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肌萎缩侧索硬化症的液体生物标志物:综述。

Fluid biomarkers for amyotrophic lateral sclerosis: a review.

机构信息

Department of Pathology, Johns Hopkins Medicine, Baltimore, MD, 21205, USA.

Department of Neuroscience, Johns Hopkins Medicine, Baltimore, MD, 21205, USA.

出版信息

Mol Neurodegener. 2024 Jan 24;19(1):9. doi: 10.1186/s13024-023-00685-6.


DOI:10.1186/s13024-023-00685-6
PMID:38267984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10809579/
Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the loss of upper and lower motor neurons. Presently, three FDA-approved drugs are available to help slow functional decline for patients with ALS, but no cure yet exists. With an average life expectancy of only two to five years after diagnosis, there is a clear need for biomarkers to improve the care of patients with ALS and to expedite ALS treatment development. Here, we provide a review of the efforts made towards identifying diagnostic, prognostic, susceptibility/risk, and response fluid biomarkers with the intent to facilitate a more rapid and accurate ALS diagnosis, to better predict prognosis, to improve clinical trial design, and to inform interpretation of clinical trial results. Over the course of 20 + years, several promising fluid biomarker candidates for ALS have emerged. These will be discussed, as will the exciting new strategies being explored for ALS biomarker discovery and development.

摘要

肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病,其特征是上下运动神经元的丧失。目前,有三种经美国食品和药物管理局批准的药物可用于帮助减缓 ALS 患者的功能下降,但尚无治愈方法。从诊断到死亡的平均预期寿命仅为 2 到 5 年,因此非常需要生物标志物来改善 ALS 患者的护理,并加速 ALS 治疗的发展。在这里,我们回顾了在识别诊断、预后、易感性/风险和反应液生物标志物方面所做的努力,旨在促进更快速和准确的 ALS 诊断,更好地预测预后,改进临床试验设计,并为临床试验结果的解释提供信息。在 20 多年的时间里,已经出现了几个有前途的 ALS 液体生物标志物候选物。本文将讨论这些候选物,以及正在探索的用于 ALS 生物标志物发现和开发的令人兴奋的新策略。

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Acta Neuropathol Commun. 2025-9-2

[2]
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[3]
The metabolic intersection between immunosenescence and neuroinflammation in amyotrophic lateral sclerosis.

J Inflamm (Lond). 2025-8-27

[4]
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosis.

Nat Med. 2025-8-19

[5]
The emerging role of cellular senescence in amyotrophic lateral sclerosis.

Front Neurosci. 2025-8-1

[6]
Large-scale RNA-Seq mining reveals ciclopirox olamine induces TDP-43 cryptic exons.

Nat Commun. 2025-7-25

[7]
Inhibition of nonsense-mediated decay in TDP-43 deficient neurons reveals novel cryptic exons.

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[8]
Emerging biomarkers in amyotrophic lateral sclerosis: from pathogenesis to clinical applications.

Front Mol Biosci. 2025-6-30

[9]
Biomarkers and therapeutic strategies targeting microglia in neurodegenerative diseases: current status and future directions.

Mol Neurodegener. 2025-7-10

[10]
Plasma proteomics links brain and immune system aging with healthspan and longevity.

Nat Med. 2025-7-9

本文引用的文献

[1]
Mis-spliced transcripts generate de novo proteins in TDP-43-related ALS/FTD.

Sci Transl Med. 2024-2-14

[2]
Advances in molecular pathology, diagnosis, and treatment of amyotrophic lateral sclerosis.

BMJ. 2023-10-27

[3]
Cerebrospinal fluid proteomics define the natural history of autosomal dominant Alzheimer's disease.

Nat Med. 2023-8

[4]
Chitinase dysregulation predicts disease aggressiveness in ALS: Insights from the D50 progression model.

J Neurol Neurosurg Psychiatry. 2023-7

[5]
Diffusion Tensor Imaging in Amyotrophic Lateral Sclerosis: Machine Learning for Biomarker Development.

Int J Mol Sci. 2023-1-18

[6]
Systematic review and meta-analysis on microRNAs in amyotrophic lateral sclerosis.

Brain Res Bull. 2023-3

[7]
Extracellular Vesicles in Amyotrophic Lateral Sclerosis.

Life (Basel). 2022-12-31

[8]
Inflammatory checkpoints in amyotrophic lateral sclerosis: From biomarkers to therapeutic targets.

Front Immunol. 2022

[9]
Neurofilament light chain in drug development for amyotrophic lateral sclerosis: a critical appraisal.

Brain. 2023-7-3

[10]
Amyotrophic Lateral Sclerosis Clinical Trials and Interpretation of Functional End Points and Fluid Biomarkers: A Review.

JAMA Neurol. 2022-12-1

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