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视网膜生物标志物在早发型阿尔茨海默病中的诊断和预后潜力

Diagnostic and Prognostic Potential of Retinal Biomarkers in Early On-Set Alzheimer's Disease.

作者信息

Shariflou Sahar, Georgevsky Dana, Mansour Hussein, Rezaeian Mahdie, Hosseini Nafiseh, Gani Fathima, Gupta Vivek, Braidy Nady, Golzan S Mojtaba

机构信息

Vision Science Group, Graduate School of Health (Orthoptics Discipline), University of Technology Sydney, Sydney. Australia.

Department of Clinical Medicine, Faculty of Medicine and Health Sciences, Macquarie University. Australia.

出版信息

Curr Alzheimer Res. 2017;14(9):1000-1007. doi: 10.2174/1567205014666170329114445.

Abstract

OBJECTIVE

Accumulating evidence suggests that the eye can be used in the assessment of early on-set Alzheimer's disease (AD). The eye offers a natural window to the brain through the retina. The retina and brain share common developmental origins and patho-physiological origins and mechanisms, having been sequestered from it during early development, but retaining its connections with the brain via the optic nerve. Therefore, it is well understood that neurological abnormalities have a direct profound impact on the retina. Recent studies suggest an array of physiological and pathological changes in the retina in dementia and specifically in AD. There are also reports on imaging the two hallmark proteins of the disease, extracellular amyloid beta peptides and intracellular hyper phosphorylated tau protein, as a proxy to neuroimaging.

RESULTS

In this review, we summarise retinal structural, functional and vascular changes reported to be associated with AD. We also review techniques employed to image these two major hall mark proteins of AD and their relevance for early detection of AD.

摘要

目的

越来越多的证据表明,眼睛可用于早期阿尔茨海默病(AD)的评估。眼睛通过视网膜为大脑提供了一个天然窗口。视网膜与大脑有着共同的发育起源以及病理生理起源和机制,在早期发育过程中从大脑分离出来,但通过视神经与大脑保持联系。因此,人们清楚地知道神经异常会对视网膜产生直接而深远的影响。最近的研究表明,痴呆症尤其是AD患者的视网膜存在一系列生理和病理变化。也有报道称,可对该疾病的两种标志性蛋白——细胞外淀粉样β肽和细胞内过度磷酸化的tau蛋白进行成像,以此作为神经成像的替代方法。

结果

在本综述中,我们总结了据报道与AD相关的视网膜结构、功能和血管变化。我们还回顾了用于对AD的这两种主要标志性蛋白进行成像的技术及其与AD早期检测的相关性。

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