Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive Tasks

Rationale: High-frequency oscillations (HFOs) in intracranial EEG (iEEG) are used to delineate the epileptogenic zone during presurgical diagnostic assessment in patients with epilepsy. HFOs are historically divided into ripples (80–250 Hz), fast ripples (FR, >250 Hz), and their co-occurrence...

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Main Authors: Ece Boran, Lennart Stieglitz, Johannes Sarnthein
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Human Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnhum.2021.613125/full
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author Ece Boran
Lennart Stieglitz
Johannes Sarnthein
Johannes Sarnthein
author_facet Ece Boran
Lennart Stieglitz
Johannes Sarnthein
Johannes Sarnthein
author_sort Ece Boran
collection DOAJ
description Rationale: High-frequency oscillations (HFOs) in intracranial EEG (iEEG) are used to delineate the epileptogenic zone during presurgical diagnostic assessment in patients with epilepsy. HFOs are historically divided into ripples (80–250 Hz), fast ripples (FR, >250 Hz), and their co-occurrence (FRandR). In a previous study, we had validated the rate of FRandRs during deep sleep to predict seizure outcome. Here, we ask whether epileptic FRandRs might be confounded by physiological FRandRs that are unrelated to epilepsy.Methods: We recorded iEEG in the medial temporal lobe MTL (hippocampus, entorhinal cortex, and amygdala) in 17 patients while they performed cognitive tasks. The three cognitive tasks addressed verbal working memory, visual working memory, and emotional processing. In our previous studies, these tasks activated the MTL. We re-analyzed the data of these studies with the automated detector that focuses on the co-occurrence of ripples and FRs (FRandR).Results: For each task, we identified those channels in which the HFO rate was modulated during the task condition compared to the control condition. However, the number of these channels did not exceed the chance level. Interestingly, even during wakefulness, the HFO rate was higher for channels within the seizure onset zone (SOZ) than for channels outside the SOZ.Conclusion: Our prospective definition of an epileptic HFO, the FRandR, is not confounded by physiological HFOs that might be elicited by our cognitive tasks. This is reassuring for the clinical use of FRandR as a biomarker of the EZ.
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spelling doaj.art-fd9d5834e7c74a089b98bc69ff703a4e2022-12-21T22:08:36ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612021-02-011510.3389/fnhum.2021.613125613125Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive TasksEce Boran0Lennart Stieglitz1Johannes Sarnthein2Johannes Sarnthein3Klinik für Neurochirurgie, Universitäts Spital und Universität Zürich, Zurich, SwitzerlandKlinik für Neurochirurgie, Universitäts Spital und Universität Zürich, Zurich, SwitzerlandKlinik für Neurochirurgie, Universitäts Spital und Universität Zürich, Zurich, SwitzerlandNeuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, SwitzerlandRationale: High-frequency oscillations (HFOs) in intracranial EEG (iEEG) are used to delineate the epileptogenic zone during presurgical diagnostic assessment in patients with epilepsy. HFOs are historically divided into ripples (80–250 Hz), fast ripples (FR, >250 Hz), and their co-occurrence (FRandR). In a previous study, we had validated the rate of FRandRs during deep sleep to predict seizure outcome. Here, we ask whether epileptic FRandRs might be confounded by physiological FRandRs that are unrelated to epilepsy.Methods: We recorded iEEG in the medial temporal lobe MTL (hippocampus, entorhinal cortex, and amygdala) in 17 patients while they performed cognitive tasks. The three cognitive tasks addressed verbal working memory, visual working memory, and emotional processing. In our previous studies, these tasks activated the MTL. We re-analyzed the data of these studies with the automated detector that focuses on the co-occurrence of ripples and FRs (FRandR).Results: For each task, we identified those channels in which the HFO rate was modulated during the task condition compared to the control condition. However, the number of these channels did not exceed the chance level. Interestingly, even during wakefulness, the HFO rate was higher for channels within the seizure onset zone (SOZ) than for channels outside the SOZ.Conclusion: Our prospective definition of an epileptic HFO, the FRandR, is not confounded by physiological HFOs that might be elicited by our cognitive tasks. This is reassuring for the clinical use of FRandR as a biomarker of the EZ.https://www.frontiersin.org/articles/10.3389/fnhum.2021.613125/fullepilepsy surgeryseizure onset zoneepileptogenic zonemedial temporal lobeworking memoryemotional processing
spellingShingle Ece Boran
Lennart Stieglitz
Johannes Sarnthein
Johannes Sarnthein
Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive Tasks
Frontiers in Human Neuroscience
epilepsy surgery
seizure onset zone
epileptogenic zone
medial temporal lobe
working memory
emotional processing
title Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive Tasks
title_full Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive Tasks
title_fullStr Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive Tasks
title_full_unstemmed Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive Tasks
title_short Epileptic High-Frequency Oscillations in Intracranial EEG Are Not Confounded by Cognitive Tasks
title_sort epileptic high frequency oscillations in intracranial eeg are not confounded by cognitive tasks
topic epilepsy surgery
seizure onset zone
epileptogenic zone
medial temporal lobe
working memory
emotional processing
url https://www.frontiersin.org/articles/10.3389/fnhum.2021.613125/full
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AT lennartstieglitz epileptichighfrequencyoscillationsinintracranialeegarenotconfoundedbycognitivetasks
AT johannessarnthein epileptichighfrequencyoscillationsinintracranialeegarenotconfoundedbycognitivetasks
AT johannessarnthein epileptichighfrequencyoscillationsinintracranialeegarenotconfoundedbycognitivetasks