Evidence map›Paper›PMID 40460352›Full record

ArticleNeurology2025

Alterations in Cortical Microstructure, Morphology, and Intrinsic Local Function in Spiking Tissue in Patients With Focal Epilepsy.

Ella Sahlas, Tamir Avigdor, Alexander Ngo, Jessica Royer, Sara Lariviere, Judy Chen, Ke Xie, Yezhou Wang, Jack Lam, Raul Rodriguez-Cruces and 6 more

Abstract read
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Ella SahlasMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0002-7119-977X
Tamir AvigdorAnalytical Neurophysiology Laboratory, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.
Alexander NgoMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0002-8999-9388
Jessica RoyerMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0002-4448-8998
Sara LariviereSherbrooke Laboratory for Integrative Connectomics, Centre de Recherche du CHUS, Université de Sherbrooke, Quebec, Canada.ORCID 0000-0001-5701-1307
Judy ChenMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0009-0004-6332-9935
Ke XieMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0002-7101-2493
Yezhou WangMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.
Jack LamMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0003-3173-7665
Raul Rodriguez-CrucesMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0002-2917-1212
Thaera ArafatMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.
Raluca PanaDepartment of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada; and.
Andrea BernasconiNeuroimaging of Epilepsy Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0001-9358-5703
Neda BernasconiNeuroimaging of Epilepsy Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0002-8947-9518
Birgit FrauscherAnalytical Neurophysiology Laboratory, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0001-6064-1529
Boris C BernhardtMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Quebec, Canada.ORCID 0000-0001-9256-6041

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesEpilepsy is increasingly conceptualized as a network disorder, and advancing methods for its diagnosis and treatment requires characterizing both the epileptic generator and related networks. Previous research has highlighted alterations in cortical structure and hemodynamics in epilepsy, but it remains unknown whether these alterations concentrate in areas generating epileptic activity. The aim of this study was to interrogate alterations in microstructure, morphology, and intrinsic local function within and beyond spiking tissue in focal epilepsy, combining multimodal MRI and high-density EEG (HD-EEG).

methodsIn this cross-sectional study, we recruited patients with focal epilepsy from the Montreal Neurological Institute's epilepsy monitoring unit. Age-matched and sex-matched control participants were recruited from the community. The 3T MRI acquisitions included T1-weighted, diffusion, quantitative T1 relaxometry, and resting-state functional MRI. Open-access processing tools derived cortex-wide maps of morphology and microstructure (cortical thickness, mean diffusivity, and quantitative T1 relaxometry) and intrinsic local function (timescales, connectivity distance, and node strength). Multivariate approaches generated structural and functional alteration scores for each cortical location. Using HD-EEG electrical source imaging, the most prominent spike type was localized and we quantified MRI alterations within spike sources, as well as in proximal and connected networks.

resultsWe included 25 patients with focal epilepsy (48% female, mean ± SD age = 31.28 ± 9.30 years) and 55 control participants: 30 for imaging feature normalization (50% female, 31.40 ± 8.74 years) and 25 for computing normative connectivity (48% female, 31.04 ± 5.65 years). Regions harboring spike sources showed increased structural MRI alterations compared with the rest of the brain (mean ± SE: 27.98% ± 6.37% vs 17.67% ± 3.32%; DISCUSSION: In a modest sample, spiking regions contained more marked alterations in microstructure and morphology than the remaining cortex. There were nevertheless broader network effects, which may relate to a cascading of structural changes to connected cortices. These results underscore the utility of combining quantitative MRI and EEG for characterizing epileptogenic tissue and assessing network effects.

Indexed as

Cerebral CortexEpilepsies, PartialAdultCross-Sectional StudiesElectroencephalographyFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedYoung Adult

Identifiers

PMID40460352
PMCPMC12141423

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LicenceCC BY-NC-ND
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Registered trials

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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.