Department of Ophthalmology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Department of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands.
JAMA Ophthalmol. 2021 Jul 1;139(7):743-750. doi: 10.1001/jamaophthalmol.2021.1407.
Treatments for geographic atrophy (GA), a late stage of age-related macular degeneration (AMD), are currently under development. Understanding the natural course is needed for optimal trial design. Although enlargement rates of GA and visual acuity (VA) in the short term are known from clinical studies, knowledge of enlargement in the long term, life expectancy, and visual course is lacking.
To determine long-term enlargement of GA.
DESIGN, SETTING, AND PARTICIPANTS: In this study, participant data were collected from 4 population-based cohort studies, with up to 25 years of follow-up and eye examinations at 5-year intervals: the Rotterdam Study cohorts 1, 2, and 3 and the Blue Mountains Eye Study. Data were collected from 1990 to 2015, and data were analyzed from January 2019 to November 2020.
Area of GA was measured pixel by pixel using all available imaging. Area enlargement and enlargement of the square root-transformed area, time until GA reached the central fovea, and time until death were assessed, and best-corrected VA, smoking status, macular lesions according to the Three Continent AMD Consortium classification, a modified version of the Wisconsin age-related maculopathy grading system, and AMD genetic variants were covariates in Spearman, Pearson, or Mann-Whitney analyses.
Of 171 included patients, 106 (62.0%) were female, and the mean (SD) age at inclusion was 82.6 (7.1) years. A total of 147 of 242 eyes with GA (60.7%) were newly diagnosed in our study. The mean area of GA at first presentation was 3.74 mm2 (95% CI, 3.11-4.67). Enlargement rate varied widely between persons (0.02 to 4.05 mm2 per year), with a mean of 1.09 mm2 per year (95% CI, 0.89-1.30). Stage of AMD in the other eye was correlated with GA enlargement (Spearman ρ = 0.34; P = .01). Foveal involvement was already present in incident GA in 55 of 147 eyes (37.4%); 23 of 42 eyes (55%) developed this after a mean (range) period of 5.6 (3-12) years, and foveal involvement did not develop before death in 11 of 42 eyes (26%). After first diagnosis, 121 of 171 patients with GA (70.8%) died after a mean (SD) period of 6.4 (5.4) years. Visual function was visually impaired (less than 20/63) in 47 of 107 patients (43.9%) at last visit before death.
In this study, enlargement of GA appeared to be highly variable in the general population. More than one-third of incident GA was foveal at first presentation; those with extrafoveal GA developed foveal GA after a mean of 5.6 years. Future intervention trials should focus on recruiting those patients who have a high chance of severe visual decline within their life expectancy.
目前正在开发治疗年龄相关性黄斑变性(AMD)晚期的地理萎缩(GA)的治疗方法。为了进行最佳的试验设计,需要了解其自然病程。尽管从临床研究中已经知道 GA 和视力(VA)在短期内的扩大率,但缺乏长期扩大、预期寿命和视觉过程的知识。
确定 GA 的长期扩大情况。
设计、地点和参与者:在这项研究中,参与者的数据来自 4 项基于人群的队列研究,随访时间长达 25 年,每 5 年进行一次眼部检查:鹿特丹研究队列 1、2 和 3 以及蓝山眼研究。数据收集于 1990 年至 2015 年,分析数据的时间为 2019 年 1 月至 2020 年 11 月。
使用所有可用的成像方法逐像素测量 GA 面积。评估 GA 的扩大和平方根变换后的面积扩大、GA 达到中央凹的时间以及死亡时间,并对最佳矫正视力(VA)、吸烟状况、根据三大陆 AMD 联合会分类的黄斑病变、威斯康星州年龄相关性黄斑病变分级系统的改良版和 AMD 遗传变异进行 Spearman、Pearson 或 Mann-Whitney 分析。
在 171 名纳入的患者中,106 名(62.0%)为女性,纳入时的平均(SD)年龄为 82.6(7.1)岁。我们的研究中共有 242 只患有 GA 的眼睛中有 147 只(60.7%)是新诊断的。首次就诊时 GA 的平均面积为 3.74mm2(95%CI,3.11-4.67)。人与人之间的扩大率差异很大(0.02 至 4.05mm2/年),平均每年为 1.09mm2(95%CI,0.89-1.30)。对侧眼 AMD 的分期与 GA 扩大相关(Spearman ρ=0.34;P=0.01)。在 147 只 GA 眼中,55 只(37.4%)已经存在黄斑中心凹受累;其中 23 只(55%)在平均(范围)5.6(3-12)年后出现这种情况,而在 42 只眼中,有 11 只(26%)在死亡前黄斑中心凹没有受累。首次诊断后,171 名 GA 患者中有 121 名(70.8%)在平均(SD)6.4(5.4)年后死亡。在死亡前最后一次就诊时,107 名视力受损(视力低于 20/63)的患者中有 47 名(43.9%)。
在这项研究中,GA 的扩大在一般人群中似乎差异很大。超过三分之一的新发 GA 最初是黄斑中心凹受累;那些存在黄斑中心凹外 GA 的患者在平均 5.6 年后发展为黄斑中心凹 GA。未来的干预试验应重点招募那些在预期寿命内有严重视力下降风险的患者。