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阿尔茨海默病的视觉特征:从基础机制到临床概述。

Visual Features in Alzheimer's Disease: From Basic Mechanisms to Clinical Overview.

机构信息

Escuela Superior de Oftalmología-Instituto Barraquer de América, Bogotá, Colombia.

Grupo de Investigación en Neurociencias (NeURos), Escuela de Medicina y Ciencias de la Salud, Universidad del Rosario, Bogotá, Colombia.

出版信息

Neural Plast. 2018 Oct 14;2018:2941783. doi: 10.1155/2018/2941783. eCollection 2018.

Abstract

Alzheimer's disease (AD) is the leading cause of dementia worldwide. It compromises patients' daily activities owing to progressive cognitive deterioration, which has elevated direct and indirect costs. Although AD has several risk factors, aging is considered the most important. Unfortunately, clinical diagnosis is usually performed at an advanced disease stage when dementia is established, making implementation of successful therapeutic interventions difficult. Current biomarkers tend to be expensive, insufficient, or invasive, raising the need for novel, improved tools aimed at early disease detection. AD is characterized by brain atrophy due to neuronal and synaptic loss, extracellular amyloid plaques composed of amyloid-beta peptide (A), and neurofibrillary tangles of hyperphosphorylated tau protein. The visual system and central nervous system share many functional components. Thus, it is plausible that damage induced by A, tau, and neuroinflammation may be observed in visual components such as the retina, even at an early disease stage. This underscores the importance of implementing ophthalmological examinations, less invasive and expensive than other biomarkers, as useful measures to assess disease progression and severity in individuals with or at risk of AD. Here, we review functional and morphological changes of the retina and visual pathway in AD from pathophysiological and clinical perspectives.

摘要

阿尔茨海默病(AD)是全球范围内导致痴呆的主要原因。由于认知功能逐渐恶化,患者的日常活动受到影响,这增加了直接和间接的成本。尽管 AD 有几个风险因素,但年龄增长被认为是最重要的因素。不幸的是,临床诊断通常在痴呆症确立的疾病晚期进行,这使得成功的治疗干预措施难以实施。目前的生物标志物往往昂贵、不足或具有侵入性,因此需要新的、改进的工具来早期发现疾病。AD 的特征是由于神经元和突触丧失导致的脑萎缩、由淀粉样β肽(A)组成的细胞外淀粉样斑块,以及过度磷酸化的tau 蛋白组成的神经原纤维缠结。视觉系统和中枢神经系统有许多功能成分。因此,A、tau 和神经炎症引起的损伤可能在视网膜等视觉成分中被观察到,即使在疾病的早期阶段也是如此。这强调了实施眼科检查的重要性,眼科检查比其他生物标志物侵入性更小、成本更低,是评估 AD 患者或有患病风险的个体疾病进展和严重程度的有用措施。在这里,我们从病理生理学和临床角度综述 AD 中视网膜和视觉通路的功能和形态变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f26/6204169/cfe8b819e53b/NP2018-2941783.001.jpg

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