斯塔加特萎缩症和地理萎缩症纵向进展的并发预测

Zubin Mishra, Ziyuan Chris Wang, Emily Xu, Sophia Xu, Iyad Majid, SriniVas Reddy Sadda, Zhihong Jewel Hu
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摘要

斯塔加特病和老年性黄斑变性分别是青少年和老年人失明的主要原因。黄斑萎缩区的形成是这两种疾病晚期的标志。这些疾病的进展可通过各种成像模式进行跟踪,其中最常见的两种模式是眼底自动荧光成像(FAF)和光谱域光学相干断层扫描(SD-OCT)。本研究旨在探讨如何利用纵向 FAF 和 SD-OCT 成像(0 个月、6 个月、12 个月和 18 个月)数据来预测 Stargardt 和地理性萎缩的未来萎缩情况。为了实现这一目标,我们开发了一套新型深度卷积神经网络,该网络利用平均强度特征之外的改进视网膜层特征,增强了用于纵向预测的递归网络单元和同时学习的集合网络单元(称为 ReConNet)。利用 FAF 图像,本文介绍的神经网络对斯塔加特萎缩的平均(标准偏差,SD)和中位数 Dice 系数分别为 0.895(0.086)和 0.922,对地理萎缩的平均(标准偏差,SD)和中位数 Dice 系数分别为 0.864(0.113)和 0.893。使用 SD-OCT 图像预测斯塔加尔特萎缩时,神经网络的平均和中位 Dice 系数分别为 0.882 (0.101) 和 0.906。当仅用 FAF 图像预测萎缩病变的间隔生长时,Stargardt 萎缩的平均(SD)和中位数 Dice 系数分别为 0.557 (0.094) 和 0.559,地理萎缩的平均(SD)和中位数 Dice 系数分别为 0.612 (0.089) 和 0.601。OCT 图像的预测性能与使用 FAF 的预测性能相当,这为临床试验和视网膜诊所评估萎缩进展打开了一扇新的、更高效、更实用的大门,超越了广泛使用的 FAF。这些结果非常鼓舞人心,当我们在临床上获得更频繁或更长期的纵向数据时,就能进行高性能的间隔生长预测。这是我们下一步研究的紧迫任务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent and Concurrent Prediction of Longitudinal Progression of Stargardt Atrophy and Geographic Atrophy
Stargardt disease and age-related macular degeneration are the leading causes of blindness in the juvenile and geriatric populations, respectively. The formation of atrophic regions of the macula is a hallmark of the end-stages of both diseases. The progression of these diseases is tracked using various imaging modalities, two of the most common being fundus autofluorescence (FAF) imaging and spectral-domain optical coherence tomography (SD-OCT). This study seeks to investigate the use of longitudinal FAF and SD-OCT imaging (month 0, month 6, month 12, and month 18) data for the predictive modelling of future atrophy in Stargardt and geographic atrophy. To achieve such an objective, we develop a set of novel deep convolutional neural networks enhanced with recurrent network units for longitudinal prediction and concurrent learning of ensemble network units (termed ReConNet) which take advantage of improved retinal layer features beyond the mean intensity features. Using FAF images, the neural network presented in this paper achieved mean (standard deviation, SD) and median Dice coefficients of 0.895 (0.086) and 0.922 for Stargardt atrophy, and 0.864 (0.113) and 0.893 for geographic atrophy. Using SD-OCT images for Stargardt atrophy, the neural network achieved mean and median Dice coefficients of 0.882 (0.101) and 0.906, respectively. When predicting only the interval growth of the atrophic lesions with FAF images, mean (SD) and median Dice coefficients of 0.557 (0.094) and 0.559 were achieved for Stargardt atrophy, and 0.612 (0.089) and 0.601 for geographic atrophy. The prediction performance in OCT images is comparably good to that using FAF which opens a new, more efficient, and practical door in the assessment of atrophy progression for clinical trials and retina clinics, beyond widely used FAF. These results are highly encouraging for a high-performance interval growth prediction when more frequent or longer-term longitudinal data are available in our clinics. This is a pressing task for our next step in ongoing research.
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