Ramon Castroviejo Institute for Ophthalmic Research, Complutense University of Madrid, 28040 Madrid, Spain.
Health Research Institute of the Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain.
Biomolecules. 2024 Jul 10;14(7):828. doi: 10.3390/biom14070828.
Alzheimer's disease (AD) may manifest retinal changes preceding brain pathology. A transversal case-control study utilized spectral-domain OCT angiography (SD-OCTA) and Angio-Tool software 0.6a to assess retinal vascular structures and OCT for inner and outer retina thickness in the AD model at 6, 9, 12, 15, 17, and 20 months old. Comparisons to age-matched wild type (WT) were performed. The analysis focused on the three vascular plexuses using AngiooTool and on retinal thickness, which was represented with the Early Treatment Diabetic Retinopathy Study (ETDRS) sectors. Compared to WT, the group exhibited both vascular and structural changes as early as 6 months persisting and evolving at 15, 17, and 20 months. Significant vascular alterations, principally in the superficial vascular complex (SVC), were observed. There was a significant decrease in the vessel area and the total vessel length in SVC, intermediate, and deep capillary plexus. The inner retina in the group predominantly decreased in thickness while the outer retina showed increased thickness in most analyzed time points compared to the control group. There are early vascular and structural retinal changes that precede the cognitive changes, which appear at later stages. Therefore, the natural history of the model may be more similar to human AD than other transgenic models.
阿尔茨海默病(AD)可能会在大脑病理学之前表现出视网膜变化。一项横断面病例对照研究利用频域光相干断层扫描血管造影(SD-OCTA)和 Angio-Tool 软件 0.6a 评估 AD 模型在 6、9、12、15、17 和 20 月龄时的视网膜血管结构和 OCT 内外视网膜厚度。与年龄匹配的野生型(WT)进行了比较。该分析使用 AngiooTool 集中在三个血管丛上,并使用早期糖尿病视网膜病变治疗研究(ETDRS)区域表示视网膜厚度。与 WT 相比,6 个月时就已经出现了血管和结构变化,这些变化在 15、17 和 20 个月时持续存在并不断发展。观察到明显的血管改变,主要是在浅层血管丛(SVC)中。SVC、中间和深层毛细血管丛中的血管面积和总血管长度显著减少。与对照组相比,AD 组的内视网膜厚度主要减少,而外视网膜在大多数分析时间点显示出增加的厚度。在认知变化出现在后期之前,存在早期的血管和结构视网膜变化。因此,该模型的自然史可能比其他转基因模型更类似于人类 AD。