生物标志物
疾病
淀粉样蛋白(真菌学)
阿尔茨海默病
β淀粉样蛋白
血清淀粉样蛋白A
痴呆
淀粉样β
生物标志物发现
载脂蛋白E
病理
特雷姆2
老年斑
脑淀粉样血管病
神经退行性变
作者
Andreas Nabers,Laura Perna,Julia Lange,Ute Mons,Jonas Schartner,Jörn Güldenhaupt,Kai Uwe Saum,Shorena Janelidze,Bernd Holleczek,Dan Rujescu,Oskar Hansson,Klaus Gerwert,Hermann Brenner
标识
DOI:10.15252/emmm.201708763
摘要
Alzheimer's disease (AD) is currently incurable, but there is general agreement that a minimally invasive blood biomarker for screening in preclinical stages would be crucial for future therapy. Diagnostic tools for detection of AD are either invasive like cerebrospinal fluid (CSF) biomarkers or expensive such as positron emission tomography (PET) scanning. Here, we determine the secondary structure change of amyloid-β (Aβ) in human blood. This change used as blood amyloid biomarker indicates prodromal AD and correlates with CSF AD biomarkers and amyloid PET imaging in the cross-sectional BioFINDER cohort. In a further population-based longitudinal cohort (ESTHER), the blood biomarker detected AD several years before clinical diagnosis in baseline samples with a positive likelihood ratio of 7.9; that is, those who were diagnosed with AD over the years were 7.9 times more likely to test positive. This assay may open avenues for blood screening of early AD stages as a funnel for further more invasive and expensive tests.
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