Controllability of nonlinear epileptic-seizure spreading dynamics in large-scale subject-specific brain networks
Closed-loop electrical stimulation has become an important alternative to resective surgery for control of pharmacologically-resistant focal epileptic seizures. Seizure spread across large-scale brain networks, rather than its focal onset, is what commonly leads to major disruptions in sensorimotor...
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Published in | Scientific reports Vol. 15; no. 1; pp. 6467 - 37 |
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Format | Journal Article |
Language | English |
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22.02.2025
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Abstract | Closed-loop electrical stimulation has become an important alternative to resective surgery for control of pharmacologically-resistant focal epileptic seizures. Seizure spread across large-scale brain networks, rather than its focal onset, is what commonly leads to major disruptions in sensorimotor and cognitive processing, as well as loss-of-consciousness, one of the main impairing aspects of the disorder. Electrical stimulation, triggered by early detection of seizure onset in epileptogenic zones (EZs), has been applied to prevent spread and its subsequent effects. Here, we show how linear feedback seizure-spread controllability in subject-specific (white-matter tractography) Epileptor network models is affected by variations in brain excitability, network coupling strength, control latency and gain, and actuation targets. Feedback control can qualitatively change the nonlinear seizure dynamics, and the paths to seizure termination and spread prevention. Notably, control onset latency is a critical parameter leading to a phase transition in spread controllability. Consequently, the efficacy of EZ-only actuation is limited depending on network excitability, coupling strength, and practical latencies for detection and actuation. Additional feedback-stabilization control of theoretically-derived optimal node subsets in the network are necessary for spread prevention. Finally, we contrast our linear-feedback controllability assessment with other measures based on minimum-energy (Gramian) controllability and nonlinear pulse-perturbation approaches. |
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AbstractList | Abstract Closed-loop electrical stimulation has become an important alternative to resective surgery for control of pharmacologically-resistant focal epileptic seizures. Seizure spread across large-scale brain networks, rather than its focal onset, is what commonly leads to major disruptions in sensorimotor and cognitive processing, as well as loss-of-consciousness, one of the main impairing aspects of the disorder. Electrical stimulation, triggered by early detection of seizure onset in epileptogenic zones (EZs), has been applied to prevent spread and its subsequent effects. Here, we show how linear feedback seizure-spread controllability in subject-specific (white-matter tractography) Epileptor network models is affected by variations in brain excitability, network coupling strength, control latency and gain, and actuation targets. Feedback control can qualitatively change the nonlinear seizure dynamics, and the paths to seizure termination and spread prevention. Notably, control onset latency is a critical parameter leading to a phase transition in spread controllability. Consequently, the efficacy of EZ-only actuation is limited depending on network excitability, coupling strength, and practical latencies for detection and actuation. Additional feedback-stabilization control of theoretically-derived optimal node subsets in the network are necessary for spread prevention. Finally, we contrast our linear-feedback controllability assessment with other measures based on minimum-energy (Gramian) controllability and nonlinear pulse-perturbation approaches. Closed-loop electrical stimulation has become an important alternative to resective surgery for control of pharmacologically-resistant focal epileptic seizures. Seizure spread across large-scale brain networks, rather than its focal onset, is what commonly leads to major disruptions in sensorimotor and cognitive processing, as well as loss-of-consciousness, one of the main impairing aspects of the disorder. Electrical stimulation, triggered by early detection of seizure onset in epileptogenic zones (EZs), has been applied to prevent spread and its subsequent effects. Here, we show how linear feedback seizure-spread controllability in subject-specific (white-matter tractography) Epileptor network models is affected by variations in brain excitability, network coupling strength, control latency and gain, and actuation targets. Feedback control can qualitatively change the nonlinear seizure dynamics, and the paths to seizure termination and spread prevention. Notably, control onset latency is a critical parameter leading to a phase transition in spread