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Enlarged perivascular space in the temporal lobe as a prognostic marker in temporal lobe epilepsy with hippocampal sclerosis
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 김경민 | - |
| dc.contributor.author | 김원주 | - |
| dc.contributor.author | 조수미 | - |
| dc.contributor.author | 허경 | - |
| dc.date.accessioned | 2025-08-18T05:45:58Z | - |
| dc.date.available | 2025-08-18T05:45:58Z | - |
| dc.date.issued | 2025-05 | - |
| dc.identifier.issn | 0013-9580 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/207181 | - |
| dc.description.abstract | Objective: 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.statementOfResponsibility | open | - |
| dc.language | English | - |
| dc.publisher | Blackwell Science | - |
| dc.relation.isPartOf | EPILEPSIA | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.subject.MESH | Adolescent | - |
| dc.subject.MESH | Adult | - |
| dc.subject.MESH | Epilepsy, Temporal Lobe* / complications | - |
| dc.subject.MESH | Epilepsy, Temporal Lobe* / diagnostic imaging | - |
| dc.subject.MESH | Epilepsy, Temporal Lobe* / drug therapy | - |
| dc.subject.MESH | Epilepsy, Temporal Lobe* / pathology | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Glymphatic System* / diagnostic imaging | - |
| dc.subject.MESH | Glymphatic System* / pathology | - |
| dc.subject.MESH | Hippocampal Sclerosis | - |
| dc.subject.MESH | Hippocampus* / diagnostic imaging | - |
| dc.subject.MESH | Hippocampus* / pathology | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Magnetic Resonance Imaging | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Middle Aged | - |
| dc.subject.MESH | Prognosis | - |
| dc.subject.MESH | Retrospective Studies | - |
| dc.subject.MESH | Sclerosis / pathology | - |
| dc.subject.MESH | Temporal Lobe* / diagnostic imaging | - |
| dc.subject.MESH | Temporal Lobe* / pathology | - |
| dc.subject.MESH | Young Adult | - |
| dc.title | Enlarged perivascular space in the temporal lobe as a prognostic marker in temporal lobe epilepsy with hippocampal sclerosis | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Neurology (신경과학교실) | - |
| dc.contributor.googleauthor | Soomi Cho | - |
| dc.contributor.googleauthor | Seungwon Song | - |
| dc.contributor.googleauthor | Jungyon Yum | - |
| dc.contributor.googleauthor | Eun Hwa Kim | - |
| dc.contributor.googleauthor | Yun Ho Roh | - |
| dc.contributor.googleauthor | Won-Joo Kim | - |
| dc.contributor.googleauthor | Kyoung Heo | - |
| dc.contributor.googleauthor | Han Kyu Na | - |
| dc.contributor.googleauthor | Kyung Min Kim | - |
| dc.identifier.doi | 10.1111/epi.18301 | - |
| dc.contributor.localId | A05748 | - |
| dc.contributor.localId | A00771 | - |
| dc.contributor.localId | A06551 | - |
| dc.contributor.localId | A04341 | - |
| dc.relation.journalcode | J00793 | - |
| dc.identifier.eissn | 1528-1167 | - |
| dc.identifier.pmid | 39985382 | - |
| dc.subject.keyword | glymphatic function | - |
| dc.subject.keyword | imaging biomarker | - |
| dc.subject.keyword | mesial temporal lobe epilepsy | - |
| dc.subject.keyword | perivascular space | - |
| dc.subject.keyword | prognosis | - |
| dc.contributor.alternativeName | Kim, Kyung Min | - |
| dc.contributor.affiliatedAuthor | 김경민 | - |
| dc.contributor.affiliatedAuthor | 김원주 | - |
| dc.contributor.affiliatedAuthor | 조수미 | - |
| dc.contributor.affiliatedAuthor | 허경 | - |
| dc.citation.volume | 66 | - |
| dc.citation.number | 5 | - |
| dc.citation.startPage | 1665 | - |
| dc.citation.endPage | 1676 | - |
| dc.identifier.bibliographicCitation | EPILEPSIA, Vol.66(5) : 1665-1676, 2025-05 | - |
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