Alzheimer's Disease: Biomarkers in the Genome, Blood, and Cerebrospinal Fluid

被引:81
作者
Huynh, Rose Ann [1 ]
Mohan, Chandra [1 ]
机构
[1] Univ Houston, Dept Biomed Engn, Houston, TX 77004 USA
来源
FRONTIERS IN NEUROLOGY | 2017年 / 8卷
关键词
Alzheimer's disease; early detection; genetic biomarkers; neurochemical biomarkers; blood-derived biomarkers; longitudinal studies; PLASMA AMYLOID-BETA; APOLIPOPROTEIN-E; COGNITIVE DECLINE; CLINICAL-TRIALS; A-BETA; PROGNOSTIC BIOMARKER; PREDICTIVE-VALUE; GENETIC RISK; TAU; DIAGNOSIS;
D O I
10.3389/fneur.2017.00102
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disorder that slowly destroys memory and thinking skills, resulting in behavioral changes. It is estimated that nearly 36 million are affected globally with numbers reaching 115 million by 2050. AD can only be definitively diagnosed at autopsy since its manifestations of senile plaques and neurofibrillary tangles throughout the brain cannot yet be fully captured with current imaging technologies. Current AD therapeutics have also been suboptimal. Besides identifying markers that distinguish AD from controls, there has been a recent drive to identify better biomarkers that can predict the rates of cognitive decline and neocortical amyloid burden in those who exhibit preclinical, prodromal, or clinical AD. This review covers biomarkers of three main types: genes, cerebrospinal fluid-derived, and blood-derived biomarkers. Looking ahead, cutting-edge OMICs technologies, including proteomics and metabolomics, ought to be fully tapped in order to mine even better biomarkers for AD that are more predictive.
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页数:15
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