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Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery
OBJECTIVE: We assessed preoperative structural brain networks and clinical characteristics of patients with drug-resistant temporal lobe epilepsy (TLE) to identify correlates of postsurgical seizure recurrences. METHODS: We examined data from 51 patients with TLE who underwent anterior temporal lobe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884990/ https://www.ncbi.nlm.nih.gov/pubmed/33361262 http://dx.doi.org/10.1212/WNL.0000000000011315 |
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author | Sinha, Nishant Wang, Yujiang Moreira da Silva, Nádia Miserocchi, Anna McEvoy, Andrew W. de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John S. Taylor, Peter N. |
author_facet | Sinha, Nishant Wang, Yujiang Moreira da Silva, Nádia Miserocchi, Anna McEvoy, Andrew W. de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John S. Taylor, Peter N. |
author_sort | Sinha, Nishant |
collection | PubMed |
description | OBJECTIVE: We assessed preoperative structural brain networks and clinical characteristics of patients with drug-resistant temporal lobe epilepsy (TLE) to identify correlates of postsurgical seizure recurrences. METHODS: We examined data from 51 patients with TLE who underwent anterior temporal lobe resection (ATLR) and 29 healthy controls. For each patient, using the preoperative structural, diffusion, and postoperative structural MRI, we generated 2 networks: presurgery network and surgically spared network. Standardizing these networks with respect to controls, we determined the number of abnormal nodes before surgery and expected to be spared by surgery. We incorporated these 2 abnormality measures and 13 commonly acquired clinical data from each patient into a robust machine learning framework to estimate patient-specific chances of seizures persisting after surgery. RESULTS: Patients with more abnormal nodes had a lower chance of complete seizure freedom at 1 year and, even if seizure-free at 1 year, were more likely to relapse within 5 years. The number of abnormal nodes was greater and their locations more widespread in the surgically spared networks of patients with poor outcome than in patients with good outcome. We achieved an area under the curve of 0.84 ± 0.06 and specificity of 0.89 ± 0.09 in predicting unsuccessful seizure outcomes (International League Against Epilepsy [ILAE] 3–5) as opposed to complete seizure freedom (ILAE 1) at 1 year. Moreover, the model-predicted likelihood of seizure relapse was significantly correlated with the grade of surgical outcome at year 1 and associated with relapses up to 5 years after surgery. CONCLUSION: Node abnormality offers a personalized, noninvasive marker that can be combined with clinical data to better estimate the chances of seizure freedom at 1 year and subsequent relapse up to 5 years after ATLR. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that node abnormality predicts postsurgical seizure recurrence. |
format | Online Article Text |
id | pubmed-7884990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-78849902021-03-02 Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery Sinha, Nishant Wang, Yujiang Moreira da Silva, Nádia Miserocchi, Anna McEvoy, Andrew W. de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John S. Taylor, Peter N. Neurology Article OBJECTIVE: We assessed preoperative structural brain networks and clinical characteristics of patients with drug-resistant temporal lobe epilepsy (TLE) to identify correlates of postsurgical seizure recurrences. METHODS: We examined data from 51 patients with TLE who underwent anterior temporal lobe resection (ATLR) and 29 healthy controls. For each patient, using the preoperative structural, diffusion, and postoperative structural MRI, we generated 2 networks: presurgery network and surgically spared network. Standardizing these networks with respect to controls, we determined the number of abnormal nodes before surgery and expected to be spared by surgery. We incorporated these 2 abnormality measures and 13 commonly acquired clinical data from each patient into a robust machine learning framework to estimate patient-specific chances of seizures persisting after surgery. RESULTS: Patients with more abnormal nodes had a lower chance of complete seizure freedom at 1 year and, even if seizure-free at 1 year, were more likely to relapse within 5 years. The number of abnormal nodes was greater and their locations more widespread in the surgically spared networks of patients with poor outcome than in patients with good outcome. We achieved an area under the curve of 0.84 ± 0.06 and specificity of 0.89 ± 0.09 in predicting unsuccessful seizure outcomes (International League Against Epilepsy [ILAE] 3–5) as opposed to complete seizure freedom (ILAE 1) at 1 year. Moreover, the model-predicted likelihood of seizure relapse was significantly correlated with the grade of surgical outcome at year 1 and associated with relapses up to 5 years after surgery. CONCLUSION: Node abnormality offers a personalized, noninvasive marker that can be combined with clinical data to better estimate the chances of seizure freedom at 1 year and subsequent relapse up to 5 years after ATLR. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that node abnormality predicts postsurgical seizure recurrence. Lippincott Williams & Wilkins 2021-02-02 /pmc/articles/PMC7884990/ /pubmed/33361262 http://dx.doi.org/10.1212/WNL.0000000000011315 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Sinha, Nishant Wang, Yujiang Moreira da Silva, Nádia Miserocchi, Anna McEvoy, Andrew W. de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John S. Taylor, Peter N. Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery |
title | Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery |
title_full | Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery |
title_fullStr | Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery |
title_full_unstemmed | Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery |
title_short | Structural Brain Network Abnormalities and the Probability of Seizure Recurrence After Epilepsy Surgery |
title_sort | structural brain network abnormalities and the probability of seizure recurrence after epilepsy surgery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884990/ https://www.ncbi.nlm.nih.gov/pubmed/33361262 http://dx.doi.org/10.1212/WNL.0000000000011315 |
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