controllability. Consequently, the efficacy of EZ-only actuation is limited depending on network excitability, coupling strength, and practical latencies for detection and actuation. Additional feedback-stabilization control of theoretically-derived optimal node subsets in the network are necessary for spread prevention. Finally, we contrast our linear-feedback controllability assessment with other measures based on minimum-energy (Gramian) controllability and nonlinear pulse-perturbation approaches. Closed-loop electrical stimulation has become an important alternative to resective surgery for control of pharmacologically-resistant focal epileptic seizures. Seizure spread across large-scale brain networks, rather than its focal onset, is what commonly leads to major disruptions in sensorimotor and cognitive processing, as well as loss-of-consciousness, one of the main impairing aspects of the disorder. Electrical stimulation, triggered by early detection of seizure onset in epileptogenic zones (EZs), has been applied to prevent spread and its subsequent effects. Here, we show how linear feedback seizure-spread controllability in subject-specific (white-matter tractography) Epileptor network models is affected by variations in brain excitability, network coupling strength, control latency and gain, and actuation targets. Feedback control can qualitatively change the nonlinear seizure dynamics, and the paths to seizure termination and spread prevention. Notably, control onset latency is a critical parameter leading to a phase transition in spread controllability. Consequently, the efficacy of EZ-only actuation is limited depending on network excitability, coupling strength, and practical latencies for detection and actuation. Additional feedback-stabilization control of theoretically-derived optimal node subsets in the network are necessary for spread prevention. Finally, we contrast our linear-feedback controllability assessment with other measures based on minimum-energy (Gramian) controllability and nonlinear pulse-perturbation approaches.Closed-loop electrical stimulation has become an important alternative to resective surgery for control of pharmacologically-resistant focal epileptic seizures. Seizure spread across large-scale brain networks, rather than its focal onset, is what commonly leads to major disruptions in sensorimotor and cognitive processing, as well as loss-of-consciousness, one of the main impairing aspects of the disorder. Electrical stimulation, triggered by early detection of seizure onset in epileptogenic zones (EZs), has been applied to prevent spread and its subsequent effects. Here, we show how linear feedback seizure-spread controllability in subject-specific (white-matter tractography) Epileptor network models is affected by variations in brain excitability, network coupling strength, control latency and gain, and actuation targets. Feedback control can qualitatively change the nonlinear seizure dynamics, and the paths to seizure termination and spread prevention. Notably, control onset latency is a critical parameter leading to a phase transition in spread controllability. Consequently, the efficacy of EZ-only actuation is limited depending on network excitability, coupling strength, and practical latencies for detection and actuation. Additional feedback-stabilization control of theoretically-derived optimal node subsets in the network are necessary for spread prevention. Finally, we contrast our linear-feedback controllability assessment with other measures based on minimum-energy (Gramian) controllability and nonlinear pulse-perturbation approaches. |
ArticleNumber | 6467 |
Author | Feldman, Jordan S. Moosavi, S. Amin Truccolo, Wilson |
Author_xml | – sequence: 1 givenname: S. Amin surname: Moosavi fullname: Moosavi, S. Amin organization: Department of Neuroscience, Brown University – sequence: 2 givenname: Jordan S. surname: Feldman fullname: Feldman, Jordan S. organization: Undergraduate Program in Applied Mathematics, Brown University – sequence: 3 givenname: Wilson surname: Truccolo fullname: Truccolo, Wilson email: wilson_truccolo@brown.edu organization: Department of Neuroscience, Brown University, Carney Institute for Brain Science, Brown University |
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SubjectTerms | 639/766/530/2801 639/766/530/2803 Brain - diagnostic imaging Brain - physiopathology Convulsions & seizures Electric Stimulation Electrical stimuli Electroencephalography Epilepsy Epilepsy - physiopathology Excitability Feedback Humanities and Social Sciences Humans Information processing Latency Models, Neurological multidisciplinary Nerve Net - physiopathology Nonlinear Dynamics Phase transitions Prevention Science Science (multidisciplinary) Seizures Seizures - physiopathology Sensorimotor system |
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Title | Controllability of nonlinear epileptic-seizure spreading dynamics in large-scale subject-specific brain networks |
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