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

Author:

Ilhan-Bayrakcı Merve1ORCID,Cabral-Calderin Yuranny2ORCID,Bergmann Til Ole13ORCID,Tüscher Oliver145ORCID,Stroh Albrecht16ORCID

Affiliation:

1. Systemic Mechanisms of Resilience , Leibniz Institute for Resilience Research (LIR), 55122 Mainz, Germany

2. Neural and Environmental Rhythms , Max Planck Institute for Empirical Aesthetics, 60322 Frankfurt, Germany

3. Neuroimaging Center (NIC), Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz , 55131 Mainz , Germany

4. Department of Psychiatry and Psychotherapy , , 55131 Mainz , Germany

5. University Medical Center of the Johannes Gutenberg University Mainz , , 55131 Mainz , Germany

6. Institute of Pathophysiology, University Medical Center of the Johannes Gutenberg University Mainz , 55131 Mainz , Germany

Abstract

Abstract 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.

Funder

Deutsche Forschungsgemeinschaft

Leibniz Gemeinschaft

Boehringer Ingelheim Foundation

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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