Evidence map›Paper›PMID 42246704›Full record

SynthesisEpilepsia2026

Use of artificial intelligence in magnetic resonance imaging across the epileptic patient's journey: A meta-analysis of four clinical applications.

Judy Chen, Ella Sahlas, Yigu Zhou, Natalie Chen, Jim Xie, Farhan Wadia, Lorenzo Caciagli, Aristides Hadjinicolaou, Alexander G Weil, Roy W Dudley and 4 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Epilepsia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Judy ChenMultimodal Imaging and Connectome Analysis Laboratory (MICA), McConnell Brain Imaging Centre and Centre for Excellence in Epilepsy at the Neuro, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0009-0004-6332-9935
Ella SahlasMultimodal Imaging and Connectome Analysis Laboratory (MICA), McConnell Brain Imaging Centre and Centre for Excellence in Epilepsy at the Neuro, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
Yigu ZhouMultimodal Imaging and Connectome Analysis Laboratory (MICA), McConnell Brain Imaging Centre and Centre for Excellence in Epilepsy at the Neuro, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
Natalie ChenTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0003-4157-2710
Jim XieTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Farhan WadiaMultimodal Imaging and Connectome Analysis Laboratory (MICA), McConnell Brain Imaging Centre and Centre for Excellence in Epilepsy at the Neuro, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
Lorenzo CaciagliDepartment of Neurology, Inselspital, Sleep-Wake-Epilepsy Center, Bern University Hospital, University of Bern, Bern, Switzerland.
Aristides HadjinicolaouCentre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montreal, Quebec, Canada.
Alexander G WeilCentre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montreal, Quebec, Canada.
Roy W DudleyMontreal Children's Hospital, McGill University, Montreal, Quebec, Canada.
Dewi V SchraderBC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Andrea BernasconiNeuroimaging of Epilepsy Laboratory (NOEL), McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0001-9358-5703
Neda BernasconiNeuroimaging of Epilepsy Laboratory (NOEL), McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-8947-9518
Boris C BernhardtMultimodal Imaging and Connectome Analysis Laboratory (MICA), McConnell Brain Imaging Centre and Centre for Excellence in Epilepsy at the Neuro, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0001-9256-6041

Funding

Centre of Excellence in Epilepsy at the NeuroCIHR CIHR MOP-123520CIHR CIHR MOP-57840CIHR FDN-154298CIHR PJT-174995CIHR PJT-191853CIHR PJT-203761CIHR PJT-206196Epilepsy CanadaNatural Sciences and Engineering Research Council of Canada NSERC Discovery-1304413Natural Sciences and Engineering Research Council of Canada NSERC Discovery-243141Natural Sciences and Engineering Research Council of Canada NSERC Discovery-24779SickKids Foundation NI17-039Vanier Scholarship
6 · The paper itself

Abstract

objectiveThe application of artificial intelligence/machine learning (AI/ML) to magnetic resonance imaging (MRI) promises to enhance and support clinical decision-making in epilepsy. However, there currently lacks an appropriate assessment of clinical utility and study rigor of current AI/ML-driven models that are targeted toward supporting decision-making within the clinical workup in epilepsy.

methodsWe systematically reviewed and examined the ability of current AI/ML-driven models in MRI across four main applications within the clinical workup(s) for epilepsy: (1) diagnosis, (2) temporal lobe epilepsy lateralization, (3) lesion (focal cortical dysplasia) localization, and (4) postsurgical outcome prediction. We additionally assessed the risk of bias for each study model. Studies that employed AI/ML classification models trained on any MRI modality or sequence type were selected for qualitative assessment; those reporting accuracy rates were subsequently included in the meta-analysis.

resultsOf 3227 searched articles, we identified 159 studies (n = 26 732 participants) for qualitative evaluation and 127 studies (n = 20 456) for inclusion in the meta-analysis. Our results reveal that AI/ML on MRI could accurately distinguish epilepsy patients from healthy controls (overall accuracy = .87, 95% confidence interval [CI] = .85-.89), lateralize temporal lobe epilepsy (.90, 95% CI = .87-.93), localize epileptogenic lesions (.82, 95% CI = .74-.87), and predict postsurgical seizure freedom (.83, 95% CI = .78-.87). However, systematic assessment indicated a very high risk of bias in the literature, suggestive of overly optimistic performance estimates. SIGNIFICANCE: Although our results support overall high accuracy of AI/ML models in epilepsy diagnostics and prognostics, the literature remains susceptible to bias in participant recruitment and validation methods. Furthermore, most models were limited by study architecture that demands strict adherence to nonstandard, highly specific data acquisition and processing protocols that cannot be easily deployed for clinical implementation. We encourage closer interdisciplinary collaboration between clinical and scientific groups to improve validation studies, and outline suggested recommendations for future study design, analysis, and reporting.

Indexed as

Artificial IntelligenceEpilepsyMagnetic Resonance ImagingClinical Decision-MakingEpilepsy, Temporal LobeFocal Cortical DysplasiaHumansMachine Learningartificial intelligenceepilepsymachine learningprognosis

Identifiers

PMID42246704
PMCPMC13525556

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.