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Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings

The slow wave state is a general state of quiescence interrupted by sudden bursts of activity or so-called slow wave events (SWEs). Recently, the relationship between SWEs and blood oxygen level–dependent (BOLD) functional magnetic resonance imaging (fMRI) signals was assessed in rodent models which...

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Detalles Bibliográficos
Autores principales: Ilhan-Bayrakcı, Merve, Cabral-Calderin, Yuranny, Bergmann, Til Ole, Tüscher, Oliver, Stroh, Albrecht
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627041/
https://www.ncbi.nlm.nih.gov/pubmed/35094045
http://dx.doi.org/10.1093/cercor/bhab516
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author Ilhan-Bayrakcı, Merve
Cabral-Calderin, Yuranny
Bergmann, Til Ole
Tüscher, Oliver
Stroh, Albrecht
author_facet Ilhan-Bayrakcı, Merve
Cabral-Calderin, Yuranny
Bergmann, Til Ole
Tüscher, Oliver
Stroh, Albrecht
author_sort Ilhan-Bayrakcı, Merve
collection PubMed
description The slow wave state is a general state of quiescence interrupted by sudden bursts of activity or so-called slow wave events (SWEs). Recently, the relationship between SWEs and blood oxygen level–dependent (BOLD) functional magnetic resonance imaging (fMRI) signals was assessed in rodent models which revealed cortex-wide BOLD activation. However, it remains unclear which macroscopic signature corresponds to these specific neurophysiological events in the human brain. Therefore, we analyzed simultaneous electroencephalographic (EEG)-fMRI data during human non-REM sleep. SWEs individually detected in the EEG data were used as predictors in event-related fMRI analyses to examine the relationship between SWEs and fMRI signals. For all 10 subjects we identified significant changes in BOLD activity associated with SWEs covering substantial parts of the gray matter. As demonstrated in rodents, we observed a direct relation of a neurophysiological event to specific BOLD activation patterns. We found a correlation between the number of SWEs and the spatial extent of these BOLD activation patterns and discovered that the amplitude of the BOLD response strongly depends on the SWE amplitude. As altered SWE propagation has recently been found in neuropsychiatric diseases, it is critical to reveal the brain’s physiological slow wave state networks to potentially establish early imaging biomarkers for various diseases long before disease onset.
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spelling pubmed-96270412022-11-04 Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings Ilhan-Bayrakcı, Merve Cabral-Calderin, Yuranny Bergmann, Til Ole Tüscher, Oliver Stroh, Albrecht Cereb Cortex Original Article The slow wave state is a general state of quiescence interrupted by sudden bursts of activity or so-called slow wave events (SWEs). Recently, the relationship between SWEs and blood oxygen level–dependent (BOLD) functional magnetic resonance imaging (fMRI) signals was assessed in rodent models which revealed cortex-wide BOLD activation. However, it remains unclear which macroscopic signature corresponds to these specific neurophysiological events in the human brain. Therefore, we analyzed simultaneous electroencephalographic (EEG)-fMRI data during human non-REM sleep. SWEs individually detected in the EEG data were used as predictors in event-related fMRI analyses to examine the relationship between SWEs and fMRI signals. For all 10 subjects we identified significant changes in BOLD activity associated with SWEs covering substantial parts of the gray matter. As demonstrated in rodents, we observed a direct relation of a neurophysiological event to specific BOLD activation patterns. We found a correlation between the number of SWEs and the spatial extent of these BOLD activation patterns and discovered that the amplitude of the BOLD response strongly depends on the SWE amplitude. As altered SWE propagation has recently been found in neuropsychiatric diseases, it is critical to reveal the brain’s physiological slow wave state networks to potentially establish early imaging biomarkers for various diseases long before disease onset. Oxford University Press 2022-01-30 /pmc/articles/PMC9627041/ /pubmed/35094045 http://dx.doi.org/10.1093/cercor/bhab516 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ilhan-Bayrakcı, Merve
Cabral-Calderin, Yuranny
Bergmann, Til Ole
Tüscher, Oliver
Stroh, Albrecht
Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings
title Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings
title_full Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings
title_fullStr Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings
title_full_unstemmed Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings
title_short Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings
title_sort individual slow wave events give rise to macroscopic fmri signatures and drive the strength of the bold signal in human resting-state eeg-fmri recordings
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627041/
https://www.ncbi.nlm.nih.gov/pubmed/35094045
http://dx.doi.org/10.1093/cercor/bhab516
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