Editorial: Functional Brain Mapping of Epilepsy Networks: Methods and Applications

With technology such as simultaneous electroencephalography and functional magnetic resonance imaging (EEG-fMRI) now more readily available, it is possible to non-invasively map epileptiform activity throughout the entire brain at millimeter resolution. In application to MTLE and healthy controls, t...

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Published inFrontiers in neuroscience Vol. 13; p. 417
Main Authors Abbott, David F., Archer, John S., Carney, Patrick W., Vaughan, David N., Jackson, Graeme D.
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Research Foundation 21.05.2019
Frontiers Media S.A
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ISSN1662-453X
1662-4548
1662-453X
DOI10.3389/fnins.2019.00417

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Abstract With technology such as simultaneous electroencephalography and functional magnetic resonance imaging (EEG-fMRI) now more readily available, it is possible to non-invasively map epileptiform activity throughout the entire brain at millimeter resolution. In application to MTLE and healthy controls, three distinct reliable networks were revealed: two that exhibited increased activity in patients (a network including hippocampus and amygdala bilaterally, and a network including postcentral gyri and temporal poles), and a network identified as specific to healthy controls (i.e., effectively decreased in patients, consisting of bilateral precuneus, anterior cingulate, thalamus, and parahippocampal gyrus). Confirming with computer modeling and phantom measurements that lead positioning can have a substantial effect on the amplitude of the MRI gradient artifact present on the EEG, they optimized the positions in a novel cap design. [...]whilst this substantially reduced gradient artifact amplitude on the phantom, it made things worse when used on human subjects. [...]improvements in model accuracy are required if one is to make accurate predictions for the human context.
AbstractList With technology such as simultaneous electroencephalography and functional magnetic resonance imaging (EEG-fMRI) now more readily available, it is possible to non-invasively map epileptiform activity throughout the entire brain at millimeter resolution. In application to MTLE and healthy controls, three distinct reliable networks were revealed: two that exhibited increased activity in patients (a network including hippocampus and amygdala bilaterally, and a network including postcentral gyri and temporal poles), and a network identified as specific to healthy controls (i.e., effectively decreased in patients, consisting of bilateral precuneus, anterior cingulate, thalamus, and parahippocampal gyrus). Confirming with computer modeling and phantom measurements that lead positioning can have a substantial effect on the amplitude of the MRI gradient artifact present on the EEG, they optimized the positions in a novel cap design. [...]whilst this substantially reduced gradient artifact amplitude on the phantom, it made things worse when used on human subjects. [...]improvements in model accuracy are required if one is to make accurate predictions for the human context.
Author Carney, Patrick W.
Archer, John S.
Jackson, Graeme D.
Vaughan, David N.
Abbott, David F.
AuthorAffiliation 3 Eastern Health Clinical School, Monash University , Melbourne, VIC , Australia
1 The Florey Institute of Neuroscience and Mental Health, Austin Hospital , Melbourne, VIC , Australia
2 Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne , Melbourne, VIC , Australia
AuthorAffiliation_xml – name: 3 Eastern Health Clinical School, Monash University , Melbourne, VIC , Australia
– name: 1 The Florey Institute of Neuroscience and Mental Health, Austin Hospital , Melbourne, VIC , Australia
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CitedBy_id crossref_primary_10_1111_epi_17890
crossref_primary_10_1016_j_seizure_2020_03_010
crossref_primary_10_3390_bs12040107
Cites_doi 10.1016/j.neuroimage.2012.12.025
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ContentType Journal Article
Copyright 2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright © 2019 Abbott, Archer, Carney, Vaughan and Jackson. 2019 Abbott, Archer, Carney, Vaughan and Jackson
Copyright_xml – notice: 2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Copyright © 2019 Abbott, Archer, Carney, Vaughan and Jackson. 2019 Abbott, Archer, Carney, Vaughan and Jackson
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Keywords epilepsy
fMRI
seizure prediction
functional connectivity
EEG
default mode network
interictal epileptiform discharge
computational modeling and simulation
Language English
License 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) and the copyright owner(s) 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.
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This article was submitted to Brain Imaging Methods, a section of the journal Frontiers in Neuroscience
Edited and reviewed by: Vince D. Calhoun, University of New Mexico, United States
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SubjectTerms Brain mapping
Brain research
Conflicts of interest
Convulsions & seizures
default mode network
Editorials
EEG
Electroencephalography
Epilepsy
fMRI
functional connectivity
Functional magnetic resonance imaging
Funding
interictal epileptiform discharge
Medical imaging
Mental health
Neuroimaging
Neuroscience
Neurosciences
NMR
Nuclear magnetic resonance
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Title Editorial: Functional Brain Mapping of Epilepsy Networks: Methods and Applications
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