Epilepsy is the world?s most prominent serious brain disorder, affecting nearly 50 million people worldwide. For about 30% of these patients, seizures remain poorly controlled despite optimal medical management, with attendant effects on health and quality of life. In order to enable advances in the therapeutic management of epilepsy, a thorough understanding of how cellular processes that drive seizures are linked to large-scale network effects is needed. While seizures impact large brain areas and often multiple lobes, the driving processes span regions on the scale of millimeters. These have been well characterized in animal models, but the relevance to human seizures, i.e. how seizures are driven by brain signals from small-scale processes remains unclear. Instead, the view that naturally-occurring seizures may be attributable instead to large-scale neural mass effects (i.e., the epileptic network) is a subject of ongoing debate. Previously, we defined a key role for surround inhibition in shaping EEG recordings of seizures at the onset site and on small spatial scales. We now propose that surround inhibition has a dual role. On a millimeter scale, its abrupt failure permits the advance of a seizure. At long distances from the seizure focus, strong local inhibition serves to mask the excitatory effects of seizures and may help to hasten seizure termination, while weakened inhibition may permit emergence of ictal activity at a distant, noncontiguous seizure site. Multiple seizure foci may go unrecognized with standard EEG interpretation methods, and are likely a critical factor in epilepsy surgery failures. We hypothesize that once established, multiple ictal generators behave as delay-coupled oscillators, demonstrating activity that is synchronized or even temporally reversed. This results in complex and at times counterintuitive network behavior that can be challenging to reverse engineer from EEG recordings. Typically, however, even intracranial EEG recordings provide only a limited view of neural activity. In this project, an interdisciplinary research group with combined expertise in epilepsy, clinical neurophysiology, computational modeling, and mathematics will conduct a comprehensive study of the neuronal contributors to epileptic networks utilizing a unique combined dataset of simultaneous microelectrode and macroelectrode recordings of human seizures. Using a machine learning approach, we will apply this information to develop a multivariate EEG biomarker based on the inferred source of EEG discharges, high frequency oscillations, and very low frequency (DC) shifts and assess its predictive value for post-resection surgical outcome. We anticipate that the project will lead to a theoretical framework for rational development of innovative strategies for developing interventions to control seizures.

Public Health Relevance

This project aims to identify the cellular mechanisms of epileptic networks, a critical barrier to developing treatments based on epileptic network analysis and manipulation. An interdisciplinary team of researchers will address this problem by analyzing and modeling multiscale voltage data from epilepsy patients, and utilizing the results to develop a new multivariate biomarker for seizure-generating brain areas.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS084142-07
Application #
9792276
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Whittemore, Vicky R
Project Start
2013-09-01
Project End
2023-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
7
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Neurology
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
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Smith, Elliot H; Schevon, Catherine A (2016) Toward a Mechanistic Understanding of Epileptic Networks. Curr Neurol Neurosci Rep 16:97

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