Centro Hospitalar de Lisboa Central EPE, Department of Ophthalmology, Lisboa, Portugal.
iNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade Nova de Lisboa, Lisboa, Portugal.
Transl Vis Sci Technol. 2023 Jul 3;12(7):22. doi: 10.1167/tvst.12.7.22.
Intermediate age-related macular degeneration (iAMD) is a risk factor for progression to advanced stages, but rates of progression vary between individuals. Predicting individual risk is advantageous for programing timely and effective treatment and for patient stratification into future clinical trials.
We conducted a prospective and noninterventional study following patients with iAMD for 24 months. Optical coherence tomography parameters related with drusen, hyper-reflective foci (HRF), presence of incomplete retinal pigment epithelial and outer retinal atrophy (iRORA) and ellipsoid zone (EZ) status were explored at the baseline. Patients were reclassified at the end of the follow-up period and divided according to their progression. A risk prediction model for progression to late AMD was developed.
A total of 135 patients were enrolled in the study and 30.4% developed late disease. A multivariate logistic regression model was created using those optical coherence tomography parameters, further optimized by backward feature elimination. Parameters offering the best fit in prediction progression were presence of iRORA, EZ status, drusen area and presence of HRF. iRORA is the feature that provides a higher probability of developing late AMD (odds ratio, 12.91; P = 0.000), followed by EZ disruption status (odds ratio, 3.54; P = 0.0018). The area under the receiver operating characteristic curve calculated for the testing set was 0.77 (95% confidence interval, 0.56-0.98).
The combination of iRORA and EZ disruption constitute a high risk of progression to complete RORA within 2 years.
We propose a practical and useful model to help clinicians in their daily practice in predicting individual progression to advanced AMD.
中度年龄相关性黄斑变性(iAMD)是进展为晚期的危险因素,但个体之间的进展速度有所不同。预测个体风险有利于及时有效地治疗,并将患者分层为未来的临床试验。
我们对 iAMD 患者进行了为期 24 个月的前瞻性非干预性研究。在基线时,研究人员探索了与玻璃膜疣、高反射焦点(HRF)、不完全视网膜色素上皮和外层视网膜萎缩(iRORA)以及椭圆体带(EZ)状态相关的光学相干断层扫描参数。在随访期末对患者进行重新分类,并根据其进展情况进行分组。开发了一种预测进展为晚期 AMD 的风险预测模型。
共有 135 名患者纳入研究,其中 30.4%的患者进展为晚期疾病。使用这些光学相干断层扫描参数创建了一个多变量逻辑回归模型,并通过向后特征消除进一步优化。在预测进展方面提供最佳拟合的参数是 iRORA 的存在、EZ 状态、玻璃膜疣面积和 HRF 的存在。iRORA 是发生晚期 AMD 的可能性更高的特征(优势比,12.91;P=0.000),其次是 EZ 破坏状态(优势比,3.54;P=0.0018)。为测试集计算的接收者操作特征曲线下面积为 0.77(95%置信区间,0.56-0.98)。
iRORA 和 EZ 破坏的结合在 2 年内构成了完全 RORA 进展的高风险。
何金津