Department of Ophthalmology, Hanyang University Hospital, Hanyang University College of Medicine, Seoul, South Korea.
Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
Invest Ophthalmol Vis Sci. 2022 Jan 3;63(1):12. doi: 10.1167/iovs.63.1.12.
The purpose of this study was to investigate the perimetric features and their associations with structural and functional features in patients with RP1L1-associated occult macular dystrophy (OMD; i.e. Miyake disease).
In this international, multicenter, retrospective cohort study, 76 eyes of 38 patients from an East Asian cohort of patients with RP1L1-associated OMD were recruited. Visual field tests were performed using standard automated perimetry, and the patients were classified into three perimetric groups based on the visual field findings: central scotoma, other scotoma (e.g. paracentral scotoma), and no scotoma. The association of the structural and functional findings with the perimetric findings was evaluated.
Fifty-four eyes (71.1%) showed central scotoma, 14 (18.4%) had other scotomata, and 8 (10.5%) had no scotoma. Central scotoma was mostly noted in both eyes (96.3%) and within the central 10 degrees (90.7%). Among the three perimetric groups, there were significant differences in visual symptoms, best-corrected visual acuity (BCVA), and structural phenotypes (i.e. severity of photoreceptor changes). The central scotoma group showed worse BCVA often with severe structural abnormalities (96.3%) and a pathogenic variant of p.R45W (72.2%). The multifocal electroretinogram (mfERG) groups largely corresponded with the perimetric groups; however, 8 (10.5%) of 76 eyes showed mfERG abnormalities preceding typical central scotoma.
The patterns of scotoma with different clinical severity were first identified in occult macular dystrophy, and central scotoma, a severe pattern, was most frequently observed. These perimetric patterns were associated with the severity of BCVA, structural phenotypes, genotype, and objective functional characteristics which may precede in some cases.
本研究旨在探讨 RP1L1 相关隐匿性黄斑营养不良(OMD;即 Miyake 病)患者的视野特征及其与结构和功能特征的相关性。
在这项国际性、多中心、回顾性队列研究中,我们招募了来自东亚 RP1L1 相关 OMD 患者队列的 38 名患者的 76 只眼。使用标准自动视野计进行视野检查,根据视野结果将患者分为三组:中心暗点、其他暗点(如旁中心暗点)和无暗点。评估结构和功能发现与视野发现的相关性。
54 只眼(71.1%)表现为中心暗点,14 只眼(18.4%)有其他暗点,8 只眼(10.5%)无暗点。中心暗点主要见于双眼(96.3%)和中央 10 度以内(90.7%)。在这三个视野组中,视觉症状、最佳矫正视力(BCVA)和结构表型(即光感受器变化的严重程度)存在显著差异。中心暗点组 BCVA 较差,常伴有严重的结构异常(96.3%)和 p.R45W 致病性变异(72.2%)。多焦视网膜电图(mfERG)组与视野组有很大的对应关系;然而,76 只眼中有 8 只(10.5%)的 mfERG 异常早于典型的中心暗点。
隐匿性黄斑营养不良中首次确定了不同临床严重程度的暗点模式,且最常观察到严重的中心暗点模式。这些视野模式与 BCVA、结构表型、基因型和客观功能特征的严重程度相关,在某些情况下这些特征可能会先出现。