Poster No:
1333
Submission Type:
Abstract Submission
Authors:
Miao Cao1, Jiayi Liu2, Wei Cui2, Xiongfei Wang3, Simon Vogrin1, Jia-hong Gao2, David White4, Chris Plummer5, Will Woods1
Institutions:
1Swinburne University of Technology, Melbourne, Victoria, 2Peking University, Beijing, Beijing, 3Capital Medical University, Beijing, Beijing, 4Centre for Mental Health and Brain Sciences, School of Health Sciences, Swinburne University of T, Melbourne, Victoria, 5Swinburne University of Technology, Melbourne, Vicrtoria
First Author:
Miao Cao
Swinburne University of Technology
Melbourne, Victoria
Co-Author(s):
Wei Cui
Peking University
Beijing, Beijing
Simon Vogrin
Swinburne University of Technology
Melbourne, Victoria
David White, A/Prof
Centre for Mental Health and Brain Sciences, School of Health Sciences, Swinburne University of T
Melbourne, Victoria
Chris Plummer
Swinburne University of Technology
Melbourne, Vicrtoria
Will Woods
Swinburne University of Technology
Melbourne, Victoria
Introduction:
Modelling neural dynamics, characterized by fast-evolving physiological and pathological activity, across multiple spatial-temporal scales is crucial to understand the underlying mechanisms that give rise to such phenomena. High dimensionality of neural recordings and complexity of fast-evolving spatio-temporal patterns remain as major challenges for computational models. Our previous attempts have enabled a unique combination of neuroimaging and neural mass models to temporospatially delineate the ictogenic brain regions that are responsible for seizure generation.
Methods:
Here, we extended the previously proposed framework (Cao et al., 2022) to three-dimensional velocity fields of the whole-brain MEG/EEG source space including cortical and subcortical structures.
Results:
We revealed the field singularities and dynamical patterns that pinpoint and track the underlying functional pathways of pathological and physiological dynamics (including visual and auditory activity).
Conclusions:
Such findings may lead to better understanding of brain's function-structure coupling as well as clinical applications, including identifying epileptogenic brain regions and preserving eloquent cortex for brain tumour and epilepsy surgery.
Modeling and Analysis Methods:
EEG/MEG Modeling and Analysis 1
Methods Development 2
Keywords:
Computational Neuroscience
Data analysis
Electroencephaolography (EEG)
Epilepsy
MEG
Modeling
Neurological
1|2Indicates the priority used for review
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Please indicate below if your study was a "resting state" or "task-activation” study.
Resting state
Task-activation
Healthy subjects only or patients (note that patient studies may also involve healthy subjects):
Patients
Was this research conducted in the United States?
No
Were any human subjects research approved by the relevant Institutional Review Board or ethics panel?
NOTE: Any human subjects studies without IRB approval will be automatically rejected.
Yes
Were any animal research approved by the relevant IACUC or other animal research panel?
NOTE: Any animal studies without IACUC approval will be automatically rejected.
Not applicable
Please indicate which methods were used in your research:
EEG/ERP
MEG
Structural MRI
For human MRI, what field strength scanner do you use?
3.0T
Which processing packages did you use for your study?
Free Surfer
Provide references using APA citation style.
Cao, M., Galvis, D., Vogrin, S. J., Woods, W. P., Vogrin, S., Wang, F., … Cook, M. J. (2022). Virtual intracranial EEG signals reconstructed from MEG with potential for epilepsy surgery. Nature Communications, 13(1), 994. doi: 10.1038/s41467-022-28640-x
No