AugenZentrum Siegburg, Europaplatz, Siegburg, Germany.
Retina. 2010 Jan;30(1):6-15. doi: 10.1097/iae.0b013e3181b8348b.
The purpose of this study was to compare near-infrared fundus autofluorescence(NIA, excitation 787 nm, emission >800 nm) with fundus autofluorescence (FAF,excitation 488 nm, emission >500 nm) in patients with age-related macular degeneration(AMD).
Fundus autofluorescence and NIA were obtained using a confocal scanning laser ophthalmoscope (HRA2) in 308 eyes (172 patients) with AMD [age-related maculopathy(n 116), geographic atrophy (n 77), and neovascular AMD (n 115)].
Retinal pigment epithelial alterations were detected with FAF and NIA in all eyes and showed a similar lesion size in 81.8%. In age-related maculopathy, spots of increased FAF (87.9%) were more frequent than spots of reduced FAF (26.7%). Spots of increased and reduced NIA were of similar frequency (66.4%). A higher relative intensity of FAF was more frequent (72.4%) than higher relative NIA intensity (16.4%), suggesting that loss of NIA usually precedes loss of FAF. The junctional zone of geographic atrophy presented with increased NIA (19.5%), increased FAF (10.4%), or an increase of both(22.1%). In neovascular AMD, exudative changes were better visualized with FAF (56.5%)compared with NIA (33.9%).
Patterns of FAF and NIA indicate different involvement of lipofuscin and melanin in the pathophysiological process and provide further insight into the development of AMD and noninvasive monitoring of future therapeutic interventions.
本研究旨在比较近红外眼底自发荧光(NIR,激发 787nm,发射>800nm)与年龄相关性黄斑变性(AMD)患者的眼底自发荧光(FAF,激发 488nm,发射>500nm)。
使用共焦扫描激光检眼镜(HRA2)在 308 只眼(172 例患者)的 AMD [年龄相关性黄斑病变(n=116)、地理萎缩(n=77)和新生血管性 AMD(n=115)]中获得眼底自发荧光和 NIR。
所有眼均通过 FAF 和 NIR 检测到视网膜色素上皮改变,81.8%的病变大小相似。在年龄相关性黄斑病变中,FAF 增加的斑点(87.9%)比 FAF 减少的斑点(26.7%)更为常见。增加和减少的 NIR 斑点频率相似(66.4%)。FAF 的相对强度较高更为常见(72.4%),而 NIR 相对强度较高的情况较少(16.4%),这表明 NIR 的损失通常先于 FAF 的损失。地理萎缩的交界区表现为 NIR 增加(19.5%)、FAF 增加(10.4%)或两者均增加(22.1%)。在新生血管性 AMD 中,与 NIR(33.9%)相比,FAF 更好地显示出渗出性改变(56.5%)。
FAF 和 NIR 的模式表明脂褐素和黑色素在病理生理过程中的不同参与,并进一步深入了解 AMD 的发生机制以及对未来治疗干预的非侵入性监测。