Evidence map›Paper›PMID 42012765›Full record

ArticleTranslational stroke research2026

Impaired Glymphatic-Meningeal Lymphatic Function in Patients with Spontaneous Subarachnoid Hemorrhage.

Jianan Lu, Miao Lin, Heping Tian, Yibo Liu, Bingrui Zhu, Jin Mao, Jiahao Zhang, Haocheng Zhang, Sixuan Tian, Xu Li and 9 more

Abstract read
PubMed Publisher
In one paragraph

Article in Translational stroke research, 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

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

2 citing papers in PubMed.

  1. Review
  2. Review
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

19 authors.

Jianan Lu *Department of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Miao Lin *Department of Radiology, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Heping Tian *Department of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Yibo LiuDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Bingrui ZhuDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Jin MaoDepartment of Radiology, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Jiahao ZhangDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Haocheng ZhangDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Sixuan TianDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Xu LiDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Ding XuDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Chenhan LingDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Jianru LiDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Hui HongDepartment of Radiology, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Peiyu HuangDepartment of Radiology, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Jianmin ZhangDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China.
Chao WangDepartment of Radiology, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China. wangchaosmart@zju.edu.cn.
Sheng ChenDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China. saintchan@zju.edu.cn.
Yuanjian FangDepartment of Neurosurgery, The Second Affiliated Hospital of Zhejiang, University School of Medicine, 88 Jiefang Road, Zhejiang, Hangzhou, 310009, China. sandman0506@zju.edu.cn.

Funding

National Natural Science Foundation of China 82302135National Natural Science Foundation of China 82371300Noncommunicable Chronic Disease National Science and Technology Major Project 2023ZD0505100
6 · The paper itself

Abstract

According to animal studies, glymphatic–meningeal lymphatic dysfunction contributes to poor prognosis and the development of chronic hydrocephalus after subarachnoid hemorrhage (SAH). This study aimed to evaluate glymphatic function and meningeal lymphatic drainage signal in patients with SAH. SAH patients and healthy controls (HCs) were enrolled and underwent multimodal MRI. Glymphatic function was assessed using the diffusion tensor imaging analysis along the perivascular space (DTI-ALPS) index, free water in white matter (FW-WM), and white matter perivascular space volume fraction (PVSVF-WM). The signal intensity (SI) of meningeal lymphatic vessels (mLVs) and deep cervical lymph nodes (dcLNs) was also quantified as an imaging surrogate of meningeal lymphatic drainage. Compared with HCs, SAH patients exhibited significant impairment of glymphatic function, characterized by a reduced DTI-ALPS index, increased FW-WM, and increased PVSVF-WM, along with reduced SI of the mLVs and dcLNs. Patients with chronic hydrocephalus showed even more pronounced impairment than those with acute SAH. Importantly, reduced DTI-ALPS index and mLV SI loss were identified as independent predictors of chronic shunt-dependent hydrocephalus. Notably, 53.8% of chronic hydrocephalus patients exhibited fluid accumulation in the mastoid air cells, inversely correlated with meningeal lymphatic drainage signal. In conclusion, SAH is associated with acute and persistent impairment of glymphatic function and reduced meningeal lymphatic drainage signal, with early MRI-derived metrics serving as potential predictors of chronic hydrocephalus and poor functional outcomes.

Indexed as

Glymphatic SystemHydrocephalusLymphatic VesselsMeningesSubarachnoid HemorrhageAdultAgedDiffusion Tensor ImagingFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedChronic hydrocephalusGlymphatic systemMeningeal lymphatic vesselsMultimodal MRISubarachnoid hemorrhage

Identifiers

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Registered trials

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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.