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Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection

OBJECTIVE: Epilepsy surgery is an effective treatment for drug‐resistant patients. However, how different surgical approaches affect long‐term brain structure remains poorly characterized. Here, we present a semiautomated method for quantifying structural changes after epilepsy surgery and compare t...

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Autores principales: Arnold, T. Campbell, Kini, Lohith G., Bernabei, John M., Revell, Andrew Y., Das, Sandhitsu R., Stein, Joel M., Lucas, Timothy H., Englot, Dario J., Morgan, Victoria L., Litt, Brian, Davis, Kathryn A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235552/
https://www.ncbi.nlm.nih.gov/pubmed/36944585
http://dx.doi.org/10.1002/epi4.12733
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author Arnold, T. Campbell
Kini, Lohith G.
Bernabei, John M.
Revell, Andrew Y.
Das, Sandhitsu R.
Stein, Joel M.
Lucas, Timothy H.
Englot, Dario J.
Morgan, Victoria L.
Litt, Brian
Davis, Kathryn A.
author_facet Arnold, T. Campbell
Kini, Lohith G.
Bernabei, John M.
Revell, Andrew Y.
Das, Sandhitsu R.
Stein, Joel M.
Lucas, Timothy H.
Englot, Dario J.
Morgan, Victoria L.
Litt, Brian
Davis, Kathryn A.
author_sort Arnold, T. Campbell
collection PubMed
description OBJECTIVE: Epilepsy surgery is an effective treatment for drug‐resistant patients. However, how different surgical approaches affect long‐term brain structure remains poorly characterized. Here, we present a semiautomated method for quantifying structural changes after epilepsy surgery and compare the remote structural effects of two approaches, anterior temporal lobectomy (ATL), and selective amygdalohippocampectomy (SAH). METHODS: We studied 36 temporal lobe epilepsy patients who underwent resective surgery (ATL = 22, SAH = 14). All patients received same‐scanner MR imaging preoperatively and postoperatively (mean 2 years). To analyze postoperative structural changes, we segmented the resection zone and modified the Advanced Normalization Tools (ANTs) longitudinal cortical pipeline to account for resections. We compared global and regional annualized cortical thinning between surgical treatments. RESULTS: Across procedures, there was significant cortical thinning in the ipsilateral insula, fusiform, pericalcarine, and several temporal lobe regions outside the resection zone as well as the contralateral hippocampus. Additionally, increased postoperative cortical thickness was seen in the supramarginal gyrus. Patients treated with ATL exhibited greater annualized cortical thinning compared with SAH cases (ATL: −0.08 ± 0.11 mm per year, SAH: −0.01 ± 0.02 mm per year, t = 2.99, P = 0.006). There were focal postoperative differences between the two treatment groups in the ipsilateral insula (P = 0.039, corrected). Annualized cortical thinning rates correlated with preoperative cortical thickness (r = 0.60, P < 0.001) and had weaker associations with age at surgery (r = −0.33, P = 0.051) and disease duration (r = −0.42, P = 0.058). SIGNIFICANCE: Our evidence suggests that selective procedures are associated with less cortical thinning and that earlier surgical intervention may reduce long‐term impacts on brain structure.
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spelling pubmed-102355522023-06-03 Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection Arnold, T. Campbell Kini, Lohith G. Bernabei, John M. Revell, Andrew Y. Das, Sandhitsu R. Stein, Joel M. Lucas, Timothy H. Englot, Dario J. Morgan, Victoria L. Litt, Brian Davis, Kathryn A. Epilepsia Open Original Articles OBJECTIVE: Epilepsy surgery is an effective treatment for drug‐resistant patients. However, how different surgical approaches affect long‐term brain structure remains poorly characterized. Here, we present a semiautomated method for quantifying structural changes after epilepsy surgery and compare the remote structural effects of two approaches, anterior temporal lobectomy (ATL), and selective amygdalohippocampectomy (SAH). METHODS: We studied 36 temporal lobe epilepsy patients who underwent resective surgery (ATL = 22, SAH = 14). All patients received same‐scanner MR imaging preoperatively and postoperatively (mean 2 years). To analyze postoperative structural changes, we segmented the resection zone and modified the Advanced Normalization Tools (ANTs) longitudinal cortical pipeline to account for resections. We compared global and regional annualized cortical thinning between surgical treatments. RESULTS: Across procedures, there was significant cortical thinning in the ipsilateral insula, fusiform, pericalcarine, and several temporal lobe regions outside the resection zone as well as the contralateral hippocampus. Additionally, increased postoperative cortical thickness was seen in the supramarginal gyrus. Patients treated with ATL exhibited greater annualized cortical thinning compared with SAH cases (ATL: −0.08 ± 0.11 mm per year, SAH: −0.01 ± 0.02 mm per year, t = 2.99, P = 0.006). There were focal postoperative differences between the two treatment groups in the ipsilateral insula (P = 0.039, corrected). Annualized cortical thinning rates correlated with preoperative cortical thickness (r = 0.60, P < 0.001) and had weaker associations with age at surgery (r = −0.33, P = 0.051) and disease duration (r = −0.42, P = 0.058). SIGNIFICANCE: Our evidence suggests that selective procedures are associated with less cortical thinning and that earlier surgical intervention may reduce long‐term impacts on brain structure. John Wiley and Sons Inc. 2023-04-25 /pmc/articles/PMC10235552/ /pubmed/36944585 http://dx.doi.org/10.1002/epi4.12733 Text en © 2023 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Arnold, T. Campbell
Kini, Lohith G.
Bernabei, John M.
Revell, Andrew Y.
Das, Sandhitsu R.
Stein, Joel M.
Lucas, Timothy H.
Englot, Dario J.
Morgan, Victoria L.
Litt, Brian
Davis, Kathryn A.
Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection
title Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection
title_full Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection
title_fullStr Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection
title_full_unstemmed Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection
title_short Remote effects of temporal lobe epilepsy surgery: Long‐term morphological changes after surgical resection
title_sort remote effects of temporal lobe epilepsy surgery: long‐term morphological changes after surgical resection
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235552/
https://www.ncbi.nlm.nih.gov/pubmed/36944585
http://dx.doi.org/10.1002/epi4.12733
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