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Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks

Objective: To evaluate local and distant blood oxygen level dependent (BOLD) signal changes related to interictal epileptiform discharges (IED) in drug-resistant temporal lobe epilepsy (TLE). Methods: Thirty-three TLE patients undergoing EEG–functional Magnetic Resonance Imaging (fMRI) as part of th...

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Autores principales: Mirandola, Laura, Ballotta, Daniela, Talami, Francesca, Giovannini, Giada, Pavesi, Giacomo, Vaudano, Anna Elisabetta, Meletti, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718871/
https://www.ncbi.nlm.nih.gov/pubmed/34975714
http://dx.doi.org/10.3389/fneur.2021.746468
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author Mirandola, Laura
Ballotta, Daniela
Talami, Francesca
Giovannini, Giada
Pavesi, Giacomo
Vaudano, Anna Elisabetta
Meletti, Stefano
author_facet Mirandola, Laura
Ballotta, Daniela
Talami, Francesca
Giovannini, Giada
Pavesi, Giacomo
Vaudano, Anna Elisabetta
Meletti, Stefano
author_sort Mirandola, Laura
collection PubMed
description Objective: To evaluate local and distant blood oxygen level dependent (BOLD) signal changes related to interictal epileptiform discharges (IED) in drug-resistant temporal lobe epilepsy (TLE). Methods: Thirty-three TLE patients undergoing EEG–functional Magnetic Resonance Imaging (fMRI) as part of the presurgical workup were consecutively enrolled. First, a single-subject spike-related analysis was performed: (a) to verify the BOLD concordance with the presumed Epileptogenic Zone (EZ); and (b) to investigate the Intrinsic Connectivity Networks (ICN) involvement. Then, a group analysis was performed to search for common BOLD changes in TLE. Results: Interictal epileptiform discharges were recorded in 25 patients and in 19 (58%), a BOLD response was obtained at the single-subject level. In 42% of the cases, BOLD changes were observed in the temporal lobe, although only one patient had a pure concordant finding, with a single fMRI cluster overlapping (and limited to) the EZ identified by anatomo-electro-clinical correlations. In the remaining 58% of the cases, BOLD responses were localized outside the temporal lobe and the presumed EZ. In every patient, with a spike-related fMRI map, at least one ICN appeared to be involved. Four main ICNs were preferentially involved, namely, motor, visual, auditory/motor speech, and the default mode network. At the single-subject level, EEG–fMRI proved to have high specificity (above 65%) in detecting engagement of an ICN and the corresponding ictal/postictal symptom, and good positive predictive value (above 67%) in all networks except the visual one. Finally, in the group analysis of BOLD changes related to IED revealed common activations at the right precentral gyrus, supplementary motor area, and middle cingulate gyrus. Significance: Interictal temporal spikes affect several distant extra-temporal areas, and specifically the motor/premotor cortex. EEG–fMRI in patients with TLE eligible for surgery is recommended not for strictly localizing purposes rather it might be useful to investigate ICNs alterations at the single-subject level.
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spelling pubmed-87188712022-01-01 Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks Mirandola, Laura Ballotta, Daniela Talami, Francesca Giovannini, Giada Pavesi, Giacomo Vaudano, Anna Elisabetta Meletti, Stefano Front Neurol Neurology Objective: To evaluate local and distant blood oxygen level dependent (BOLD) signal changes related to interictal epileptiform discharges (IED) in drug-resistant temporal lobe epilepsy (TLE). Methods: Thirty-three TLE patients undergoing EEG–functional Magnetic Resonance Imaging (fMRI) as part of the presurgical workup were consecutively enrolled. First, a single-subject spike-related analysis was performed: (a) to verify the BOLD concordance with the presumed Epileptogenic Zone (EZ); and (b) to investigate the Intrinsic Connectivity Networks (ICN) involvement. Then, a group analysis was performed to search for common BOLD changes in TLE. Results: Interictal epileptiform discharges were recorded in 25 patients and in 19 (58%), a BOLD response was obtained at the single-subject level. In 42% of the cases, BOLD changes were observed in the temporal lobe, although only one patient had a pure concordant finding, with a single fMRI cluster overlapping (and limited to) the EZ identified by anatomo-electro-clinical correlations. In the remaining 58% of the cases, BOLD responses were localized outside the temporal lobe and the presumed EZ. In every patient, with a spike-related fMRI map, at least one ICN appeared to be involved. Four main ICNs were preferentially involved, namely, motor, visual, auditory/motor speech, and the default mode network. At the single-subject level, EEG–fMRI proved to have high specificity (above 65%) in detecting engagement of an ICN and the corresponding ictal/postictal symptom, and good positive predictive value (above 67%) in all networks except the visual one. Finally, in the group analysis of BOLD changes related to IED revealed common activations at the right precentral gyrus, supplementary motor area, and middle cingulate gyrus. Significance: Interictal temporal spikes affect several distant extra-temporal areas, and specifically the motor/premotor cortex. EEG–fMRI in patients with TLE eligible for surgery is recommended not for strictly localizing purposes rather it might be useful to investigate ICNs alterations at the single-subject level. Frontiers Media S.A. 2021-12-17 /pmc/articles/PMC8718871/ /pubmed/34975714 http://dx.doi.org/10.3389/fneur.2021.746468 Text en Copyright © 2021 Mirandola, Ballotta, Talami, Giovannini, Pavesi, Vaudano and Meletti. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Mirandola, Laura
Ballotta, Daniela
Talami, Francesca
Giovannini, Giada
Pavesi, Giacomo
Vaudano, Anna Elisabetta
Meletti, Stefano
Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks
title Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks
title_full Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks
title_fullStr Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks
title_full_unstemmed Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks
title_short Temporal Lobe Spikes Affect Distant Intrinsic Connectivity Networks
title_sort temporal lobe spikes affect distant intrinsic connectivity networks
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718871/
https://www.ncbi.nlm.nih.gov/pubmed/34975714
http://dx.doi.org/10.3389/fneur.2021.746468
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