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Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations
Temporal lobe epilepsy (TLE) is a prevalent neurological disorder resulting in disruptive seizures. In the case of drug resistant epilepsy resective surgery is often considered. This is a procedure hampered by unpredictable success rates, with many patients continuing to have seizures even after sur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675531/ https://www.ncbi.nlm.nih.gov/pubmed/26657566 http://dx.doi.org/10.1371/journal.pcbi.1004642 |
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author | Hutchings, Frances Han, Cheol E. Keller, Simon S. Weber, Bernd Taylor, Peter N. Kaiser, Marcus |
author_facet | Hutchings, Frances Han, Cheol E. Keller, Simon S. Weber, Bernd Taylor, Peter N. Kaiser, Marcus |
author_sort | Hutchings, Frances |
collection | PubMed |
description | Temporal lobe epilepsy (TLE) is a prevalent neurological disorder resulting in disruptive seizures. In the case of drug resistant epilepsy resective surgery is often considered. This is a procedure hampered by unpredictable success rates, with many patients continuing to have seizures even after surgery. In this study we apply a computational model of epilepsy to patient specific structural connectivity derived from diffusion tensor imaging (DTI) of 22 individuals with left TLE and 39 healthy controls. We validate the model by examining patient-control differences in simulated seizure onset time and network location. We then investigate the potential of the model for surgery prediction by performing in silico surgical resections, removing nodes from patient networks and comparing seizure likelihood post-surgery to pre-surgery simulations. We find that, first, patients tend to transit from non-epileptic to epileptic states more often than controls in the model. Second, regions in the left hemisphere (particularly within temporal and subcortical regions) that are known to be involved in TLE are the most frequent starting points for seizures in patients in the model. In addition, our analysis also implicates regions in the contralateral and frontal locations which may play a role in seizure spreading or surgery resistance. Finally, the model predicts that patient-specific surgery (resection areas chosen on an individual, model-prompted, basis and not following a predefined procedure) may lead to better outcomes than the currently used routine clinical procedure. Taken together this work provides a first step towards patient specific computational modelling of epilepsy surgery in order to inform treatment strategies in individuals. |
format | Online Article Text |
id | pubmed-4675531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46755312015-12-31 Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations Hutchings, Frances Han, Cheol E. Keller, Simon S. Weber, Bernd Taylor, Peter N. Kaiser, Marcus PLoS Comput Biol Research Article Temporal lobe epilepsy (TLE) is a prevalent neurological disorder resulting in disruptive seizures. In the case of drug resistant epilepsy resective surgery is often considered. This is a procedure hampered by unpredictable success rates, with many patients continuing to have seizures even after surgery. In this study we apply a computational model of epilepsy to patient specific structural connectivity derived from diffusion tensor imaging (DTI) of 22 individuals with left TLE and 39 healthy controls. We validate the model by examining patient-control differences in simulated seizure onset time and network location. We then investigate the potential of the model for surgery prediction by performing in silico surgical resections, removing nodes from patient networks and comparing seizure likelihood post-surgery to pre-surgery simulations. We find that, first, patients tend to transit from non-epileptic to epileptic states more often than controls in the model. Second, regions in the left hemisphere (particularly within temporal and subcortical regions) that are known to be involved in TLE are the most frequent starting points for seizures in patients in the model. In addition, our analysis also implicates regions in the contralateral and frontal locations which may play a role in seizure spreading or surgery resistance. Finally, the model predicts that patient-specific surgery (resection areas chosen on an individual, model-prompted, basis and not following a predefined procedure) may lead to better outcomes than the currently used routine clinical procedure. Taken together this work provides a first step towards patient specific computational modelling of epilepsy surgery in order to inform treatment strategies in individuals. Public Library of Science 2015-12-10 /pmc/articles/PMC4675531/ /pubmed/26657566 http://dx.doi.org/10.1371/journal.pcbi.1004642 Text en © 2015 Hutchings 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hutchings, Frances Han, Cheol E. Keller, Simon S. Weber, Bernd Taylor, Peter N. Kaiser, Marcus Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations |
title | Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations |
title_full | Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations |
title_fullStr | Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations |
title_full_unstemmed | Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations |
title_short | Predicting Surgery Targets in Temporal Lobe Epilepsy through Structural Connectome Based Simulations |
title_sort | predicting surgery targets in temporal lobe epilepsy through structural connectome based simulations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675531/ https://www.ncbi.nlm.nih.gov/pubmed/26657566 http://dx.doi.org/10.1371/journal.pcbi.1004642 |
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