Post-Ictal Sleep Changes in Human Focal Epilepsy.
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.
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
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PMC12962774Similar content
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Pilot Trial of the Picostim® Deep Brain Stimulation System for Children With Epilepsy: A Prospective, Open-Label Medical Device Study of a System Optimised for Paediatric Neuromodulation
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Towards network-guided neuromodulation for epilepsy.
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Free Full Text at Europe PMC
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A cardiac pulse signal affects local field potentials recorded from deep brain stimulation electrodes across clinical targets
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