Neuroimaging Biomarkers for Alzheimer's Disease

被引:136
|
作者
Marquez, Freddie [1 ]
Yassa, Michael A. [1 ]
机构
[1] Univ Calif Irvine, Ctr Neurobiol Learning & Memory, Dept Neurobiol & Behav, Irvine, CA 92697 USA
关键词
MILD COGNITIVE IMPAIRMENT; POSITRON-EMISSION-TOMOGRAPHY; MEDIAL TEMPORAL-LOBE; APICAL NEUROPIL ATROPHY; WHITE-MATTER DISRUPTION; ENTORHINAL CORTEX; TRANSLOCATOR PROTEIN; HIPPOCAMPAL ATROPHY; DEFAULT-MODE; AGED RATS;
D O I
10.1186/s13024-019-0325-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Currently, over five million Americans suffer with Alzheimer's disease (AD). In the absence of a cure, this number could increase to 13.8 million by 2050. A critical goal of biomedical research is to establish indicators of AD during the preclinical stage (i.e. biomarkers) allowing for early diagnosis and intervention. Numerous advances have been made in developing biomarkers for AD using neuroimaging approaches. These approaches offer tremendous versatility in terms of targeting distinct age-related and pathophysiological mechanisms such as structural decline (e.g. volumetry, cortical thinning), functional decline (e.g. fMRI activity, network correlations), connectivity decline (e.g. diffusion anisotropy), and pathological aggregates (e.g. amyloid and tau PET). In this review, we survey the state of the literature on neuroimaging approaches to developing novel biomarkers for the amnestic form of AD, with an emphasis on combining approaches into multimodal biomarkers. We also discuss emerging methods including imaging epigenetics, neuroinflammation, and synaptic integrity using PET tracers. Finally, we review the complementary information that neuroimaging biomarkers provide, which highlights the potential utility of composite biomarkers as suitable outcome measures for proof-of-concept clinical trials with experimental therapeutics.
引用
收藏
页数:14
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