Department of Ophthalmology, Inselspital, Bern University Hospital, and Department of Biomedical Research, University of Bern, Bern, Switzerland,
Department of Ophthalmology, Inselspital, Bern University Hospital, and Department of Biomedical Research, University of Bern, Bern, Switzerland.
Ophthalmologica. 2020;243(3):195-206. doi: 10.1159/000503567. Epub 2019 Nov 19.
To investigate whether autofluorescence lifetime patterns within retinal pigment epithelium (RPE) atrophy differ between age-related macular degeneration (AMD) and Stargardt disease (STGD).
Mean retinal autofluorescence lifetimes were measured in a short and a long spectral channel (SSC: 498-560 nm; LSC: 560-720 nm). Mean retinal fluorescence lifetimes were analyzed with corresponding clinical features, fundus images, fundus autofluorescence intensity images, and optical coherence tomography. Mean fluorescence lifetime values of atrophic areas were compared between the two cohorts and within the same patient to adjacent nonatrophic regions.
Mean fluorescence lifetimes within areas with RPE atrophy of 13 patients with STGD (mean age ± SEM 43.7 ± 5 years) and 30 patients with geographic atrophy (mean age: 78 ± 2 years) were analyzed and compared to age-matched healthy participants. The mean area of RPE atrophy in STGD and AMD was 6.6 ± 2.3 mm2 (range: 0.66-33.17 mm2) and 17.5 ± 3.8 mm2 (range: 0.58-50.02 mm2), respectively. In patients with AMD, atrophic areas revealed significantly longer mean fluorescence lifetime values as compared with patients with STGD (SSC: 997 ± 60 vs. 363 ± 26 ps; LSC: 880 ± 46 vs. 393 ± 23 ps; p < 0.0001).
This study established that RPE atrophy in patients secondary to STGD and AMD display distinctive mean fluorescence lifetime characteristics. As retinal fluorescence lifetimes within areas of RPE atrophy were significantly longer in AMD patients, the analysis of specific lifetime patterns may provide additional insight into the disease processes and the pathogenetic mechanisms in the development of atrophic patches in AMD and STGD.
研究年龄相关性黄斑变性(AMD)和斯特格病(STGD)的视网膜色素上皮(RPE)萎缩中的自发荧光寿命模式是否不同。
在短和长光谱通道(SSC:498-560nm;LSC:560-720nm)中测量平均视网膜自发荧光寿命。用相应的临床特征、眼底图像、眼底自发荧光强度图像和光学相干断层扫描分析平均视网膜荧光寿命。将两个队列之间以及同一患者的萎缩区域与相邻非萎缩区域的平均荧光寿命值进行比较。
分析了 13 名 STGD(平均年龄±SEM 43.7±5 岁)和 30 名地理萎缩(平均年龄:78±2 岁)患者的 RPE 萎缩区的平均荧光寿命,并与年龄匹配的健康参与者进行了比较。STGD 和 AMD 的 RPE 萎缩平均面积分别为 6.6±2.3mm2(范围:0.66-33.17mm2)和 17.5±3.8mm2(范围:0.58-50.02mm2)。与 STGD 患者相比,AMD 患者的萎缩区显示出明显更长的平均荧光寿命值(SSC:997±60 对 363±26 ps;LSC:880±46 对 393±23 ps;p<0.0001)。
本研究确立了 STGD 和 AMD 继发的 RPE 萎缩显示出独特的平均荧光寿命特征。由于 AMD 患者 RPE 萎缩区的视网膜荧光寿命明显较长,因此分析特定的寿命模式可能为 AMD 和 STGD 萎缩斑发展中的疾病过程和发病机制提供额外的见解。