Rahimy Ehsan, Khan M Ali, Ho Allen C, Hatfield Meghan, Nguyen Thai Hien, Jones Daniel, McKeown Alex, Borkar Durga, Leng Theodore, Ribeiro Ramiro, Holekamp Nancy
Palo Alto Medical Foundation, Palo Alto, California.
Byers Eye Institute at Stanford, Stanford University School of Medicine, Palo Alto, California.
Ophthalmol Sci. 2023 Apr 19;3(4):100318. doi: 10.1016/j.xops.2023.100318. eCollection 2023 Dec.
To evaluate disease progression and associated vision changes in patients with geographic atrophy (GA) secondary to age-related macular degeneration (AMD) in 1 eye and GA or neovascular AMD (nAMD) in the fellow eye using a large dataset from routine clinical practice.
Retrospective analysis of clinical data over 24 months.
A total of 256 635 patients with GA from the American Academy of Ophthalmology (Academy) IRIS® Registry (Intelligent Research in Sight) Registry (January 2016 to December 2017).
Patients with ≥ 24 months of follow-up were grouped by fellow-eye status: Cohort 1, GA:GA; Cohort 2, GA:nAMD, each with (subfoveal) and without subfoveal (nonsubfoveal) involvement. Eyes with history of retinal disease other than AMD were excluded. Sensitivity analysis included patients who were managed by retina specialists and had a record of imaging within 30 days of diagnosis.
Change in visual acuity (VA), occurrence of new-onset nAMD, and GA progression from nonsubfoveal to subfoveal.
In total, 69 441 patients were included: 44 120 (64%) GA:GA and 25 321 (36%) GA:nAMD. Otherwise eligible patients (57 788) were excluded due to follow-up < 24 months. In both GA:GA and GA:nAMD cohorts, nonsubfoveal study eyes had better mean (standard deviation) VA at index (67 [19.3] and 66 [20.3] letters) than subfoveal eyes (59 [23.9] and 47 [26.9] letters), and 24-month mean VA changes were similar for nonsubfoveal (-7.6 and -6.2) and subfoveal (-7.9 and -6.5) subgroups. Progression to subfoveal GA occurred in 16.7% of nonsubfoveal study eyes in the GA:GA cohort and 12.5% in the GA:nAMD cohort. More new-onset study-eye nAMD was observed in the GA:nAMD (21.6%) versus GA:GA (8.2%) cohorts. Sensitivity analysis supported the robustness of the observations in the study.
This retrospective analysis describes the natural progression of GA lesions and the decline in VA associated with the disease.
Proprietary or commercial disclosure may be found after the references.
利用来自常规临床实践的大型数据集,评估单眼患有年龄相关性黄斑变性(AMD)继发地图样萎缩(GA)且对侧眼患有GA或新生血管性AMD(nAMD)患者的疾病进展及相关视力变化。
对24个月内的临床数据进行回顾性分析。
来自美国眼科学会(眼科学会)IRIS®注册库(视力智能研究)(2016年1月至2017年12月)的总共256635例GA患者。
随访时间≥24个月的患者按对侧眼情况分组:队列1,GA:GA;队列2,GA:nAMD,每组又分为(黄斑中心凹下)累及和未累及黄斑中心凹下(非黄斑中心凹下)。排除有AMD以外视网膜疾病史的眼。敏感性分析纳入由视网膜专科医生诊治且在诊断后30天内有影像学记录的患者。
视力(VA)变化、新发nAMD的发生情况以及GA从非黄斑中心凹下进展至黄斑中心凹下。
总共纳入69441例患者:44120例(64%)GA:GA和25321例(36%)GA:nAMD。另有符合条件但因随访时间<24个月而被排除的患者57788例。在GA:GA和GA:nAMD队列中,非黄斑中心凹下研究眼在基线时的平均(标准差)VA(分别为67[19.3]和66[20.3]个字母)均优于黄斑中心凹下眼(分别为59[23.9]和47[26.9]个字母),非黄斑中心凹下亚组(-7.6和-6.2)和黄斑中心凹下亚组(-7.9和-6.5)的24个月平均VA变化相似。GA:GA队列中16.7%的非黄斑中心凹下研究眼进展为黄斑中心凹下GA,GA:nAMD队列中这一比例为12.5%。GA:nAMD队列(21.6%)中观察到的新发研究眼nAMD比GA:GA队列(8.2%)更多。敏感性分析支持了本研究观察结果的稳健性。
这项回顾性分析描述了GA病变的自然进展以及与该疾病相关的VA下降情况。
专有或商业披露信息可在参考文献之后找到。