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Spectral organization of focal seizures within the thalamotemporal network

OBJECTIVE: To investigate dynamic changes in neural activity between the anterior nucleus of the thalamus (ANT) and the seizure onset zone (SOZ) in patients with drug‐resistant temporal lobe epilepsy (TLE) based on anatomic location, seizure subtype, and state of vigilance (SOV). METHODS: Eleven pat...

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Autores principales: Pizarro, Diana, Ilyas, Adeel, Chaitanya, Ganne, Toth, Emilia, Irannejad, Auriana, Romeo, Andrew, Riley, Kristen O., Iasemidis, Leonidas, Pati, Sandipan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764631/
https://www.ncbi.nlm.nih.gov/pubmed/31468745
http://dx.doi.org/10.1002/acn3.50880
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author Pizarro, Diana
Ilyas, Adeel
Chaitanya, Ganne
Toth, Emilia
Irannejad, Auriana
Romeo, Andrew
Riley, Kristen O.
Iasemidis, Leonidas
Pati, Sandipan
author_facet Pizarro, Diana
Ilyas, Adeel
Chaitanya, Ganne
Toth, Emilia
Irannejad, Auriana
Romeo, Andrew
Riley, Kristen O.
Iasemidis, Leonidas
Pati, Sandipan
author_sort Pizarro, Diana
collection PubMed
description OBJECTIVE: To investigate dynamic changes in neural activity between the anterior nucleus of the thalamus (ANT) and the seizure onset zone (SOZ) in patients with drug‐resistant temporal lobe epilepsy (TLE) based on anatomic location, seizure subtype, and state of vigilance (SOV). METHODS: Eleven patients undergoing stereoelectroencephalography for seizure localization were recruited prospectively for local field potential (LFP) recording directly from the ANT. The SOZ was identified using line length and epileptogenicity index. Changes in power spectral density (PSD) were compared between the two anatomic sites as seizures (N = 53) transitioned from interictal baseline to the posttermination stage. RESULTS: At baseline, the thalamic LFPs were significantly lower and distinct from the SOZ with the presence of higher power in the fast ripple band (P < 0.001). Temporal changes in ictal power of neural activity within ANT mimic those of the SOZ, are increased significantly at seizure onset (P < 0.05), and are distinct for seizures that impaired awareness or that secondarily generalized (P < 0.05). The onset of seizure was preceded by a decrease in the mean power spectral density (PSD) in ANT and SOZ (P < 0.05). Neural activity correlated with different states of vigilance at seizure onset within the ANT but not in the SOZ (P = 0.005). INTERPRETATION: The ANT can be recruited at the onset of mesial temporal lobe seizures, and the recruitment pattern differs with seizure subtypes. Furthermore, changes in neural dynamics precede seizure onset and are widespread to involve temporo‐thalamic regions, thereby providing an opportunity to intervene early with closed‐loop DBS.
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spelling pubmed-67646312019-09-30 Spectral organization of focal seizures within the thalamotemporal network Pizarro, Diana Ilyas, Adeel Chaitanya, Ganne Toth, Emilia Irannejad, Auriana Romeo, Andrew Riley, Kristen O. Iasemidis, Leonidas Pati, Sandipan Ann Clin Transl Neurol Research Articles OBJECTIVE: To investigate dynamic changes in neural activity between the anterior nucleus of the thalamus (ANT) and the seizure onset zone (SOZ) in patients with drug‐resistant temporal lobe epilepsy (TLE) based on anatomic location, seizure subtype, and state of vigilance (SOV). METHODS: Eleven patients undergoing stereoelectroencephalography for seizure localization were recruited prospectively for local field potential (LFP) recording directly from the ANT. The SOZ was identified using line length and epileptogenicity index. Changes in power spectral density (PSD) were compared between the two anatomic sites as seizures (N = 53) transitioned from interictal baseline to the posttermination stage. RESULTS: At baseline, the thalamic LFPs were significantly lower and distinct from the SOZ with the presence of higher power in the fast ripple band (P < 0.001). Temporal changes in ictal power of neural activity within ANT mimic those of the SOZ, are increased significantly at seizure onset (P < 0.05), and are distinct for seizures that impaired awareness or that secondarily generalized (P < 0.05). The onset of seizure was preceded by a decrease in the mean power spectral density (PSD) in ANT and SOZ (P < 0.05). Neural activity correlated with different states of vigilance at seizure onset within the ANT but not in the SOZ (P = 0.005). INTERPRETATION: The ANT can be recruited at the onset of mesial temporal lobe seizures, and the recruitment pattern differs with seizure subtypes. Furthermore, changes in neural dynamics precede seizure onset and are widespread to involve temporo‐thalamic regions, thereby providing an opportunity to intervene early with closed‐loop DBS. John Wiley and Sons Inc. 2019-08-30 /pmc/articles/PMC6764631/ /pubmed/31468745 http://dx.doi.org/10.1002/acn3.50880 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Pizarro, Diana
Ilyas, Adeel
Chaitanya, Ganne
Toth, Emilia
Irannejad, Auriana
Romeo, Andrew
Riley, Kristen O.
Iasemidis, Leonidas
Pati, Sandipan
Spectral organization of focal seizures within the thalamotemporal network
title Spectral organization of focal seizures within the thalamotemporal network
title_full Spectral organization of focal seizures within the thalamotemporal network
title_fullStr Spectral organization of focal seizures within the thalamotemporal network
title_full_unstemmed Spectral organization of focal seizures within the thalamotemporal network
title_short Spectral organization of focal seizures within the thalamotemporal network
title_sort spectral organization of focal seizures within the thalamotemporal network
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764631/
https://www.ncbi.nlm.nih.gov/pubmed/31468745
http://dx.doi.org/10.1002/acn3.50880
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