Automated and Interpretable Detection of Hippocampal Sclerosis in Temporal Lobe Epilepsy: AID-HS

dc.contributor.authorRipart, Mathildees_ES
dc.contributor.authorDeKraker, Jordanes_ES
dc.contributor.authorEriksson, Maria H.es_ES
dc.contributor.authorPiper, Rory J.es_ES
dc.contributor.authorGopinath, Sibyes_ES
dc.contributor.authorParasuram, Harilales_ES
dc.contributor.authorMo, Jiajiees_ES
dc.contributor.authorLikeman, Marcuses_ES
dc.contributor.authorCiobotaru, Georgianes_ES
dc.contributor.authorSequeiros-Peggs, Philipes_ES
dc.contributor.authorHamandi, Khalides_ES
dc.contributor.authorXie, Huaes_ES
dc.contributor.authorCohen, Nathan T.es_ES
dc.contributor.authorSu, Ting-Yues_ES
dc.contributor.authorRojas-Costa, Gonzalo M.es_ES
dc.contributor.funderNational Institutes of Health, EEUUes_ES
dc.contributor.funderMedical Research Council, Reino Unidoes_ES
dc.contributor.funderCanadian Institutes of Health Researches_ES
dc.contributor.funderMinistero dell'Università e della Ricercaes_ES
dc.contributor.funderNational Institute for Health Research, Reino Unidoes_ES
dc.contributor.funderNatural Sciences and Engineering Research Council of Canadaes_ES
dc.contributor.funderFondo Nacional de Desarrollo Científico y Tecnológico, Chilees_ES
dc.date.accessioned2025-10-27T20:23:23Z
dc.date.available2025-10-27T20:23:23Z
dc.date.issued2025-01es_ES
dc.description.abstract[EN] Objective: Hippocampal sclerosis (HS), the most common pathology associated with temporal lobe epilepsy (TLE), is not always visible on magnetic resonance imaging (MRI), causing surgical delays and reduced postsurgical seizurefreedom. We developed an open-source software to characterize and localize HS to aid the presurgical evaluation of children and adults with suspected TLE. Methods: We included a multicenter cohort of 365 participants (154 HS; 90 disease controls; 121 healthy controls). HippUnfold was used to extract morphological surface-based features and volumes of the hippocampus from T1-weighted MRI scans. We characterized pathological hippocampi in patients by comparing them to normative growth charts and analyzing within-subject feature asymmetries. Feature asymmetry scores were used to train a logistic regression classifier to detect and lateralize HS. The classifier was validated on an independent multicenter cohort of 275 patients with HS and 161 healthy and disease controls. Results: HS was characterized by decreased volume, thickness, and gyrification alongside increased mean and intrinsic curvature. The classifier detected 90.1% of unilateral HS patients and lateralized lesions in 97.4%. In patients with MRI negative histopathologically-confirmed HS, the classifier detected 79.2% (19/24) and lateralized 91.7% (22/24). The model achieved similar performances on the independent cohort, demonstrating its ability to generalize to new data. Individual patient reports contextualize a patient¿s hippocampal features in relation to normative growth trajectories, visualise feature asymmetries, and report classifier predictions. Interpretation: Automated and Interpretable Detection of Hippocampal Sclerosis (AID-HS) is an open-source pipeline for detecting and lateralizing HS and outputting clinically-relevant reports.en_EN
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationRipart, M.; Dekraker, J.; Eriksson, MH.; Piper, RJ.; Gopinath, S.; Parasuram, H.; Mo, J.... (2025). Automated and Interpretable Detection of Hippocampal Sclerosis in Temporal Lobe Epilepsy: AID-HS. Annals of Neurology. 97(1):62-75. https://doi.org/10.1002/ana.27089es_ES
dc.description.issue1es_ES
dc.description.sponsorshipM.R. and S.A. are supported by the Rosetrees Trust (A2665) and Epilepsy Research Institute (P2208). K.W. is supported by the Wellcome Trust (301991/Z/23/Z). JD is supported by a Canada Research Chairs program (#950-231964), CIHR Project Grant (366062), and NSERC Discovery Grant (RGPIN-2023-05558). MHE is supported by the Sigrid Jusélius Foundation. S.G. and H.P. are supported by a Seed grant from Amrita Institute of Medical Sciences, Kochi. P.S. and K.H. are supported by Health and Care Research Wales. HX is supported by the Hess Foundation. N.T.C. is supported by an AAN Career Development Award, Hess Foundation. I.W. is supported by NIH R01 NS109439. G.M.R. is supported by FONDECYT grants (#1210195, #1210176, #1220995). A.R. is supported by Ministero dell'Università e della Ricerca PE0000006. A.V. and R.T. are supported by Fundación Iniciativa Para las Neurociencias. H.R.P. is supported by the NIH (R21NS117990). G.P.W. is supported by the Medical Research Council (G0802012, MR/M00841X/1). J.S.D. is supported by the NIHR. A.R.K. is supported by the Natural Sciences and Engineering Research Council of Canada. This work is supported by the NIHR Great Ormond Street Hospital Children's Charity BRC. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health.es_ES
dc.description.upvformatpfin75es_ES
dc.description.upvformatpinicio62es_ES
dc.description.volume97es_ES
dc.identifier.doi10.1002/ana.27089es_ES
dc.identifier.issn0364-5134es_ES
dc.identifier.pmcidPMC11683179es_ES
dc.identifier.pmid39543853es_ES
dc.identifier.urihttps://riunet.upv.es/handle/10251/229473
dc.languageIngléses_ES
dc.publisherJohn Wiley & Sonses_ES
dc.relation.ispartofAnnals of Neurologyes_ES
dc.relation.pasarelaS\562350es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/NSERC//RGPIN-2023-05558/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/FONDECYT//1210176/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/FONDECYT//1210195/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/FONDECYT//1220995/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MRC//MR%2FM00841X%2F1/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MRC//G0802012/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/NIH//R21NS117990/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/NIH//R01 NS109439/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/CIHR//366062/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MUR//PE0000006/es_ES
dc.relation.publisherversionhttps://doi.org/10.1002/ana.27089es_ES
dc.rightsReconocimiento (by)es_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectHippocampal sclerosises_ES
dc.subjectTemporal lobe epilepsyes_ES
dc.subjectMagnetic resonance imaginges_ES
dc.subjectAutomated detectiones_ES
dc.subjectMachine learninges_ES
dc.subjectClinical decision supportes_ES
dc.titleAutomated and Interpretable Detection of Hippocampal Sclerosis in Temporal Lobe Epilepsy: AID-HSes_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dspace.entity.typePublicationes_ES
upv.uuid483f8bc3-30b6-4826-b73c-9739eabaed92es_ES

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