Noisy network attractor models for transitions between EEG microstates

This is the final version. Available on open access from Springer via the DOI in this recordAvailability of data and material: The data used in this paper are published in [18] and are available from JB on reasonable request.The brain is intrinsically organized into large-scale networks that constantly re-organize on multiple timescales, even when the brain is at rest. The timing of these dynamics is crucial for sensation, perception, cognition and ultimately consciousness, but the underlying dynamics governing the constant reorganization and switching between networks are not yet well understood. Functional magnetic resonance imaging (fMRI) and electroencephalography (EEG) provide anatomical and temporal information about the resting-state networks (RSNs), respectively. EEG microstates are brief periods of stable scalp topography, and four distinct configurations with characteristic switching patterns between them are reliably identified at rest. Microstates have been identified as the electrophysiological correlate of fMRI-defined RSNs, this link could be established because EEG microstate sequences are scale-free and have long-range temporal correlations. This property is crucial for any approach to model EEG microstates. This paper proposes a novel modeling approach for microstates: we consider nonlinear stochastic differential equations (SDEs) that exhibit a noisy network attractor between nodes that represent the microstates. Using a single layer network between four states, we can reproduce the transition probabilities between microstates but not the heavy tailed residence time distributions. Introducing a two layer network with a hidden layer gives the flexibility to capture these heavy tails and their long-range temporal correlations. We fit these models to capture the statistical properties of microstate sequences from EEG data recorded inside and outside the MRI scanner and show that the processing required to separate the EEG signal from the fMRI machine noise results in a loss of information which is reflected in differences in the long tail of the dwell-time distributions.Engineering and Physical Sciences Research Council (EPSRC)Medical Research Council (MRC)Marsden Fund, Royal Society of New Zealan

EEG microstate complexity for aiding early diagnosis of Alzheimer’s disease

The dynamics of the resting brain exhibit transitions between a small number of discrete networks, each remaining stable for tens to hundreds of milliseconds. These functional microstates are thought to be the building blocks of spontaneous consciousness. The electroencephalogram (EEG) is a useful tool for imaging microstates, and EEG microstate analysis can potentially give insight into altered brain dynamics underpinning cognitive impairment in disorders such as Alzheimer’s disease (AD). Since EEG is non-invasive and relatively inexpensive, EEG microstates have the potential to be useful clinical tools for aiding early diagnosis of AD. In this study, EEG was collected from two independent cohorts of probable AD and cognitively healthy control participants, and a cohort of mild cognitive impairment (MCI) patients with four-year clinical follow-up. The microstate associated with the frontoparietal working-memory/attention network was altered in AD due to parietal inactivation. Using a novel measure of complexity, we found microstate transitioning was slower and less complex in AD. When combined with a spectral EEG measure, microstate complexity could classify AD with sensitivity and specificity >80%, which was tested on an independent cohort, and could predict progression from MCI to AD in a small preliminary test cohort of 11 participants. EEG microstates therefore have potential to be a non-invasive functional biomarker of AD

MEG cortical microstates: Spatiotemporal characteristics, dynamic functional connectivity and stimulus-evoked responses

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

MEG cortical microstates: spatiotemporal characteristics, dynamic functional connectivity and stimulus-evoked responses

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