion z scores were strongly correlated with the FC of hyper‐, and separately, hypoperfused ROIs across patients. High interictal connectivity was observed between hyperperfused brain regions inside and outside the resected area. High connectivity was also observed between regions of ictal hypoperfusion. Importantly, the ictally hypoperfused regions had a low interictal connectivity to regions that became hyperperfused during seizures. We conclude that brain regions exhibiting hyperperfusion during seizures highlight a preferentially connected interictal network, whereas regions of ictal hypoperfusion highlight a separate, discrete and interconnected, interictal network. John Wiley & Sons, Inc. 2022-12-08 /pmc/articles/PMC9921232/ /pubmed/36480260 http://dx.doi.org/10.1002/hbm.26168 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Krishnan, Balu
Tousseyn, Simon
Wang, Zhong Irene
Murakami, Hiroatsu
Wu, Guiyun
Burgess, Richard
Iasemidis, Leonidas
Najm, Imad
Alexopoulos, Andreas V.
Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics
title Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics
title_full Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics
title_fullStr Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics
title_full_unstemmed Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics
title_short Novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: Linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics
title_sort novel noninvasive identification of patient‐specific epileptic networks in focal epilepsies: linking single‐photon emission computed tomography perfusion during seizures with resting‐state magnetoencephalography dynamics
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9921232/
https://www.ncbi.nlm.nih.gov/pubmed/36480260
http://dx.doi.org/10.1002/hbm.26168
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