Visualization of Focal Thinning of the Ganglion Cell–Inner Plexiform Layer in Patients with Mild Cognitive Impairment and Alzheimer’s Disease

内丛状层 神经纤维层 神经节 视网膜 外层核层 内核层 外丛状层 眼科 医学 神经节细胞层 视网膜 神经退行性变 病理 解剖 神经科学 心理学 疾病
作者
Yi Shao,Hong Jiang,Yantao Wei,Yingying Shi,Ce Shi,Clinton B. Wright,Xiaoyan Sun,Elizabeth A. Vanner,Anny D Rodriguez,Byron L. Lam,Tatjana Rundek,Barry S. Baumel,Giovana Rosa Gameiro,Chuanhui Dong,Jianhua Wang
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
卷期号:64 (4): 1261-1273 被引量:36
标识
DOI:10.3233/jad-180070
摘要

A detailed analysis of the tomographic thickness of intraretinal layers may provide more information on neurodegeneration in patients with mild cognitive impairment (MCI) and Alzheimer's disease (AD).The goal was to analyze tomographic thickness patterns of intraretinal layers in patients with AD andMCI.Forty-nine patients (25 AD and 24 MCI) and 21 cognitively normal (CN) controls were imaged using ultra-high-resolution optical coherence tomography to obtain volumetric data centered on the fovea. The segmented intraretinal layers were retinal nerve fiber layer (RNFL), ganglion cell- inner plexiform layer (GCIPL), inner nuclear layer (INL), outer nuclear layer (ONL), outer plexiform layer (OPL), and retinal photoreceptor (PR), in addition to the total retinal thickness(TRT).The thickness differences were negative (thinning) mainly in TRT, RNFL, and GCIPL in both AD and MCI groups in comparison to CN, while the thickness differences were positive (thickening) mainly in ONL and PR in AD. GCIPL of AD and MCI was thinner in superior, nasal superior, and temporal superior quadrants, compared to CN (p < 0.05). GCIPL of the inner superior, inner nasal superior, inner temporal superior, and outer nasal superior sectors was significantly thinner in AD than CN (p < 0.05). GCIPL of the outer superior, inner temporal superior, outer nasal, and temporal superior sectors was significantly thinner in MCI than CN (p < 0.05).Focal thinning of the GCIPL was visualized and quantified by detailed partitions in AD and MCI, which provides specific information about neurodegeneration in MCI and AD.
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