Evidence map›Paper›PMID 39056406›Full record

ArticleEpilepsia2024

Network signatures define consciousness state during focal seizures.

Derek J Doss, Graham W Johnson, Ghassan S Makhoul, Rohan V Rashingkar, Jared S Shless, Camden E Bibro, Danika L Paulo, Abhijeet Gummadavelli, Tyler J Ball, Shilpa B Reddy and 8 more

Abstract read
In one paragraph

Article in Epilepsia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Derek J DossDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-2685-0762
Graham W JohnsonDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-9154-4315
Ghassan S MakhoulDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0002-9281-541X
Rohan V RashingkarVanderbilt University Institute of Imaging Science, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0004-8231-5782
Jared S ShlessVanderbilt University Institute of Imaging Science, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0003-0702-4454
Camden E BibroVanderbilt University Institute of Imaging Science, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0006-6440-9245
Danika L PauloDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-2292-1164
Abhijeet GummadavelliDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-0505-7511
Tyler J BallDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Shilpa B ReddyDepartment of Pediatrics, Vanderbilt Children's Hospital, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-3172-0102
Robert P NaftelDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-4344-503X
Kevin F HaasDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Benoit M DawantDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-3804-8400
Christos ConstantinidisDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0001-7441-022X
Shawniqua Williams RobersonDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0003-1331-380X
Sarah K BickDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0003-0753-1720
Victoria L MorganDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0001-8263-2324
Dario J EnglotDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0001-8373-690X

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey L Neul · 2020 to 2026
$10.3M
Medical Scientist Training ProgramT32GM152284 · NIGMS · VANDERBILT UNIVERSITY · PI Christopher S. Williams · 2024 to 2026
$4.8M
Relating Vigilance to Connectivity and Neurocognition in Temporal Lobe EpilepsyR01NS112252 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ENGLOT, DARIO J · 2019 to 2023
$3.0M
MRI Connectivity Biomarkers of Treatment Response in Focal EpilepsyR01NS108445 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MORGAN, VICTORIA L · 2019 to 2024
$2.5M
Training Program for Innovative Engineering Research in Surgery and InterventionT32EB021937 · NIBIB · VANDERBILT UNIVERSITY · PI Dario J Englot, Michael Ian Miga · 2016 to 2026
$2.3M
Development of multimodal network analyses to improve epilepsy surgery outcomesR01NS134625 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Dario J Englot · 2024 to 2026
$2.0M
Dynamic multimodal connectivity analysis of brain networks in focal epilepsyF31NS131056 · NINDS · VANDERBILT UNIVERSITY · PI DOSS, DEREK J · 2023 to 2024
$60k
Directed connectivity analysis of resting-state SEEG and DWI to improve lateralization and localization in focal epilepsyF31NS120401 · NINDS · VANDERBILT UNIVERSITY · PI JOHNSON, GRAHAM WALTER · 2021 to 2022
$52k
NIBIB NIH HHS T32 EB021937NIBIB NIH HHS T32EB021937NICHD NIH HHS P50 HD103537NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32GM007347NIGMS NIH HHS T32 GM152284NINDS NIH HHS F31 NS120401NINDS NIH HHS F31NS120401NINDS NIH HHS F31 NS131056NINDS NIH HHS F31NS131056NINDS NIH HHS R01 NS108445NINDS NIH HHS R01NS108445NINDS NIH HHS R01 NS112252NINDS NIH HHS R01NS112252NINDS NIH HHS R01 NS134625NINDS NIH HHS R01NS134625
6 · The paper itself

Abstract

objectiveEpilepsy is a common neurological disorder affecting 1% of the global population. Loss of consciousness in focal impaired awareness seizures (FIASs) and focal-to-bilateral tonic-clonic seizures (FBTCSs) can be devastating, but the mechanisms are not well understood. Although ictal activity and interictal connectivity changes have been noted, the network states of focal aware seizures (FASs), FIASs, and FBTCSs have not been thoroughly evaluated with network measures ictally.

methodsWe obtained electrographic data from 74 patients with stereoelectroencephalography (SEEG). Sliding window band power, functional connectivity, and segregation were computed on preictal, ictal, and postictal data. Five-minute epochs of wake, rapid eye movement sleep, and deep sleep were also extracted. Connectivity of subcortical arousal structures was analyzed in a cohort of patients with both SEEG and functional magnetic resonance imaging (fMRI). Given that custom neuromodulation of seizures is predicated on detection of seizure type, a convolutional neural network was used to classify seizure types.

resultsWe found that in the frontoparietal association cortex, an area associated with consciousness, both consciousness-impairing seizures (FIASs and FBTCSs) and deep sleep had increases in slow wave delta (1-4 Hz) band power. However, when network measures were employed, we found that only FIASs and deep sleep exhibited an increase in delta segregation and a decrease in gamma segregation. Furthermore, we found that only patients with FIASs had reduced subcortical-to-neocortical functional connectivity with fMRI versus controls. Finally, our deep learning network demonstrated an area under the curve of .75 for detecting consciousness-impairing seizures. SIGNIFICANCE: This study provides novel insights into ictal network measures in FASs, FIASs, and FBTCSs. Importantly, although both FIASs and FBTCSs result in loss of consciousness, our results suggest that ictal network changes in FIASs uniquely resemble those that occur during deep sleep. Our results may inform novel neuromodulation strategies for preservation of consciousness in epilepsy.

Indexed as

ConsciousnessElectroencephalographyMagnetic Resonance ImagingSeizuresAdolescentAdultEpilepsies, PartialFemaleHumansMaleMiddle AgedNerve NetUnconsciousnessYoung Adultconsciousness‐impairing seizuresfocal epilepsyfunctional connectivitynetwork analysis of epilepsystereoelectroencephalography

Identifiers

PMID39056406
PMCPMC11534508

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.