Multivariate regression methods for estimating velocity of ictal discharges from human microelectrode recordings
Abstract
Objective. Epileptiform discharges, an electrophysiological hallmark of seizures, can propagate across cortical tissue in a manner similar to traveling waves. Recent work has focused attention on the origination and propagation patterns of these discharges, yielding important clues to their source location and mechanism of travel. However, systematic studies of methods for measuring propagation are lacking. Approach. We analyzed epileptiform discharges in microelectrode array recordings of human seizures. The array records multiunit activity and local field potentials at 400-micron spatial resolution, from a small cortical site free of obstructions. We evaluated several computationally efficient statistical methods for calculating traveling wave velocity, benchmarking them to analyses of associated neuronal burst firing. Main results. Over 90% of discharges met statistical criteria for propagation across the sampled cortical territory. Detection rate, direction and speed estimates derived from a multiunit estimator were compared to four field potential-based estimators: negative peak, maximum descent, high gamma power, and cross-correlation. Interestingly, the methods that were computationally simplest and most efficient (negative peak and maximal descent) offer non-inferior results in predicting neuronal traveling wave velocities compared to the other two, more complex methods. Moreover, the negative peak and maximal descent methods proved to be more robust against reduced spatial sampling challenges. Using least absolute deviation in place of least squares error minimized the impact of outliers, and reduced the discrepancies between local field potential-based and multiunit estimators. Significance. Our findings suggest that ictal epileptiform discharges typically take the form of exceptionally strong, rapidly traveling waves, with propagation detectable across millimeter distances. The sequential activation of neurons in space can be inferred from clinically-observable EEG data, with a variety of straightforward computation methods available. This opens possibilities for systematic assessments of ictal discharge propagation in clinical and research settings.
Additional Information
© 2017 IOP Publishing Ltd. Received 18 July 2016; Revised 21 March 2017; Accepted 23 March 2017; Accepted Manuscript online 23 March 2017. Published 13 June 2017. This work was supported by the National Institutes of Health, through National Institute of Neurological Disorders and Stroke grants R01-NS084142 and R01-NS095368, and the Simons Foundation. We thank Larry Abbott, Sean Escola, Dar Gilboa, and John P. Cunningham for their useful discussions and suggestions.Attached Files
Accepted Version - nihms873434.pdf
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Additional details
- PMCID
- PMC5728389
- Eprint ID
- 75425
- Resolver ID
- CaltechAUTHORS:20170327-134405082
- NIH
- R01-NS084142
- NIH
- R01-NS095368
- Simons Foundation
- Created
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2017-03-27Created from EPrint's datestamp field
- Updated
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2022-03-23Created from EPrint's last_modified field