Department of Ophthalmology, University of Bonn, Bonn, Nordrhein-Westfalen, Germany
Institute for Medical Biometry, Informatics and Epidemiology, University Hospital Bonn, Bonn, Nordrhein-Westfalen, Germany.
Br J Ophthalmol. 2021 Feb;105(2):239-245. doi: 10.1136/bjophthalmol-2020-316004. Epub 2020 Apr 8.
To characterise early stages of geographic atrophy (GA) development in age-related macular degeneration (AMD) and to determine the prognostic value of structural precursor lesions in eyes with intermediate (i) AMD on the subsequent GA progression.
Structural precursor lesions for atrophic areas (lesion size at least 0.5 mm² in fundus autofluorescence images) were retrospectively identified based on multimodal imaging and evaluated for association with the subsequent GA enlargement rates (square-root transformed, sqrt). A linear mixed-effects model was used to account for the hierarchical nature of the data with a Tukey post hoc test to assess the impact of the local precursor on the subsequent GA progression rate.
A total of 39 eyes with GA of 34 patients with a mean age of 74.4±6.7 (±SD) years were included in this study. Five precursor lesions (phenotypes 1-5) preceding GA development were identified: large, sub-retinal pigment epithelial drusen (n=19), reticular pseudodrusen (RPD, n=10), refractile deposits (n=4), pigment epithelial detachment (n=4) and vitelliform lesions (n=2). Precursor lesions exhibited a significant association with the subsequent (sqrt) GA progression rates (p=0.0018) with RPD (phenotype 2) being associated with the fastest GA enlargement (2.29±0.52 (±SE) mm/year.
The results indicate the prognostic relevance of iAMD phenotyping for subsequent GA progression highlighting the role of structural AMD features across different AMD stages.
本研究旨在描述年龄相关性黄斑变性(AMD)中地理萎缩(GA)的早期阶段,并确定中间型(i)AMD 眼中的结构前体病变与随后 GA 进展的相关性。
基于多模态成像,回顾性地识别出萎缩区域的结构前体病变(眼底自发荧光图像中病变大小至少为 0.5mm²),并评估其与随后 GA 扩大率(平方根转换,sqrt)的相关性。采用线性混合效应模型来解释数据的层次结构,并采用 Tukey 事后检验来评估局部前体病变对随后 GA 进展速率的影响。
本研究共纳入了 39 只眼睛(34 名患者),平均年龄为 74.4±6.7(±SD)岁。研究发现了 5 种 GA 发生前的前体病变(表型 1-5):大的、位于视网膜色素上皮下的玻璃膜疣(n=19)、网状假性玻璃膜疣(RPD,n=10)、折光性沉积物(n=4)、色素上皮脱离(n=4)和卵黄样病变(n=2)。前体病变与随后的(sqrt)GA 进展率显著相关(p=0.0018),其中 RPD(表型 2)与 GA 扩大速度最快相关(2.29±0.52(±SE)mm/年)。
这些结果表明 iAMD 表型对随后 GA 进展具有预测价值,突出了结构 AMD 特征在不同 AMD 阶段的作用。