Post-Ictal Sleep Changes in Human Focal Epilepsy.

Kremen V
Sladky V
Gerla V
Cao Y
Mivalt F
St Louis EK
Bower MR
Brinkmann B
Miller KD
Van Gompel J
Cook M
Leyde K
Worrell G

Scientific Abstract

Bidirectional interactions between sleep, seizures, and epilepsy remain incompletely understood. Evidence from animal models and people with focal epilepsy suggest that seizures may engage mechanisms of memory consolidation during post-ictal sleep to reinforce and strengthen synaptic connections within the pathological networks that generates seizures, termed seizure-related consolidation (SRC). Human studies of post-ictal sleep changes supportive of SRC, however, are limited by small sample size and restricted observations of post-ictal sleep. We investigated the interplay between seizures and sleep by analyzing sleep-wake and seizure catalogs derived from continuous local field potential (LFP) recordings in 11 people (6 males and 5 females) with drug-resistant focal epilepsy implanted with novel investigational devices and living in their natural environments. Our findings demonstrate that post-ictal rapid-eye-movement sleep duration is reduced, whereas slow-wave sleep duration, slow-wave LFP spectral power, and waveform slope are increased compared with inter-ictal nights without preceding seizures. The most significant changes localize to the epileptogenic networks generating the participants' habitual seizures. These results reveal parallels between SRC and physiological memory consolidation, providing novel insights into the potential role of post-ictal sleep in strengthening epileptic neural engrams and may have implications for targeted disruption of post-ictal sleep and SRC in focal epilepsy.

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Post-Ictal Sleep Changes in Human Focal Epilepsy.

Kremen V
Sladky V
Gerla V
Cao Y
Mivalt F
St Louis EK
Bower MR
Brinkmann B
Miller KD
Van Gompel J
Cook M
Leyde K
Worrell G

Scientific Abstract

Bidirectional interactions between sleep, seizures, and epilepsy remain incompletely understood. Evidence from animal models and people with focal epilepsy suggest that seizures may engage mechanisms of memory consolidation during post-ictal sleep to reinforce and strengthen synaptic connections within the pathological networks that generates seizures, termed seizure-related consolidation (SRC). Human studies of post-ictal sleep changes supportive of SRC, however, are limited by small sample size and restricted observations of post-ictal sleep. We investigated the interplay between seizures and sleep by analyzing sleep-wake and seizure catalogs derived from continuous local field potential (LFP) recordings in 11 people (6 males and 5 females) with drug-resistant focal epilepsy implanted with novel investigational devices and living in their natural environments. Our findings demonstrate that post-ictal rapid-eye-movement sleep duration is reduced, whereas slow-wave sleep duration, slow-wave LFP spectral power, and waveform slope are increased compared with inter-ictal nights without preceding seizures. The most significant changes localize to the epileptogenic networks generating the participants' habitual seizures. These results reveal parallels between SRC and physiological memory consolidation, providing novel insights into the potential role of post-ictal sleep in strengthening epileptic neural engrams and may have implications for targeted disruption of post-ictal sleep and SRC in focal epilepsy.

Citation

2026. J Neurosci, 46(9).

DOI

10.1523/JNEUROSCI.0303-25.2026

Free Full Text at Europe PMC

PMC12962774

Similar content

Preprint
Piper RJ, Fleming JE, van Rheede JJ, Marks VS, Landin K, Costache D, Hasegawa H, Selway R, Richardson H, Seunarine K, D'Arco F, Carter S, Arcaro C, Moeller F, Moulay-Dehbi H, Valentin A, Kaliakatsos M, Denison T, Tisdall MM

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