Evidence map›Paper›PMID 42813903›Full record

ArticleBrain and behavior2026

Glymphatic System Dysfunction and its Associated Factors in Wilson's Disease: A DTI-ALPS Study.

Ling Zhu, Tong Wu, Liang-Jie Zhang, Qin-Yuan Liu, Liang-Liang Zhang, Bin Song, Yu-Long Zhu, Lei Hua, Long Zhang, Bo Li and 5 more

Abstract read
In one paragraph

Article in Brain and behavior, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Ling ZhuInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Tong WuInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Liang-Jie ZhangDepartment of Radiology, The Fourth Clinical Medical College of Guangzhou University of Chinese Medicine (Shenzhen Traditional Chinese Medicine Hospital), Shenzhen, China.
Qin-Yuan LiuInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Liang-Liang ZhangInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Bin SongInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Yu-Long ZhuInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Lei HuaInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Long ZhangInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Bo LiInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Quan SunInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Ben-Chun XueInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Yin XuInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Yong-Zhu HanInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.
Yong-Sheng HanInstitute of Neurology, Anhui University of Chinese Medicine, Hefei, China.

Funding

Anhui Provincial Clinical Translational Special Project: Research on Integrated Evaluation ModelAnhui Provincial Department of Science and Technology 202204295107020047Anhui University of Chinese Medicine 2023CXMMTCM002
6 · The paper itself

Abstract

backgroundWilson's disease (WD) is a genetic disorder of copper (Cu) metabolism that causes Cu accumulation in multiple organs, particularly the liver and brain, resulting in progressive multisystem damage. This study investigated glymphatic system function and its associated factors in patients with WD.

methodsSeventy-one patients with WD (19 hepatic, 52 neurological) and 15 healthy controls (HCs) were enrolled. The analysis along the perivascular space (ALPS) index was quantified using diffusion tensor imaging (DTI-ALPS). Comparisons were performed between patients and than HCs, and across WD phenotypes, and correlations with clinical characteristics were analyzed.

resultsCompared with HCs, patients with WD exhibited significantly reduced ALPS index (p < 0.001). Patients with neurological WD had a significantly lower ALPS index than those with hepatic WD (p = 0.018) and HCs (p < 0.001). No significant difference was observed between patients with hepatic WD and HCs (p = 0.077). In neurological WD, the ALPS index was significantly higher on the left side than that on the right (p < 0.001), whereas no significant interhemispheric differences were found in hepatic WD or HCs (p > 0.05). In neurological WD, the ALPS index correlated positively with albumin, fasting blood glucose, and the white matter volume-to-total intracranial volume ratio (V_WM/TIV ratio), and negatively with age, alanine aminotransferase, aspartate aminotransferase (AST), and the unified WD rating scale-part I (UWDRS-I) score. Multiple regression identified age, AST, and the UWDRS-I score as independent predictors of reduced ALPS index.

conclusionsNeurological WD was associated with impaired glymphatic system function and altered lateralization. Age, AST, and the UWDRS-I score were independently associated with dysfunction.Glymphatic function, assessed by DTI-ALPS index, was impaired in neurological WD compared with the hepatic phenotype and controls. Age, AST, and UWDRS-I score independently predicted dysfunction, linking neurodegeneration, liver injury, and altered glymphatic activity.

Indexed as

Glymphatic SystemHepatolenticular DegenerationAdolescentAdultBrainDiffusion Tensor ImagingFemaleHumansLiverMaleYoung Adultanalysis along the perivascular space indexdiffusion tensor imagingglymphatic systemWilson's disease

Identifiers

PMID42813903
PMCPMC13625821

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