Kurokawa Kazuhiro, Nemeth Morgan
Discoveries in Sight Research Laboratories, Devers Eye Institute, Legacy Research Institute, Legacy Health, Portland, OR 97232, USA.
Biomed Opt Express. 2024 Jan 31;15(2):1331-1354. doi: 10.1364/BOE.505395. eCollection 2024 Feb 1.
Clinicians are unable to detect glaucoma until substantial loss or dysfunction of retinal ganglion cells occurs. To this end, novel measures are needed. We have developed an optical imaging solution based on adaptive optics optical coherence tomography (AO-OCT) to discern key clinical features of glaucoma and other neurodegenerative diseases at the cellular scale in the living eye. Here, we test the feasibility of measuring AO-OCT-based reflectance, retardance, optic axis orientation, and angiogram at specifically targeted locations in the living human retina and optic nerve head. Multifunctional imaging, combined with focus stacking and global image registration algorithms, allows us to visualize cellular details of retinal nerve fiber bundles, ganglion cell layer somas, glial septa, superior vascular complex capillaries, and connective tissues. These are key histologic features of neurodegenerative diseases, including glaucoma, that are now measurable in vivo with excellent repeatability and reproducibility. Incorporating this noninvasive cellular-scale imaging with objective measurements will significantly enhance existing clinical assessments, which is pivotal in facilitating the early detection of eye disease and understanding the mechanisms of neurodegeneration.
在视网膜神经节细胞出现大量损失或功能障碍之前,临床医生无法检测到青光眼。为此,需要新的检测方法。我们开发了一种基于自适应光学光学相干断层扫描(AO-OCT)的光学成像解决方案,以在活体眼睛的细胞尺度上辨别青光眼和其他神经退行性疾病的关键临床特征。在此,我们测试了在活体人类视网膜和视神经乳头的特定目标位置测量基于AO-OCT的反射率、相位延迟、光轴方向和血管造影的可行性。多功能成像结合聚焦堆叠和全局图像配准算法,使我们能够可视化视网膜神经纤维束、神经节细胞层胞体、神经胶质隔膜、上血管复合体毛细血管和结缔组织的细胞细节。这些是包括青光眼在内的神经退行性疾病的关键组织学特征,现在可以在体内进行测量,具有出色的可重复性和再现性。将这种非侵入性细胞尺度成像与客观测量相结合,将显著增强现有的临床评估,这对于促进眼病的早期检测和理解神经退行性变机制至关重要。