Thee Eric F, Meester-Smoor Magda A, Luttikhuizen Daniel T, Colijn Johanna M, Enthoven Clair A, Haarman Annechien E G, Rizopoulos Dimitris, Klaver Caroline C W
Department of Ophthalmology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Department of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Transl Vis Sci Technol. 2020 Apr 24;9(2):26. doi: 10.1167/tvst.9.2.26. eCollection 2020 Apr.
To compare frequently used classification systems for age-related macular degeneration (AMD) in their abilty to predict late AMD.
In total, 9066 participants from the population-based Rotterdam Study were followed up for progression of AMD during a study period up to 30 years. AMD lesions were graded on color fundus photographs after confirmation on other image modalities and grouped at baseline according to six classification systems. Late AMD was defined as geographic atrophy or choroidal neovascularization. Incidence rate (IR) and cumulative incidence (CuI) of late AMD were calculated, and Kaplan-Meier plots and area under the operating characteristics curves (AUCs) were constructed.
A total of 186 persons developed incident late AMD during a mean follow-up time of 8.7 years. The AREDS simplified scale showed the highest IR for late AMD at 104 cases/1000 py for ages <75 years. The Rotterdam classification showed the highest IR at 89 cases/1000 py >75 years. The 3-Continent harmonization classification provided the most stable progression. Drusen area >10% ETDRS grid (hazard ratio 30.05, 95% confidence interval [CI] 19.25-46.91) was most prognostic of progression. The highest AUC of late AMD (0.8372, 95% CI: 0.8070-0.8673) was achieved when all AMD features present at baseline were included.
Highest turnover rates from intermediate to late AMD were provided by the AREDS simplified scale and the Rotterdam classification. The 3-Continent harmonization classification showed the most stable progression. All features, especially drusen area, contribute to late AMD prediction.
Findings will help stakeholders select appropriate classification systems for screening, deep learning algorithms, or trials.
比较常用于年龄相关性黄斑变性(AMD)的分类系统预测晚期AMD的能力。
在长达30年的研究期间,对基于人群的鹿特丹研究中的9066名参与者进行随访,观察AMD的进展情况。在通过其他影像模式确认后,根据彩色眼底照片对AMD病变进行分级,并在基线时根据六种分类系统进行分组。晚期AMD定义为地图样萎缩或脉络膜新生血管形成。计算晚期AMD的发病率(IR)和累积发病率(CuI),并绘制Kaplan-Meier曲线和构建操作特征曲线下面积(AUC)。
在平均8.7年的随访时间内,共有186人发生了晚期AMD。年龄<75岁时,年龄相关性眼病研究(AREDS)简化量表显示晚期AMD的发病率最高,为104例/1000人年。鹿特丹分类法显示年龄>75岁时发病率最高,为89例/1000人年。三大洲协调分类法显示进展最为稳定。玻璃膜疣面积>10%早期治疗糖尿病性视网膜病变研究(ETDRS)方格(风险比30.05,95%置信区间[CI]19.25-46.91)对进展的预测性最强。当纳入基线时存在的所有AMD特征时,晚期AMD的AUC最高(0.8372,95%CI:0.8070-0.8673)。
AREDS简化量表和鹿特丹分类法显示从中期到晚期AMD的转化率最高。三大洲协调分类法显示进展最为稳定。所有特征,尤其是玻璃膜疣面积,有助于晚期AMD的预测。
研究结果将有助于利益相关者选择合适的分类系统用于筛查、深度学习算法或试验。