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延迟的视杆介导暗适应与年龄相关性黄斑变性的发病率及早期进展相关:阿拉巴马州早期年龄相关性黄斑变性研究2

Delayed Rod-Mediated Dark Adaptation Is Associated with Incidence and Early Progression of Age-Related Macular Degeneration: Alabama Study on Early Age-Related Macular Degeneration 2.

作者信息

Owsley Cynthia, McGwin Gerald, Clark Mark E, Gao Liyan, Gooden Lindsay, Thomas Tracy N, Goerdt Lukas, Curcio Christine A

机构信息

Department of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Birmingham, Alabama.

Department of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Birmingham, Alabama; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama.

出版信息

Ophthalmology. 2025 Jun 16. doi: 10.1016/j.ophtha.2025.06.013.


DOI:10.1016/j.ophtha.2025.06.013
PMID:40532855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12377478/
Abstract

PURPOSE: To examine whether delayed rod-mediated dark adaptation (RMDA) in healthy older eyes and those with early age-related macular degeneration (AMD) is associated with AMD incidence and progression at follow-up, as compared with other visual functions reliant on rods, cones, or mixed rod-cone mediation. DESIGN: Longitudinal study over 3 years. PARTICIPANTS: Eyes from adults ≥60 years of age with normal macular health or with early AMD at baseline. METHODS: At baseline, eyes underwent fundus photography to establish AMD presence and severity using the Age-Related Eye Disease Study (AREDS) 9-step classification system. The following visual functions were tested in 1 eye at baseline (the study eye): RMDA, scotopic sensitivity, low-luminance acuity, mesopic contrast sensitivity, mesopic light sensitivity, visual acuity, and contrast sensitivity. Three years later at follow-up, fundus photography and the AREDS classification were repeated. Age-adjusted relative risks and 95% confidence intervals measured the association between visual functions and AMD incidence and progression for the study eye and the fellow eye at follow-up. MAIN OUTCOME MEASURES: Presence and severity of AMD at the 3-year follow-up visit in the study and fellow eyes. RESULTS: Healthy older eyes at baseline with delayed RMDA were 3.54 or 3.40 times more likely to have incident AMD at the 3-year follow-up in the study eye and the fellow eye, respectively, compared with eyes without delays. No other visual functions were associated with AMD incidence, except for low-luminance visual acuity in the study eye. Eyes with early AMD at baseline with delayed RMDA were 3.89 or 2.65 times more likely to have progressed at follow-up for the study and fellow eye, respectively. No other visual functions were associated with AMD progression at follow-up. CONCLUSIONS: Rod-mediated dark adaptation is the only visual function of those tested that was associated with AMD incidence and progression over 3 years in healthy eyes or those with early AMD at baseline. Our results suggest that other visual functions are not useful for understanding AMD incidence and early progression risk. Interventions that eventually are designed to arrest early AMD progression or preventative measures in those at risk should consider RMDA a functional outcome measure. FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的:与其他依赖视杆细胞、视锥细胞或混合视杆-视锥细胞介导的视觉功能相比,研究健康老年眼和早期年龄相关性黄斑变性(AMD)患者的延迟视杆细胞介导的暗适应(RMDA)是否与随访时AMD的发病率和进展相关。 设计:为期3年的纵向研究。 参与者:≥60岁的成年人的眼睛,基线时黄斑健康正常或患有早期AMD。 方法:在基线时,对眼睛进行眼底照相,使用年龄相关性眼病研究(AREDS)9级分类系统确定AMD的存在和严重程度。在基线时对1只眼睛(研究眼)进行以下视觉功能测试:RMDA、暗视敏感度、低亮度视力、中间视觉对比敏感度、中间视觉光敏感度、视力和对比敏感度。3年后随访时,重复进行眼底照相和AREDS分类。年龄调整后的相对风险和95%置信区间测量了研究眼和随访时对侧眼的视觉功能与AMD发病率和进展之间的关联。 主要观察指标:研究眼和对侧眼在3年随访时AMD的存在和严重程度。 结果:与无延迟的眼睛相比,基线时RMDA延迟的健康老年眼在研究眼和对侧眼中发生AMD的可能性分别为3.54倍或3.40倍。除研究眼中的低亮度视力外,没有其他视觉功能与AMD发病率相关。基线时患有早期AMD且RMDA延迟的眼睛在随访时研究眼和对侧眼进展的可能性分别为3.89倍或2.65倍。随访时没有其他视觉功能与AMD进展相关。 结论:视杆细胞介导的暗适应是所测试的视觉功能中唯一与健康眼或基线时患有早期AMD的眼睛在3年内AMD发病率和进展相关的功能。我们的结果表明,其他视觉功能对于理解AMD发病率和早期进展风险没有帮助。最终旨在阻止早期AMD进展的干预措施或针对高危人群的预防措施应将RMDA视为一种功能结局指标。 财务披露:在本文末尾的脚注和披露中可能会发现专有或商业披露信息。

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本文引用的文献

[1]
Fluorescence Lifetime Imaging Ophthalmoscopy, Vision, and Chorioretinal Asymmetries in Aging and Age-Related Macular Degeneration: ALSTAR2.

Invest Ophthalmol Vis Sci. 2025-4-1

[2]
Polygenic Risk Score Impact on Visual Function in Older Individuals with Healthy Macula: The Northern Ireland Sensory Ageing Study.

Eye (Lond). 2025-6

[3]
Acetyl-CoA carboxylase inhibition increases retinal pigment epithelial cell fatty acid flux and restricts apolipoprotein efflux.

J Biol Chem. 2024-10

[4]
Extent and Topography of Subretinal Drusenoid Deposits Associate With Rod-Mediated Vision in Aging and AMD: ALSTAR2 Baseline.

Invest Ophthalmol Vis Sci. 2024-8-1

[5]
Choriocapillaris Impairment, Visual Function, and Distance to Fovea in Aging and Age-Related Macular Degeneration: ALSTAR2 Baseline.

Invest Ophthalmol Vis Sci. 2024-7-1

[6]
Age-Related Macular Degeneration, a Mathematically Tractable Disease.

Invest Ophthalmol Vis Sci. 2024-3-5

[7]
Repeatability of Rod-Mediated Dark Adaptation Testing in Normal Aging and Early and Intermediate Age-Related Macular Degeneration.

Curr Eye Res. 2024-7

[8]
Potential Structural Biomarkers in 3D Images Validated by the First Functional Biomarker for Early Age-Related Macular Degeneration - ALSTAR2 Baseline.

Invest Ophthalmol Vis Sci. 2024-2-1

[9]
Pegcetacoplan for the treatment of geographic atrophy secondary to age-related macular degeneration (OAKS and DERBY): two multicentre, randomised, double-masked, sham-controlled, phase 3 trials.

Lancet. 2023-10-21

[10]
Choriocapillaris Impairment Is Associated With Delayed Rod-Mediated Dark Adaptation in Age-Related Macular Degeneration.

Invest Ophthalmol Vis Sci. 2023-9-1

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