Evidence map›Paper›PMID 39963843›Full record

ArticleCNS neuroscience & therapeutics2025

Relationships Between Glymphatic System Activity and Tau Burden, Dopaminergic Impairment, Abnormal Glucose Metabolism in Progressive Supranuclear Palsy.

Fangyang Jiao, Qingmin Wang, Jiayi Zhong, Huamei Lin, Jiaying Lu, Luyao Wang, Min Wang, Fengtao Liu, Jiehui Jiang, Chuantao Zuo

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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  4. 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

10 authors.

Fangyang JiaoDepartment of Nuclear Medicine & PET Center, National Clinical Research Center for Aging and Medicine & National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.ORCID 0000-0002-2246-0951
Qingmin WangInstitute of Biomedical Engineering, School of Life Science, Shanghai University, Shanghai, China.
Jiayi ZhongInstitute of Biomedical Engineering, School of Life Science, Shanghai University, Shanghai, China.
Huamei LinDepartment of Nuclear Medicine & PET Center, National Clinical Research Center for Aging and Medicine & National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.
Jiaying LuDepartment of Nuclear Medicine & PET Center, National Clinical Research Center for Aging and Medicine & National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.ORCID 0000-0003-0927-0042
Luyao WangInstitute of Biomedical Engineering, School of Life Science, Shanghai University, Shanghai, China.
Min WangInstitute of Biomedical Engineering, School of Life Science, Shanghai University, Shanghai, China.
Fengtao LiuDepartment of Neurology, National Clinical Research Center for Aging and Medicine & National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.
Jiehui JiangInstitute of Biomedical Engineering, School of Life Science, Shanghai University, Shanghai, China.ORCID 0000-0003-4948-3683
Chuantao ZuoDepartment of Nuclear Medicine & PET Center, National Clinical Research Center for Aging and Medicine & National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.

Funding

National Natural Science Foundation of China 62376150National Natural Science Foundation of China 81971641National Natural Science Foundation of China 82020108013National Natural Science Foundation of China 82021002National Natural Science Foundation of China 82272039National Natural Science Foundation of China 82394434Shanghai Industrial Collaborative Innovation Project XTCX-KJ-2023-37STI2030-Major Projects 2022ZD0211606
6 · The paper itself

Abstract

backgroundProgressive supranuclear palsy (PSP) is a primary tauopathy characterized by dopaminergic impairment and abnormal glucose metabolism. The glymphatic system can promote the elimination of tau protein. The association between glymphatic function and pathological hallmark in neuroimaging remains unknown.

methodsDiffusion tensor imaging (DTI) and positron emission tomography (PET) scanning with

resultsPSP patients exhibited changes in ALPS index and tau deposition. ALPS index, tau deposition, and PSPRP expression showed significant correlations with clinical scores. Additionally, ALPS index was correlated with tau deposition and PSPRP expression. However, neither ALPS index nor the clinical scores were correlated with striatum dysfunction. Finally, tau deposition in subcortical regions and PSPRP expression exhibited mediating effects between ALPS index and clinical scores.

conclusionThe glymphatic dysfunction is associated with tau deposition and abnormal metabolic brain network activity and is independent of dopaminergic impairment in PSP.

Indexed as

DopamineGlucoseGlymphatic SystemSupranuclear Palsy, Progressivetau ProteinsAgedAged, 80 and overBrainDiffusion Tensor ImagingFemaleHumansMaleMiddle AgedPositron-Emission TomographyDopamineGlucosetau Proteinsdopamine systemglucose metabolismglymphatic systemprogressive supranuclear palsytau protein

Identifiers

PMID39963843
PMCPMC11833299

What OpenQuestion holds

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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.