从OCT/OCTA图像诊断痴呆的视网膜生物标志物的系统综述

IF 2.8 Q2 NEUROSCIENCES
Yehia Ibrahim, Jianyang Xie, Antonella Macerollo, Rodolfo Sardone, Yaochun Shen, Vito Romano, Yalin Zheng
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引用次数: 0

摘要

背景:传统的痴呆症诊断方法昂贵、耗时,而且有一定的侵入性。由于视网膜与大脑具有显著的解剖相似性,通过光学相干断层扫描(OCT)和OCT血管造影(OCTA)检测视网膜异常已被研究作为神经退行性疾病的潜在非侵入性诊断工具;然而,最有效的视网膜改变在这篇综述中仍然是一个谜。目的:探讨OCT/OCTA图像视网膜异常与认知能力下降的关系,评价生物标志物在神经退行性疾病检测中的有效性。方法:在PubMed、Web of Science和Scopus上进行系统检索,直到2022年12月,使用商定的搜索关键词和纳入/排除标准获得64篇论文。结果:上乳头状周围视网膜神经纤维层(pRNFL)是识别大多数阿尔茨海默病(AD)的可靠生物标志物;然而,在治疗轻度AD和轻度认知障碍(MCI)时,它是无效的。全球pRNFL (pRNFL- g)是另一个可靠的生物标志物,可区分额颞叶痴呆与轻度AD和健康对照(hc),中度AD和MCI与hcc,以及识别认知健康个体的病理性Aβ42/tau。相反,pRNFL-G不能实现轻度AD和AD的进展。pRNFL平均厚度变化被认为是监测AD进展的可行生物标志物。最后,优越和平均的pRNFL厚度被认为与晚期AD一致,但与早期/轻度AD不一致。结论:视网膜变化可能预示着痴呆,但需要进一步的研究来确认早期和轻度AD最有效的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Systematic Review on Retinal Biomarkers to Diagnose Dementia from OCT/OCTA Images
Background: Traditional methods for diagnosing dementia are costly, time-consuming, and somewhat invasive. Since the retina shares significant anatomical similarities with the brain, retinal abnormalities detected via optical coherence tomography (OCT) and OCT angiography (OCTA) have been studied as a potential non-invasive diagnostic tool for neurodegenerative disorders; however, the most effective retinal changes remain a mystery to be unraveled in this review. Objective: This study aims to explore the relationship between retinal abnormalities in OCT/OCTA images and cognitive decline as well as evaluating biomarkers’ effectiveness in detecting neurodegenerative diseases. Methods: A systematic search was conducted on PubMed, Web of Science, and Scopus until December 2022, resulted in 64 papers using agreed search keywords, and inclusion/exclusion criteria. Results: The superior peripapillary retinal nerve fiber layer (pRNFL) is a trustworthy biomarker to identify most Alzheimer’s disease (AD) cases; however, it is inefficient when dealing with mild AD and mild cognitive impairment (MCI). The global pRNFL (pRNFL-G) is another reliable biomarker to discriminate frontotemporal dementia from mild AD and healthy controls (HCs), moderate AD and MCI from HCs, as well as identifing pathological Aβ42/tau in cognitively healthy individuals. Conversely, pRNFL-G fails to realize mild AD and the progression of AD. The average pRNFL thickness variation is considered a viable biomarker to monitor the progression of AD. Finally, the superior and average pRNFL thicknesses are considered consistent for advanced AD but not for early/mild AD. Conclusions: Retinal changes may indicate dementia, but further research is needed to confirm the most effective biomarkers for early and mild AD.
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