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Seizure pathways: A model-based investigation

We present the results of a model inversion algorithm for electrocorticography (ECoG) data recorded during epileptic seizures. The states and parameters of neural mass models were tracked during a total of over 3000 seizures from twelve patients with focal epilepsy. These models provide an estimate...

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Autores principales: Karoly, Philippa J., Kuhlmann, Levin, Soudry, Daniel, Grayden, David B., Cook, Mark J., Freestone, Dean R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199000/
https://www.ncbi.nlm.nih.gov/pubmed/30307937
http://dx.doi.org/10.1371/journal.pcbi.1006403
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author Karoly, Philippa J.
Kuhlmann, Levin
Soudry, Daniel
Grayden, David B.
Cook, Mark J.
Freestone, Dean R.
author_facet Karoly, Philippa J.
Kuhlmann, Levin
Soudry, Daniel
Grayden, David B.
Cook, Mark J.
Freestone, Dean R.
author_sort Karoly, Philippa J.
collection PubMed
description We present the results of a model inversion algorithm for electrocorticography (ECoG) data recorded during epileptic seizures. The states and parameters of neural mass models were tracked during a total of over 3000 seizures from twelve patients with focal epilepsy. These models provide an estimate of the effective connectivity within intracortical circuits over the time course of seizures. Observing the dynamics of effective connectivity provides insight into mechanisms of seizures. Estimation of patients seizure dynamics revealed: 1) a highly stereotyped pattern of evolution for each patient, 2) distinct sub-groups of onset mechanisms amongst patients, and 3) different offset mechanisms for long and short seizures. Stereotypical dynamics suggest that, once initiated, seizures follow a deterministic path through the parameter space of a neural model. Furthermore, distinct sub-populations of patients were identified based on characteristic motifs in the dynamics at seizure onset. There were also distinct patterns between long and short duration seizures that were related to seizure offset. Understanding how these different patterns of seizure evolution arise may provide new insights into brain function and guide treatment for epilepsy, since specific therapies may have preferential effects on the various parameters that could potentially be individualized. Methods that unite computational models with data provide a powerful means to generate testable hypotheses for further experimental research. This work provides a demonstration that the hidden connectivity parameters of a neural mass model can be dynamically inferred from data. Our results underscore the power of theoretical models to inform epilepsy management. It is our hope that this work guides further efforts to apply computational models to clinical data.
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spelling pubmed-61990002018-11-05 Seizure pathways: A model-based investigation Karoly, Philippa J. Kuhlmann, Levin Soudry, Daniel Grayden, David B. Cook, Mark J. Freestone, Dean R. PLoS Comput Biol Research Article We present the results of a model inversion algorithm for electrocorticography (ECoG) data recorded during epileptic seizures. The states and parameters of neural mass models were tracked during a total of over 3000 seizures from twelve patients with focal epilepsy. These models provide an estimate of the effective connectivity within intracortical circuits over the time course of seizures. Observing the dynamics of effective connectivity provides insight into mechanisms of seizures. Estimation of patients seizure dynamics revealed: 1) a highly stereotyped pattern of evolution for each patient, 2) distinct sub-groups of onset mechanisms amongst patients, and 3) different offset mechanisms for long and short seizures. Stereotypical dynamics suggest that, once initiated, seizures follow a deterministic path through the parameter space of a neural model. Furthermore, distinct sub-populations of patients were identified based on characteristic motifs in the dynamics at seizure onset. There were also distinct patterns between long and short duration seizures that were related to seizure offset. Understanding how these different patterns of seizure evolution arise may provide new insights into brain function and guide treatment for epilepsy, since specific therapies may have preferential effects on the various parameters that could potentially be individualized. Methods that unite computational models with data provide a powerful means to generate testable hypotheses for further experimental research. This work provides a demonstration that the hidden connectivity parameters of a neural mass model can be dynamically inferred from data. Our results underscore the power of theoretical models to inform epilepsy management. It is our hope that this work guides further efforts to apply computational models to clinical data. Public Library of Science 2018-10-11 /pmc/articles/PMC6199000/ /pubmed/30307937 http://dx.doi.org/10.1371/journal.pcbi.1006403 Text en © 2018 Karoly 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
Karoly, Philippa J.
Kuhlmann, Levin
Soudry, Daniel
Grayden, David B.
Cook, Mark J.
Freestone, Dean R.
Seizure pathways: A model-based investigation
title Seizure pathways: A model-based investigation
title_full Seizure pathways: A model-based investigation
title_fullStr Seizure pathways: A model-based investigation
title_full_unstemmed Seizure pathways: A model-based investigation
title_short Seizure pathways: A model-based investigation
title_sort seizure pathways: a model-based investigation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199000/
https://www.ncbi.nlm.nih.gov/pubmed/30307937
http://dx.doi.org/10.1371/journal.pcbi.1006403
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