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Mapping Lesion-Related Epilepsy to a Human Brain Network

Schaper Frederic L. W. V. J.; Nordberg Janne; Cohen Alexander L.; Lin Christopher; Hsu Joey; Horn Andreas; Ferguson Michael A.; Siddiqi Shan H.; Drew William; Soussand Louis; Winkler Anderson M.; Simo Marta; Bruna Jordi; Rheims Sylvain; Guenot Marc; Bucci Marco; Nummenmaa Lauri; Staals Julie; Colon Albert J.; Ackermans Linda; Bubrick Ellen J.; Peters Jurriaan M.; Wu Ona; Rost Natalia S.; Grafman Jordan; Blumenfeld Hal; Temel Yasin; Rouhl Rob P. W.; Joutsa Juho; Fox Michael D.

Mapping Lesion-Related Epilepsy to a Human Brain Network

Schaper Frederic L. W. V. J.
Nordberg Janne
Cohen Alexander L.
Lin Christopher
Hsu Joey
Horn Andreas
Ferguson Michael A.
Siddiqi Shan H.
Drew William
Soussand Louis
Winkler Anderson M.
Simo Marta
Bruna Jordi
Rheims Sylvain
Guenot Marc
Bucci Marco
Nummenmaa Lauri
Staals Julie
Colon Albert J.
Ackermans Linda
Bubrick Ellen J.
Peters Jurriaan M.
Wu Ona
Rost Natalia S.
Grafman Jordan
Blumenfeld Hal
Temel Yasin
Rouhl Rob P. W.
Joutsa Juho
Fox Michael D.
Katso/Avaa
jamaneurology_schaper_2023_oi_230041_1686684664.68314.pdf (4.507Mb)
Lataukset: 

AMER MEDICAL ASSOC
doi:10.1001/jamaneurol.2023.1988
URI
https://jamanetwork.com/journals/jamaneurology/fullarticle/2806404
Näytä kaikki kuvailutiedot
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082791670
Tiivistelmä

IMPORTANCE 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.

OBJECTIVE To assess whether lesion locations associated with epilepsy map to specific brain regions and networks.

DESIGN, SETTING, AND PARTICIPANTS 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.

MAIN OUTCOMES AND MEASURES Epilepsy or no epilepsy.

RESULTS 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; P < .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).

CONCLUSIONS AND RELEVANCE 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.

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