Bakkar Nadine, Boehringer Ashley, Bowser Robert
Divisions of Neurology and Neurobiology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ 85013, USA.
Divisions of Neurology and Neurobiology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ 85013, USA.
Brain Res. 2015 May 14;1607:94-107. doi: 10.1016/j.brainres.2014.10.031. Epub 2014 Oct 24.
The past decade has seen a dramatic increase in the discovery of candidate biomarkers for ALS. These biomarkers typically can either differentiate ALS from control subjects or predict disease course (slow versus fast progression). At the same time, late-stage clinical trials for ALS have failed to generate improved drug treatments for ALS patients. Incorporation of biomarkers into the ALS drug development pipeline and the use of biologic and/or imaging biomarkers in early- and late-stage ALS clinical trials have been absent and only recently pursued in early-phase clinical trials. Further clinical research studies are needed to validate biomarkers for disease progression and develop biomarkers that can help determine that a drug has reached its target within the central nervous system. In this review we summarize recent progress in biomarkers across ALS model systems and patient population, and highlight continued research directions for biomarkers that stratify the patient population to enrich for patients that may best respond to a drug candidate, monitor disease progression and track drug responses in clinical trials. It is crucial that we further develop and validate ALS biomarkers and incorporate these biomarkers into the ALS drug development process. This article is part of a Special Issue entitled ALS complex pathogenesis.
在过去十年中,肌萎缩侧索硬化症(ALS)候选生物标志物的发现急剧增加。这些生物标志物通常能够将ALS患者与对照受试者区分开来,或者预测疾病进程(缓慢进展与快速进展)。与此同时,ALS的晚期临床试验未能为ALS患者带来更好的药物治疗。生物标志物尚未纳入ALS药物研发流程,在ALS早期和晚期临床试验中也未使用生物和/或成像生物标志物,直到最近才在早期临床试验中有所探索。需要进一步开展临床研究,以验证用于疾病进展的生物标志物,并开发能够帮助确定药物是否已作用于中枢神经系统靶点的生物标志物。在本综述中,我们总结了ALS模型系统和患者群体中生物标志物的最新进展,并强调了生物标志物的持续研究方向,这些生物标志物可对患者群体进行分层,以富集可能对候选药物反应最佳的患者,监测疾病进展并在临床试验中跟踪药物反应。进一步开发和验证ALS生物标志物并将这些生物标志物纳入ALS药物研发过程至关重要。本文是名为“ALS复杂发病机制”的特刊的一部分。