In vivo imaging of human retinal ganglion cells using optical coherence tomography without adaptive optics

被引:0
|
作者
Zhang, Furu [1 ]
Kovalick, Katherine [1 ]
Raghavendra, Achyut [1 ]
Soltanian-Zadeh, Somayyeh [1 ,2 ]
Farsiu, Sina
Hammer, Daniel X. [1 ]
Liu, Zhuolin [1 ]
机构
[1] US FDA, Ctr Devices & Radiol Hlth CDRH, Silver Spring, MD 20993 USA
[2] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
来源
BIOMEDICAL OPTICS EXPRESS | 2024年 / 15卷 / 08期
基金
美国国家卫生研究院;
关键词
SUBRETINAL DRUSENOID DEPOSITS; SCANNING LASER OPHTHALMOSCOPY; HIGH-RESOLUTION; AUTOFLUORESCENCE; OCT; SUPERRESOLUTION; DEGENERATION; NEURONS; IMAGES;
D O I
10.1364/BOE.533249
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Retinal ganglion cells play an important role in human vision, and their degeneration results in glaucoma and other neurodegenerative diseases. Imaging these cells in the living human retina can greatly improve the diagnosis and treatment of glaucoma. However, owing to their translucent soma and tight packing arrangement within the ganglion cell layer (GCL), successful imaging has only been achieved with sophisticated research-grade adaptive optics (AO) systems. For the first time we demonstrate that GCL somas can be resolved and cell morphology can be quantified using non-AO optical coherence tomography (OCT) devices with optimal parameter configuration and post-processing. (c) 2024 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
引用
收藏
页码:4675 / 4688
页数:14
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