认知障碍和痴呆中的视网膜生物标志物:结构、功能和分子见解

IF 11.1 1区 医学 Q1 CLINICAL NEUROLOGY
Yan Min, Hongyu Zhou, Zixiao Li, Yongjun Wang
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引用次数: 0

摘要

认知障碍和痴呆症,包括阿尔茨海默病(AD),构成全球健康危机,需要非侵入性生物标志物进行早期检测。这篇综述强调了视网膜作为中枢神经系统(CNS)的可及延伸部分,通过结构、功能和分子改变作为大脑病理的窗口。通过综合跨学科的证据,我们确定视网膜生物标志物作为早期诊断和风险分层的有前途的工具。然而,将生物标志物转化为临床实践面临着重大的翻译障碍,包括方法学的异质性、混淆变量、缺乏标准化的协议,以及在不同人群中的纵向验证不足。通过严格的标准化和强有力的验证研究来克服这些挑战对于建立视网膜生物标志物的临床应用至关重要。突出阶段特异性诊断潜力:视网膜生物标志物(如OCT/OCTA变化,眼球运动,分子沉积)显示与认知障碍阶段(临床前AD到痴呆)相关的改变,有助于阶段区分。反映大脑病理:多模态视网膜改变(结构、功能、分子)与关键脑病理(淀粉样蛋白/tau负担、萎缩、小血管疾病)相关,表明共享通路。翻译差距和未来:临床采用面临障碍(方法异质性、混杂因素、有限的验证)。未来需要严格筛选候选视网膜生物标志物,广泛的多中心验证,以及人工智能(AI)促进的临床翻译。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Retinal biomarkers in cognitive impairment and dementia: Structural, functional, and molecular insights

Retinal biomarkers in cognitive impairment and dementia: Structural, functional, and molecular insights

Retinal biomarkers in cognitive impairment and dementia: Structural, functional, and molecular insights

Retinal biomarkers in cognitive impairment and dementia: Structural, functional, and molecular insights

Retinal biomarkers in cognitive impairment and dementia: Structural, functional, and molecular insights

Cognitive impairment and dementia, including Alzheimer's disease (AD), pose a global health crisis, necessitating non-invasive biomarkers for early detection. This review highlights the retina, an accessible extension of the central nervous system (CNS), as a window to cerebral pathology through structural, functional, and molecular alterations. By synthesizing interdisciplinary evidence, we identify retinal biomarkers as promising tools for early diagnosis and risk stratification. Nevertheless, translating biomarkers into clinical practice faces significant translational hurdles, including methodological heterogeneity, confounding variables, lack of standardized protocols, and insufficient longitudinal validation in diverse populations. Overcoming these challenges through rigorous standardization and robust validation studies is essential to establish the clinical utility of retinal biomarkers.

Highlights

  • Stage-specific diagnostic potential: Retinal biomarkers (e.g., OCT/OCTA changes, eye movements, molecular deposits) show alterations correlating with cognitive impairment stages (preclinical AD to dementia), assisting stage differentiation.
  • Reflecting cerebral pathology: Multimodal retinal alterations (structural, functional, molecular) correlate with key brain pathologies (amyloid/tau burden, atrophy, small vessel disease), indicating shared pathways.
  • Translation gaps and future: Clinical adoption faces barriers (method heterogeneity, confounders, limited validation). Future requires rigorous screening of candidate retinal biomarkers, extensive multicenter validation, and artificial intelligence (AI)-facilitated clinical translation.
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来源期刊
Alzheimer's & Dementia
Alzheimer's & Dementia 医学-临床神经学
CiteScore
14.50
自引率
5.00%
发文量
299
审稿时长
3 months
期刊介绍: Alzheimer's & Dementia is a peer-reviewed journal that aims to bridge knowledge gaps in dementia research by covering the entire spectrum, from basic science to clinical trials to social and behavioral investigations. It provides a platform for rapid communication of new findings and ideas, optimal translation of research into practical applications, increasing knowledge across diverse disciplines for early detection, diagnosis, and intervention, and identifying promising new research directions. In July 2008, Alzheimer's & Dementia was accepted for indexing by MEDLINE, recognizing its scientific merit and contribution to Alzheimer's research.
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