Intracortical neural activity distal to seizure-onset-areas predicts human focal seizures.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 22 01 2019
accepted: 04 07 2019
entrez: 23 7 2019
pubmed: 23 7 2019
medline: 19 2 2020
Statut: epublish

Résumé

The apparent unpredictability of epileptic seizures has a major impact in the quality of life of people with pharmacologically resistant seizures. Here, we present initial results and a proof-of-concept of how focal seizures can be predicted early in advance based on intracortical signals recorded from small neocortical patches away from identified seizure onset areas. We show that machine learning algorithms can discriminate between interictal and preictal periods based on multiunit activity (i.e. thresholded action potential counts) and multi-frequency band local field potentials recorded via 4 X 4 mm2 microelectrode arrays. Microelectrode arrays were implanted in 5 patients undergoing neuromonitoring for resective surgery. Post-implant analysis revealed arrays were outside the seizure onset areas. Preictal periods were defined as the 1-hour period leading to a seizure. A 5-minute gap between the preictal period and the putative seizure onset was enforced to account for potential errors in the determination of actual seizure onset times. We used extreme gradient boosting and long short-term memory networks for prediction. Prediction accuracy based on the area under the receiver operating characteristic curves reached 90% for at least one feature type in each patient. Importantly, successful prediction could be achieved based exclusively on multiunit activity. This result indicates that preictal activity in the recorded neocortical patches involved not only subthreshold postsynaptic potentials, perhaps driven by the distal seizure onset areas, but also neuronal spiking in distal recurrent neocortical networks. Beyond the commonly identified seizure onset areas, our findings point to the engagement of large-scale neuronal networks in the neural dynamics building up toward a seizure. Our initial results obtained on currently available human intracortical microelectrode array recordings warrant new studies on larger datasets, and open new perspectives for seizure prediction and control by emphasizing the contribution of multiscale neural signals in large-scale neuronal networks.

Identifiants

pubmed: 31329587
doi: 10.1371/journal.pone.0211847
pii: PONE-D-19-02056
pmc: PMC6645464
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0211847

Subventions

Organisme : RRD VA
ID : I01 RX000668
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS079533
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS062092
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Timothée Proix (T)

Department of Neuroscience, Brown University, Providence, Rhode Island, United States of America.
Carney Institute for Brain Science, Brown University, Providence, Rhode Island, United States of America.
Center for Neurorestoration & Neurotechnology, U.S. Department of Veterans Affairs, Providence, Rhode Island, United States of America.

Mehdi Aghagolzadeh (M)

Department of Neuroscience, Brown University, Providence, Rhode Island, United States of America.
Carney Institute for Brain Science, Brown University, Providence, Rhode Island, United States of America.
Center for Neurorestoration & Neurotechnology, U.S. Department of Veterans Affairs, Providence, Rhode Island, United States of America.

Joseph R Madsen (JR)

Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.

Rees Cosgrove (R)

Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.

Emad Eskandar (E)

Department of Neurosurgery and Nayef Al-Rodhan Laboratories for Cellular Neurosurgery and Neurosurgical Technology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.

Leigh R Hochberg (LR)

Carney Institute for Brain Science, Brown University, Providence, Rhode Island, United States of America.
Center for Neurorestoration & Neurotechnology, U.S. Department of Veterans Affairs, Providence, Rhode Island, United States of America.
School of Engineering, Brown University, Providence, Rhode Island, United States of America.
Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.

Sydney S Cash (SS)

Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.

Wilson Truccolo (W)

Department of Neuroscience, Brown University, Providence, Rhode Island, United States of America.
Carney Institute for Brain Science, Brown University, Providence, Rhode Island, United States of America.
Center for Neurorestoration & Neurotechnology, U.S. Department of Veterans Affairs, Providence, Rhode Island, United States of America.

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