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Brunovsky, M.

Publications and source records attributed to Brunovsky, M..

4 recordsLinked to original sources

EEG microstate dynamics during psilocybin intoxication relate to acute experience and persisting psychological changes

Psilocybin and other serotonergic psychedelics show therapeutic promise for psychiatric disorders, yet objective neural correlates linking the acute psychedelic state to persisting psychological outcomes remain limited. Electroencephalography (EEG) microstate analysis characterizes the rapid spatiotemporal organization of large-scale brain activity, offering a millisecond-resolution window into neural dynamics. Here, we examined resting-state EEG microstates in 15 healthy volunteers who participated in a double-blind, randomized, placebo-controlled crossover study of psilocybin, using both data-driven (three-microstate) and canonical (four-microstate) analysis solutions. EEG was recorded at five time points spanning pre-drug baseline, peak intoxication, and recovery. Psilocybin significantly increased the number of global field power (GFP) peaks and reduced microstate lifespan while increasing frequency of occurrence during peak intoxication (50-100 min post-administration), consistent with accelerated transitions between brain states. Notably, microstate coverage was largely preserved, with only a transient difference at peak intoxication in the 2-20 Hz band-width, suggesting that access to the repertoire of canonical brain states is broadly maintained despite altered temporal dynamics. Critically, individual differences in microstate dynamics during peak intoxication correlated with both acute subjective experience intensity and self-reported psychological changes measured 28 days post-administration, providing exploratory evidence for a link between acute neural dynamics and longer-term experiential outcomes in healthy volunteers. These findings suggest that psilocybin is associated with altered temporal organization of large-scale brain dynamics with largely preserved microstate coverage, and identify EEG microstates as candidate neural markers for psychedelic-induced alterations in consciousness with potential relevance to therapeutic research.

neuroscience↗

EEG connectivity changes in early response to antidepressant treatment

ObjectiveFinding indicators of early response to antidepressant treatment in EEG signals recorded from patients suffering from major depressive disorder. MethodsFunctional brain connectivity networks based on weighted imaginary coherence and weighted imaginary mean phase coherence were computed for 176 patients for 6 different EEG frequency bands. Cross-hemispheric connectivity (CH) and lateral asymmetry (LA) were estimated from these networks based on EEG signals recorded before the beginning of treatment (V is1) and one week after the start of the treatment (V is2). Repeated measures ANOVA was used to check for statistically significant changes in connectivity based on these measures at V is2 w.r.t. V is1. Post-hoc analysis was performed with multiple pairwise comparison tests to determine which group means were significantly different. ResultsIt was found that CHV is2 was significantly reduced w.r.t. CHV is1 in the {beta}1 [12.5 - 17.5 Hz] frequency band for the responders to treatment. Also, LAV is2 was significantly increased w.r.t. LAV is1 in the {beta}1 frequency band for the responders. No such significant changes were observed for the non-responders. Brain networks constructed using both weighted imaginary coherence and weighted imaginary mean phase coherence were found to exhibit these results. For the CH connectivity changes, binarized networks and for the LA connectivity changes, weighted networks were found to be more reliable. ConclusionsResponders were found to show a reduction in cross-hemispheric connectivity and an increase in lateral asymmetry, both in the {beta}1 band while no such change was observed for the non-responders. SignificanceDecrease in cross-hemispheric connectivity and increase in lateral asymmetry in the {beta}1 band may represent candidate neurophysiological indicators of early treatment response, but they require independent replication before any clinical application can be considered.

neuroscience↗

Graph-Based EEG Symmetry Features from the Temporal Lobe as Markers of Antidepressant Treatment Response

Major Depressive Disorder (MDD) is a mental disorder that affects millions globally and has highly individualized responses to antidepressant treatment. Identifying objective early markers that can distinguish responders from non-responders remains a critical challenge in personalized psychiatry. In this study, we investigate the role of brain symmetry in EEG-derived functional connectivity as a potential early marker of treatment response. Using resting-state EEG recordings from 176 patients diagnosed with MDD at baseline (Visit 1) and after one week of treatment (Visit 2), we construct graph-based representations of functional connectivity and define region-wise and electrode-wise temporal-lobe symmetry features. We focus on symmetry change scores (Visit 2 - Visit 1) across typical EEG frequency bands in both weighted and binary forms. Statistical analyses reveal a consistent group-level pattern in the and {beta} bands: responders show negative symmetry change scores, whereas non-responders show relative stability or weakly positive change scores. The contrast is strongest in the {beta}1 band and is more pronounced for binary symmetry metrics, while the band shows the same direction with slightly weaker significance. Physiologically, these opposite trajectories are consistent with a treatment-related shift toward more lateralized temporal-lobe network organization in responders and a more bilateral coupling pattern in nonresponders; however, these neurophysiological interpretations remain hypothesis-generating given the resting-state design and the absence of direct behavioral or task-based validation. To quantify whether temporal symmetry change scores contain reproducible discriminative signal under strict validation, we benchmark the proposed features in a supervised classification pipeline using repeated nested cross-validation. The best-performing configuration achieved a median out-of-sample AUC of 0.690 with a 95% bootstrap confidence interval of [0.611, 0.711], indicating modest but reproducible separability. Overall, temporal-lobe symmetry change features provide interpretable candidate markers of early antidepressant-related neurophysiological change that may complement existing EEG predictors in future multi-marker models, but they are not yet sufficient for standalone clinical decision support and require external validation in independent cohorts.

neuroscience↗

Unveiling Stimulus Transduction Artifacts in Auditory Steady-State Response Experiments: Characterization, Risks, and Mitigation Strategies

This scientific paper addresses the potential risk of spurious responses in neuroscientific auditory steady-state response (ASSR) experiments attributed to transduction artifacts. The focus is particularly on click train stimuli, given their spectral content in the frequency range of interest (e.g., 40 Hz). Building upon a pilot experiment demonstrating the existence of the artifact in a phantom head, this study focuses on the characterization of stimulus artifacts in extended measurements with phantoms and the evaluation of associated risks in experiments involving human subjects. The investigation is divided into two parts: the first part scrutinizes stimulus artifact properties crucial for mitigation, while the second part assesses risks in ASSR experiments with human subjects based on the characterized artifact. The discussion covers stimulus characterization, experimental setups with phantoms, and experiments with human subjects, exploring potential sources of the artifact, its spatial properties, and the influence of re-referencing. The results reveal the role of headphone cables as a source of stimulus artifacts, along with the surprising impact of headphone transducers. The study emphasizes the need for careful experimental design and data analysis to avoid misinterpretations of stimulus artifacts as genuine brain responses in ASSR experiments.

neuroscience↗