Biomarkers for Alzheimer's disease-preparing for a new era of disease-modifying therapies

被引:251
作者
Zetterberg, Henrik [1 ,2 ,3 ,4 ]
Bendlin, Barbara B. [5 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Molndal, Sweden
[2] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[3] UCL Inst Neurol, Dept Neurodegenerat Dis, Queen Sq, London, England
[4] UCL, UK Dementia Res Inst, London, England
[5] Univ Wisconsin Madison, Univ Wisconsin Sch Med & Publ Hlth, Wisconsin Alzheimers Dis Res Ctr, Madison, WI 53706 USA
基金
欧洲研究理事会; 瑞典研究理事会; 英国医学研究理事会;
关键词
CEREBROSPINAL-FLUID LEVELS; AMYLOID-BETA; SYNAPTIC PROTEIN; BRAIN; TAU; PLASMA; NEUROGRANIN; DIAGNOSIS; CSF; ATROPHY;
D O I
10.1038/s41380-020-0721-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Clinical trial results presented in 2019 suggest that antibody-based removal of cerebral amyloid beta (A beta) plaques may possibly clear tau tangles and modestly slow cognitive decline in symptomatic Alzheimer's disease (AD). Although regulatory approval of this approach is still pending, preparing the healthcare system for the advent of disease-modifying therapies against AD is imperative. In particular, it will be necessary to identify the most suitable biomarkers to facilitate appropriate treatment of AD. Here, we give an update on recent developments in fluid and imaging biomarkers for AD-related pathologies and discuss potential approaches that could be adopted to screen for and clarify the underlying pathology in people seeking medical advice because of cognitive symptoms. We succinctly review recent data regarding biomarkers for A beta and tau pathology, neurodegeneration, synaptic dysfunction, and inflammation, highlight the need for further research into common copathologies, and suggest how different biomarkers could be used (most likely in combination) to facilitate the development and clinical implementation of novel drug candidates against AD.
引用
收藏
页码:296 / 308
页数:13
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