Evidence map›Paper›PMID 37152597›Full record

ArticleFrontiers in neuroscience2023

Microstructural and functional impairment of the basal ganglia in Wilson's disease: a multimodal neuroimaging study.

Dongning Su, Zhijin Zhang, Zhe Zhang, Yawen Gan, Yingkui Zhang, Xinyao Liu, Jingfeng Bi, Lingyan Ma, Huiqing Zhao, Xuemei Wang and 8 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2023. 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
1.6field-weighted citation impact, top 19% of its field
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, 10 citations in OpenAlex.

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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

18 authors at 5 institutions in 3 countries.

Dongning Su *Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zhijin Zhang *Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zhe Zhang *China National Clinical Research Center for Neurological Diseases, Beijing, China.
Yawen GanDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Yingkui ZhangChina National Clinical Research Center for Neurological Diseases, Beijing, China.
Xinyao LiuChina National Clinical Research Center for Neurological Diseases, Beijing, China.
Jingfeng BiChina National Clinical Research Center for Neurological Diseases, Beijing, China.
Lingyan MaDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Huiqing ZhaoDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Xuemei WangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zhan WangDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Huizi MaDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Shairy SifatDjavad Mowafaghian Centre for Brain Health, Pacific Parkinson's Research Centre, University of British Columbia and Vancouver Coastal Health, Vancouver, BC, Canada.
Junhong ZhouHinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Roslindale, MA, United States.
Wei LiDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Tao WuDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Jing JingDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Tao FengDepartment of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Capital Medical University · CNBeijing Tian Tan Hospital · CNNational Clinical Research Center for Digestive Diseases · CNHebrew SeniorLife · USVancouver Coastal Health · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Magnetic susceptibility changes in brain MRI of Wilson's disease (WD) patients have been described in subcortical nuclei especially the basal ganglia. The objectives of this study were to investigate its relationship with other microstructural and functional alterations of the subcortical nuclei and the diagnostic utility of these MRI-related metrics. Methods: A total of 22 WD patients and 20 healthy controls (HCs) underwent 3.0T multimodal MRI scanning. Susceptibility, volume, diffusion microstructural indices and whole-brain functional connectivity of the putamen (PU), globus pallidus (GP), caudate nucleus (CN), and thalamus (TH) were analyzed. Receiver operating curve (ROC) was applied to evaluate the diagnostic value of the imaging data. Correlation analysis was performed to explore the connection between susceptibility change and microstructure and functional impairment of WD and screen for neuroimaging biomarkers of disease severity. Results: Wilson's disease patients demonstrated increased susceptibility in the PU, GP, and TH, and widespread atrophy and microstructural impairments in the PU, GP, CN, and TH. Functional connectivity decreased within the basal ganglia and increased between the PU and cortex. The ROC model showed higher diagnostic value of isotropic volume fraction (ISOVF, in the neurite orientation dispersion and density imaging model) compared with susceptibility. Severity of neurological symptoms was correlated with volume and ISOVF. Susceptibility was positively correlated with ISOVF in GP. Conclusion: Microstructural impairment of the basal ganglia is related to excessive metal accumulation in WD. Brain atrophy and microstructural impairments are useful neuroimaging biomarkers for the neurological impairment of WD.

Indexed as

basal gangliaironmultimodal MRIneuroimaging biomarkerWilson’s disease

Identifiers

PMID37152597
PMCPMC10157043
OpenAlexW4366598916

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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.