Cargando…
Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study
OBJECTIVE: To characterise temporal lobe epilepsy (TLE) surgery-induced changes in brain network properties, as measured using diffusion weighted MRI, and investigate their association with postoperative seizure-freedom. METHODS: For 48 patients who underwent anterior temporal lobe resection, diffus...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334605/ https://www.ncbi.nlm.nih.gov/pubmed/32623138 http://dx.doi.org/10.1016/j.nicl.2020.102320 |
_version_ | 1783553961090875392 |
---|---|
author | da Silva, Nádia Moreira Forsyth, Rob McEvoy, Andrew Miserocchi, Anna de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John Wang, Yujiang Taylor, Peter N. |
author_facet | da Silva, Nádia Moreira Forsyth, Rob McEvoy, Andrew Miserocchi, Anna de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John Wang, Yujiang Taylor, Peter N. |
author_sort | da Silva, Nádia Moreira |
collection | PubMed |
description | OBJECTIVE: To characterise temporal lobe epilepsy (TLE) surgery-induced changes in brain network properties, as measured using diffusion weighted MRI, and investigate their association with postoperative seizure-freedom. METHODS: For 48 patients who underwent anterior temporal lobe resection, diffusion weighted MRI was acquired pre-operatively, 3–4 months post-operatively (N = 48), and again 12 months post-operatively (N = 13). Data for 17 controls were also acquired over the same period. After registering all subjects to a common space, we performed two complementary analyses of the subjects’ quantitative anisotropy (QA) maps. 1) A connectometry analysis which is sensitive to changes in subsections of fasciculi. 2) A graph theory approach which integrates connectivity information across the wider brain network. RESULTS: We found significant postoperative alterations in QA in patients relative to controls measured over the same period. Reductions were primarily located in the uncinate fasciculus and inferior fronto-occipital fasciculus ipsilaterally for all patients. Larger reductions were associated with postoperative seizure-freedom in left TLE. Increased QA was mainly located in corona radiata and corticopontine tracts. Graph theoretic analysis revealed widespread increases in nodal betweenness centrality, which were not associated with patient outcomes. CONCLUSION: Substantial alterations in QA occur in the months after epilepsy surgery, suggesting Wallerian degeneration and strengthening of specific white matter tracts. Greater reductions in QA were related to postoperative seizure freedom in left TLE. |
format | Online Article Text |
id | pubmed-7334605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-73346052020-07-07 Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study da Silva, Nádia Moreira Forsyth, Rob McEvoy, Andrew Miserocchi, Anna de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John Wang, Yujiang Taylor, Peter N. Neuroimage Clin Regular Article OBJECTIVE: To characterise temporal lobe epilepsy (TLE) surgery-induced changes in brain network properties, as measured using diffusion weighted MRI, and investigate their association with postoperative seizure-freedom. METHODS: For 48 patients who underwent anterior temporal lobe resection, diffusion weighted MRI was acquired pre-operatively, 3–4 months post-operatively (N = 48), and again 12 months post-operatively (N = 13). Data for 17 controls were also acquired over the same period. After registering all subjects to a common space, we performed two complementary analyses of the subjects’ quantitative anisotropy (QA) maps. 1) A connectometry analysis which is sensitive to changes in subsections of fasciculi. 2) A graph theory approach which integrates connectivity information across the wider brain network. RESULTS: We found significant postoperative alterations in QA in patients relative to controls measured over the same period. Reductions were primarily located in the uncinate fasciculus and inferior fronto-occipital fasciculus ipsilaterally for all patients. Larger reductions were associated with postoperative seizure-freedom in left TLE. Increased QA was mainly located in corona radiata and corticopontine tracts. Graph theoretic analysis revealed widespread increases in nodal betweenness centrality, which were not associated with patient outcomes. CONCLUSION: Substantial alterations in QA occur in the months after epilepsy surgery, suggesting Wallerian degeneration and strengthening of specific white matter tracts. Greater reductions in QA were related to postoperative seizure freedom in left TLE. Elsevier 2020-06-26 /pmc/articles/PMC7334605/ /pubmed/32623138 http://dx.doi.org/10.1016/j.nicl.2020.102320 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Regular Article da Silva, Nádia Moreira Forsyth, Rob McEvoy, Andrew Miserocchi, Anna de Tisi, Jane Vos, Sjoerd B. Winston, Gavin P. Duncan, John Wang, Yujiang Taylor, Peter N. Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study |
title | Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study |
title_full | Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study |
title_fullStr | Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study |
title_full_unstemmed | Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study |
title_short | Network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: A longitudinal study |
title_sort | network reorganisation following anterior temporal lobe resection and relation with post-surgery seizure relapse: a longitudinal study |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334605/ https://www.ncbi.nlm.nih.gov/pubmed/32623138 http://dx.doi.org/10.1016/j.nicl.2020.102320 |
work_keys_str_mv | AT dasilvanadiamoreira networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT forsythrob networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT mcevoyandrew networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT miserocchianna networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT detisijane networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT vossjoerdb networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT winstongavinp networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT duncanjohn networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT wangyujiang networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy AT taylorpetern networkreorganisationfollowinganteriortemporalloberesectionandrelationwithpostsurgeryseizurerelapsealongitudinalstudy |