Evidence map›Paper›PMID 40221240›Full record

ArticleThe journal of prevention of Alzheimer's disease2025

Poor glymphatic function is associated with mild cognitive impairment and its progression to Alzheimer's disease: A DTI-ALPS study.

Cuiping Bao, Hongbin Luo, Jiao Wang, Xuehuan Liu, Yiming Li, Jun Yang, Chong Chen, Rongrong Yang, Weili Ba, Xinying Lian and 3 more

Abstract read
In one paragraph

Article in The journal of prevention of Alzheimer's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
–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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

13 authors.

Cuiping BaoDepartment of Radiology, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin 300121, China.
Hongbin LuoTianjin Jinnan District Center for Disease Control and Prevention, 28 Highway Road, Jinnan District, Tianjin 300350, China.
Jiao WangCenter of Gerontology and Geriatrics, West China Hospital, Sichuan University, Chengdu, China; National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, China; Aging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Skockholm, Sweden.
Xuehuan LiuDepartment of Radiology, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin 300121, China.
Yiming LiDepartment of Radiology, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin 300121, China.
Jun YangDepartment of Radiology, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin 300121, China.
Chong ChenDepartment of Clinical Laboratory, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin 300121, China.
Rongrong YangPublic Health Science and Engineering College, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Weili BaDepartment of Radiology, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin 300121, China.
Xinying LianTianjin Fourth Central Hospital, The Affiliated Hospital of Tianjin Medical University, Zhongshan Rord 1st Tianjin 300140, China.
Michelle DunkAging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Skockholm, Sweden.
Jun LiuTianjin Fourth Central Hospital, The Affiliated Hospital of Tianjin Medical University, Zhongshan Rord 1st Tianjin 300140, China; Tianjin Fourth Central Hospital, Tianjin University, Zhongshan Rord 1st, Tianjin 300140, China; The Institute of Translational Medicine, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin, 300121, China. Electronic address: cjr.liujun@vip.163.com.
Weili XuAging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Skockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to explore the association between ALPS index and both risks of MCI from cognitively normal (CN) and incident AD progressed from MCI, as well as potential mediating factors.

methodsThis study included 519 adults including 253 (48.75 %) CN and 266 (51.25 %) MCI participants from Alzheimer's Disease Neuroimaging Initiative. Glymphatic function (assessed by along the perivascular space [ALPS] index) was measured by diffusion tensor image at baseline. Neurobiomarkers (Aβ and tau from CSF, plasma and PET) and cognitive functions were served as mediators. Data were analyzed using Cox and Laplace regression and mediation analysis.

resultsDuring follow-up (median 3.6 years, interquartile range [IQR]: 2.0-4.9 years), 30 (11.86 %) participants developed MCI in the CN cohort and 73 (27.4 %) participants progressed to AD in the MCI cohort. The hazard ratios (95 % confidence intervals [CIs]) of the higher ALPS index was 0.605 (0.386-0.948) for MCI and 0.501 (0.356-0.706) for AD. In addition, participants with high ALPS index had 3.837 and 3.466 years prolonged onset of MCI and AD, separately. Aβ in choroid plexus (17.1 %), tau in cortex [Inferiortemporal (21.1 %), Middletemporal (AV1451:17.0 %, FTP:15.5 %), Superiortemporal(7.7 %), Meta_temporal (AV1451:17.5 %, FTP:16.6 %)], and executive function (14.1 %) mediated the association between ALPS and MCI-AD progression.

conclusionHigh ALPS index decreases MCI risk and delays MCI progression to AD by approximately 3.5 years. Aβ in choroid plexus, tau in cortex, and executive function may partially mediate the MCI-AD progression in relation to ALPS index.

Indexed as

Alzheimer DiseaseCognitive DysfunctionDiffusion Tensor ImagingGlymphatic SystemAgedAged, 80 and overAmyloid beta-PeptidesBiomarkersCognitionDisease ProgressionFemaleFollow-Up StudiesHumansMaleMediation AnalysisPeptide FragmentsAmyloid beta-Peptidesamyloid beta-protein (1-42)BiomarkersPeptide Fragmentstau ProteinsAlong the perivascular spacesAlzheimer's diseaseGlymphatic function

Identifiers

PMID40221240
PMCPMC12321638

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.