Medical Retina and Visual Science Laboratories, Institute of Health and Biomedical Innovation, Queensland University of Technology (QUT), Brisbane, QLD, Australia.
School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD, Australia.
Acta Ophthalmol. 2016 Dec;94(8):e772-e778. doi: 10.1111/aos.13112. Epub 2016 May 26.
To determine whether decreasing illumination of the Pelli-Robson contrast sensitivity (CS) chart and MP-1 microperimeter to low mesopic conditions is more sensitive to vision changes occurring with healthy ageing and in early and intermediate age-related macular degeneration (AMD) and whether these mesopic tests can differentiate visual function between healthy older participants with and without AMD risk genotypes.
Retinal sensitivity was measured in 98 healthy participants (19-85 years) and 21 AMD (AREDS Grade 2/3) patients (73.9 ± 6.5 years) using the Pelli-Robson CS chart and MP-1 microperimeter under low mesopic and standard illumination. The effect of ageing and AMD on retinal sensitivity was estimated using regression analysis. Healthy older participants (>50 years; n = 24) were genotyped for AMD risk genes CFH and/or ARMS2 and retinal sensitivity was compared between genotypes.
With healthy ageing, photopic and mesopic Pelli-Robson CS showed a similar decline (-0.004 log CS/year). In AMD, photopic CS showed a similar decline to healthy ageing (-0.004 log CS/year) while mesopic CS was significantly reduced (-0.007 log CS/year). Both standard and low mesopic microperimetry showed a significant decline (-0.51 and -0.73% contrast/year) with healthy ageing and greater decline (-0.73 and -0.99% contrast/year) with AMD onset. Pelli-Robson CS and microperimetry sensitivity did not differ between AMD risk genotypes in healthy participants.
Mesopic Pelli-Robson CS detects functional deficits before photopic CS in early and intermediate AMD that can be differentiated from ageing. This test can be easily administered in clinical practice and may provide a means for early detection of retinal dysfunction.
确定在低中间光条件下降低 Pelli-Robson 对比敏感度 (CS) 图表和 MP-1 微视野计的照明度是否对健康衰老以及早期和中期年龄相关性黄斑变性 (AMD) 中发生的视力变化更敏感,以及这些中间光测试是否可以区分健康的老年参与者中是否存在 AMD 风险基因型的视觉功能。
使用 Pelli-Robson CS 图表和 MP-1 微视野计,在低中间光和标准照明条件下,对 98 名健康参与者(19-85 岁)和 21 名 AMD(AREDS 2/3 级)患者(73.9±6.5 岁)测量视网膜敏感性。使用回归分析估计年龄和 AMD 对视网膜敏感性的影响。对年龄超过 50 岁的健康老年参与者(n=24)进行 AMD 风险基因 CFH 和/或 ARMS2 的基因分型,并比较基因型之间的视网膜敏感性。
随着健康衰老,明视和中间光 Pelli-Robson CS 显示出相似的下降(-0.004 log CS/年)。在 AMD 中,明视 CS 与健康衰老的下降相似(-0.004 log CS/年),而中间光 CS 则明显降低(-0.007 log CS/年)。标准和低中间光微视野计在健康衰老时都显示出明显的下降(-0.51%和-0.73%对比度/年),而在 AMD 发作时下降更大(-0.73%和-0.99%对比度/年)。在健康参与者中,Pelli-Robson CS 和微视野计的敏感性在 AMD 风险基因型之间没有差异。
中间光 Pelli-Robson CS 在早期和中期 AMD 中比明视 CS 更早地检测到功能缺陷,这些缺陷可以与衰老区分开来。该测试可以在临床实践中轻松进行,并且可能为视网膜功能障碍的早期检测提供一种手段。