肌萎缩侧索硬化
利鲁唑
医学
SOD1
疾病
重症监护医学
临床试验
运动神经元
梅德林
疾病管理
物理医学与康复
物理疗法
病理
政治学
帕金森病
法学
作者
David O’Brien,Pamela J. Shaw
出处
期刊:British Medical Bulletin
[Oxford University Press]
日期:2024-09-29
摘要
Abstract Introduction Motor neuron disease (MND) is a devastating neurodegenerative disease characterized by progressive muscle weakness. Sources of data PubMed, MEDLINE, and Cochrane databases were searched for articles to March 2024. Searches involved the terms ‘motor neuron disease’ or ‘amyotrophic lateral sclerosis’ and ‘epidemiology’, ‘diagnosis’, ‘clinical’, ‘genetic’, ‘management’, ‘treatment’, or ‘trial’. Areas of agreement Evidence-based management involves riluzole, multidisciplinary care, provision of noninvasive ventilation and gastrostomy, and symptomatic treatments. Tofersen should be offered to treat SOD1-MND. Areas of controversy Edaravone and Relyvrio are approved treatments in the USA, but insufficient evidence was found to support approval in the UK and Europe. Growing points The discovery of neurofilaments as MND biomarkers, growth of platform trials and development of novel therapies provide optimism for more powerful neuroprotective therapies. Areas timely for developing research Further work should focus on the elucidation of environmental causes of MND, gene–environment interactions, and advanced cellular models of disease.
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