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Bastiaens, S. P.

Publications and source records attributed to Bastiaens, S. P..

5 recordsLinked to original sources

Excitation-Inhibition Balance and Fronto-Limbic Connectivity Drive TMS Treatment Outcomes in Refractory Depression

Depression affects over 350 million people worldwide, with treatment resistance occurring in up to 30% of cases. Intermittent theta burst stimulation (iTBS) targeting the left dorsolateral prefrontal cortex (DLPFC) has emerged as a promising intervention, yet the neurophysiological mechanisms determining which patients will respond remain poorly understood. Here, we combined transcranial magnetic stimulation with electroencephalography and whole-brain computational modeling to uncover the mechanistic basis of treatment efficacy in 90 patients with treatment-resistant depression. We identified two distinct neurophysiological signatures that differentiate responders from non-responders: (1) post-treatment shifts in excitation-inhibition balance toward greater inhibitory control, and (2) a pre-treatment brain state characterized by anticorrelated dynamics between subgenual anterior cingulate cortex and DLPFC. These features were significantly correlated with clinical improvement and could not be explained by non-specific factors. Our findings provide a neurophysiologically-informed framework for developing personalized and optimized neuromodulation approaches in treatment-resistant depression.

neuroscience↗

Assessing the Validity and Reliability of HD-DOT TD-fNIRS Resting-State Measurements in Rapid Succession Data Collection Settings

AO_SCPLOWBSTRACTC_SCPLOWFunctional magnetic resonance imaging (fMRI) has long been a cornerstone in the study of brain activity, but its high operational costs, limited availability, and restricted practical applicability have led researchers to seek alternative neuroimaging technologies. Recent advancements in high-density diffuse optical tomography (HD-DOT) and Time-Domain (TD) functional near-infrared spectroscopy (fNIRS) have emerged as promising solutions, offering the ability to generate detailed tomographic maps of hemodynamic fluctuations associated with neural activity. In this study, using the Kernel Flow device, we assess the performance of HD-DOT TD-fNIRS in terms of signal validity and reliability, particularly in rapid succession data collection settings. We conducted a multiple test-retest experiment involving fNIRS recordings from three participants across 20 ten-minute sessions of eyes-open resting-state brain activity over six days. Our findings indicate that HD-DOT TD-fNIRS systems like the Kernel Flow can reproduce hemodynamic patterns identified by fMRI, albeit with less spatial detail, and can detect resting state networks overall, though some individual network detections are not significant. The system performs consistently over days, with more variability within the time of day, and can capture subject-specific patterns with high accuracy as identified through FC fingerprinting analysis. We conclude that the new generation of HD-DOT TD-fNIRS systems holds significant promise for enhancing and expanding the measurement of functional brain data in both clinical and more naturalistic research settings. This study represents an important step towards a comprehensive understanding of the data quality and consistency achievable with these innovative neuroimaging devices.

neuroscience↗

The Role of Inhibition in fMRI Resting-State Negative Correlations

Resting-state brain activity, as observed via functional magnetic resonance imaging (fMRI), displays non-random fluctuations whose functional connectivity (FC) is commonly parsed into spatial patterns of positive and negative correlations (PCs and NCs). Mapping NC patterns for certain key seed regions has shown considerable promise in recent years as a tool for enhancing neuro-navigated targeting and clinical outcomes of repetitive transcranial magnetic stimulation (rTMS) therapies in psychiatry. These successes bring to the fore several major outstanding questions about the neurophysiological origins of fMRI NCs. In this work, we studied candidate mechanisms for the emergence of fMRI NCs using connectome-based brain network modeling. Simulations of fMRI data under manipulation of inhibitory parameters WI and {lambda}, representing local and network-mediated inhibition respectively, were explored, focusing on the impact of inhibition levels on the emergence of NCs. Despite the considerable difference in time scales between GABAergic neuronal inhibition and fMRI FC, a clear relationship was observed, whereby the greater levels of overall inhibition led to significantly greater magnitude and spatial extent of NCs. We show that this effect is due to a leftward shift in the FC correlation distribution, leading to a reduction in the number of PCs and a concomitant increase in the number of NCs. Relatedly, we observed that those connections available for recruitment as NCs were precisely those with the weakest corresponding structural connectivity. Relative to nominally default values for the models used, greater levels of inhibition also improved, quantitatively and qualitatively, single-subject fits of simulated to empirical FC matrices. Our results provide new insights into how individual variability in anatomical connectivity strengths and neuronal inhibition levels may determine individualized expression of NCs in fMRI data. These, in turn, may offer new directions for optimization and personalization of rTMS therapies and other clinical applications of fMRI NC patterns. Author SummaryResting-state brain activity, as detected through functional magnetic resonance imaging (fMRI), demonstrates non-random fluctuations in its covariance structure, often characterized as functional connectivity (FC), which is further divided into spatial patterns of positive and negative correlations (NCs). Mapping patterns of NCs of specific key seed regions have demonstrated significant potential as a method for improving the precision of neuro-navigated targeting and enhancing clinical outcomes in the application of repetitive transcranial magnetic stimulation therapies within the field of psychiatry. In our study, we employed the reduced Wong-Wang neural mass model to investigate the physiological underpinnings of NCs observed in resting-state fMRI (rs-fMRI). Our simulated data partially captures the dynamics of empirical rs-fMRI data, revealing that increased inhibition levels correlate with a higher number of NCs. We also observed differential effects on model stability and NCs with varying levels of excitation and inhibition. These findings shed light on the complex interplay between neural dynamics and rs-fMRI connectivity patterns. Importantly, our work contributes to refining model parameters and offers insights for future validation with empirical clinical data. Understanding the factors influencing NCs in rs-fMRI FC has implications for optimizing therapeutic interventions and advancing our understanding of brain function.

