Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Transl Vis Sci Technol. 2024 Sep 3;13(9):29. doi: 10.1167/tvst.13.9.29.
Choroideremia is an X-linked outer retinal degeneration. Early symptoms include nyctalopia and progressive visual field loss, but visual acuity is preserved until late disease stages. Dark-adapted two-color fundus-controlled perimetry (also known as scotopic microperimetry) has been developed to enable spatial assessment of rod and cone photoreceptor function. This study explores the use of scotopic microperimetry in patients with choroideremia.
Twenty patients with choroideremia and 21 age-matched healthy controls completed visual acuity and scotopic microperimetry testing, which used the Scotopic Macular Integrity Assessment (S-MAIA) microperimeter. A subset of participants completed repeat scotopic testing to enable Bland-Altman repeatability analyses. Test reliability was assessed using fixation stability, fixation losses, and assessment of the rod-free zones. Pointwise sensitivity, mean sensitivity, and volume sensitivity indices were analyzed.
False positive responses were the main source of poor test reliability, indicated by stimuli responses in the physiological blind spot and lack of rod-free mapping. Scotopic cyan and red sensitivities were significantly reduced in choroideremia participants (n = 17) compared to healthy controls (n = 16) (P < 0.01, Mann-Whitney U test). Scotopic cyan sensitivity was statistically lower than scotopic red sensitivity in both healthy controls and choroideremia (P < 0.01, Wilcoxon signed rank test). Interpretation of scotopic cyan-red differences should be used with caution due to high test-retest variability.
Scotopic microperimetry could be a useful outcome measure in patients with early choroideremia. Careful selection of test grid design and sensitivity indices is required.
Scotopic microperimetry may be a useful outcome measure in clinical trials for patients with early stage choroideremia.
脉络膜视网膜变性是一种 X 连锁的外视网膜退行性疾病。早期症状包括夜盲和进行性视野丧失,但视力在疾病晚期才会受到影响。暗适应双色眼底控制视野计(也称为暗视野微视野计)已被开发出来,用于评估杆状和锥状光感受器的功能。本研究探讨了暗适应微视野计在脉络膜视网膜变性患者中的应用。
20 名脉络膜视网膜变性患者和 21 名年龄匹配的健康对照者完成了视力和暗适应微视野计检查,使用 Scotopic Macular Integrity Assessment(S-MAIA)微视野计。部分参与者完成了重复暗适应测试,以进行 Bland-Altman 重复性分析。通过评估固视稳定性、固视丢失和杆状光感受器无映射区来评估测试可靠性。分析了点敏感性、平均敏感性和体积敏感性指数。
假阳性反应是测试可靠性差的主要原因,表现为刺激反应出现在生理盲点内,并且缺乏杆状光感受器无映射区。与健康对照组(n=16)相比,脉络膜视网膜变性患者(n=17)的暗适应蓝和红敏感度显著降低(P<0.01,Mann-Whitney U 检验)。在健康对照组和脉络膜视网膜变性患者中,暗适应蓝敏感度均显著低于暗适应红敏感度(P<0.01,Wilcoxon 符号秩检验)。由于测试-复测变异性较大,因此应谨慎解释暗适应蓝-红差异。
暗适应微视野计可能是早期脉络膜视网膜变性患者的一种有用的疗效评估指标。需要仔细选择测试网格设计和敏感性指数。
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