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Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients

OBJECTIVE: Memory deficits are frequent among patients with epilepsies affecting the temporal lobe. Hippocampal interictal epileptic discharges (hIEDs), the presumed epileptic exaggeration of sharp wave‐ripples (SWRs), are known to contribute to memory dysfunction, but the potential underlying mecha...

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Autores principales: Sákovics, Anna, Csukly, Gábor, Borbély, Csaba, Virág, Márta, Kelemen, Anna, Bódizs, Róbert, Erőss, Loránd, Fabó, Dániel
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/PMC9796153/
https://www.ncbi.nlm.nih.gov/pubmed/35723195
http://dx.doi.org/10.1111/epi.17337
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author Sákovics, Anna
Csukly, Gábor
Borbély, Csaba
Virág, Márta
Kelemen, Anna
Bódizs, Róbert
Erőss, Loránd
Fabó, Dániel
author_facet Sákovics, Anna
Csukly, Gábor
Borbély, Csaba
Virág, Márta
Kelemen, Anna
Bódizs, Róbert
Erőss, Loránd
Fabó, Dániel
author_sort Sákovics, Anna
collection PubMed
description OBJECTIVE: Memory deficits are frequent among patients with epilepsies affecting the temporal lobe. Hippocampal interictal epileptic discharges (hIEDs), the presumed epileptic exaggeration of sharp wave‐ripples (SWRs), are known to contribute to memory dysfunction, but the potential underlying mechanism is unknown. The precise temporal coordination between hippocampal SWRs and corticothalamic spindles during sleep is critical for memory consolidation. Moreover, previous investigation indicated that hIEDs induce neocortical spindlelike oscillation. In the present study, we aimed to assess the influence of hIEDs on neocortical spindles. METHODS: We analyzed the spindle characteristics (duration, amplitude, frequency) of 21 epilepsy patients implanted with foramen ovale (FO) electrodes during a whole night sleep. Scalp sleep spindles were categorized based on their temporal relationship to hIEDs detected on the FO electrodes. Three groups were created: (1) spindles coinciding with hIEDs, (2) spindles “induced” by hIEDs, and (3) spindles without hIED co‐occurrence. RESULTS: We found that spindles co‐occurring with hIEDs had altered characteristics in all measured properties, lasted longer by 126 ± 48 ms (mean ± SD), and had higher amplitude by 3.4 ± 3.2 μV, and their frequency range shifted toward the higher frequencies within the 13–15‐Hz range. Also, hIED‐induced spindles had identical oscillatory properties to spindles without any temporal relationships with hIEDs. In more than half of our subjects, clear temporal coherence was revealed between hIEDs and spindles, but the direction of the coupling was patient‐specific. SIGNIFICANCE: We investigated the effect of hippocampal IEDs on neocortical spindle activity and found spindle alterations in cases of spindle–hIED co‐occurrence, but not in cases of hIED‐initiated spindles. We propose that this is a marker of a pathologic process, where IEDs may have direct effect on spindle generation. It could mark a potential mechanism whereby IEDs disrupt memory processes, and also provide a potential therapeutic target to treat memory disturbances in epilepsy.
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spelling pubmed-97961532022-12-30 Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients Sákovics, Anna Csukly, Gábor Borbély, Csaba Virág, Márta Kelemen, Anna Bódizs, Róbert Erőss, Loránd Fabó, Dániel Epilepsia Research Articles OBJECTIVE: Memory deficits are frequent among patients with epilepsies affecting the temporal lobe. Hippocampal interictal epileptic discharges (hIEDs), the presumed epileptic exaggeration of sharp wave‐ripples (SWRs), are known to contribute to memory dysfunction, but the potential underlying mechanism is unknown. The precise temporal coordination between hippocampal SWRs and corticothalamic spindles during sleep is critical for memory consolidation. Moreover, previous investigation indicated that hIEDs induce neocortical spindlelike oscillation. In the present study, we aimed to assess the influence of hIEDs on neocortical spindles. METHODS: We analyzed the spindle characteristics (duration, amplitude, frequency) of 21 epilepsy patients implanted with foramen ovale (FO) electrodes during a whole night sleep. Scalp sleep spindles were categorized based on their temporal relationship to hIEDs detected on the FO electrodes. Three groups were created: (1) spindles coinciding with hIEDs, (2) spindles “induced” by hIEDs, and (3) spindles without hIED co‐occurrence. RESULTS: We found that spindles co‐occurring with hIEDs had altered characteristics in all measured properties, lasted longer by 126 ± 48 ms (mean ± SD), and had higher amplitude by 3.4 ± 3.2 μV, and their frequency range shifted toward the higher frequencies within the 13–15‐Hz range. Also, hIED‐induced spindles had identical oscillatory properties to spindles without any temporal relationships with hIEDs. In more than half of our subjects, clear temporal coherence was revealed between hIEDs and spindles, but the direction of the coupling was patient‐specific. SIGNIFICANCE: We investigated the effect of hippocampal IEDs on neocortical spindle activity and found spindle alterations in cases of spindle–hIED co‐occurrence, but not in cases of hIED‐initiated spindles. We propose that this is a marker of a pathologic process, where IEDs may have direct effect on spindle generation. It could mark a potential mechanism whereby IEDs disrupt memory processes, and also provide a potential therapeutic target to treat memory disturbances in epilepsy. John Wiley and Sons Inc. 2022-07-17 2022-09 /pmc/articles/PMC9796153/ /pubmed/35723195 http://dx.doi.org/10.1111/epi.17337 Text en © 2022 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Sákovics, Anna
Csukly, Gábor
Borbély, Csaba
Virág, Márta
Kelemen, Anna
Bódizs, Róbert
Erőss, Loránd
Fabó, Dániel
Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients
title Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients
title_full Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients
title_fullStr Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients
title_full_unstemmed Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients
title_short Prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients
title_sort prolongation of cortical sleep spindles during hippocampal interictal epileptiform discharges in epilepsy patients
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796153/
https://www.ncbi.nlm.nih.gov/pubmed/35723195
http://dx.doi.org/10.1111/epi.17337
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