Evidence map›Paper›PMID 40790774›Full record

ArticleOrphanet journal of rare diseases2025

Distribution of perivascular spaces distribution and relate to the clinical features of SCA3.

Xinyuan Chen, Yanhua Lian, Wei Lin, Xiaoyue Xia, Lin Zhang, Zhuoying Huang, Maolin Cui, Ruying Yuan, Mengcheng Li, Ziqiang Huang and 6 more

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Xinyuan Chen *Department of Rehabilitation Medicine, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Yanhua Lian *Fuzhou Second General Hospital, Fuzhou, 350007, China.
Wei Lin *Department of Neurology, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, 350005, China.
Xiaoyue Xia *Department of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Lin ZhangDepartment of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Zhuoying HuangDepartment of Neurology, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, 350005, China.
Maolin CuiDepartment of Neurology, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, 350005, China.
Ruying YuanDepartment of Neurology, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, 350005, China.
Mengcheng LiDepartment of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Ziqiang HuangDepartment of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Naping ChenDepartment of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Yuqing TuDepartment of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Jianping HuDepartment of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China. fmrihjp@163.com.
Ning WangDepartment of Neurology, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, 350005, China. ningwang@fjmu.edu.cn.
Qunlin ChenDepartment of Radiology, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China. fychenqunlin@126.com.
Shirui GanDepartment of Neurology, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, 350005, China. ganshirui@fjmu.edu.cn.ORCID 0000-0001-7552-5141

Funding

Fujian Provincial Clinical Medical Research Center for First Aid and Rehabilitation in Orthopedic Trauma 2020Y2014National Natural Science Foundation of China 82230039National Natural Science Foundation of China 82371879National Natural Science Foundation of China 82402952
6 · The paper itself

Abstract

backgroundSpinocerebellar ataxia type 3 (SCA3) is a rare neurodegenerative condition. Prior research has established perivascular spaces (PVS) expansion has been implicated in the pathogenesis and prognosis of various neurodegenerative diseases. To examine PVS changes in SCA3 by comparing patients and matched healthy controls and to identify potential connection of PVS for clinical features.

methodsWe conducted MRI scans on 91 SCA3 patients and 64 healthy controls. We utilized visual semi-quantitative methods to assess PVS in various brain regions, including the center of the semiovale (CSO), basal ganglia (BG), and midbrain-pons, as well as combinations (BG + CSO, BG + CSO + midbrain-pons). To differentiate SCA3 patients from healthy controls, we compared the area under the curve (AUC) of the receiver operating characteristic curve between the two groups. Additionally, we employed Pearson's correlation coefficient to examine the relationship between PVS scores in each brain region and clinical indicators among SCA3 patients.

resultsIn the SCA3 group, we observed higher levels of PVS in the BG, CSO + BG, and three brain regions compared to the healthy control group. PVS in the CSO and CSO + BG also showed positive correlations with age and disease duration, and negative correlations with the number of CAG repeats. Furthermore, PVS in three brain regions exhibited negative correlation with the number of CAG repeats.

conclusionsThis study represents an initial investigation into the relationship between PVS and SCA3 disease. Our findings suggest that PVS might indicate the degree of cerebellar ataxia to a certain extent.

Indexed as

Glymphatic SystemMachado-Joseph DiseaseAdultAgedBrainFemaleHumansMagnetic Resonance ImagingMaleMiddle Aged

Identifiers

PMID40790774
PMCPMC12341106

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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.