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Role of Retinal Amyloid-β in Neurodegenerative Diseases: Overlapping Mechanisms and Emerging Clinical Applications

机译:视网膜淀粉样蛋白-β在神经变性疾病中的作用:重叠机制和新兴临床应用

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摘要

Amyloid-β (Aβ) accumulations have been identified in the retina for neurodegeneration-associated disorders like Alzheimer’s disease (AD), glaucoma, and age-related macular degeneration (AMD). Elevated retinal Aβ levels were associated with progressive retinal neurodegeneration, elevated cerebral Aβ accumulation, and increased disease severity with a decline in cognition and vision. Retinal Aβ accumulation and its pathological effects were demonstrated to occur prior to irreversible neurodegeneration, which highlights its potential in early disease detection and intervention. Using the retina as a model of the brain, recent studies have focused on characterizing retinal Aβ to determine its applicability for population-based screening of AD, which warrants a further understanding of how Aβ manifests between these disorders. While current treatments directly targeting Aβ accumulations have had limited results, continued exploration of Aβ-associated pathological pathways may yield new therapeutic targets for preserving cognition and vision. Here, we provide a review on the role of retinal Aβ manifestations in these distinct neurodegeneration-associated disorders. We also discuss the recent applications of retinal Aβ for AD screening and current clinical trial outcomes for Aβ-associated treatment approaches. Lastly, we explore potential future therapeutic targets based on overlapping mechanisms of pathophysiology in AD, glaucoma, and AMD.
机译:淀粉样蛋白-β(Aβ)累积已在视网膜中鉴定为患有阿尔茨海默病(Ad),青光眼和年龄相关的黄斑变性(AMD)的神经变性相关疾病的视网膜。视网膜Aβ水平升高与渐进式视网膜神经变性,脑Aβ积累升高,疾病严重程度增加,具有认知和视力下降。视网膜Aβ积累及其病理学效应被证明在不可逆神经变性之前发生,这突出了其早期疾病检测和干预的潜力。使用视网膜作为大脑的模型,最近的研究侧重于表征视网膜Aβ,以确定其对广告的基于人口的筛查适用性,这是进一步了解这些疾病之间的Aβ如何表现如何。虽然目前直接靶向Aβ累积的治疗具有有限的结果,但持续探索Aβ相关的病理途径可以产生新的治疗目标,以保护认知和视觉。在这里,我们对这些不同神经变性相关疾病中视网膜Aβ表现的作用提供了综述。我们还讨论了视网膜Aβ的最近应用于AD筛选和目前用于Aβ相关治疗方法的临床试验结果。最后,我们根据广告,青光眼和AMD的病理生理学重叠机制探索潜在的未来治疗目标。

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