TY - JOUR
T1 - Early Ictal Dynamics in Childhood Absence Epilepsy
T2 - Scalp EEG Detection of Direct Current Shifts and High-Frequency Oscillations
AU - Maeda, Keisuke
AU - Yamaguchi, Shunta
AU - Tsuboi, Himari
AU - Ichino, Naohiro
AU - Osakabe, Keisuke
AU - Sugimoto, Keiko
AU - Furukawa, Gen
AU - Ishihara, Naoko
N1 - Publisher Copyright:
© EEG and Clinical Neuroscience Society (ECNS) 2026
PY - 2026
Y1 - 2026
N2 - Introduction: Absence seizures are characterized by the appearance of generalized spike-and-wave complexes (SWCs) on scalp electroencephalography (EEG), but the EEG-level physiological changes that precede the onset of SWCs remain poorly understood. Advances in scalp wide-band EEG have enabled the simultaneous visualization of ultraslow and high-frequency activity, providing an opportunity to examine early ictal dynamics in childhood absence epilepsy (CAE). Here, we report two cases of pediatric CAE in which scalp EEG captured ictal direct current (DC) shifts and ictal high-frequency oscillations (HFOs) within the same seizure epoch. Patients and Methods: We report two pediatric patients with CAE who exhibited typical absence seizures during hyperventilation-provoked scalp EEG recordings. Across three seizures, the same wide-band EEG methodology enabled the evaluation of ictal DC shifts and HFOs. Results: Across three seizures, a reproducible temporal sequence was observed: a negative DC shift emerged several hundred milliseconds before the first SWC, followed by spike-locked HFOs shortly after ictal onset. The DC shift progressively deepened during this interval, whereas HFOs appeared as discrete, band-limited events with modest frequency evolution. Despite differences in seizure duration and clinical background, this pattern was consistent across seizures and between patients. Discussion: These findings suggest that ictal DC shifts reflect slow network changes preceding thalamocortical hypersynchrony, whereas ictal HFOs index the fast dynamics involved in SWC generation. As both components can be detected noninvasively, scalp wide-band EEG may offer a foundation for developing early ictal biomarkers in CAE.
AB - Introduction: Absence seizures are characterized by the appearance of generalized spike-and-wave complexes (SWCs) on scalp electroencephalography (EEG), but the EEG-level physiological changes that precede the onset of SWCs remain poorly understood. Advances in scalp wide-band EEG have enabled the simultaneous visualization of ultraslow and high-frequency activity, providing an opportunity to examine early ictal dynamics in childhood absence epilepsy (CAE). Here, we report two cases of pediatric CAE in which scalp EEG captured ictal direct current (DC) shifts and ictal high-frequency oscillations (HFOs) within the same seizure epoch. Patients and Methods: We report two pediatric patients with CAE who exhibited typical absence seizures during hyperventilation-provoked scalp EEG recordings. Across three seizures, the same wide-band EEG methodology enabled the evaluation of ictal DC shifts and HFOs. Results: Across three seizures, a reproducible temporal sequence was observed: a negative DC shift emerged several hundred milliseconds before the first SWC, followed by spike-locked HFOs shortly after ictal onset. The DC shift progressively deepened during this interval, whereas HFOs appeared as discrete, band-limited events with modest frequency evolution. Despite differences in seizure duration and clinical background, this pattern was consistent across seizures and between patients. Discussion: These findings suggest that ictal DC shifts reflect slow network changes preceding thalamocortical hypersynchrony, whereas ictal HFOs index the fast dynamics involved in SWC generation. As both components can be detected noninvasively, scalp wide-band EEG may offer a foundation for developing early ictal biomarkers in CAE.
KW - absence epilepsy
KW - absence seizure
KW - biomarker
KW - DC shifts
KW - electroencephalography (EEG)
KW - epilepsy
KW - high-frequency oscillations
KW - wide-band EEG
UR - https://www.scopus.com/pages/publications/105047746686
UR - https://www.scopus.com/pages/publications/105047746686#tab=citedBy
U2 - 10.1177/15500594261475856
DO - 10.1177/15500594261475856
M3 - Article
C2 - 42606319
AN - SCOPUS:105047746686
SN - 1550-0594
JO - Clinical EEG and Neuroscience
JF - Clinical EEG and Neuroscience
M1 - 15500594261475856
ER -