Applied Vision Research Group, Faculty of Optics and Optometry, Universidad Complutense de Madrid, Madrid, Spain.
Centre for Applied Vision Research, The Henry Wellcome Laboratories for Vision Science, School of Health Sciences, City, University of London, London, UK.
Transl Vis Sci Technol. 2021 Oct 4;10(12):16. doi: 10.1167/tvst.10.12.16.
Early detection of structural changes in retinal ganglion cells (RGCs) and corresponding changes in visual function is important in early degenerative diseases of the retina, but the sensitivity of both measurements is limited by the inherent variability in healthy subjects. This study investigates the relationships between RGC-related layer thicknesses and foveal and parafoveal flicker modulation sensitivity (FMS) across photopic and mesopic light levels in healthy subjects.
Photopic and mesopic FMS was measured in 56 young adults, at the point of fixation and at an eccentricity of 5 degrees, in each of the four quadrants. Spectral-domain optical coherence tomography (SD-OCT) was used to measure retinal thicknesses. Relationships between foveal and parafoveal FMS and the retinal thickness in the corresponding region were examined after adjusting for confounding variables.
Total macular and inner retinal layer (IRL) thicknesses in the parafoveal ring were significant predictors of photopic (P = 0.034) and mesopic (P = 0.034) parafoveal FMS, respectively. The superior peripapillary retinal nerve fiber layer (pRNFL) thickness was a contributing factor to the inferior parafoveal FMS (photopic: P = 0.006 and mesopic: P = 0.021) and the inferior pRNFL thickness was also a contributing factor to the superior parafoveal FMS (photopic: P < 0.001 and mesopic: P = 0.015).
The pRNFL thicknesses predict parafoveal FMS for both mesopic and photopic conditions in healthy eyes.
The measurement of rapid flicker sensitivity in the parafoveal retina together with the pRNFL thickness profiles measured before the onset of disease, may provide a more sensitive biomarker for detecting loss of sensitivity caused by the earliest neurodegenerative changes in the eyes.
在视网膜退行性疾病的早期,检测视网膜神经节细胞(RGC)的结构变化和相应的视觉功能变化很重要,但这两种测量方法的敏感性都受到健康受试者固有变异性的限制。本研究旨在探讨健康受试者在明适应和中间适应光水平下,RGC 相关层厚度与中心凹和旁中心区闪烁调制敏感度(FMS)之间的关系。
在 56 名年轻成年人中,在注视点和每个象限的 5 度偏距处,测量明适应和中间适应的 FMS。使用频域光学相干断层扫描(SD-OCT)测量视网膜厚度。在调整混杂变量后,检查中心凹和旁中心区 FMS 与相应区域视网膜厚度之间的关系。
在旁中心区,黄斑区和内层视网膜(IRL)厚度是明适应(P = 0.034)和中间适应(P = 0.034)旁中心区 FMS 的显著预测因素。上方视盘周围神经纤维层(pRNFL)厚度是下方旁中心区 FMS 的影响因素(明适应:P = 0.006 和中间适应:P = 0.021),下方 pRNFL 厚度也是上方旁中心区 FMS 的影响因素(明适应:P < 0.001 和中间适应:P = 0.015)。
在健康眼的明适应和中间适应条件下,pRNFL 厚度可以预测旁中心区 FMS。
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