Spatiotemporal EEG Dynamics Across Early and Late Preictal Periods in Pediatric Focal Epilepsy
Abstract
Objective: This study aimed to quantify the temporal and spatial dynamics of preictal cortical networks in pediatric refractory focal epilepsy using scale-independent EEG measurements. Method: For this purpose, the preictal (−35 to −5 min), interictal, early preictal (−35 to −20 min), and late preictal (−20 to −5 min) periods were examined in long-term scalp EEG recordings from pediatric patients in the CHB–MIT database. For the selected segments, the detrended fluctuation analysis (DFA) scale exponent, median power frequency (MPF), and aperiodic 1/f exponent (β) were calculated using SpecParam/FOOOF and IRASA. The metrics were summarized on an individual basis and analyzed using two-way repeated measures ANOVA with Šídák-corrected post-hoc tests and topographic mapping. Findings: The preictal period was characterized by increased DFA-α and MPF in fronto-temporal regions compared to the interictal period; during the interictal period, MPF foci shifted to posterior areas. Aperiodic β values showed steepening in frontal regions during the preictal period and exhibited a posterior-temporal gradient during the interictal period. Critically, during the transition from the early to late preictal period, fronto-temporal DFA-α and MPF values decreased, accompanied by a posterior-to-anterior spread of aperiodic β steepening. Conclusion: These findings indicate that cortical networks experience a collapse in long-range temporal correlations and a reorganization of the aperiodic spectral structure as seizure onset approaches. The observed loss of complexity, spectral slowing, and frontal aperiodic steepening, occurring simultaneously, suggest a heterogeneous nature of the preictal process and highlight the potential of scale-independent metrics in monitoring seizure risk.
Keywords
- Aperiodic 1/f activity
- EEG dynamics
- epilepsy
- Long-range temporal correlations
- Median power frequency
- Preictal brain states
- Seizure prediction
Supporting Institution
Ethical Statement
Thanks
References
- Mormann F, Andrzejak RG, Elger CE, Lehnertz K. Seizure prediction: the long and winding road. Brain 2007;130:314–33. https://doi.org/10.1093/BRAIN/AWL241.
- [2]. Donoghue T, Haller M, Peterson EJ, Varma P, Sebastian P, Gao R, et al. Parameterizing neural power spectra into periodic and aperiodic components. Nat Neurosci 2020;23:1655–65. https://doi.org/10.1038/S41593-020-00744-X.
- [3]. Wen H, Liu Z. Separating Fractal and Oscillatory Components in the Power Spectrum of Neurophysiological Signal. Brain Topogr 2016;29:13–26. https://doi.org/10.1007/S10548-015-0448-0.
- [4]. He BJ, Zempel JM, Snyder AZ, Raichle ME. The temporal structures and functional significance of scale-free brain activity. Neuron 2010;66:353. https://doi.org/10.1016/J.NEURON.2010.04.020.
- [5]. Gadhoumi K, Gotman J, Lina JM. Scale Invariance Properties of Intracerebral EEG Improve Seizure Prediction in Mesial Temporal Lobe Epilepsy 2015. https://doi.org/10.1371/journal.pone.0121182.
- [6]. Maturana MI, Meisel C, Dell K, Karoly PJ, D’Souza W, Grayden DB, et al. Critical slowing down as a biomarker for seizure susceptibility. Nature Communications 2020 11:1 2020;11:2172-. https://doi.org/10.1038/s41467-020-15908-3.
- [7]. Linkenkaer-Hansen K, Nikouline V V., Palva JM, Ilmoniemi RJ. Long-range temporal correlations and scaling behavior in human brain oscillations. J Neurosci 2001;21:1370–7. https://doi.org/10.1523/JNEUROSCI.21-04-01370.2001.
- [8]. Castiglioni P, Faini A. A Fast DFA Algorithm for Multifractal Multiscale Analysis of Physiological Time Series. Front Physiol 2019;10. https://doi.org/10.3389/fphys.2019.00115.
Details
Primary Language
English
Subjects
Biomedical Diagnosis, Computational Physiology
Journal Section
Research Article
Authors
Publication Date
June 30, 2026
Submission Date
November 25, 2025
Acceptance Date
March 5, 2026
Published in Issue
Year 2026 Volume: 22 Number: 2