Seizure recruitment properties are dependent upon dynamotype: A modeling study
- 1Department of Biomedical Engineering, BioInterfaces Institute, University of Michigan, Ann Arbor, Michigan, United States of America
- 2Aix Marseille Univ, INSERM, INS, Inst Neurosci Syst, Marseille, France
- 3Department of Neurology, University of Michigan, Ann Arbor, Michigan, United States of America
Abstract
Seizure propagation – how epileptogenic brain tissue recruits less excitable tissue – is poorly understood. Previous studies have used dynamical modeling to study seizure propagation and to create patient-specific whole-brain models of seizure spread. However, these studies focused on seizures of a single dynamotype (onset and offset bifurcation pair). Here, we implement a novel coupling method to investigate seizure propagation in a diverse array of dynamotypes. We utilize the Multiclass Epileptor, a recently proposed model that captures a wide range of seizure dynamotypes in a cortical mass (“node”). We consider two nodes: the seizure onset zone (node 1), which bursts autonomously, and the potential propagation zone (node 2), which is not independently epileptogenic but can be recruited by node 1. We examine the impact of intrinsic and coupling factors on the likelihood and speed of recruitment, with particular attention to the onset bifurcation of node 1. We also measure the range of onset behaviors observed in node 2 with respect to the onset behavior of node 1. The model predicted that seizures that display baseline shifts at onset are less likely to spread, and spread more slowly, compared to seizures that do not exhibit baseline shifts at onset. Seizures that present with amplitude scaling at onset were unlikely to propagate. Further, the model predicted the potential for unusual combinations of onset dynamics, such as a baseline shift in node 2 but not node 1. We confirmed the possibility for several of these unusual recruitment behaviors in humans using intracranial electroencephalography data. The results of the study provide a theoretical framework for seizure propagation, establishing a basis for innovations in characterization of patients’ seizure networks and identification of the seizure onset zone. Author summary: In this work, we examined how a seizure spreads from one part of the brain to another using a computational model. We modeled two brain regions using the Multiclass Epileptor, which reproduces a range of brain activity patterns associated with seizures. In the model, the first brain node was able to recruit the second brain node into a seizure. The model predicted that the likelihood and speed of seizure spread differ depending on the pattern of brain activity observed at the start of the seizure. We also found that the pattern of brain activity at seizure onset is not necessarily the same pattern seen when the seizure spreads. We confirmed this possibility for mismatched patterns in recordings from human brain. The findings of the study improve our understanding of seizure spread, which lays the groundwork for development of tools to quantify seizure spread and may inform future work in patient-specific brain modeling.
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BibTeX
@article{karosas2026seizure,
title = {{Seizure recruitment properties are dependent upon dynamotype: A modeling study}},
author = {Diana M. Karosas and Marisa Saggio and William C. Stacey},
journal = {PLOS Computational Biology},
year = {2026},
month = sep,
doi = {10.1371/journal.pcbi.1013975},
url = {https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1013975},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Seizure recruitment properties are dependent upon dynamotype: A modeling study
AU - Diana M. Karosas
AU - Marisa Saggio
AU - William C. Stacey
PY - 2026
DA - 2026/09/21
JO - PLOS Computational Biology
DO - 10.1371/journal.pcbi.1013975
UR - https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1013975
AB - Seizure propagation – how epileptogenic brain tissue recruits less excitable tissue – is poorly understood. Previous studies have used dynamical modeling to study seizure propagation and to create patient-specific whole-brain models of seizure spread. However, these studies focused on seizures of a single dynamotype (onset and offset bifurcation pair). Here, we implement a novel coupling method to investigate seizure propagation in a diverse array of dynamotypes. We utilize the Multiclass Epileptor, a recently proposed model that captures a wide range of seizure dynamotypes in a cortical mass (“node”). We consider two nodes: the seizure onset zone (node 1), which bursts autonomously, and the potential propagation zone (node 2), which is not independently epileptogenic but can be recruited by node 1. We examine the impact of intrinsic and coupling factors on the likelihood and speed of recruitment, with particular attention to the onset bifurcation of node 1. We also measure the range of onset behaviors observed in node 2 with respect to the onset behavior of node 1. The model predicted that seizures that display baseline shifts at onset are less likely to spread, and spread more slowly, compared to seizures that do not exhibit baseline shifts at onset. Seizures that present with amplitude scaling at onset were unlikely to propagate. Further, the model predicted the potential for unusual combinations of onset dynamics, such as a baseline shift in node 2 but not node 1. We confirmed the possibility for several of these unusual recruitment behaviors in humans using intracranial electroencephalography data. The results of the study provide a theoretical framework for seizure propagation, establishing a basis for innovations in characterization of patients’ seizure networks and identification of the seizure onset zone. Author summary: In this work, we examined how a seizure spreads from one part of the brain to another using a computational model. We modeled two brain regions using the Multiclass Epileptor, which reproduces a range of brain activity patterns associated with seizures. In the model, the first brain node was able to recruit the second brain node into a seizure. The model predicted that the likelihood and speed of seizure spread differ depending on the pattern of brain activity observed at the start of the seizure. We also found that the pattern of brain activity at seizure onset is not necessarily the same pattern seen when the seizure spreads. We confirmed this possibility for mismatched patterns in recordings from human brain. The findings of the study improve our understanding of seizure spread, which lays the groundwork for development of tools to quantify seizure spread and may inform future work in patient-specific brain modeling.
SN - 1553-7358
ER -