生命银行
神经化学
肌萎缩侧索硬化
医学
神经科学
疾病
临床试验
生物信息学
病理
心理学
生物
作者
Markus Otto,Robert Bowser,Martin R. Turner,James Berry,Johannes Brettschneider,James R. Connor,Júlia Costa,Merit Cudkowicz,Jonathan D. Glass,Olaf Jahn,Stefan Lehnert,Andrea Malaspina,Lucilla Parnetti,Axel Petzold,Pamela J. Shaw,Alexander Sherman,Petra Steinacker,Sigurd D. Süßmuth,Charlotte E. Teunissen,Hayrettin Tumani,Anna Wuolikainen,Albert C. Ludolph
标识
DOI:10.3109/17482968.2011.627589
摘要
Despite major advances in deciphering the neuropathological hallmarks of amyotrophic lateral sclerosis (ALS), validated neurochemical biomarkers for monitoring disease activity, earlier diagnosis, defining prognosis and unlocking key pathophysiological pathways are lacking. Although several candidate biomarkers exist, translation into clinical application is hindered by small sample numbers, especially longitudinal, for independent verification. This review considers the potential routes to the discovery of neurochemical markers in ALS, and provides a consensus statement on standard operating procedures that will facilitate multicenter collaboration, validation and ultimately clinical translation.
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