Key result
Standardized auditory perturbations elicited substantial inter-individual variability in coordinated frontal beta activity and heart rate variability, with no significant group-level effects detected (p > 0.05).
Why the study?
Psychiatric research needs objective, biologically grounded markers, but EEG approaches are typically brain-centric and static, with limited integration of autonomic dynamics.
Do brief standardized auditory perturbations elicit coordinated changes in frontal EEG activity and heart rate variability in healthy adults?
Do brief standardized auditory perturbations elicit coordinated changes in frontal EEG activity and heart rate variability in healthy adults?
This exploratory pilot study demonstrated substantial inter-individual variability in coordinated EEG and HRV responses to auditory perturbations, providing a methodological foundation for future physiology-informed precision psychiatry research.
Marked inter-individual EEG-HRV variability to auditory stimuli; hypothesis-generating for multimodal frameworks, should not yet change practice.
Background Contemporary psychiatric research increasingly emphasizes the need for objective, biologically grounded markers to complement symptom-based diagnostic frameworks. While electroencephalography (EEG) has been widely used to investigate neural dynamics associated with attention, arousal, and cognitive control, these approaches are typically brain-centric and rely on static or resting-state paradigms. Integration of autonomic dynamics remains limited despite theoretical models highlighting brain–body interactions. Methods In the present pilot study, we employed a multimodal, perturbation-based paradigm combining wearable EEG and heart rate variability (HRV) to examine cortico–autonomic regulatory dynamics. Ten healthy participants were exposed to brief auditory conditions (silence, noise-based stimulation, and binaural-beat auditory input). Frontal upper-beta activity (β 2 ; 21–30 Hz) and vagally mediated HRV indices (RMSSD, HF power) were analyzed to characterize within-subject regulatory responses across conditions. Results Condition-related variation was observed descriptively in both cortical and autonomic measures, although no statistically significant group-level effects were detected. Substantial inter-individual variability emerged in the direction and magnitude of these responses. Notably, substantial inter-individual variability emerged in both the direction and magnitude of physiological responses. In several participants, coordinated changes between EEG and HRV measures suggested multimodal cortico–autonomic response patterns, whereas others exhibited divergent or minimal response profiles. Coordinated decreases in frontal β 2 activity together with increases in RMSSD were observed in 4 of the 10 participants. Given the exploratory nature of the study and the limited sample size, these observations should be interpreted as preliminary and hypothesis-generating. Conclusion These findings support the potential utility of multimodal, stimulus-dependent approaches for characterizing dynamic brain–body responses beyond static biomarkers. The observed multimodal response configurations are consistent with coordinated cortico–autonomic response patterns and provide a useful framework for generating hypotheses regarding individual variability in brain–body regulation. As an exploratory pilot study, the present findings require validation in larger and clinically diverse cohorts before conclusions regarding physiological subgroups or clinical applications can be drawn. This perturbation-based multimodal EEG–HRV framework may contribute to future physiology-informed precision psychiatry research by providing a methodological foundation for characterizing individual brain–body response variability.
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Hauber et al. (2026) studied Healthy (n=10). Standardized auditory perturbations (noise and binaural-beat) vs. Silence (baseline) was evaluated on Baseline-corrected frontal asymmetry (ΔAIb2) (p=>0.05). Standardized auditory perturbations elicited substantial inter-individual variability in coordinated frontal beta activity and heart rate variability, with no significant group-level effects detected (p > 0.05).
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