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Synaptic inhibitory dynamics drive benzodiazepine response in pediatric status epilepticus

Abstract:
Objective: Pediatric status epilepticus (SE) is a medical emergency associated with significant morbidity. Benzodiazepines (BZPs) are the current first‐line treatment, but do not work in more than one third of children presenting with SE. Animal studies have shown that SE can cause changes in synaptic inhibition signaling that can ultimately lead to BZPs becoming ineffective. However, the relevance of these mechanisms in pediatric patients with SE remains unknown. Methods: To test this hypothesis, we combine clinical electroencephalographic (EEG) recordings with dynamic causal modeling (DCM). This approach allows model‐based inference of cortical synaptic coupling parameters based on EEG recorded across distinct oscillatory states. Results: Our DCM revealed that dynamic changes in inhibitory synaptic coupling explain differences in EEG power spectra associated with BZP treatment responsiveness and guide the transition from ictal to interictal state. Furthermore, in silico simulations demonstrate that there are alternative routes to seizure termination even in cortical circuit models unresponsive to BZPs. Significance: Together, our findings confirm that alterations in synaptic inhibition underlie BZP response during pediatric SE. More broadly, this work further demonstrates the utility of computational modeling to validate insights from basic science in clinically accessible recordings in neurological disorders characterized by abnormal brain states.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1111/epi.18398

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Role:
Author
ORCID:
0000-0002-9019-3760
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Institution:
University of Oxford
Role:
Author
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Role:
Author
ORCID:
0000-0002-7931-2327


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Funder identifier:
https://ror.org/029chgv08


Publisher:
Wiley
Journal:
Epilepsia: Official journal of the International League Against Epilepsy More from this journal
Publication date:
2025-04-15
Acceptance date:
2025-03-21
DOI:
EISSN:
1528-1167
ISSN:
0013-9580


Language:
English
Keywords:
Source identifiers:
2860353
Deposit date:
2025-04-15
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