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. 2021 Feb 5;10(2):28. doi: 10.1167/tvst.10.2.28.
Choroideremia and RPGR-associated retinitis pigmentosa (RP) are two distinct inherited rod-cone degenerations, where good visual acuity (VA) is maintained until late disease stages, limiting its usefulness as a disease marker. Low luminance VA and low luminance deficit (standard VA minus low luminance VA) may be more sensitive visual function measures.
Standard VA was obtained using Early Treatment Diabetic Retinopathy Study letter charts (Precision Vision, Bloomington, IL, USA). Low luminance VA was assessed using a 2.0-log unit neutral density filter, with the same chart setup, without formal dark adaptation. Mean central retinal sensitivity was assessed using MAIA microperimetry (Centervue SpA, Padova, Italy). Optical coherence tomography imaging was attained with Heidelberg Eye Explorer software (Heidelberg Engineering, Heidelberg, Germany).
Twenty-four male participants with confirmed pathogenic RPGR mutations, 44 male participants with confirmed pathogenic CHM mutations, and 62 age-matched controls underwent clinical assessment prior to clinical trial recruitment. Low luminance VA was significantly reduced in both disease groups compared to controls. The low luminance deficit correlated with microperimetry retinal sensitivity and ellipsoid zone width. Eleven participants with moderate VA had poor low luminance VA (subsequently a large low luminance deficit), no detectable microperimetry sensitivity, and severely constricted ellipsoid zone widths.
Low luminance VA and subsequently low luminance deficit are useful markers of central macular visual function in both choroideremia and RPGR-associated RP, when standard VA is preserved.
Low luminance visual acuity and low luminance deficit are useful vision measures in two distinct rod-cone degenerations and may be useful in other retinal degenerations.
脉络膜视网膜变性(Choroideremia)和 RPGR 相关的视网膜色素变性(RP)是两种不同的遗传性杆锥细胞退行性疾病,在疾病的晚期,良好的视力(VA)仍能维持,这限制了其作为疾病标志物的作用。低亮度 VA 和低亮度缺损(标准 VA 减去低亮度 VA)可能是更敏感的视觉功能测量指标。
使用早期糖尿病视网膜病变研究字母图表(Precision Vision,Bloomington,IL,USA)获得标准 VA。使用 2.0 对数单位中性密度滤光片评估低亮度 VA,使用相同的图表设置,但不进行正式的暗适应。使用 MAIA 微视野计(Centervue SpA,Padova,Italy)评估中央视网膜敏感性。使用海德堡眼探索者软件(Heidelberg Engineering,Heidelberg,Germany)获得光学相干断层扫描成像。
在临床试验招募前,对 24 名确诊有致病性 RPGR 突变的男性参与者、44 名确诊有致病性 CHM 突变的男性参与者和 62 名年龄匹配的对照者进行了临床评估。与对照组相比,低亮度 VA 在两个疾病组中均显著降低。低亮度缺损与微视野视网膜敏感性和椭圆体带宽度相关。11 名中度 VA 的参与者存在低亮度 VA 差(随后出现较大的低亮度缺损)、无法检测到微视野敏感性和严重受限的椭圆体带宽度。
当标准 VA 保持时,低亮度 VA 及其随后的低亮度缺损是脉络膜视网膜变性和 RPGR 相关 RP 中心黄斑视觉功能的有用标志物。
低亮度视力和低亮度缺损是两种不同的杆锥细胞变性的有用视力测量指标,在其他视网膜变性中也可能有用。