Cusumano Andrea, Falsini Benedetto, D'Ambrosio Michele, D'Apolito Fabian, Sebastiani Jacopo, Levialdi Ghiron Jung Hee, Giardina Emiliano, Cascella Raffaella
Department of Ophthalmology, Tor Vergata University, Rome, Italy.
Macula and Genoma Foundation, Rome, Italy.
Case Rep Ophthalmol. 2023 Nov 23;14(1):626-639. doi: 10.1159/000534579. eCollection 2023 Jan-Dec.
Doyne honeycomb retinal dystrophy (DHRD), or autosomal dominant radial drusen, is a genetic disease caused by pathogenic variants of the epidermal growth factor (EGF)-containing fibulin-like extracellular matrix protein 1 gene and is characterized by the formation of subretinal drusenoid deposits. In a previous study, we reported the short-term beneficial effects of nanosecond laser treatment (2RT) on retinal function in DHRD. The aim of the present report was to describe the findings of a long-term follow-up of retinal structure/function in a small case series of patients with DHRD who underwent 2RT treatment.
Three DHRD patients (case 1, male and cases 2 and 3, two sister females, age range 41-46) with pathogenic variant (c.1033C>T; p.R345W) and drusenoid deposits at the posterior pole were examined at baseline and after 2RT treatment, at regular intervals (every 2-4 months) up to 30 months. All 3 patients underwent one or two treatment sessions in one or both eyes during the follow-up period. Case 3 was treated with only the left eye (LE). Each patient underwent a full ophthalmologic examination, spectral domain optical coherence tomography (OCT), central perimetry with frequency doubling technology, and mesopic and photopic Ganzfeld electroretinograms. Compared to baseline findings, during follow-up, visual acuity improved in both eyes in case 1 and LE in case 2, while it decreased in the right eye in case 2 and LE in case 3; perimetric sensitivity was stable in case 1 and improved in both eyes in cases 2 and 3; and electroretinogram amplitude improved in cases 1 and 2 and was stable in case 3 (both eyes). OCT central macular thickness and retinal structure were stable in all cases. None of the patients had treatment-related side effects.
This is the first report showing that in a long-term follow-up, 2RT treatment in DHRD may improve or stabilize some retinal function parameters without significant structural changes.
多伊内蜂窝状视网膜营养不良(DHRD),即常染色体显性遗传性放射性玻璃疣,是一种由含表皮生长因子(EGF)的类纤连蛋白细胞外基质蛋白1基因的致病变异引起的遗传性疾病,其特征是视网膜下玻璃疣样沉积物的形成。在先前的一项研究中,我们报告了纳秒激光治疗(2RT)对DHRD患者视网膜功能的短期有益效果。本报告的目的是描述一小例接受2RT治疗的DHRD患者视网膜结构/功能的长期随访结果。
三名DHRD患者(病例1为男性,病例2和病例3为姐妹女性,年龄范围41 - 46岁),携带致病变异(c.1033C>T;p.R345W)且后极部有玻璃疣样沉积物,在基线时以及2RT治疗后,每隔2 - 4个月定期检查,直至30个月。在随访期间,所有3名患者的一只或两只眼睛接受了一或两个疗程的治疗。病例3仅左眼接受治疗。每位患者均接受了全面的眼科检查、光谱域光学相干断层扫描(OCT)、频率加倍技术中心视野检查以及明视和暗视全视野视网膜电图检查。与基线检查结果相比,随访期间,病例1的双眼和病例2的左眼视力提高,而病例2的右眼和病例3的左眼视力下降;病例1的视野敏感度稳定,病例2和病例3的双眼视野敏感度提高;病例1和病例2的视网膜电图振幅提高,病例3(双眼)的视网膜电图振幅稳定。所有病例的OCT中心黄斑厚度和视网膜结构均稳定。所有患者均未出现与治疗相关的副作用。
这是第一份表明在长期随访中,DHRD患者接受2RT治疗可能改善或稳定一些视网膜功能参数且无明显结构变化的报告。