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Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study
OBJECTIVE: To investigate the functional correlates of recurrent secondarily generalized seizures in temporal lobe epilepsy (TLE) using task-based fMRI as a framework to test for epilepsy-specific network rearrangements. Because the thalamus modulates propagation of temporal lobe onset seizures and...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682917/ https://www.ncbi.nlm.nih.gov/pubmed/32847951 http://dx.doi.org/10.1212/WNL.0000000000010645 |
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author | Caciagli, Lorenzo Allen, Luke A. He, Xiaosong Trimmel, Karin Vos, Sjoerd B. Centeno, Maria Galovic, Marian Sidhu, Meneka K. Thompson, Pamela J. Bassett, Danielle S. Winston, Gavin P. Duncan, John S. Koepp, Matthias J. Sperling, Michael R. |
author_facet | Caciagli, Lorenzo Allen, Luke A. He, Xiaosong Trimmel, Karin Vos, Sjoerd B. Centeno, Maria Galovic, Marian Sidhu, Meneka K. Thompson, Pamela J. Bassett, Danielle S. Winston, Gavin P. Duncan, John S. Koepp, Matthias J. Sperling, Michael R. |
author_sort | Caciagli, Lorenzo |
collection | PubMed |
description | OBJECTIVE: To investigate the functional correlates of recurrent secondarily generalized seizures in temporal lobe epilepsy (TLE) using task-based fMRI as a framework to test for epilepsy-specific network rearrangements. Because the thalamus modulates propagation of temporal lobe onset seizures and promotes cortical synchronization during cognition, we hypothesized that occurrence of secondarily generalized seizures, i.e., focal to bilateral tonic-clonic seizures (FBTCS), would relate to thalamic dysfunction, altered connectivity, and whole-brain network centrality. METHODS: FBTCS occur in a third of patients with TLE and are a major determinant of disease severity. In this cross-sectional study, we analyzed 113 patients with drug-resistant TLE (55 left/58 right), who performed a verbal fluency fMRI task that elicited robust thalamic activation. Thirty-three patients (29%) had experienced at least one FBTCS in the year preceding the investigation. We compared patients with TLE-FBTCS to those without FBTCS via a multiscale approach, entailing analysis of statistical parametric mapping (SPM) 12–derived measures of activation, task-modulated thalamic functional connectivity (psychophysiologic interaction), and graph-theoretical metrics of centrality. RESULTS: Individuals with TLE-FBTCS had less task-related activation of bilateral thalamus, with left-sided emphasis, and left hippocampus than those without FBTCS. In TLE-FBTCS, we also found greater task-related thalamotemporal and thalamomotor connectivity, and higher thalamic degree and betweenness centrality. Receiver operating characteristic curves, based on a combined thalamic functional marker, accurately discriminated individuals with and without FBTCS. CONCLUSIONS: In TLE-FBTCS, impaired task-related thalamic recruitment coexists with enhanced thalamotemporal connectivity and whole-brain thalamic network embedding. Altered thalamic functional profiles are proposed as imaging biomarkers of active secondary generalization. |
format | Online Article Text |
id | pubmed-7682917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-76829172020-11-24 Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study Caciagli, Lorenzo Allen, Luke A. He, Xiaosong Trimmel, Karin Vos, Sjoerd B. Centeno, Maria Galovic, Marian Sidhu, Meneka K. Thompson, Pamela J. Bassett, Danielle S. Winston, Gavin P. Duncan, John S. Koepp, Matthias J. Sperling, Michael R. Neurology Article OBJECTIVE: To investigate the functional correlates of recurrent secondarily generalized seizures in temporal lobe epilepsy (TLE) using task-based fMRI as a framework to test for epilepsy-specific network rearrangements. Because the thalamus modulates propagation of temporal lobe onset seizures and promotes cortical synchronization during cognition, we hypothesized that occurrence of secondarily generalized seizures, i.e., focal to bilateral tonic-clonic seizures (FBTCS), would relate to thalamic dysfunction, altered connectivity, and whole-brain network centrality. METHODS: FBTCS occur in a third of patients with TLE and are a major determinant of disease severity. In this cross-sectional study, we analyzed 113 patients with drug-resistant TLE (55 left/58 right), who performed a verbal fluency fMRI task that elicited robust thalamic activation. Thirty-three patients (29%) had experienced at least one FBTCS in the year preceding the investigation. We compared patients with TLE-FBTCS to those without FBTCS via a multiscale approach, entailing analysis of statistical parametric mapping (SPM) 12–derived measures of activation, task-modulated thalamic functional connectivity (psychophysiologic interaction), and graph-theoretical metrics of centrality. RESULTS: Individuals with TLE-FBTCS had less task-related activation of bilateral thalamus, with left-sided emphasis, and left hippocampus than those without FBTCS. In TLE-FBTCS, we also found greater task-related thalamotemporal and thalamomotor connectivity, and higher thalamic degree and betweenness centrality. Receiver operating characteristic curves, based on a combined thalamic functional marker, accurately discriminated individuals with and without FBTCS. CONCLUSIONS: In TLE-FBTCS, impaired task-related thalamic recruitment coexists with enhanced thalamotemporal connectivity and whole-brain thalamic network embedding. Altered thalamic functional profiles are proposed as imaging biomarkers of active secondary generalization. Lippincott Williams & Wilkins 2020-10-27 /pmc/articles/PMC7682917/ /pubmed/32847951 http://dx.doi.org/10.1212/WNL.0000000000010645 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 Caciagli, Lorenzo Allen, Luke A. He, Xiaosong Trimmel, Karin Vos, Sjoerd B. Centeno, Maria Galovic, Marian Sidhu, Meneka K. Thompson, Pamela J. Bassett, Danielle S. Winston, Gavin P. Duncan, John S. Koepp, Matthias J. Sperling, Michael R. Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study |
title | Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study |
title_full | Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study |
title_fullStr | Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study |
title_full_unstemmed | Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study |
title_short | Thalamus and focal to bilateral seizures: A multiscale cognitive imaging study |
title_sort | thalamus and focal to bilateral seizures: a multiscale cognitive imaging study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682917/ https://www.ncbi.nlm.nih.gov/pubmed/32847951 http://dx.doi.org/10.1212/WNL.0000000000010645 |
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