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Enlarged perivascular space in the temporal lobe as a prognostic marker in temporal lobe epilepsy with hippocampal sclerosis

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dc.contributor.author김경민-
dc.contributor.author김원주-
dc.contributor.author조수미-
dc.contributor.author허경-
dc.date.accessioned2025-08-18T05:45:58Z-
dc.date.available2025-08-18T05:45:58Z-
dc.date.issued2025-05-
dc.identifier.issn0013-9580-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/207181-
dc.description.abstractObjective: This study was undertaken to investigate the regional burden of enlarged perivascular spaces (EPVSs) in patients with temporal lobe epilepsy with hippocampal sclerosis (TLE-HS) and explore its prognostic relevance. Methods: In this retrospective observational study, EPVSs in the temporal lobe (T-EPVS), centrum semiovale (CS-EPVS), basal ganglia (BG-EPVS), midbrain, and hippocampus were visually rated in 68 treatment-naïve patients with TLE-HS. Regional EPVS burden was dichotomized into high and low degrees (cutoff: >10 for BG-EPVS/T-EPVS; >20 for CS-EPVS). Cox proportional hazards models were used to determine the potential predictors of seizure freedom (SF; no seizure for >1 year) and delayed SF (SF achieved >6 months after initiating antiseizure medication [ASM]). Multivariate logistic regression using stepwise variable selection based on the Akaike information criterion was performed to investigate whether EPVS burden was associated with medical refractoriness (never achieving SF). Results: Of the 68 patients, 20 were classified into the refractory group (29.4%). The high T-EPVS group had an older epilepsy onset (37.3 ± 12.3 vs. 26.5 ± 13.0 years, p = .005), higher pretreatment seizure density (median = 12.0, interquartile range [IQR] = 5.0-20.0 vs. 4.0, IQR = 2.0-10.5, p = .008), and lower focal to bilateral tonic-clonic seizure prevalence (13.3% vs. 73.6%, p < .001) than the low T-EPVS group. High T-EPVS burden (odds ratio [OR] = 10.908, 95% confidence interval [CI] = 1.895-62.789) was an independent predictor of medial refractoriness, along with female sex (OR = 12.906, 95% CI = 2.214-75.220) and ASM treatment duration (OR = .985, 95% CI = .971-.999). The low T-EPVS group had higher probability of achieving delayed SF than the high T-EPVS group (pLog-rank = .030, pCox regression = .038), whereas the probability of achieving SF was comparable between the two groups (pLog-rank = .053, pCox regression = .146). Significance: Increased T-EPVS burden may serve as an imaging marker of unfavorable prognosis in patients with TLE-HS, underscoring the potential role of perivascular dysfunction in diminished ASM response.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherBlackwell Science-
dc.relation.isPartOfEPILEPSIA-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHEpilepsy, Temporal Lobe* / complications-
dc.subject.MESHEpilepsy, Temporal Lobe* / diagnostic imaging-
dc.subject.MESHEpilepsy, Temporal Lobe* / drug therapy-
dc.subject.MESHEpilepsy, Temporal Lobe* / pathology-
dc.subject.MESHFemale-
dc.subject.MESHGlymphatic System* / diagnostic imaging-
dc.subject.MESHGlymphatic System* / pathology-
dc.subject.MESHHippocampal Sclerosis-
dc.subject.MESHHippocampus* / diagnostic imaging-
dc.subject.MESHHippocampus* / pathology-
dc.subject.MESHHumans-
dc.subject.MESHMagnetic Resonance Imaging-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPrognosis-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHSclerosis / pathology-
dc.subject.MESHTemporal Lobe* / diagnostic imaging-
dc.subject.MESHTemporal Lobe* / pathology-
dc.subject.MESHYoung Adult-
dc.titleEnlarged perivascular space in the temporal lobe as a prognostic marker in temporal lobe epilepsy with hippocampal sclerosis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorSoomi Cho-
dc.contributor.googleauthorSeungwon Song-
dc.contributor.googleauthorJungyon Yum-
dc.contributor.googleauthorEun Hwa Kim-
dc.contributor.googleauthorYun Ho Roh-
dc.contributor.googleauthorWon-Joo Kim-
dc.contributor.googleauthorKyoung Heo-
dc.contributor.googleauthorHan Kyu Na-
dc.contributor.googleauthorKyung Min Kim-
dc.identifier.doi10.1111/epi.18301-
dc.contributor.localIdA05748-
dc.contributor.localIdA00771-
dc.contributor.localIdA06551-
dc.contributor.localIdA04341-
dc.relation.journalcodeJ00793-
dc.identifier.eissn1528-1167-
dc.identifier.pmid39985382-
dc.subject.keywordglymphatic function-
dc.subject.keywordimaging biomarker-
dc.subject.keywordmesial temporal lobe epilepsy-
dc.subject.keywordperivascular space-
dc.subject.keywordprognosis-
dc.contributor.alternativeNameKim, Kyung Min-
dc.contributor.affiliatedAuthor김경민-
dc.contributor.affiliatedAuthor김원주-
dc.contributor.affiliatedAuthor조수미-
dc.contributor.affiliatedAuthor허경-
dc.citation.volume66-
dc.citation.number5-
dc.citation.startPage1665-
dc.citation.endPage1676-
dc.identifier.bibliographicCitationEPILEPSIA, Vol.66(5) : 1665-1676, 2025-05-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers

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