Department of Ophthalmology, University of Bonn, Bonn, Germany.
Invest Ophthalmol Vis Sci. 2018 Mar 20;59(4):AMD1-AMD11. doi: 10.1167/iovs.17-23315.
To evaluate the development of central atrophy in eyes with age-related macular degeneration (AMD).
Six-year longitudinal multimodal retinal imaging data (MODIAMD study) from 98 eyes of 98 subjects with non-late-stage AMD in the study eye at baseline were analyzed for the presence of central atrophy at each annual follow-up visit. Development, manifestation, and further progression of complete retinal pigment epithelium and outer retinal atrophy (cRORA) by multimodal imaging data were compared with atrophy detection based on color fundus photography only.
Seventeen study eyes with development of central cRORA within 6 years (cumulative rate: 17.4%) were identified based on multimodal imaging. In 10 (60%) of these eyes, presence of central manifest atrophy was initially not detectable by color fundus photography. In six (35%) eyes, central cRORA occurred by the spread of existing paracentral atrophy toward the fovea. Drusen-associated atrophy development was noted in eight eyes. In two eyes, atrophy development was associated with refractile deposits, while only pigmentary changes in absence of large drusen or refractile deposits were detectable before atrophy occurrence in one eye.
The earlier and more precise detection of central cRORA by multimodal imaging as compared to atrophy detection solely based on color fundus photography allows for more accurate detection and identification of different pathways for atrophy development. In accordance with previous clinical and histopathologic reports, the results confirm that different precursor lesions may independently proceed to central cRORA in AMD.
评估与年龄相关的黄斑变性(AMD)相关的中心萎缩的发展。
对基线时研究眼中无晚期 AMD 的 98 例 98 只眼的 6 年纵向多模态视网膜成像数据(MODIAMD 研究)进行分析,以在每次年度随访时评估中心萎缩的存在。通过多模态成像数据比较完全视网膜色素上皮和外层视网膜萎缩(cRORA)的发展、表现和进一步进展与仅基于眼底彩色照相的萎缩检测。
根据多模态成像,在 6 年内发现 17 只眼出现中心 cRORA(累积率:17.4%)。在这些眼中的 10 只(60%),眼底彩色照相最初无法检测到中心显性萎缩。在 6 只眼(35%)中,中心 cRORA 通过向黄斑扩展现有的旁中心萎缩而发生。在 8 只眼中发现了与玻璃膜疣相关的萎缩发展。在 2 只眼中,萎缩发展与折射沉积物有关,而在一只眼发生萎缩之前,仅在缺乏大玻璃膜疣或折射沉积物的情况下可检测到色素变化。
与仅基于眼底彩色照相的萎缩检测相比,多模态成像更早且更精确地检测中心 cRORA,从而可以更准确地检测和识别萎缩发展的不同途径。与以前的临床和组织病理学报告一致,结果证实不同的前体病变可能独立地进展为 AMD 中的中心 cRORA。