Minella Andrea Louise, Occelli Laurence Mireille, Narfström Kristina, Petersen-Jones Simon Michael
Department of Small Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI, USA.
Department of Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, MO, USA.
Vet Ophthalmol. 2018 May;21(3):224-232. doi: 10.1111/vop.12495. Epub 2017 Aug 30.
Children with Leber congenital amaurosis (LCA) due to CEP290 mutations show characteristic macular preservation. Spectral domain-optical coherence tomography (SD-OCT) is a noninvasive technique to investigate retinal structural changes. Loss of integrity of the ellipsoid zone (EZ) on OCT in people with retinal disease has been associated with loss of visual function and is a useful measure of retinal disease progression. We hypothesized that rdAc felines with Cep290 mutation would have a similar pattern of degeneration, with relative central retinal preservation associated with maintenance of the EZ.
Fundus imaging, confocal scanning laser ophthalmoscopy, and SD-OCT cross-sectional imaging was performed on 11 rdAc cats ranging from 6 months to 10 years of age. Images were collected from the area centralis, visual streak, and the mid-superior and mid-inferior retina. Receptor plus (REC+, encompassing the entire length of photoreceptors) thicknesses were measured. Regional rates of degeneration were determined by regression analysis and compared using unpaired t-tests. The EZ was evaluated for the presence, absence, or loss of definition.
RdAc cats showed REC+ thinning over time in all regions. The area centralis and visual streak had a slower rate of thinning than the mid-peripheral retina. There was loss of integrity of the EZ initially in the more peripheral regions, while its integrity was maintained in the area centralis and visual streak at all ages studied.
rdAc cats show preservation of the central retina with maintenance of EZ integrity, which recapitulates findings in human patients.
因CEP290基因突变导致的莱伯先天性黑蒙(LCA)患儿表现出特征性的黄斑保留。光谱域光学相干断层扫描(SD - OCT)是一种用于研究视网膜结构变化的非侵入性技术。视网膜疾病患者OCT上椭圆体带(EZ)完整性的丧失与视觉功能丧失相关,是评估视网膜疾病进展的一项有用指标。我们推测,具有Cep290突变的rdAc猫会有类似的退化模式,相对中央视网膜的保留与EZ的维持有关。
对11只年龄在6个月至10岁之间的rdAc猫进行眼底成像、共焦扫描激光眼底镜检查和SD - OCT横断面成像。从中央凹、视条纹以及视网膜中上部和中下部区域采集图像。测量受体加(REC +,涵盖光感受器的全长)厚度。通过回归分析确定区域退化率,并使用不成对t检验进行比较。评估EZ的存在、缺失或清晰度丧失情况。
随着时间的推移,rdAc猫所有区域的REC +均变薄。中央凹和视条纹的变薄速度比视网膜中周边区域慢。最初,EZ的完整性在更周边区域丧失,而在所有研究年龄的中央凹和视条纹区域,其完整性得以维持。
rdAc猫表现出中央视网膜的保留以及EZ完整性的维持,这与人类患者的研究结果一致。