Abstract

EEG microstate analysis is an approach to study brain states and their fast transitions in healthy cognition and disease. A key limitation of conventional microstate analysis is that it must be performed at the sensor level, and therefore gives limited anatomical insight. Here, we generalise the microstate methodology to be applicable to source-reconstructed electrophysiological data. Using simulations of a neural-mass network model, we first established the validity and robustness of the proposed method. Using MEG resting-state data, we uncovered ten microstates with distinct spatial distributions of cortical activation. Multivariate pattern analysis demonstrated that source-level microstates were associated with distinct functional connectivity patterns. We further demonstrated that the occurrence probability of MEG microstates were altered by auditory stimuli, exhibiting a hyperactivity of the microstate including the auditory cortex. Our results support the use of source-level microstates as a method for investigating brain dynamic activity and connectivity at the millisecond scale.

Highlights

  • Whole-brain, non-invasive functional neuroimaging of the human brain is a useful tool for uncovering the mechanisms underpinning cognitive functions and neurological disease 1–6

  • In functional MRI data, techniques to study functional brain-states have included independent component analysis (ICA) 7;20 and sliding-window analysis 21, uncovering a small number of reproducible networks known as resting-state networks (RSNs) 7

  • It follows that alternative methods are required to uncover faster time-scale dynamics in EEG/MEG data 10, and it is currently unclear the extent to which spatiotemporal properties of millisecond scale non-stationarity reflect those of slower RSNs

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Summary

Introduction

Whole-brain, non-invasive functional neuroimaging of the human brain is a useful tool for uncovering the mechanisms underpinning cognitive functions and neurological disease 1–6. It follows that alternative methods are required to uncover faster time-scale (on the order of milliseconds) dynamics in EEG/MEG data 10 , and it is currently unclear the extent to which spatiotemporal properties of millisecond scale non-stationarity reflect those of slower RSNs

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