Suppr超能文献

神经丝蛋白在肌萎缩侧索硬化症中的当前应用及未来展望。

Current application of neurofilaments in amyotrophic lateral sclerosis and future perspectives.

作者信息

Falzone Yuri Matteo, Russo Tommaso, Domi Teuta, Pozzi Laura, Quattrini Angelo, Filippi Massimo, Riva Nilo

机构信息

Neuropathology Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute; Neurology and Neurorehabilitation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Neuropathology Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.

出版信息

Neural Regen Res. 2021 Oct;16(10):1985-1991. doi: 10.4103/1673-5374.308072.

Abstract

Motor neuron disease includes a heterogeneous group of relentless progressive neurological disorders defined and characterized by the degeneration of motor neurons. Amyotrophic lateral sclerosis is the most common and aggressive form of motor neuron disease with no effective treatment so far. Unfortunately, diagnostic and prognostic biomarkers are lacking in clinical practice. Neurofilaments are fundamental structural components of the axons and neurofilament light chain and phosphorylated neurofilament heavy chain can be measured in both cerebrospinal fluid and serum. Neurofilament light chain and phosphorylated neurofilament heavy chain levels are elevated in amyotrophic lateral sclerosis, reflecting the extensive damage of motor neurons and axons. Hence, neurofilaments are now increasingly recognized as the most promising candidate biomarker in amyotrophic lateral sclerosis. The potential usefulness of neurofilaments regards various aspects, including diagnosis, prognosis, patient stratification in clinical trials and evaluation of treatment response. In this review paper, we review the body of literature about neurofilaments measurement in amyotrophic lateral sclerosis. We also discuss the open issues concerning the use of neurofilaments clinical practice, as no overall guideline exists to date; finally, we address the most recent evidence and future perspectives.

摘要

运动神经元病包括一组异质性的、持续进展的神经系统疾病,其定义和特征为运动神经元的变性。肌萎缩侧索硬化症是运动神经元病最常见且进展迅速的形式,目前尚无有效治疗方法。不幸的是,临床实践中缺乏诊断和预后生物标志物。神经丝是轴突的基本结构成分,神经丝轻链和磷酸化神经丝重链可在脑脊液和血清中检测到。肌萎缩侧索硬化症患者的神经丝轻链和磷酸化神经丝重链水平升高,反映了运动神经元和轴突的广泛损伤。因此,神经丝现在越来越被认为是肌萎缩侧索硬化症中最有前景的候选生物标志物。神经丝的潜在用途涉及多个方面,包括诊断、预后、临床试验中的患者分层以及治疗反应评估。在这篇综述文章中,我们回顾了有关肌萎缩侧索硬化症中神经丝测量的文献。我们还讨论了神经丝在临床实践中使用的未决问题,因为迄今为止尚无总体指南;最后,我们阐述了最新证据和未来展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eadb/8343335/a822335eaad6/NRR-16-1985-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验