Evidence map›Paper›PMID 39620262›Full record

ArticleEuropean journal of neurology2025

Connectivity-based striatal subregion microstructural changes in sporadic amyotrophic lateral sclerosis patients: Relation to motor disability, cognitive deficits, and serum biomarkers.

Yujing Chen, Sujuan Sun, Yan Yun, Xiaohan Sun, Jiaxiang Xin, Kai Shao, Pengfei Lin, Dexin Yu, Chuanzhu Yan, Shuangwu Liu

Abstract read
In one paragraph

Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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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

10 authors.

Yujing ChenDepartment of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Shandong Provincial Key Laboratory of Mitochondrial Medicine and Rare Diseases, Qilu Hospital of Shandong University, Jinan, China.
Sujuan SunDepartment of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Shandong Provincial Key Laboratory of Mitochondrial Medicine and Rare Diseases, Qilu Hospital of Shandong University, Jinan, China.
Yan YunDepartment of Radiology, Cheeloo College of Medicine, Qilu Hospital, Shandong University, Jinan, China.
Xiaohan SunDepartment of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Shandong Provincial Key Laboratory of Mitochondrial Medicine and Rare Diseases, Qilu Hospital of Shandong University, Jinan, China.
Jiaxiang XinMR Research Collaboration Siemens Healthineers Ltd, Shanghai, China.
Kai ShaoDepartment of Clinical Laboratory, Cheeloo College of Medicine, Qilu Hospital (Qingdao), Shandong University, Qingdao, China.
Pengfei LinDepartment of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Shandong Provincial Key Laboratory of Mitochondrial Medicine and Rare Diseases, Qilu Hospital of Shandong University, Jinan, China.
Dexin YuDepartment of Radiology, Cheeloo College of Medicine, Qilu Hospital, Shandong University, Jinan, China.ORCID 0000-0002-3430-4817
Chuanzhu YanDepartment of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Shandong Provincial Key Laboratory of Mitochondrial Medicine and Rare Diseases, Qilu Hospital of Shandong University, Jinan, China.ORCID 0000-0002-2191-5184
Shuangwu LiuDepartment of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Shandong Provincial Key Laboratory of Mitochondrial Medicine and Rare Diseases, Qilu Hospital of Shandong University, Jinan, China.ORCID 0000-0002-9179-1543

Funding

China Postdoctoral Science Foundation 2020M672067National Natural Science Foundation of China NSFC82001354National Natural Science Foundation of China NSFC82471395Shandong Provincial Natural Science Foundation ZR2023LSW020
6 · The paper itself

Abstract

background and purposeTo date, no previous studies have used multishell diffusion MRI to identify striatal microstructural damage in vivo in amyotrophic lateral sclerosis (ALS) patients. Thus, in the present study, we aimed to comprehensively explore connectivity-based selective striatal subregion microstructural damage in sporadic ALS patients and its associations with motor disability, cognitive deficits, and serum biomarkers.

methodsIn this retrospective study, 79 ALS patients and 53 healthy controls (HCs) who underwent clinical assessment, serum neurofilament light (NfL) measurement, genetic testing, and multishell diffusion MRI scanning were included. Using a probabilistic tractography approach, the striatum was segmented into six subregions based on their corticostriatal connectivity. Three neurite orientation dispersion and density imaging (NODDI) parameters, the neurite density index (NDI), orientation dispersion index (ODI), and isotropic volume fraction (ISO), of the connectivity-based striatal subregions were measured.

resultsCompared with HCs, ALS patients had a significantly lower NDI in the bilateral motor and right frontal subregions, a significantly lower ODI in the right motor and frontal subregions, and a significantly higher ISO in the bilateral motor and frontal subregions of the striatum after familywise error (p < 0.05). Moreover, striatal subregion microstructural damage was significantly correlated with motor disabilities, cognitive deficits, and serum NfL levels in ALS patients (p = 0.020-0.002).

conclusionsOur study provides clear evidence demonstrating that connectivity-based selective striatal subregion microstructural damage is a definite feature of sporadic ALS patients and suggesting that striatal damage may play an important role in motor disability and cognitive deficits in ALS patients.

Indexed as

Amyotrophic Lateral SclerosisBiomarkersCognitive DysfunctionCorpus StriatumAdultAgedDiffusion Magnetic Resonance ImagingDiffusion Tensor ImagingFemaleHumansMaleMiddle AgedNeurofilament ProteinsRetrospective StudiesBiomarkersneurofilament protein LNeurofilament ProteinsALSNfLNODDIstriatum

Identifiers

PMID39620262
PMCPMC11609743

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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.