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血浆神经丝轻链作为肝豆状核变性神经受累的生物标志物。

Plasma Neurofilament Light as a Biomarker of Neurological Involvement in Wilson's Disease.

机构信息

Department of Clinical and Movement Neurosciences, Reta Lila Weston Institute, UCL Queen Square Institute of Neurology, London, United Kingdom.

Dementia Research Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London, United Kingdom.

出版信息

Mov Disord. 2021 Feb;36(2):503-508. doi: 10.1002/mds.28333. Epub 2020 Oct 20.


DOI:10.1002/mds.28333
PMID:33078859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8436757/
Abstract

BACKGROUND: Outcomes are unpredictable for neurological presentations of Wilson's disease (WD). Dosing regimens for chelation therapy vary and monitoring depends on copper indices, which do not reflect end-organ damage. OBJECTIVE: To identify a biomarker for neurological involvement in WD. METHODS: Neuronal and glial-specific proteins were measured in plasma samples from 40 patients and 38 age-matched controls. Patients were divided into neurological or hepatic presentations and those with recent neurological presentations or deterioration associated with non-adherence were subcategorized as having active neurological disease. Unified WD Rating Scale scores and copper indices were recorded. RESULTS: Unlike copper indices, neurofilament light (NfL) concentrations were higher in neurological than hepatic presentations. They were also higher in those with active neurological disease when controlling for severity and correlated with neurological examination subscores in stable patients. CONCLUSION: NfL is a biomarker of neurological involvement with potential use in guiding chelation therapy and clinical trials for novel treatments. © 2020 University College London. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

摘要

背景:威尔逊病(WD)的神经表现结果难以预测。螯合疗法的剂量方案各不相同,而监测则依赖于不能反映终末器官损伤的铜指标。 目的:寻找 WD 神经受累的生物标志物。 方法:检测了 40 名患者和 38 名年龄匹配对照者的血浆样本中的神经元和神经胶质特异性蛋白。患者分为神经或肝脏表现,近期有神经表现或与不依从相关的恶化者被细分为有活动性神经疾病。记录了统一 WD 评分量表评分和铜指标。 结果:与铜指标不同,神经丝轻链(NfL)浓度在神经表现中高于肝脏表现。在控制严重程度的情况下,与有活动性神经疾病的患者的 NfL 浓度也更高,并且与稳定患者的神经检查子评分相关。 结论:NfL 是神经受累的生物标志物,可能有助于指导螯合治疗和新型治疗的临床试验。 © 2020 伦敦大学学院。运动障碍学会代表国际帕金森病和运动障碍学会由 Wiley 期刊出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0675/8436757/8f1c487543b6/MDS-36-503-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0675/8436757/8f1c487543b6/MDS-36-503-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0675/8436757/8f1c487543b6/MDS-36-503-g001.jpg

相似文献

[1]
Plasma Neurofilament Light as a Biomarker of Neurological Involvement in Wilson's Disease.

Mov Disord. 2021-2

[2]
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[3]
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[4]
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[7]
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[8]
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引用本文的文献

[1]
Biomarker Discovery in Wilson's Disease-A Path Toward Improved Diagnosis and Management: A Comprehensive Review.

Mol Neurobiol. 2025-6-18

[2]
Effect of primary copper metabolism disturbance on elemental, protein, and lipid composition of the organs in Jackson toxic milk mouse.

Biometals. 2025-2

[3]
Non-ceruloplasmin copper and urinary copper in clinically stable Wilson disease: Alignment with recommended targets.

JHEP Rep. 2024-5-6

[4]
The Role of Glia in Wilson's Disease: Clinical, Neuroimaging, Neuropathological and Molecular Perspectives.

Int J Mol Sci. 2024-7-9

[5]
Nano-Mediated Molecular Targeting in Diagnosis and Mitigation of Wilson Disease.

Mol Neurobiol. 2024-7

[6]
Blood Based Biomarkers of Central Nervous System Involvement in Wilson's Disease.

Diagnostics (Basel). 2023-4-26

[7]
Brain microstructural abnormalities in patients with Wilson's disease: A systematic review of diffusion tenor imaging studies.

Brain Imaging Behav. 2022-12

[8]
Serum neurofilament light chain and initial severity of neurological disease predict the early neurological deterioration in Wilson's disease.

Acta Neurol Belg. 2023-6

[9]
The Role of Zinc in the Treatment of Wilson's Disease.

Int J Mol Sci. 2022-8-18

[10]
The 2022 Lady Estelle Wolfson lectureship on neurofilaments.

J Neurochem. 2022-11

本文引用的文献

[1]
Biological and clinical characteristics of gene carriers far from predicted onset in the Huntington's disease Young Adult Study (HD-YAS): a cross-sectional analysis.

Lancet Neurol. 2020-5-26

[2]
Biomarkers for diagnosis of Wilson's disease.

Cochrane Database Syst Rev. 2019-11-19

[3]
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study.

Lancet Neurol. 2019-12

[4]
Targeting Higher Levels of Tau Protein in Ukrainian Patients with Wilson's Disease.

Neurol Ther. 2019-6

[5]
Neurofilaments as biomarkers in neurological disorders.

Nat Rev Neurol. 2018-10

[6]
Peripheral blood neurofilament light chain levels: the neurologist's C-reactive protein?

Brain. 2018-8-1

[7]
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BMC Neurol. 2018-4-5

[8]
Exchangeable copper: a reflection of the neurological severity in Wilson's disease.

Eur J Neurol. 2017-1

[9]
Long-term metabolic correction of Wilson's disease in a murine model by gene therapy.

J Hepatol. 2016-2

[10]
Early neurological worsening in patients with Wilson's disease.

J Neurol Sci. 2015-8-15

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