PhD ThesisBackground: Epilepsy is a neurological disorder of abnormal brain network in which
seizures originate and spread via patient-specific spatial and temporal pathways. Disrupting
these epileptic networks can enable seizure control; therefore, it is crucial to map, quantify,
and understand these networks. This thesis aims to quantify the whole-brain structural
network abnormalities of patients with focal and generalised epilepsy along with patientspecific
network disruptions caused by epilepsy surgery.
Method: We developed a novel patient-specific metric to quantify structural network abnormality
at every brain region by standardising whole-brain structural networks of patients
with healthy structural networks. To quantify local changes in the white-matter structure, we
applied quantitative neuroimaging techniques and a computational model for making predictions
on mechanisms of epilepsy development. We combined the network-based measures
in robust cross-validated machine learning models to predict neurosurgical outcomes and
seizure spread.
Results: In drug-resistant focal epilepsy patients, structural network abnormality associated
with post-surgical seizure recurrence and patient history of focal to bilateral tonic-clonic
seizures. Combined with routinely acquired clinical variables, we predicted the patientspecific
probability of seizure recurrence after surgery. In patients with idiopathic generalised
epilepsy, we found localised abnormalities in major white-matter fascicles. The thalamocortical
computer model of spike-wave seizures implicated the role of cortico-reticular
connections in mechanism of epileptogenesis.
Significance: This thesis highlighted the heterogeneity between patients that may be making
them susceptible to a varied response for the same treatment. We offer practical tools to
quantify these heterogeneities to complement clinical decision-making for effective patient
stratification and tailored treatments
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