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Invest Ophthalmol Vis Sci. 2020 Jun 3;61(6):11. doi: 10.1167/iovs.61.6.11.
To investigate the impact of subretinal drusenoid deposits (SDD) and photoreceptor integrity on global and local geographic atrophy (GA) progression.
Eighty-three eyes of 49 patients, aged 50 years and older with GA secondary to age-related macular degeneration (AMD), were prospectively included in this study. Participants underwent spectral-domain optical coherence tomography (SD-OCT) and fundus autofluorescence (FAF) imaging at baseline and after 12 months. The junctional zone and presence of SDD were delineated on SD-OCT and FAF images. Linear mixed models were calculated to investigate the association between GA progression and the junctional zone area, baseline GA area, age, global and local presence of SDD and unifocal versus multifocal lesions.
The area of the junctional zone was significantly associated with the progression of GA, both globally and locally (all P < 0.001). SDD were associated with faster growth in the overall model (P = 0.039), as well as in the superior-temporal (P = 0.005) and temporal (P = 0.002) sections. Faster progression was associated with GA baseline area (P < 0.001). No difference was found between unifocal and multifocal lesions (P > 0.05). Age did not have an effect on GA progression (P > 0.05).
Photoreceptor integrity and SDD are useful for predicting global and local growth in GA. Investigation of the junctional zone is merited because this area is destined to become atrophic. Photoreceptor loss visible on SD-OCT might lead to new structural outcome measurements visible before irreversible loss of retinal pigment epithelium occurs.
研究视网膜下类脂沉积(SDD)和光感受器完整性对全局和局部地图状萎缩(GA)进展的影响。
本前瞻性研究纳入了 49 名年龄在 50 岁及以上的与年龄相关性黄斑变性(AMD)相关 GA 患者的 83 只眼。参与者在基线和 12 个月时接受了频域光学相干断层扫描(SD-OCT)和眼底自发荧光(FAF)成像。在 SD-OCT 和 FAF 图像上描绘了交界区和 SDD 的存在。线性混合模型用于研究 GA 进展与交界区面积、基线 GA 面积、年龄、全局和局部 SDD 以及单灶与多灶病变之间的关系。
交界区面积与 GA 的全局和局部进展均显著相关(均 P < 0.001)。SDD 在整体模型中与更快的增长相关(P = 0.039),在上方颞部(P = 0.005)和颞部(P = 0.002)也是如此。GA 基线面积与更快的进展相关(P < 0.001)。在单灶和多灶病变之间未发现差异(P > 0.05)。年龄对 GA 进展无影响(P > 0.05)。
光感受器完整性和 SDD 可用于预测 GA 的全局和局部增长。交界区的研究是有价值的,因为这个区域注定会发生萎缩。SD-OCT 上可见的光感受器损失可能会导致新的结构终点测量,在视网膜色素上皮不可逆丢失之前就可以观察到。