医学
生物标志物发现
疾病
临床试验
精密医学
鉴定(生物学)
生物标志物
药物开发
生物信息学
重症监护医学
病理
蛋白质组学
药理学
基因
生物
化学
植物
生物化学
药品
作者
Harald Hampel,Sid E. O’Bryant,José Luís Molinuevo,Henrik Zetterberg,Colin L. Masters,Simone Lista,Steven J. Kiddle,Richard Batrla,Kaj Blennow
标识
DOI:10.1038/s41582-018-0079-7
摘要
Biomarker discovery and development for clinical research, diagnostics and therapy monitoring in clinical trials have advanced rapidly in key areas of medicine - most notably, oncology and cardiovascular diseases - allowing rapid early detection and supporting the evolution of biomarker-guided, precision-medicine-based targeted therapies. In Alzheimer disease (AD), breakthroughs in biomarker identification and validation include cerebrospinal fluid and PET markers of amyloid-β and tau proteins, which are highly accurate in detecting the presence of AD-associated pathophysiological and neuropathological changes. However, the high cost, insufficient accessibility and/or invasiveness of these assays limit their use as viable first-line tools for detecting patterns of pathophysiology. Therefore, a multistage, tiered approach is needed, prioritizing development of an initial screen to exclude from these tests the high numbers of people with cognitive deficits who do not demonstrate evidence of underlying AD pathophysiology. This Review summarizes the efforts of an international working group that aimed to survey the current landscape of blood-based AD biomarkers and outlines operational steps for an effective academic-industry co-development pathway from identification and assay development to validation for clinical use.
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