论文标题
使用深度学习预测晚期相关黄斑变性的风险
Predicting risk of late age-related macular degeneration using deep learning
论文作者
论文摘要
到2040年,与年龄相关的黄斑变性(AMD)将影响全球约2.88亿人。识别出高风险发展到AMD后期的个体,即视力危及阶段,对于临床行动,包括医疗干预和及时监测至关重要。尽管深度学习已经显示出使用彩色眼睛照片诊断/筛选AMD的希望,但仍然很难准确预测个人的后期AMD风险。对于这两项任务,这些最初的深度学习尝试在很大程度上仍然是独立人群中未验证的。在这里,我们证明了如何使用3,298名参与者(超过80,000张图像)从与年龄相关的眼病研究AREDS和AREDS2(AREDS2)(AMD中最大的纵向临床试验)中预测到AMD的后期AMD的可能性。当对601名参与者的独立测试数据集进行验证时,我们的模型实现了很高的预后准确性(五年C统计86.4(95%置信区间86.2-86.6)),使用两个现有的临床标准(81.3(81.1.1-81.5)和82.0.82.0.81.8-82),该数据实质上超过了视网膜专家的预后准确性。有趣的是,我们的方法为AMD预后的现有临床标准提供了更多优势(例如,风险确定高于50%),鉴于美国82个美国视网膜特种诊所的培训数据广度,可能是高度概括的。实际上,在外部验证期间,通过对AREDS进行培训和对AREDS2作为独立队列的测试,我们的模型保留了比现有临床标准更高的预后准确性。这些结果突出了深度学习系统增强AMD患者临床决策的潜力。
By 2040, age-related macular degeneration (AMD) will affect approximately 288 million people worldwide. Identifying individuals at high risk of progression to late AMD, the sight-threatening stage, is critical for clinical actions, including medical interventions and timely monitoring. Although deep learning has shown promise in diagnosing/screening AMD using color fundus photographs, it remains difficult to predict individuals' risks of late AMD accurately. For both tasks, these initial deep learning attempts have remained largely unvalidated in independent cohorts. Here, we demonstrate how deep learning and survival analysis can predict the probability of progression to late AMD using 3,298 participants (over 80,000 images) from the Age-Related Eye Disease Studies AREDS and AREDS2, the largest longitudinal clinical trials in AMD. When validated against an independent test dataset of 601 participants, our model achieved high prognostic accuracy (five-year C-statistic 86.4 (95% confidence interval 86.2-86.6)) that substantially exceeded that of retinal specialists using two existing clinical standards (81.3 (81.1-81.5) and 82.0 (81.8-82.3), respectively). Interestingly, our approach offers additional strengths over the existing clinical standards in AMD prognosis (e.g., risk ascertainment above 50%) and is likely to be highly generalizable, given the breadth of training data from 82 US retinal specialty clinics. Indeed, during external validation through training on AREDS and testing on AREDS2 as an independent cohort, our model retained substantially higher prognostic accuracy than existing clinical standards. These results highlight the potential of deep learning systems to enhance clinical decision-making in AMD patients.