Centre for Public Health, Queen's University Belfast Faculty of Medicine Health and Life Sciences, Belfast, UK
Centre for Public Health, Queen's University Belfast Faculty of Medicine Health and Life Sciences, Belfast, UK.
Br J Ophthalmol. 2023 Nov 22;107(12):1873-1879. doi: 10.1136/bjo-2021-320469.
To report prevalence and risk factor associations for age-related macular degeneration (AMD) and AMD features from multimodal retinal grading in a multidisciplinary longitudinal population-based study of aging in Northern Ireland.
Population-based longitudinal cohort study.
Retinal imaging at the Norther Ireland Cohort for the Longitudinal Aging Study health assessment included stereo Colour Fundus Photography (CFP) (Canon CX-1, Tokyo, Japan) and Spectral-Domain Optical Coherence Tomography (SD-OCT) ((Heidelberg Retinal Angopgraph (HRA)+OCT; Heidelberg Engineering, Heidelberg, Germany). Medical history and demographic information was obtained during a home interview. Descriptive statistics were used to describe the prevalence of AMD and individual AMD features. Multiple imputation followed by multiple regression modelling was used to explore risk factor associations including relationships with AMD genetic risk score.
Retinal images from 3386 participants were available for analysis. Mean age of the sample was 63.4 (SD 9.01, range: 36-99). Population weighted prevalence of AMD using colour grading in those over 55 years was: no drusen: 6 0.4%; drusen <63 μm: 15.9%; drusen 63-125 µm: 13.7%; drusen >125 µm or pigmentary changes: 8.3%; late AMD: 1.6%. Prevalence of AMD features in those over 55 years was: OCT drusen 27.5%, complete outer retinal pigment epithelium and outer retinal atrophy (cRORA) on OCT was 4.3%, reticular drusen 3.2% and subretinal drusenoid deposits 25.7%. The genetic risk score was significantly associated with drusen and cRORA but less so for SDD alone and non-significant for hyperpigmentation or vitelliform lesions.
Multimodal imaging-based classification has provided evidence of some divergence of genetic risk associations between classical drusen and SDD. Our findings support an urgent review of current AMD severity classification systems.
在北爱尔兰老龄化多学科纵向人群研究中,报告多模态视网膜分级中与年龄相关性黄斑变性(AMD)和 AMD 特征相关的患病率和危险因素。
基于人群的纵向队列研究。
北爱尔兰纵向老龄化研究健康评估中的视网膜成像包括立体彩色眼底照相(CFP)(佳能 CX-1,东京,日本)和谱域光相干断层扫描(SD-OCT)(海德堡视网膜血管造影(HRA)+OCT;海德堡工程,海德堡,德国)。在家庭访谈期间获得了病史和人口统计学信息。描述性统计用于描述 AMD 和个体 AMD 特征的患病率。多重插补后进行多元回归模型分析,以探讨危险因素相关性,包括与 AMD 遗传风险评分的关系。
对 3386 名参与者的视网膜图像进行了分析。样本的平均年龄为 63.4(SD 9.01,范围:36-99)。55 岁以上人群使用彩色分级的 AMD 总体患病率为:无玻璃膜疣:60.4%;<63μm 玻璃膜疣:15.9%;63-125μm 玻璃膜疣:13.7%;>125μm 或色素改变:8.3%;晚期 AMD:1.6%。55 岁以上人群 AMD 特征的患病率为:OCT 玻璃膜疣 27.5%,OCT 上完全性外层视网膜色素上皮和外层视网膜萎缩(cRORA)为 4.3%,网状玻璃膜疣为 3.2%,视网膜下类脂质沉积为 25.7%。遗传风险评分与玻璃膜疣和 cRORA 显著相关,但与单独的 SDD 相关程度较低,与色素沉着或类 vitelliform 病变无显著相关性。
基于多模态成像的分类提供了一些证据,表明经典玻璃膜疣和 SDD 之间的遗传风险关联存在一些差异。我们的研究结果支持对当前 AMD 严重程度分类系统进行紧急审查。