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Scalp HFO rates are higher for larger lesions

High‐frequency oscillations (HFO) in scalp EEG are a new and promising noninvasive epilepsy biomarker, providing added prognostic value, particularly in pediatric lesional epilepsy. However, it is unclear if lesion characteristics, such as lesion volume, depth, type, and localization, impact scalp H...

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Autores principales: Cserpan, Dorottya, Gennari, Antonio, Gaito, Luca, Lo Biundo, Santo Pietro, Tuura, Ruth, Sarnthein, Johannes, Ramantani, Georgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436296/
https://www.ncbi.nlm.nih.gov/pubmed/35357778
http://dx.doi.org/10.1002/epi4.12596
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author Cserpan, Dorottya
Gennari, Antonio
Gaito, Luca
Lo Biundo, Santo Pietro
Tuura, Ruth
Sarnthein, Johannes
Ramantani, Georgia
author_facet Cserpan, Dorottya
Gennari, Antonio
Gaito, Luca
Lo Biundo, Santo Pietro
Tuura, Ruth
Sarnthein, Johannes
Ramantani, Georgia
author_sort Cserpan, Dorottya
collection PubMed
description High‐frequency oscillations (HFO) in scalp EEG are a new and promising noninvasive epilepsy biomarker, providing added prognostic value, particularly in pediatric lesional epilepsy. However, it is unclear if lesion characteristics, such as lesion volume, depth, type, and localization, impact scalp HFO rates. We analyzed scalp EEG from 13 children and adolescents with focal epilepsy associated with focal cortical dysplasia (FCD), low‐grade tumors, or hippocampal sclerosis. We applied a validated automated detector to determine HFO rates in bipolar channels. We identified the lesion characteristics in MRI. Larger lesions defined by MRI volumetric analysis corresponded to higher cumulative scalp HFO rates (P = .01) that were detectable in a higher number of channels (P = .05). Both superficial and deep lesions generated HFO detectable in the scalp EEG. Lesion type (FCD vs tumor) and lobar localization (temporal vs extratemporal) did not affect scalp HFO rates in our study. Our observations support that all lesions may generate HFO detectable in scalp EEG, irrespective of their characteristics, whereas larger epileptogenic lesions generate higher scalp HFO rates over larger areas that are thus more accessible to detection. Our study provides crucial insight into scalp HFO detectability in pediatric lesional epilepsy, facilitating their implementation as an epilepsy biomarker in a clinical setting.
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spelling pubmed-94362962022-09-09 Scalp HFO rates are higher for larger lesions Cserpan, Dorottya Gennari, Antonio Gaito, Luca Lo Biundo, Santo Pietro Tuura, Ruth Sarnthein, Johannes Ramantani, Georgia Epilepsia Open Short Research Articles High‐frequency oscillations (HFO) in scalp EEG are a new and promising noninvasive epilepsy biomarker, providing added prognostic value, particularly in pediatric lesional epilepsy. However, it is unclear if lesion characteristics, such as lesion volume, depth, type, and localization, impact scalp HFO rates. We analyzed scalp EEG from 13 children and adolescents with focal epilepsy associated with focal cortical dysplasia (FCD), low‐grade tumors, or hippocampal sclerosis. We applied a validated automated detector to determine HFO rates in bipolar channels. We identified the lesion characteristics in MRI. Larger lesions defined by MRI volumetric analysis corresponded to higher cumulative scalp HFO rates (P = .01) that were detectable in a higher number of channels (P = .05). Both superficial and deep lesions generated HFO detectable in the scalp EEG. Lesion type (FCD vs tumor) and lobar localization (temporal vs extratemporal) did not affect scalp HFO rates in our study. Our observations support that all lesions may generate HFO detectable in scalp EEG, irrespective of their characteristics, whereas larger epileptogenic lesions generate higher scalp HFO rates over larger areas that are thus more accessible to detection. Our study provides crucial insight into scalp HFO detectability in pediatric lesional epilepsy, facilitating their implementation as an epilepsy biomarker in a clinical setting. John Wiley and Sons Inc. 2022-05-06 /pmc/articles/PMC9436296/ /pubmed/35357778 http://dx.doi.org/10.1002/epi4.12596 Text en © 2022 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Short Research Articles
Cserpan, Dorottya
Gennari, Antonio
Gaito, Luca
Lo Biundo, Santo Pietro
Tuura, Ruth
Sarnthein, Johannes
Ramantani, Georgia
Scalp HFO rates are higher for larger lesions
title Scalp HFO rates are higher for larger lesions
title_full Scalp HFO rates are higher for larger lesions
title_fullStr Scalp HFO rates are higher for larger lesions
title_full_unstemmed Scalp HFO rates are higher for larger lesions
title_short Scalp HFO rates are higher for larger lesions
title_sort scalp hfo rates are higher for larger lesions
topic Short Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436296/
https://www.ncbi.nlm.nih.gov/pubmed/35357778
http://dx.doi.org/10.1002/epi4.12596
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