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Predicting geographic atrophy growth rate from fundus autofluorescence images using deep neural networks

机译:使用深神经网络预测来自眼底自发荧光图像的地理萎缩生长率

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Geographic atrophy (GA) is late-stage dry age-related macular degeneration (AMD). Improved predictors of GA progression would be useful in clinical trial design and may be relevant for clinical practice. The purpose of this study was to accurately predict GA progression over time from baseline fundus autofluorescence (FAF) images (Heidelberg Engineering, Inc., Germany) using deep learning. Study eyes of patients (n = 1312) enrolled in the Lampalizumab trials1,2 (NCT02479386, NCT02247479, NCT02247531) were included. The dataset was split by patient into training (n = 1047) and holdout sets (n = 265). GA progression, defined as GA lesion growth rate, was derived by a linear fit on all available measurements of GA lesion area (mm~2, measured from manually graded FAF images). The model performance was evaluated using 5-fold cross-validation (CV). Coefficient of determination (R~2) computed as the square of Pearson correlation coefficient was used as the performance metric. Multiple modeling approaches were implemented, and the best performance was observed using cascade learning. In this approach, pre-trained weights on ImageNet were fine-tuned to predict GA lesion area followed by further fine-tuning to predict GA growth rate. The 5-folds had an average CV R~2 of 0.44, and the holdout showed R~2 of 0.50 (95% confidence interval: 0.41 - 0.61). In comparison, a linear model using only baseline GA lesion area in the same holdout showed an R~2 of 0.18. Further investigation with visualization techniques might help understand the pathophysiology behind the predictions. The predictions may be improved by combining with imaging modalities like near-infrared and/or optical coherence tomography.
机译:地理萎缩(GA)是晚期干燥年龄相关的黄斑变性(AMD)。 GA进展的改进预测因子在临床试验设计中是有用的,并且可能与临床实践相关。本研究的目的是准确地预测从基线眼底自发荧光(FAF)图像(FAF)图像(德国海德尔伯格工程,Inc.)的时间随着时间的推移来预测GA进展。包括患者的患者(N = 1312)的研究眼睛,纳入甘露出者试验1,2(NCT02479386,NCT02247479,NCT02247531)。数据集通过患者分割成训练(n = 1047)并阻止集合(n = 265)。定义为GA病变生长速率的GA进展,通过线性配合来源于GA病变区域的所有可用测量(MM〜2,从手动分级的FAF图像测量)。使用5倍交叉验证(CV)进行评估模型性能。用作Pearson相关系数的平方计算的确定系数(R〜2)用作性能度量。实施多种建模方法,使用级联学习观察到最佳性能。在这种方法中,微调上预先训练的Imagenet的重量以预测GA病变区域,然后进一步微调以预测GA生长速率。 5倍的平均CV r〜2为0.44,并且熔断显示R〜2的0.50(95%置信区间:0.41-0.61)。相比之下,仅使用相同阻滞的基线GA病变区域的线性模型显示了0.18的R〜2。通过可视化技术进一步调查可能有助于了解预测背后的病理生理学。通过与近红外和/或光学相干断层扫描等成像方式组合,可以改善预测。

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