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Inferring neural dynamics during burst suppression using a neurophysiology-inspired switching state-space model
Name
2012.02246.pdf
Description
Accepted version
Size
2.11 MB
Format
Adobe PDF
Checksum (MD5)
e26e2801412a05a1e20478970c92b95e
Author(s)
Schamberg, Gabriel
Chakravarty, Sourish
Baum, Taylor E
Brown, Emery N
Date Issued
2020
Journal
2020 54th Asilomar Conference on Signals, Systems, and Computers
Publisher
Institute of Electrical and Electronics Engineers (IEEE)
Citation
Schamberg, Gabriel, Chakravarty, Sourish, Baum, Taylor E and Brown, Emery N. 2020. "Inferring neural dynamics during burst suppression using a neurophysiology-inspired switching state-space model." 2020 54th Asilomar Conference on Signals, Systems, and Computers.
Version
Author's final manuscript
Abstract
Burst suppression is an electroencephalography (EEG) pattern associated with profoundly inactivated brain states characterized by cerebral metabolic depression. Its distinctive feature is alternation between short temporal segments of near-isoelectric inactivity (suppressions) and relatively high-voltage activity (bursts). Prior modeling studies suggest that burst-suppression EEG is a manifestation of two alternating brain states associated with consumption (during a burst) and production (during a suppression) of adenosine triphosphate (ATP). This finding motivates us to infer latent states characterizing alternating brain states and underlying ATP kinetics from instantaneous power of multichannel EEG using a switching state-space model. Our model assumes Gaussian distributed data as a broadcast network manifestation of one of two global brain states. The two brain states are allowed to stochastically alternate with transition probabilities that depend on the instantaneous ATP level, which evolves according to first-order kinetics. The rate constants governing the ATP kinetics are allowed to vary as first- order autoregressive processes. Our latent state estimates are determined from data using a sequential Monte Carlo algorithm. Our neurophysiology-informed model not only provides unsupervised segmentation of multi-channel burst-suppression EEG but can also generate additional insights on the level of brain inactivation during anesthesia.
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Creative Commons Attribution-Noncommercial-Share Alike
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DOI of Published Version
10.1109/IEEECONF51394.2020.9443373
