Altered interictal alpha-band organization in childhood absence epilepsy
6 affiliations
- 1Department of Biomedical Engineering, Wroclaw University of Science and Technology, Wrocław, Poland
- 2Department of Pediatric Neurology, T. Marciniak Hospital, Wrocław, Poland
- 3Department of Child Neurology, "Promyk Słońca" Diagnostic and Rehabilitation Center, Wroclaw, Poland
- 4Neonatal and Pediatric Intensive Care Unit, University Hospital in Opole, Opole, Poland
- 5Department of Child Neurology, Jagiellonian University Medical College, Kraków, Poland
- 6Department of Neurology, Upper Silesian Child Health Center, Silesian Medical University, Katowice, Poland
Abstract
ObjectiveInterictal background EEG in childhood absence epilepsy (CAE) may appear normal. We asked whether drug-naive children with CAE differ from controls in alpha frequency and the regional distribution of phase-lagged synchronization, and how these differences depend on participant-specific surrogate baselines and analysis frequency.MethodsWe analyzed eyes-closed resting EEG (19 channels, 26 s) from 49 drug-naive children with CAE and 83 controls. Individual alpha frequency (IAF) was estimated by spectral parameterization of posterior channels. Weighted phase-lag index (wPLI) at 12 Hz was summarized globally and as the frontal–posterior log-ratio λFP = ln(wPLIF/wPLIP), where F and P denote frontal and posterior within-region means. Participant-specific baselines were obtained from 100 circular-shift surrogates, preserving each channel's wavelet-coefficient sequence up to circular translation while altering inter-channel alignment. Group comparisons used studentized permutation tests. The regional contrast was also evaluated at each participant's IAF.ResultsIAF was lower in patients (8.80 versus 9.42 Hz; p = 0.002). At 12 Hz, controls showed posterior predominance of synchronization (λFP = −0.352), which was largely removed by circular shifting (−0.036), whereas patients' mean regional balance was near zero. After baseline subtraction, the patient-minus-control difference in λFP was 0.332 (95 % CI [0.181, 0.483]; p < 0.001; Hedges' g = 0.79). In the 131 participants with identifiable IAF, the contrast was 0.316 at 12 Hz and 0.124 at IAF (p = 0.139). A direct comparison using within-participant changes supported a larger contrast at 12 Hz (difference 0.192, 95 % CI [0.017, 0.367]; exploratory, unadjusted p = 0.032). The global wPLI difference after baseline subtraction remained uncertain (−0.021, 95 % CI [−0.044, 0.001]; p = 0.069).ConclusionsDrug-naive CAE was associated with slower alpha activity and reduced posterior predominance of phase-lagged synchronization at 12 Hz. Circular shifting largely removed the controls' posterior predominance, supporting a difference in regional organization sensitive to inter-channel alignment. The smaller contrast at IAF indicates that analysis frequency materially affects this finding, without establishing that alpha slowing alone explains it.
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BibTeX
@article{latka2026altered,
title = {{Altered interictal alpha-band organization in childhood absence epilepsy}},
author = {Miroslaw Latka and Pawel Glaba and Marta Kuryło and Beata Jędrzejczyk-Góral and Wojciech Walas and Sławomir Kroczka and Justyna Paprocka},
journal = {Frontiers in Neuroinformatics},
year = {2026},
month = oct,
doi = {10.3389/fninf.2026.1875377},
url = {https://doi.org/10.3389/fninf.2026.1875377},
note = {CC BY},
}
RIS
TY - JOUR
TI - Altered interictal alpha-band organization in childhood absence epilepsy
AU - Miroslaw Latka
AU - Pawel Glaba
AU - Marta Kuryło
AU - Beata Jędrzejczyk-Góral
AU - Wojciech Walas
AU - Sławomir Kroczka
AU - Justyna Paprocka
PY - 2026
DA - 2026/10/23
JO - Frontiers in Neuroinformatics
DO - 10.3389/fninf.2026.1875377
UR - https://doi.org/10.3389/fninf.2026.1875377
AB - ObjectiveInterictal background EEG in childhood absence epilepsy (CAE) may appear normal. We asked whether drug-naive children with CAE differ from controls in alpha frequency and the regional distribution of phase-lagged synchronization, and how these differences depend on participant-specific surrogate baselines and analysis frequency.MethodsWe analyzed eyes-closed resting EEG (19 channels, 26 s) from 49 drug-naive children with CAE and 83 controls. Individual alpha frequency (IAF) was estimated by spectral parameterization of posterior channels. Weighted phase-lag index (wPLI) at 12 Hz was summarized globally and as the frontal–posterior log-ratio λFP = ln(wPLIF/wPLIP), where F and P denote frontal and posterior within-region means. Participant-specific baselines were obtained from 100 circular-shift surrogates, preserving each channel's wavelet-coefficient sequence up to circular translation while altering inter-channel alignment. Group comparisons used studentized permutation tests. The regional contrast was also evaluated at each participant's IAF.ResultsIAF was lower in patients (8.80 versus 9.42 Hz; p = 0.002). At 12 Hz, controls showed posterior predominance of synchronization (λFP = −0.352), which was largely removed by circular shifting (−0.036), whereas patients' mean regional balance was near zero. After baseline subtraction, the patient-minus-control difference in λFP was 0.332 (95 % CI [0.181, 0.483]; p < 0.001; Hedges' g = 0.79). In the 131 participants with identifiable IAF, the contrast was 0.316 at 12 Hz and 0.124 at IAF (p = 0.139). A direct comparison using within-participant changes supported a larger contrast at 12 Hz (difference 0.192, 95 % CI [0.017, 0.367]; exploratory, unadjusted p = 0.032). The global wPLI difference after baseline subtraction remained uncertain (−0.021, 95 % CI [−0.044, 0.001]; p = 0.069).ConclusionsDrug-naive CAE was associated with slower alpha activity and reduced posterior predominance of phase-lagged synchronization at 12 Hz. Circular shifting largely removed the controls' posterior predominance, supporting a difference in regional organization sensitive to inter-channel alignment. The smaller contrast at IAF indicates that analysis frequency materially affects this finding, without establishing that alpha slowing alone explains it.
SN - 1662-5196
ER -