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早产儿视网膜病变中的黄斑精细结构:一项自适应光学傅里叶域光学相干断层扫描研究。

Foveal fine structure in retinopathy of prematurity: an adaptive optics Fourier domain optical coherence tomography study.

作者信息

Hammer Daniel X, Iftimia Nicusor V, Ferguson R Daniel, Bigelow Chad E, Ustun Teoman E, Barnaby Amber M, Fulton Anne B

机构信息

Physical Sciences Inc., 20 New England Business Center, Andover, MA 01810, USA.

出版信息

Invest Ophthalmol Vis Sci. 2008 May;49(5):2061-70. doi: 10.1167/iovs.07-1228. Epub 2008 Jan 25.

Abstract

PURPOSE

To describe the fine structure of the fovea in subjects with a history of mild retinopathy of prematurity (ROP) using adaptive optics-Fourier domain optical coherence tomography (AO-FDOCT).

METHODS

High-speed, high-resolution AO-FDOCT videos were recorded in subjects with a history of ROP (n = 5; age range, 14-26 years) and in control subjects (n = 5; age range, 18-25 years). Custom software was used to extract foveal pit depth and volume from three-dimensional (3-D) retinal maps. The thickness of retinal layers as a function of retinal eccentricity was measured manually. The retinal vasculature in the parafoveal region was assessed.

RESULTS

The foveal pit was wider and shallower in ROP than in control subjects. Mean pit depth, defined from the base to the level at which the pit reaches a lateral radius of 728 microm, was 121 microm compared with 53 microm. Intact, contiguous inner retinal layers overlay the fovea in ROP subjects but were absent in the control subjects. Mean full retinal thickness at the fovea was greater in the subjects with ROP (279.0 microm vs. 190.2 microm). The photoreceptor layer thickness did not differ between ROP and control subjects. An avascular zone was not identified in the subjects with ROP but was present in all the control subjects.

CONCLUSIONS

The foveas of subjects with a history of mild ROP have significant structural abnormalities that are probably a consequence of perturbations of neurovascular development.

摘要

目的

使用自适应光学-傅里叶域光学相干断层扫描(AO-FDOCT)描述有轻度早产儿视网膜病变(ROP)病史的受试者黄斑中心凹的精细结构。

方法

对有ROP病史的受试者(n = 5;年龄范围14 - 26岁)和对照受试者(n = 5;年龄范围18 - 25岁)记录高速、高分辨率的AO-FDOCT视频。使用定制软件从三维(3-D)视网膜地图中提取黄斑中心凹的深度和体积。手动测量视网膜层厚度随视网膜离心率的变化。评估黄斑旁区域的视网膜血管系统。

结果

与对照受试者相比,ROP患者的黄斑中心凹更宽且更浅。从基底到中心凹达到728微米横向半径处的平均中心凹深度,ROP患者为121微米,而对照受试者为53微米。在ROP受试者中,完整、连续的视网膜内层覆盖在黄斑中心凹上,但对照受试者中则没有。ROP受试者黄斑中心凹处的平均全视网膜厚度更大(279.0微米对190.2微米)。ROP患者和对照受试者之间的光感受器层厚度没有差异。在ROP受试者中未发现无血管区,但所有对照受试者中均存在。

结论

有轻度ROP病史的受试者的黄斑中心凹存在明显的结构异常,这可能是神经血管发育受到干扰的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d367/2923467/5ef400f5f93d/nihms224891f1.jpg

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