Heterogeneity of Preictal Dynamics in Human Epileptic Seizures.

Connectivity eigenvector centrality (EC) electrocorticography (ECoG) latent inputs multivariate Gaussian partial correlation sparse-plus-latent-regularized precision matrix (SLRPM)

Journal

IEEE access : practical innovations, open solutions
ISSN: 2169-3536
Titre abrégé: IEEE Access
Pays: United States
ID NLM: 101639462

Informations de publication

Date de publication:
2020
Historique:
entrez: 16 5 2020
pubmed: 16 5 2020
medline: 16 5 2020
Statut: ppublish

Résumé

It is generally understood that there is a preictal phase in the development of a seizure and this precictal period is the basis for seizure prediction attempts. The focus of this study is the preictal global spatiotemporal dynamics and its intra-patient variability. We analyzed preictal broadband brain connectivity from human electrocorticography (ECoG) recordings of 185 seizures (which included 116 clinical seizures) collected from 12 patients. ECoG electrodes record from only a part of the cortex, leaving large regions of the brain unobserved. Brain connectivity was therefore estimated using the sparse-plus-latent-regularized precision matrix (SLRPM) method, which calculates connectivity from partial correlations of the conditional statistics of the observed regions given the unobserved latent regions. Brain connectivity was quantified using eigenvector centrality (EC), from which a degree of heterogeneity was calculated for the preictal periods of all seizures in each patient. Results from the SLRPM method are compared to those from the sparse-regularized precision matrix (SRPM) and correlation methods, which do not account for the unobserved inputs when estimating brain connectivity. The degree of heterogeneity estimated by the SLRPM method is higher than those estimated by the SRPM and correlation methods for the preictal periods in most patients. These results reveal substantial heterogeneity or desynchronization among brain areas in the preictal period of human epileptic seizures. Furthermore, the SLRPM method identifies more onset channels from the preictal active electrodes compared to the SRPM and correlation methods. Finally, the correlation between the degree of heterogeneity and seizure severity of patients for SLRPM and SRPM methods were lower than that obtained from the correlation method. These results support recent findings suggesting that inhibitory neurons can have anti-seizure effects by inducing variability or heterogeneity across seizures. Understanding how this variability is linked to seizure initiation may lead to better predictions and controlling therapies.

Identifiants

pubmed: 32411567
doi: 10.1109/access.2020.2981017
pmc: PMC7224217
mid: NIHMS1579038
doi:

Types de publication

Journal Article

Langues

eng

Pagination

52738-52748

Subventions

Organisme : NIBIB NIH HHS
ID : R01 EB009282
Pays : United States

Déclaration de conflit d'intérêts

Conflict-of-interest statement Due to HIPPAA regulations and other research protocols involved, we are unable to make the dataset used in this study publicly available at this time.

Références

J Neurophysiol. 2008 May;99(5):2431-42
pubmed: 18322007
Clin Neurophysiol. 2005 Mar;116(3):506-16
pubmed: 15721064
Epilepsia. 2018 Jul;59(7):1398-1409
pubmed: 29897628
Nat Rev Neurol. 2018 Oct;14(10):618-630
pubmed: 30131521
PLoS One. 2013 Nov 19;8(11):e80972
pubmed: 24260523
J Neurosci. 2010 Feb 3;30(5):1619-30
pubmed: 20130172
Proc Natl Acad Sci U S A. 2011 May 24;108(21):8832-7
pubmed: 21555565
Epilepsia. 2005 Jun;46(6):956-60
pubmed: 15946339
Neuropsychopharmacology. 2005 Jul;30(7):1334-44
pubmed: 15856081
Nat Rev Neurosci. 2014 Oct;15(10):683-95
pubmed: 25186238
Nature. 2016 Aug 11;536(7615):171-178
pubmed: 27437579
Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):2035-40
pubmed: 19188601
J Neurosci Methods. 2014 Feb 15;223:50-68
pubmed: 24200508
Neuroimage. 2012 Feb 15;59(4):3852-61
pubmed: 22155039
Epilepsy Res. 2003 Mar;53(3):173-85
pubmed: 12694925
PLoS Comput Biol. 2015 Mar 31;11(3):e1004083
pubmed: 25826696
Neuroimage. 2015 Jan 15;105:493-506
pubmed: 25463459
J Neurophysiol. 2007 Mar;97(3):2525-32
pubmed: 17021032
Neural Comput. 2019 Jul;31(7):1271-1326
pubmed: 31113298
Epilepsia. 2010 Aug;51(8):1598-606
pubmed: 20067499
Neural Comput. 2017 Mar;29(3):603-642
pubmed: 28095202
Biostatistics. 2008 Jul;9(3):432-41
pubmed: 18079126
Neural Comput. 2013 Aug;25(8):2172-98
pubmed: 23607561
Neuron. 2017 Jan 18;93(2):291-298
pubmed: 28041880
Front Neurosci. 2016 Mar 31;10:123
pubmed: 27242395
Lancet Neurol. 2002 May;1(1):22-30
pubmed: 12849542
Cereb Cortex. 2012 Aug;22(8):1862-75
pubmed: 21968567
Proc Natl Acad Sci U S A. 2014 Dec 9;111(49):E5321-30
pubmed: 25404339
Magn Reson Med. 1995 Oct;34(4):537-41
pubmed: 8524021
J Neurosci. 2010 Jul 28;30(30):10076-85
pubmed: 20668192
Nat Commun. 2018 Mar 14;9(1):1088
pubmed: 29540685
Neuroimage. 2010 Sep;52(3):1059-69
pubmed: 19819337
J Neurosci. 2012 Feb 15;32(7):2499-512
pubmed: 22396423
Brain. 2010 Jun;133(Pt 6):1668-81
pubmed: 20511283
J Neurosci. 2009 Jul 1;29(26):8512-24
pubmed: 19571142
Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):253-8
pubmed: 12506194
PLoS One. 2010 Aug 16;5(8):e12200
pubmed: 20808943
J Nucl Med. 1998 Jun;39(6):978-82
pubmed: 9627329
PLoS One. 2010 Apr 27;5(4):e10232
pubmed: 20436911
Nat Neurosci. 2011 May;14(5):635-41
pubmed: 21441925

Auteurs

Anup DAS (A)

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford University, Stanford, CA 94305 USA.

Sydney S Cash (SS)

Massachusetts General Hospital, Boston, MA 02114 USA.

Terrence J Sejnowski (TJ)

Division of Biological Sciences and Institute of Neural Computation, University of California, San Diego, La Jolla, CA 92093 USA.

Classifications MeSH