Evidence map›Paper›PMID 42204548›Full record

ArticleBMC medicine2026

Putative glymphatic dysfunction links extracellular fluid dysregulation to white matter degeneration and clinical impairment in amyotrophic lateral sclerosis.

Xin Jin, Yan Fu, Ting Qiu, Jianyu Li, Huixiong Zhang, Yifan Chen, Kewei Chen, Yuanchao Zhang, Junling Wang, Xiaoping Yi and 2 more

Abstract read
In one paragraph

Article in BMC medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Potential Roles of Neuroimaging in Motor Neuron Disease.Current neurology and neuroscience reports · 2026
    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

12 authors.

Xin Jin *The Clinical Hospital of Chengdu Brain Science Institute, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, Sichuan, P. R. China.
Yan Fu *Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, P. R. China.
Ting QiuDouglas Mental Health University Institute, McGill University, Montreal, QC, Canada.
Jianyu LiSchool of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, Sichuan, P. R. China.
Huixiong ZhangSchool of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, Sichuan, P. R. China.
Yifan ChenSchool of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, Sichuan, P. R. China.
Kewei ChenCollege of Health Solutions, Arizona State University, Phoenix, AZ, 85287, USA.
Yuanchao ZhangThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Lab for Neuroinformation, University of Electronic Science and Technology of China, Chengdu, Sichuan, P. R. China. yuanchao.zhang8@gmail.com.
Junling WangDepartment of Neurology, Xiangya Hospital, Central South University, Jiangxi. (National Regional Center for Neurological Diseases), Nanchang, 330038, Jiangxi, P. R. China. junling.wang@csu.edu.cn.
Xiaoping Yi *Department of Nuclear Medicine and Department of Radiology, Chongqing University Three Gorges Hospital, Chongqing University, Chongqing, 404000, P. R. China. yixiaoping@cqu.edu.cn.
Lena Palaniyappan *Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada.
B Blair Braden *College of Health Solutions, Arizona State University, Phoenix, AZ, 85287, USA.

Funding

Fundamental Research Funds for the Central Universities of Central South University 2024ZZTS0954National Natural Science Foundation of China U22A20377Project Program of National Clinical Research Center for Geriatric Disorders No. 2022LNJJ09Santé CB-C2022Scientific Research Program of FuRong Laboratory No.2024PT5109
6 · The paper itself

Abstract

backgroundAmyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by progressive motor neuron degeneration and prominent extra-motor involvement. Impaired clearance of neurotoxic proteins has led to increasing interest in the brain glymphatic system; however, its in vivo associations with brain microstructure and clinical heterogeneity remain incompletely understood.

methodsOne hundred forty-six patients with ALS and 149 demographically matched healthy controls (HCs) underwent multimodal MRI and comprehensive clinical assessments. Putative glymphatic function was quantified using diffusion tensor imaging along perivascular space (DTI-ALPS). Extracellular free water fraction (FWF) and free-water-corrected fractional anisotropy (fwcFA) were derived to characterize extracellular fluid and white matter microstructure. Group differences were assessed using vertex-wise and voxel-wise analyses with correction for multiple comparisons. Associations among imaging metrics and clinical measures were evaluated using correlation and serial mediation analyses.

resultsCompared with HCs, patients with ALS exhibited significantly reduced DTI-ALPS index, widespread increases in cortical FWF, bidirectional alterations in white matter FWF, and extensive reductions in fwcFA across major white matter tracts. Reduced DTI-ALPS was associated with changes in extracellular free water and white matter microstructural integrity, whereas FWF and fwcFA measures were associated with functional, cognitive, and emotional outcomes. Mediation analyses identified significant indirect associations between DTI-ALPS and both functional and cognitive measures through a pathway involving cortical FWF, white matter FWF, and fwcFA, although direct associations were not observed.

conclusionsThese findings provide in vivo evidence that putative glymphatic dysfunction co-occurs with extracellular fluid alterations, white matter microstructural changes, and clinical impairment in ALS. Multi-compartment diffusion imaging may offer complementary markers for characterizing brain microstructure and its clinical relevance in ALS.

Indexed as

Amyotrophic Lateral SclerosisExtracellular FluidGlymphatic SystemWhite MatterAgedDiffusion Tensor ImagingFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedALSDTI-ALPSFree-water fractionGlymphatic systemWhite matter integrity

Identifiers

PMID42204548
PMCPMC13397807

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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.