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肌萎缩侧索硬化症的命名和诊断概述。

Overview of nomenclature and diagnosis of amyotrophic lateral sclerosis.

机构信息

Department of Neurology, Jiangxi Provincial People's Hospital, Clinical College of Nanchang Medical College, First Affiliated Hospital of Nanchang Medical College, National Regional Medical Center for Neurological Diseases, Xiangya Hospital of Central South University Jiangxi Hospital, Nanchang, Jiangxi, China.

出版信息

Ann Med. 2024 Dec;56(1):2422572. doi: 10.1080/07853890.2024.2422572. Epub 2024 Oct 29.

DOI:10.1080/07853890.2024.2422572
PMID:39470153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11523246/
Abstract

The nomenclature of amyotrophic lateral sclerosis (ALS) currently is blurred, indistinct and no accurate and haven't been properly updated since the first description, which is far from being suitable for the current implementation of clinical practise and scientific research of ALS, and urgently need an solution. Furthermore, the current diagnostic criteria need also further been improved, because the current clinical diagnosis of ALS majorly depends on the clinical manifestations yet. Up to now, no any objective clinical auxiliary examination can be helpful to diagnose ALS besides the electromyogram identifying the lower motor neuron damage, which isn't conducive to early diagnosis and prolongs the time of ALS confirmed diagnosis. In this mini review, we discussed the current doubt about the nomenclature and diagnostic criteria of ALS, and prospected in order to further improve and normalize the nomenclature and diagnosis of ALS.

摘要

肌萎缩侧索硬化症(ALS)的命名目前较为模糊、不明确,且自首次描述以来一直没有得到准确更新,远不能适应目前 ALS 的临床实践和科学研究,急需解决。此外,目前的诊断标准也需要进一步改进,因为目前 ALS 的临床诊断主要依赖于临床表现。迄今为止,除了肌电图识别下运动神经元损伤外,没有任何客观的临床辅助检查有助于诊断 ALS,这不利于早期诊断,延长了 ALS 确诊的时间。在这篇综述中,我们讨论了目前对 ALS 命名和诊断标准的质疑,并展望了进一步完善和规范 ALS 命名和诊断的方向。

相似文献

1
Overview of nomenclature and diagnosis of amyotrophic lateral sclerosis.肌萎缩侧索硬化症的命名和诊断概述。
Ann Med. 2024 Dec;56(1):2422572. doi: 10.1080/07853890.2024.2422572. Epub 2024 Oct 29.
2
A review of electrophysiological studies of lower motor neuron involvement in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中运动神经元受累的电生理学研究综述。
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[Objective markers for upper motor neuron involvement in amyotrophic lateral sclerosis].[肌萎缩侧索硬化症上运动神经元受累的客观标志物]
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From suspicion to diagnosis: exploration strategy for suspected amyotrophic lateral sclerosis.从怀疑到诊断:疑似肌萎缩侧索硬化症的探索性诊断策略。
Ann Med. 2024 Dec;56(1):2398199. doi: 10.1080/07853890.2024.2398199. Epub 2024 Sep 5.
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Medical technology assessment. Electrodiagnosis in motor neuron diseases and amyotrophic lateral sclerosis.医学技术评估。运动神经元疾病和肌萎缩侧索硬化症的电诊断
Neurophysiol Clin. 2001 Oct;31(5):341-8. doi: 10.1016/s0987-7053(01)00272-6.
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Motor unit number estimation as a complementary test to routine electromyography in the diagnosis of amyotrophic lateral sclerosis.运动单位数量估计作为肌萎缩侧索硬化症诊断中常规肌电图的补充检查。
J Electromyogr Kinesiol. 2016 Feb;26:60-5. doi: 10.1016/j.jelekin.2015.11.001. Epub 2015 Nov 11.

本文引用的文献

1
Clinical and genetic factors affecting diagnostic timeline of amyotrophic lateral sclerosis: a 15-year retrospective study.影响肌萎缩侧索硬化症诊断时间线的临床和遗传因素:一项长达 15 年的回顾性研究。
Neurol Res. 2024 Sep;46(9):859-867. doi: 10.1080/01616412.2024.2362578. Epub 2024 Jun 2.
2
In Vitro Models of Amyotrophic Lateral Sclerosis.体外肌萎缩侧索硬化症模型。
Cell Mol Neurobiol. 2023 Nov;43(8):3783-3799. doi: 10.1007/s10571-023-01423-8. Epub 2023 Oct 23.
3
Neuropsychological impairment in amyotrophic lateral sclerosis-frontotemporal spectrum disorder.
肌萎缩侧索硬化-额颞叶变性的神经心理学损害。
Nat Rev Neurol. 2023 Nov;19(11):655-667. doi: 10.1038/s41582-023-00878-z. Epub 2023 Oct 12.
4
Pathogenesis underlying hexanucleotide repeat expansions in gene in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中基因六核苷酸重复扩展的发病机制。
Rev Neurosci. 2023 Aug 2;35(1):85-97. doi: 10.1515/revneuro-2023-0060. Print 2024 Jan 29.
5
Cognitive and behavioral involvement in ALS has been known for more than a century.肌萎缩侧索硬化症的认知和行为参与已经有一个多世纪的历史了。
Neurol Sci. 2022 Dec;43(12):6741-6760. doi: 10.1007/s10072-022-06340-0. Epub 2022 Sep 2.
6
A multivariate Bayesian classification algorithm for cerebral stage prediction by diffusion tensor imaging in amyotrophic lateral sclerosis.基于弥散张量成像的多变量贝叶斯分类算法在肌萎缩侧索硬化症中的脑分期预测。
Neuroimage Clin. 2022;35:103094. doi: 10.1016/j.nicl.2022.103094. Epub 2022 Jun 21.
7
Recent advances in the diagnosis and prognosis of amyotrophic lateral sclerosis.肌萎缩侧索硬化症诊断与预后的最新进展
Lancet Neurol. 2022 May;21(5):480-493. doi: 10.1016/S1474-4422(21)00465-8. Epub 2022 Mar 22.
8
Neuromuscular Junction Dysfunction in Amyotrophic Lateral Sclerosis.肌萎缩侧索硬化症中的神经肌肉接头功能障碍。
Mol Neurobiol. 2022 Mar;59(3):1502-1527. doi: 10.1007/s12035-021-02658-6. Epub 2022 Jan 8.
9
Diagnostic criteria of ALS. Are the gold coast criteria the ultimate solution?
Clin Neurophysiol. 2021 Dec;132(12):3177-3178. doi: 10.1016/j.clinph.2021.09.001. Epub 2021 Sep 24.
10
Diagnostic Utility of Gold Coast Criteria in Amyotrophic Lateral Sclerosis.黄金海岸标准在肌萎缩侧索硬化症中的诊断效用。
Ann Neurol. 2021 May;89(5):979-986. doi: 10.1002/ana.26045. Epub 2021 Feb 24.