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Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study

INTRODUCTION: Epilepsy is defined as non-lesional (NLE) when a lesion cannot be localized via standard neuroimaging. NLE is known to have a poor response to surgery. Stereotactic electroencephalography (sEEG) can detect functional connectivity (FC) between zones of seizure onset (OZ) and early (ESZ)...

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Autores principales: Sathe, Anish V., Matias, Caio M., Kogan, Michael, Ailes, Isaiah, Syed, Mashaal, Kang, KiChang, Miao, Jingya, Talekar, Kiran, Faro, Scott, Mohamed, Feroze B., Tracy, Joseph, Sharan, Ashwini, Alizadeh, Mahdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194331/
https://www.ncbi.nlm.nih.gov/pubmed/37206659
http://dx.doi.org/10.3389/fnimg.2023.1109546
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author Sathe, Anish V.
Matias, Caio M.
Kogan, Michael
Ailes, Isaiah
Syed, Mashaal
Kang, KiChang
Miao, Jingya
Talekar, Kiran
Faro, Scott
Mohamed, Feroze B.
Tracy, Joseph
Sharan, Ashwini
Alizadeh, Mahdi
author_facet Sathe, Anish V.
Matias, Caio M.
Kogan, Michael
Ailes, Isaiah
Syed, Mashaal
Kang, KiChang
Miao, Jingya
Talekar, Kiran
Faro, Scott
Mohamed, Feroze B.
Tracy, Joseph
Sharan, Ashwini
Alizadeh, Mahdi
author_sort Sathe, Anish V.
collection PubMed
description INTRODUCTION: Epilepsy is defined as non-lesional (NLE) when a lesion cannot be localized via standard neuroimaging. NLE is known to have a poor response to surgery. Stereotactic electroencephalography (sEEG) can detect functional connectivity (FC) between zones of seizure onset (OZ) and early (ESZ) and late (LSZ) spread. We examined whether resting-state fMRI (rsfMRI) can detect FC alterations in NLE to see whether noninvasive imaging techniques can localize areas of seizure propagation to potentially target for intervention. METHODS: This is a retrospective study of 8 patients with refractory NLE who underwent sEEG electrode implantation and 10 controls. The OZ, ESZ, and LSZ were identified by generating regions around sEEG contacts that recorded seizure activity. Amplitude synchronization analysis was used to detect the correlation of the OZ to the ESZ. This was also done using the OZ and ESZ of each NLE patient for each control. Patients with NLE were compared to controls individually using Wilcoxon tests and as a group using Mann-Whitney tests. Amplitude of low-frequency fluctuations (ALFF), fractional ALFF (fALFF), regional homogeneity (ReHo), degree of centrality (DoC), and voxel-mirrored homotopic connectivity (VMHC) were calculated as the difference between NLE and controls and compared between the OZ and ESZ and to zero. A general linear model was used with age as a covariate with Bonferroni correction for multiple comparisons. RESULTS: Five out of 8 patients with NLE showed decreased correlations from the OZ to the ESZ. Group analysis showed patients with NLE had lower connectivity with the ESZ. Patients with NLE showed higher fALFF and ReHo in the OZ but not the ESZ, and higher DoC in the OZ and ESZ. Our results indicate that patients with NLE show high levels of activity but dysfunctional connections in seizure-related areas. DISCUSSION: rsfMRI analysis showed decreased connectivity directly between seizure-related areas, while FC metric analysis revealed increases in local and global connectivity in seizure-related areas. FC analysis of rsfMRI can detect functional disruption that may expose the pathophysiology underlying NLE.
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spelling pubmed-101943312023-05-18 Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study Sathe, Anish V. Matias, Caio M. Kogan, Michael Ailes, Isaiah Syed, Mashaal Kang, KiChang Miao, Jingya Talekar, Kiran Faro, Scott Mohamed, Feroze B. Tracy, Joseph Sharan, Ashwini Alizadeh, Mahdi Front Neuroimaging Neuroimaging INTRODUCTION: Epilepsy is defined as non-lesional (NLE) when a lesion cannot be localized via standard neuroimaging. NLE is known to have a poor response to surgery. Stereotactic electroencephalography (sEEG) can detect functional connectivity (FC) between zones of seizure onset (OZ) and early (ESZ) and late (LSZ) spread. We examined whether resting-state fMRI (rsfMRI) can detect FC alterations in NLE to see whether noninvasive imaging techniques can localize areas of seizure propagation to potentially target for intervention. METHODS: This is a retrospective study of 8 patients with refractory NLE who underwent sEEG electrode implantation and 10 controls. The OZ, ESZ, and LSZ were identified by generating regions around sEEG contacts that recorded seizure activity. Amplitude synchronization analysis was used to detect the correlation of the OZ to the ESZ. This was also done using the OZ and ESZ of each NLE patient for each control. Patients with NLE were compared to controls individually using Wilcoxon tests and as a group using Mann-Whitney tests. Amplitude of low-frequency fluctuations (ALFF), fractional ALFF (fALFF), regional homogeneity (ReHo), degree of centrality (DoC), and voxel-mirrored homotopic connectivity (VMHC) were calculated as the difference between NLE and controls and compared between the OZ and ESZ and to zero. A general linear model was used with age as a covariate with Bonferroni correction for multiple comparisons. RESULTS: Five out of 8 patients with NLE showed decreased correlations from the OZ to the ESZ. Group analysis showed patients with NLE had lower connectivity with the ESZ. Patients with NLE showed higher fALFF and ReHo in the OZ but not the ESZ, and higher DoC in the OZ and ESZ. Our results indicate that patients with NLE show high levels of activity but dysfunctional connections in seizure-related areas. DISCUSSION: rsfMRI analysis showed decreased connectivity directly between seizure-related areas, while FC metric analysis revealed increases in local and global connectivity in seizure-related areas. FC analysis of rsfMRI can detect functional disruption that may expose the pathophysiology underlying NLE. Frontiers Media S.A. 2023-05-05 /pmc/articles/PMC10194331/ /pubmed/37206659 http://dx.doi.org/10.3389/fnimg.2023.1109546 Text en Copyright © 2023 Sathe, Matias, Kogan, Ailes, Syed, Kang, Miao, Talekar, Faro, Mohamed, Tracy, Sharan and Alizadeh. 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 Neuroimaging
Sathe, Anish V.
Matias, Caio M.
Kogan, Michael
Ailes, Isaiah
Syed, Mashaal
Kang, KiChang
Miao, Jingya
Talekar, Kiran
Faro, Scott
Mohamed, Feroze B.
Tracy, Joseph
Sharan, Ashwini
Alizadeh, Mahdi
Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study
title Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study
title_full Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study
title_fullStr Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study
title_full_unstemmed Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study
title_short Resting-state fMRI can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study
title_sort resting-state fmri can detect alterations in seizure onset and spread regions in patients with non-lesional epilepsy: a pilot study
topic Neuroimaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194331/
https://www.ncbi.nlm.nih.gov/pubmed/37206659
http://dx.doi.org/10.3389/fnimg.2023.1109546
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