Department of Ophthalmology, Shamir Medical Center (formerly Assaf Harofeh Medical Center), Zerifin, Israel.
Matlow's Ophthalmogenetic Laboratory, Department of Ophthalmology, Shamir Medical Center (formerly Assaf Harofeh Medical Center), Zerifin, Israel.
Graefes Arch Clin Exp Ophthalmol. 2020 Mar;258(3):529-536. doi: 10.1007/s00417-019-04578-7. Epub 2020 Jan 2.
Diurnal variations in foveal thickness have been reported in several ocular pathologies including X-linked retinoschisis (XLRS), but its underlying mechanism is poorly understood. Rods are active under scotopic conditions with high metabolic demand, and its decrease may have positive effect on metabolic activity and macular thickness. The purpose of this study is to evaluate whether exposure to light and diurnal variation influence macular thickness in XLRS patients.
Five patients with clinical suspicion of XLRS underwent RS1 gene sequencing and optical coherence tomography measurements at three consecutive times: morning following sleep in a dark room, morning following sleep in an illuminated room, and late afternoon following sleep in an illuminated room. Central macular thickness (CMT) was compared between measurements, and molecular analysis was performed.
Five RS1 mutations were identified: p.Gly140Arg, p.Arg141Cys, p.Gly109Glu, p.Pro193Leu, and p.Arg200His in patients 1-5, respectively. Two patients (4-5) had atrophied macula and were excluded from macular thickness variation analysis. A significant decrease in CMT between morning and afternoon measurements was observed in all patients (1-3: mean: 455.0 ± 32 μm to 342.17 ± 39 μm, 25%). Morning measurements following sleep in an illuminated room show a CMT reduction in all eyes of all patients with a mean reduction of 113 μm (mean: 547.17 ± 105 μm to 455.0 ± 32 μm, 17%).
Among XLRS patients, CMT decreased at the afternoon compared to the morning of the same day and may be reduced following sleep in an illuminated room. These results help shed light on the pathophysiologic process underlying intraretinal fluid accumulation involved with the disease.
在包括 X 连锁性视网膜炎劈裂症(XLRS)在内的几种眼部疾病中,已经报道了黄斑厚度的昼夜变化,但该机制尚未得到很好的理解。在暗适应条件下,视杆细胞活跃,代谢需求较高,其减少可能对代谢活动和黄斑厚度产生积极影响。本研究旨在评估光照和昼夜变化是否会影响 XLRS 患者的黄斑厚度。
5 名疑似 XLRS 的患者连续 3 次接受 RS1 基因测序和光学相干断层扫描测量:在黑暗房间睡眠后的早晨、在光照房间睡眠后的早晨和在光照房间睡眠后的傍晚。比较各次测量的中心黄斑厚度(CMT),并进行分子分析。
确定了 5 种 RS1 突变:患者 1-5 分别为 p.Gly140Arg、p.Arg141Cys、p.Gly109Glu、p.Pro193Leu 和 p.Arg200His。2 名患者(4-5)黄斑萎缩,排除在黄斑厚度变化分析之外。所有患者(1-3:平均 455.0±32μm 至 342.17±39μm,25%)均观察到早晨和傍晚测量之间 CMT 的显著下降。所有患者的光照房间睡眠后早晨测量显示 CMT 降低,平均降低 113μm(平均 547.17±105μm 至 455.0±32μm,17%)。
在 XLRS 患者中,与同一天的早晨相比,下午 CMT 下降,并且在光照下睡眠后可能会进一步降低。这些结果有助于阐明与疾病相关的视网膜内液体积聚的病理生理过程。