Evidence map›Paper›PMID 41134131›Full record

ArticleEpilepsia open2025

Differential glymphatic dysfunction and memory correlation in temporal lobe epilepsy subtypes.

Ruotong Chen, Hong Li, Pu Miao, Hongyi Ye, Xiao Chen, Yuyu Yang, Jinqi Zhou, Yihe Chen, Yi Ge, Chenmin He and 10 more

Abstract read
In one paragraph

Article in Epilepsia open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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  5. A Novel HNeurochemical research · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Ruotong ChenDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Hong LiDepartment of Radiology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Pu MiaoDepartment of Pediatrics, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0000-0001-5165-2613
Hongyi YeDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0009-0004-6499-9455
Xiao ChenDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yuyu YangDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Jinqi ZhouDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yihe ChenDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yi GeDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0009-0009-1408-2864
Chenmin HeDepartment of Radiology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xiaotong ShaoDepartment of Radiology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Zijian WangDepartment of Radiology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yuting GongDepartment of Radiology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Cong ChenDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Shan WangDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Lingli HuDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Lingqi YeDepartment of Neurology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yao DingDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0000-0002-0599-8872
Shuang WangDepartment of Neurology, Epilepsy Center, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0000-0001-5211-9036
Linglin YangDepartment of Psychiatry, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0000-0002-6794-5987

Funding

National Natural Science Foundation of China 81901319National Natural Science Foundation of China 82171437National Natural Science Foundation of China 82171889National Natural Science Foundation of China 82471469
6 · The paper itself

Abstract

objectiveThis study aims to evaluate the glymphatic system (GS) in different temporal lobe epilepsy (TLE) subtypes using diffusion tensor imaging analysis along the perivascular space (DTI-ALPS) and to explore its correlation with clinical factors and memory performance.

methodsThe study encompassed 112 TLE patients with hippocampal sclerosis (TLE-HS), 73 TLE patients with no lesions on magnetic resonance imaging (TLE-NL), and 55 healthy controls. The DTI-ALPS index was calculated based on 3.0T diffusion tensor image sequences, and the memory performance was assessed using the Wechsler Memory Scale-Revised. The DTI-ALPS index was compared among the three groups, and its relationships with clinical characteristics and memory performance were explored.

resultsTLE-HS group showed a significantly lower DTI-ALPS index compared with healthy controls in both hemispheres (ipsilateral: p < 0.001; contralateral: p = 0.002). By contrast, TLE-NL group exhibited a reduced DTI-ALPS index solely in the ipsilateral hemisphere (p < 0.001). Within TLE-NL cohort, those with a history of focal to bilateral tonic-clonic seizures showed reduced DTI-ALPS indices in both hemispheres (ipsilateral: p = 0.037; contralateral: p = 0.004). In the TLE-HS group, DTI-ALPS index positively correlated with memory performance (ps < 0.05). A multiple regression analysis indicated that the average DTI-ALPS index was significantly associated with memory quotient (β = 0.309, p < 0.001; R SIGNIFICANCE: The patterns of reduced DTI-ALPS index differed between TLE-HS and TLE-NL patients. The extent of GS impairment in TLE-HS patients correlated with memory decline, suggesting its potential as a therapeutic target for memory enhancement. PLAIN LANGUAGE SUMMARY: This study employed the DTI-ALPS index, a neuroimaging marker, to assess glymphatic system function in distinct subtypes of temporal lobe epilepsy (TLE). Glymphatic impairment was observed in both TLE with hippocampal sclerosis (TLE-HS) and nonlesional TLE (TLE-NL), exhibiting distinct patterns. Notably, this dysfunction was associated with memory deficits, suggesting that targeting glymphatic clearance may represent a novel therapeutic strategy for memory improvement in epilepsy.

Indexed as

Epilepsy, Temporal LobeGlymphatic SystemHippocampusMemory DisordersAdultDiffusion Tensor ImagingFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedSclerosisYoung Adultglymphatic systemhippocampal sclerosismemoryno lesions on magnetic resonance imagingtemporal lobe epilepsy

Identifiers

PMID41134131
PMCPMC12716296

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.