neuroscience↗

A comprehensive investigation of intracortical and corticothalamic models of alpha rhythms

The electroencephalographic alpha rhythm is one of the most robustly observed and widely studied empirical phenomena in all of neuroscience. However, despite its extensive implication in a wide range of cognitive processes and clinical pathologies, the mechanisms underlying alpha generation in neural circuits remain poorly understood. In this paper we offer a renewed foundation for research on this question, by undertaking a systematic comparison and synthesis of the most prominent theoretical models of alpha rhythmogenesis in the published literature. We focus on four models, each studied intensively by multiple authors over the past three decades: i) Jansen-Rit, ii) Moran-David-Friston, iii) Robinson-Rennie-Wright, and iv) Liley-Wright. Several common elements are identified, such as the use of second-order differential equations and sigmoidal potential-to-rate operators to represent population-level neural activity. Major differences are seen in other features such as wiring topologies and conduction delays. Through a series of mathematical analyses and numerical simulations, we nevertheless demonstrate that the selected models can be meaningfully compared, by associating parameters and circuit motifs of analogous biological significance. With this established, we conduct explorations of rate constant and synaptic connectivity parameter spaces, with the aim of identifying common patterns in key behaviours, such as the role of excitatory-inhibitory interactions in the generation of oscillations. Finally, using linear stability analysis we identify two qualitatively different alpha-generating dynamical regimes across the models: i) noise-driven fluctuations, and ii) self-sustained limit-cycle oscillations, emerging due to an Andronov-Hopf bifurcation. The comprehensive survey and synthesis developed here can, we suggest, be used to help guide future theoretical and experimental work aimed at disambiguating these and other candidate theories of alpha rhythmogenesis.

neuroscience↗

Corticothalamic modelling of sleep neurophysiology with applications to mobile EEG

AO_SCPLOWBSTRACTC_SCPLOWRecent developments in mathematical modelling of EEG enable the tracking of otherwise-inaccessible neurophysiological parameters throughout sleep. Likewise, advancements in wearable electronics have enabled easy & affordable collection of sleep EEG at home. The convergence of these two advances, namely neurophysiological modelling for mobile sleep EEG, can boost preclinical and clinical assessments of sleep. However, this subject area has received limited attention in existing literature. To address this, we used an established model of the corticothalamic system to analyze EEG power spectra from 5 datasets, spanning from research-grade systems to at-home mobile EEG. In the present work, we compare the convergent and divergent features of the data and the estimated physiological model parameters. While data quality and characteristics differ considerably, key patterns consistent with previous theoretical and empirical work are observed. During the transition from lighter to deeper NREM, i) exponent of the aperiodic (1/f) spectral component is increased, ii) bottom-up thalamocortical drive is reduced, iii) corticocortical connection strengths are increased. This effect is observed in healthy subjects but is interestingly absent when taking SSRI antidepressants, suggesting possible effects of ascending neuromodulation on corticothalamic oscillations. We further show a month-long increase in REM% in one mobile EEG subject, associated with boosted high-frequency activity in spectra and higher thalamothalamic gains in the model, pointing to possible changes of thalamic inhibition in REM parasomnias. Our results provide a proof-of-principle for the utility and feasibility of this physiological modelling-based approach to analyzing mobile EEG data, providing a mechanistic measure of brain physiology during sleep. Statement of significanceWe employ a physiological model of the corticothalamic circuitry to model the EEG power spectra in sleep. We fit this model to 5 EEG datasets, and demonstrate that while mobile and non-mobile EEG recordings differ in their characteristics and quality, they can both robustly represent the changes along sleep stages using the aperiodic (1/f) component. We observe an increased corticocortical connection strength and decreased corticothalamic connection strength as the subject goes into deeper stages of NREM sleep; an effect that is, importantly, not observed in subjects taking SSRIs. This work provides a proof-of-concept for using mathematical modelling, working well for large mobile and non-mobile datasets providing valuable insight into the mechanisms generating sleep EEG.

neuroscience↗