Fluid and imaging biomarkers for Alzheimer's disease: Where we stand and where to head to

被引:37
作者
Henriques, Adriane Dallanora [1 ]
Benedet, Andrea Lessa [2 ]
Camargos, Einstein Francisco [1 ]
Rosa-Neto, Pedro [2 ,3 ]
Nobrega, Otavio Toledo [1 ]
机构
[1] Univ Brasilia UnB, Univ Hosp, Med Ctr Elderly, BR-70910900 Brasilia, DF, Brazil
[2] McGill Univ, Douglas Hosp, Res Ctr Studies Aging, Translat Neuroimaging Lab, Montreal, PQ H4H 1R3, Canada
[3] Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
Alzheimer; Mild cognitive impairment; Biomarker; Cerebrospinal fluid; Diagnosis; Neuroimaging; MILD COGNITIVE IMPAIRMENT; POSITRON-EMISSION-TOMOGRAPHY; BETA-AMYLOID; 1-42; NATIONAL INSTITUTE; CSF BIOMARKERS; NIA-AA; GLUCOSE HYPOMETABOLISM; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; HYPOTHETICAL MODEL;
D O I
10.1016/j.exger.2018.01.002
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
There is increasing evidence that a number of potentially informative biomarkers for Alzheimer disease (AD) can improve the accuracy of diagnosing this form of dementia, especially when used as a panel of diagnostic assays and interpreted in the context of neuroimaging and clinical data. Moreover, by combining the power of CSF biomarkers with neuroimaging techniques to visualize A beta deposits (or neurodegenerative lesions), it might be possible to better identify individuals at greatest risk for developing MCI and converting to AD. The objective of this article was to review recent progress in selected imaging and chemical biomarkers for prediction, early diagnosis and progression of AD. We present our view point of a scenario that places CSF and imaging markers on the verge of general utility based on accuracy levels that already match (or even surpass) current clinical precision.
引用
收藏
页码:169 / 177
页数:9
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