Brandon J. Thio

Epilepsy surgery can eliminate seizures in patients with drug-resistant focal epilepsy. Surgical intervention requires proper identification of the epileptic network and often involves implanting stereo-EEG electrodes in patients where non-invasive methods are insufficient. However, only ∼60% of patients achieve seizure-freedom following surgery. Quantitative methods have been developed to help improve surgical outcomes. However, previous quantitative methods that localized interictal spike and seizure activity using stereo-EEG recordings did not account for the propagation path encoded by the temporal dynamics of stereo-EEG recordings. Reconstructing the seizure propagation path can aid in determining whether a signal originated from the seizure onset or propagation zone, which directly informs treatment decisions. We developed a novel source reconstruction algorithm, Temporally Dependent Iterative Expansion (TEDIE), that accurately reconstructs propagating and expanding neural sources over time. TEDIE iteratively optimizes the number, location and size of neural sources to minimize the differences between the reconstructed and recorded stereo-EEG signals using temporal information to refine the reconstructions. The TEDIE output comprises a movie of seizure activity projected onto patient-specific brain anatomy. We analysed data from 46 epilepsy patients implanted with stereo-EEG electrodes at Duke Hospital (12 patients) and the Hospital of the University of Pennsylvania (34 patients). We reconstructed seizure recordings and found that TEDIE’s seizure onset zone reconstructions were closer to the resected brain region for Engel 1 compared to Engel 2–4 patients, retrospectively validating the clinical utility of TEDIE. We also demonstrated that TEDIE has prospective clinical value, whereby metrics that can be determined presurgically accurately predict whether a patient would achieve seizure-freedom following surgery. Furthermore, we used TEDIE to delineate new potential surgical targets in 12/23 patients who are currently Engel 2–4. We validated TEDIE by accurately reconstructing various dynamic synthetic neural sources with known locations and sizes. TEDIE generated more accurate, focal and interpretable dynamic reconstructions of seizures compared to other algorithms (sLORETA and IRES). Our findings demonstrate that TEDIE is a promising clinical tool that can greatly improve epileptogenic zone localization and epilepsy surgery outcomes.

Unmyelinated C-fibers constitute the vast majority of axons in peripheral nerves and play key roles in homeostasis and signaling pain. However, little is known about their ion channel expression, which controls their firing properties. Also, because of their small diameters (~ 1 μm), it has not been possible to characterize their membrane properties using voltage clamp. We developed a novel library of isoform-specific ion channel models to serve as the basis functions of our C-fiber models. We then developed a particle swarm optimization (PSO) framework that used the isoform-specific ion channel models to reverse engineer C-fiber membrane properties from measured autonomic and cutaneous C-fiber conduction responses. Our C-fiber models reproduced experimental conduction velocity, chronaxie, action potential duration, intracellular threshold, and paired pulse recovery cycle. The models also matched experimental activity-dependent slowing, a property not included in model optimization. We found that simple conduction responses, characterizing the action potential, were controlled by similar membrane properties in both the autonomic and cutaneous C-fiber models, but complicated conduction response, characterizing the afterpotenials, were controlled by differential membrane properties. The unmyelinated C-fiber models constitute important tools to study autonomic signaling, assess the mechanisms of pain, and design bioelectronic devices. Additionally, the novel reverse engineering approach can be applied to generate models of other neurons where voltage clamp data are not available.

Peripheral nerves are primarily composed of unmyelinated axons, and there is growing interest in electrical stimulation of the autonomic nervous system to treat various diseases. We present the first cable model of an unmyelinated vagal nerve fiber and compare its ion channel isoforms and conduction responses with other published models of unmyelinated axons, establishing important tools for advancing modeling of autonomic nerves.