在鸡的光谱域光学相干断层成像中使用三维分割的新方法揭示了离焦引起的脉络膜厚度的区域和时间敏感不对称性。

IF 1.1 4区 医学 Q4 NEUROSCIENCES
Diane R Nava, Bhavna Antony, L I Zhang, Michael D Abràmoff, Christine F Wildsoet
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引用次数: 9

摘要

对新生儿屈光不正被纠正的主动正视过程机制的研究,已经描述了对施加的光学离焦的响应中脉络膜层厚度的快速补偿性变化。高频a超扫描,作为传统上用来表征这种变化的方法,提供了很好的中心(轴上)变化的分辨率,但局部视网膜控制机制的证据使得更多的外围、离轴变化也必须被跟踪。在这项研究中,我们使用体内高分辨率光谱域光学相干断层扫描(SD-OCT)成像结合爱荷华参考算法进行三维分割,以更全面地表征这些变化,从空间和时间上,在7日龄的雏鸡(n = 15)中,安装单眼+15 D离焦透镜来诱导脉络膜增厚。通过这些工具,我们还能够定位视网膜中央区域,该区域与眼果胶一起用作标准化扫描位置的地标,并对齐它们,以便后续分析脉络膜厚度(CT)随时间和眼睛之间的变化。以中心区域为中心的四个象限的每个象限的值都得到了,并且还得到了所有眼睛的全局CT值。将超声测量的数据与轴上变化进行比较。晶状体磨损仅一天(~ 190µm)就检测到显著的轴上脉络膜增厚,也发现了脉络膜反应的区域(象限相关)差异,以及治疗后1天的整体厚度变化。全球与轴上脉络膜厚度之比(用作响应区域变异性的指标)也发生了显著变化,反映了显著的中心变化。总之,我们证明了体内高分辨率SD-OCT成像,结合分割算法,是一种可行的、信息丰富的方法,用于表征区域(空间)、时间敏感的CT变化,如小鸡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel method using 3-dimensional segmentation in spectral domain-optical coherence tomography imaging in the chick reveals defocus-induced regional and time-sensitive asymmetries in the choroidal thickness.

Studies into the mechanisms underlying the active emmetropization process by which neonatal refractive errors are corrected, have described rapid, compensatory changes in the thickness of the choroidal layer in response to imposed optical defocus. While high frequency A-scan ultrasonography, as traditionally used to characterize such changes, offers good resolution of central (on-axis) changes, evidence of local retinal control mechanisms make it imperative that more peripheral, off-axis changes also be tracked. In this study, we used in vivo high resolution spectral domain-optical coherence tomography (SD-OCT) imaging in combination with the Iowa Reference Algorithms for 3-dimensional segmentation, to more fully characterize these changes, both spatially and temporally, in young, 7-day old chicks (n = 15), which were fitted with monocular +15 D defocusing lenses to induce choroidal thickening. With these tools, we were also able to localize the retinal area centralis, which was used as a landmark along with the ocular pectin in standardizing the location of scans and aligning them for subsequent analyses of choroidal thickness (CT) changes across time and between eyes. Values were derived for each of four quadrants, centered on the area centralis, and global CT values were also derived for all eyes. Data were compared with on-axis changes measured using ultrasonography. There were significant on-axis choroidal thickening that was detected after just one day of lens wear (∼190 µm), and regional (quadrant-related) differences in choroidal responses were also found, as well as global thickness changes 1 day after treatment. The ratio of global to on-axis choroidal thicknesses, used as an index of regional variability in responses, was also found to change significantly, reflecting the significant central changes. In summary, we demonstrated in vivo high resolution SD-OCT imaging, used in combination with segmentation algorithms, to be a viable and informative approach for characterizing regional (spatial), time-sensitive changes in CT in small animals such as the chick.

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来源期刊
Visual Neuroscience
Visual Neuroscience 医学-神经科学
CiteScore
2.20
自引率
5.30%
发文量
8
审稿时长
>12 weeks
期刊介绍: Visual Neuroscience is an international journal devoted to the publication of experimental and theoretical research on biological mechanisms of vision. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of all aspects of neuroscience research relating to the visual system. Contributions may address molecular, cellular or systems-level processes in either vertebrate or invertebrate species. The journal publishes work based on a wide range of technical approaches, including molecular genetics, anatomy, physiology, psychophysics and imaging, and utilizing comparative, developmental, theoretical or computational approaches to understand the biology of vision and visuo-motor control. The journal also publishes research seeking to understand disorders of the visual system and strategies for restoring vision. Studies based exclusively on clinical, psychophysiological or behavioral data are welcomed, provided that they address questions concerning neural mechanisms of vision or provide insight into visual dysfunction.
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