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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
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.
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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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