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An optimal strategy for epilepsy surgery: Disruption of the rich-club?

Surgery is a therapeutic option for people with epilepsy whose seizures are not controlled by anti-epilepsy drugs. In pre-surgical planning, an array of data modalities, often including intra-cranial EEG, is used in an attempt to map regions of the brain thought to be crucial for the generation of s...

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Autores principales: Lopes, Marinho A., Richardson, Mark P., Abela, Eugenio, Rummel, Christian, Schindler, Kaspar, Goodfellow, Marc, Terry, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560820/
https://www.ncbi.nlm.nih.gov/pubmed/28817568
http://dx.doi.org/10.1371/journal.pcbi.1005637
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author Lopes, Marinho A.
Richardson, Mark P.
Abela, Eugenio
Rummel, Christian
Schindler, Kaspar
Goodfellow, Marc
Terry, John R.
author_facet Lopes, Marinho A.
Richardson, Mark P.
Abela, Eugenio
Rummel, Christian
Schindler, Kaspar
Goodfellow, Marc
Terry, John R.
author_sort Lopes, Marinho A.
collection PubMed
description Surgery is a therapeutic option for people with epilepsy whose seizures are not controlled by anti-epilepsy drugs. In pre-surgical planning, an array of data modalities, often including intra-cranial EEG, is used in an attempt to map regions of the brain thought to be crucial for the generation of seizures. These regions are then resected with the hope that the individual is rendered seizure free as a consequence. However, post-operative seizure freedom is currently sub-optimal, suggesting that the pre-surgical assessment may be improved by taking advantage of a mechanistic understanding of seizure generation in large brain networks. Herein we use mathematical models to uncover the relative contribution of regions of the brain to seizure generation and consequently which brain regions should be considered for resection. A critical advantage of this modeling approach is that the effect of different surgical strategies can be predicted and quantitatively compared in advance of surgery. Herein we seek to understand seizure generation in networks with different topologies and study how the removal of different nodes in these networks reduces the occurrence of seizures. Since this a computationally demanding problem, a first step for this aim is to facilitate tractability of this approach for large networks. To do this, we demonstrate that predictions arising from a neural mass model are preserved in a lower dimensional, canonical model that is quicker to simulate. We then use this simpler model to study the emergence of seizures in artificial networks with different topologies, and calculate which nodes should be removed to render the network seizure free. We find that for scale-free and rich-club networks there exist specific nodes that are critical for seizure generation and should therefore be removed, whereas for small-world networks the strategy should instead focus on removing sufficient brain tissue. We demonstrate the validity of our approach by analysing intra-cranial EEG recordings from a database comprising 16 patients who have undergone epilepsy surgery, revealing rich-club structures within the obtained functional networks. We show that the postsurgical outcome for these patients was better when a greater proportion of the rich club was removed, in agreement with our theoretical predictions.
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spelling pubmed-55608202017-08-25 An optimal strategy for epilepsy surgery: Disruption of the rich-club? Lopes, Marinho A. Richardson, Mark P. Abela, Eugenio Rummel, Christian Schindler, Kaspar Goodfellow, Marc Terry, John R. PLoS Comput Biol Research Article Surgery is a therapeutic option for people with epilepsy whose seizures are not controlled by anti-epilepsy drugs. In pre-surgical planning, an array of data modalities, often including intra-cranial EEG, is used in an attempt to map regions of the brain thought to be crucial for the generation of seizures. These regions are then resected with the hope that the individual is rendered seizure free as a consequence. However, post-operative seizure freedom is currently sub-optimal, suggesting that the pre-surgical assessment may be improved by taking advantage of a mechanistic understanding of seizure generation in large brain networks. Herein we use mathematical models to uncover the relative contribution of regions of the brain to seizure generation and consequently which brain regions should be considered for resection. A critical advantage of this modeling approach is that the effect of different surgical strategies can be predicted and quantitatively compared in advance of surgery. Herein we seek to understand seizure generation in networks with different topologies and study how the removal of different nodes in these networks reduces the occurrence of seizures. Since this a computationally demanding problem, a first step for this aim is to facilitate tractability of this approach for large networks. To do this, we demonstrate that predictions arising from a neural mass model are preserved in a lower dimensional, canonical model that is quicker to simulate. We then use this simpler model to study the emergence of seizures in artificial networks with different topologies, and calculate which nodes should be removed to render the network seizure free. We find that for scale-free and rich-club networks there exist specific nodes that are critical for seizure generation and should therefore be removed, whereas for small-world networks the strategy should instead focus on removing sufficient brain tissue. We demonstrate the validity of our approach by analysing intra-cranial EEG recordings from a database comprising 16 patients who have undergone epilepsy surgery, revealing rich-club structures within the obtained functional networks. We show that the postsurgical outcome for these patients was better when a greater proportion of the rich club was removed, in agreement with our theoretical predictions. Public Library of Science 2017-08-17 /pmc/articles/PMC5560820/ /pubmed/28817568 http://dx.doi.org/10.1371/journal.pcbi.1005637 Text en © 2017 Lopes et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lopes, Marinho A.
Richardson, Mark P.
Abela, Eugenio
Rummel, Christian
Schindler, Kaspar
Goodfellow, Marc
Terry, John R.
An optimal strategy for epilepsy surgery: Disruption of the rich-club?
title An optimal strategy for epilepsy surgery: Disruption of the rich-club?
title_full An optimal strategy for epilepsy surgery: Disruption of the rich-club?
title_fullStr An optimal strategy for epilepsy surgery: Disruption of the rich-club?
title_full_unstemmed An optimal strategy for epilepsy surgery: Disruption of the rich-club?
title_short An optimal strategy for epilepsy surgery: Disruption of the rich-club?
title_sort optimal strategy for epilepsy surgery: disruption of the rich-club?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560820/
https://www.ncbi.nlm.nih.gov/pubmed/28817568
http://dx.doi.org/10.1371/journal.pcbi.1005637
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