Mapping Lesion-Related Epilepsy to a Human Brain Network

dc.contributor.authorSchaper Frederic L. W. V. J.
dc.contributor.authorNordberg Janne
dc.contributor.authorCohen Alexander L.
dc.contributor.authorLin Christopher
dc.contributor.authorHsu Joey
dc.contributor.authorHorn Andreas
dc.contributor.authorFerguson Michael A.
dc.contributor.authorSiddiqi Shan H.
dc.contributor.authorDrew William
dc.contributor.authorSoussand Louis
dc.contributor.authorWinkler Anderson M.
dc.contributor.authorSimo Marta
dc.contributor.authorBruna Jordi
dc.contributor.authorRheims Sylvain
dc.contributor.authorGuenot Marc
dc.contributor.authorBucci Marco
dc.contributor.authorNummenmaa Lauri
dc.contributor.authorStaals Julie
dc.contributor.authorColon Albert J.
dc.contributor.authorAckermans Linda
dc.contributor.authorBubrick Ellen J.
dc.contributor.authorPeters Jurriaan M.
dc.contributor.authorWu Ona
dc.contributor.authorRost Natalia S.
dc.contributor.authorGrafman Jordan
dc.contributor.authorBlumenfeld Hal
dc.contributor.authorTemel Yasin
dc.contributor.authorRouhl Rob P. W.
dc.contributor.authorJoutsa Juho
dc.contributor.authorFox Michael D.
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code2607321
dc.converis.publication-id180336040
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/180336040
dc.date.accessioned2025-08-28T01:25:20Z
dc.date.available2025-08-28T01:25:20Z
dc.description.abstract<p><strong>IMPORTANCE </strong>It remains unclear why lesions in some locations cause epilepsy while others do not. Identifying the brain regions or networks associated with epilepsy by mapping these lesions could inform prognosis and guide interventions.<br></p><p><strong>OBJECTIVE </strong>To assess whether lesion locations associated with epilepsy map to specific brain regions and networks.<br></p><p><strong>DESIGN, SETTING, AND PARTICIPANTS </strong>This case-control study used lesion location and lesion network mapping to identify the brain regions and networks associated with epilepsy in a discovery data set of patients with poststroke epilepsy and control patients with stroke. Patients with stroke lesions and epilepsy (n = 76) or no epilepsy (n = 625) were included. Generalizability to other lesion types was assessed using 4 independent cohorts as validation data sets. The total numbers of patients across all datasets (both discovery and validation datasets) were 347 with epilepsy and 1126 without. Therapeutic relevance was assessed using deep brain stimulation sites that improve seizure control. Data were analyzed from September 2018 through December 2022. All shared patient data were analyzed and included; no patients were excluded.<br></p><p><strong>MAIN OUTCOMES AND MEASURES </strong>Epilepsy or no epilepsy.<br></p><p><strong>RESULTS </strong>Lesion locations from 76 patients with poststroke epilepsy (39 [51%] male; mean [SD] age, 61.0 [14.6] years; mean [SD] follow-up, 6.7 [2.0] years) and 625 control patients with stroke (366 [59%] male; mean [SD] age, 62.0 [14.1] years; follow-up range, 3-12 months) were included in the discovery data set. Lesions associated with epilepsy occurred in multiple heterogenous locations spanning different lobes and vascular territories. However, these same lesion locations were part of a specific brain network defined by functional connectivity to the basal ganglia and cerebellum. Findings were validated in 4 independent cohorts including 772 patients with brain lesions (271 [35%] with epilepsy; 515 [67%] male; median [IQR] age, 60 [50-70] years; follow-up range, 3-35 years). Lesion connectivity to this brain network was associated with increased risk of epilepsy after stroke (odds ratio [OR], 2.82; 95% CI, 2.02-4.10; <em>P</em> < .001) and across different lesion types (OR, 2.85; 95% CI, 2.23-3.69; P < .001). Deep brain stimulation site connectivity to this same network was associated with improved seizure control (r, 0.63; P < .001) in 30 patients with drug-resistant epilepsy (21 [70%] male; median [IQR] age, 39 [32-46] years; median [IQR] follow-up, 24 [16-30] months).<br></p><p><strong>CONCLUSIONS AND RELEVANCE </strong>The findings in this study indicate that lesion-related epilepsy mapped to a human brain network, which could help identify patients at risk of epilepsy after a brain lesion and guide brain stimulation therapies.<br></p>
dc.identifier.eissn2168-6157
dc.identifier.jour-issn2168-6149
dc.identifier.olddbid207526
dc.identifier.oldhandle10024/190553
dc.identifier.urihttps://www.utupub.fi/handle/11111/51981
dc.identifier.urlhttps://jamanetwork.com/journals/jamaneurology/fullarticle/2806404
dc.identifier.urnURN:NBN:fi-fe2025082791670
dc.language.isoen
dc.okm.affiliatedauthorNordberg, Janne
dc.okm.affiliatedauthorJoutsa, Juho
dc.okm.affiliatedauthorNummenmaa, Lauri
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3124 Neurology and psychiatryen_GB
dc.okm.discipline3124 Neurologia ja psykiatriafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAMER MEDICAL ASSOC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1001/jamaneurol.2023.1988
dc.relation.ispartofjournalJAMA Neurology
dc.source.identifierhttps://www.utupub.fi/handle/10024/190553
dc.titleMapping Lesion-Related Epilepsy to a Human Brain Network
dc.year.issued2023

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