Evidence map›Paper›PMID 41928687›Full record

ArticleEpilepsia2026

Glymphatic dysfunction couples with cortical excitation-inhibition imbalance in epilepsy: Evidence from Rasmussen encephalitis.

Cong Fu, Yujiao Yang, Pan Gong, Kun Lv, Yilin Liu, Chongyang Tang, Xiongfei Wang, Lixin Cai, Qingzhu Liu, Yuwu Jiang and 2 more

Abstract read
In one paragraph

Article in Epilepsia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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

12 authors.

Cong FuDepartment of Neurosurgery, Epilepsy Center, Sanbo Brain Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0002-8937-3326
Yujiao YangLaboratory for Clinical Medicine, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0001-5550-2858
Pan GongDepartment of Pediatrics, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-2459-124X
Kun LvDepartment of Neurosurgery, Epilepsy Center, Sanbo Brain Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0009-0001-7704-8577
Yilin LiuDepartment of Neurosurgery, Epilepsy Center, Sanbo Brain Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0009-0003-4227-6718
Chongyang TangDepartment of Neurosurgery, Epilepsy Center, Sanbo Brain Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0001-7464-400X
Xiongfei WangDepartment of Neurosurgery, Epilepsy Center, Sanbo Brain Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0002-0095-9612
Lixin CaiDepartment of Pediatrics, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0001-8231-6428
Qingzhu LiuPediatric Epilepsy Center, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-9695-2246
Yuwu JiangDepartment of Pediatrics, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-5179-9807
Taoyun JiDepartment of Pediatrics, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-0098-3257
Guoming LuanDepartment of Neurosurgery, Epilepsy Center, Sanbo Brain Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0001-5084-2458

Funding

Capital Health Research and Development of Special Fund 2022-1-8011Laboratory for Clinical Medicine of Capital Medical University 2025LCMCMU02National Natural Science Foundation of China 82471476
6 · The paper itself

Abstract

objectiveThe glymphatic system (GS) facilitates perivascular clearance of interstitial solutes and is modulated in part by neuronal activity. However, its relationship to cortical excitability in epilepsy remains unclear. We aim to clarify the mechanistic link between GS function and cortical excitation-inhibition (E-I) balance in patients with epilepsy.

methodsWe investigated this coupling in patients with Rasmussen encephalitis (RE), a rare epileptic disorder with unilateral cortical pathology. Using a hemispheric within-subject design (N = 20), we compared the affected hemisphere (AH) and unaffected hemisphere (UH) within each patient, assessing glymphatic function via diffusion MRI (diffusion tensor imaging-analysis along the perivascular space [DTI-ALPS] index) and E-I dynamics via resting-state EEG spectral decomposition.

resultsThe AH exhibited reduced DTI-ALPS indices, elevated aperiodic exponents, and increased delta-theta oscillatory power. Across individuals, lower ALPS values in the AH correlated with higher aperiodic exponents (r = -.496, p = .026), but not with periodic EEG features. Principal component analysis (PCA) of channel-level aperiodic asymmetry (exponent-informed PCA) revealed a spatial pattern localized to atrophic cortical regions, which also showed strong correspondence with interhemispheric ALPS asymmetry (r = -.570, p = .009). SIGNIFICANCE: These findings demonstrate a spatially convergent link between glymphatic dysfunction, cortical activity with predominant inhibitory tone, and focal atrophy in the AH. Our results indicate that impaired perivascular clearance is correlated with altered cortical excitability, highlighting the potential role of the GS in maintaining neural stability in the epilepsy.

Indexed as

Cerebral CortexEncephalitisEpilepsyGlymphatic SystemNeural InhibitionAdolescentAdultDiffusion Tensor ImagingElectroencephalographyFemaleHumansMaleMiddle AgedYoung Adultepilepsyexcitation–inhibition balanceglymphatic systemRasmussen encephalitis

Identifiers

PMID41928687
PMCPMC13360925

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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.