Interpretable-by-design Deep Survival Analysis for Disease Progression Modeling

Julius Gervelmeyer, Sarah Mueller, Kerol Djoumessi, David Merle, Simon J Clark, Lisa Koch, Philipp Berens
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Abstract

In the elderly, degenerative diseases often develop differently over time for individual patients. For optimal treatment, physicians and patients would like to know how much time is left for them until symptoms reach a certain stage. However, compared to simple disease detection tasks, disease progression modeling has received much less attention. In addition, most existing models are black-box models which provide little insight into the mechanisms driving the prediction. Here, we introduce an interpretable-by-design survival model to predict the progression of age-related macular degeneration (AMD) from fundus images. Our model not only achieves state-of-the-art prediction performance compared to black-box models but also provides a sparse map of local evidence of AMD progression for individual patients. Our evidence map faithfully reflects the decision-making process of the model in contrast to widely used post-hoc saliency methods. Furthermore, we show that the identified regions mostly align with established clinical AMD progression markers. We believe that our method may help to inform treatment decisions and may lead to better insights into imaging biomarkers indicative of disease progression. The project's code is available at github.com/berenslab/interpretable-deep-survival-analysis.
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用于疾病进展建模的可解释设计深度生存分析
在老年人中,退行性疾病随着时间的推移往往会因人而异。为了达到最佳治疗效果,医生和患者都希望知道,在症状达到某个阶段之前,他们还能活多久。然而,与简单的疾病检测任务相比,疾病进展建模受到的关注要少得多。此外,现有的大多数模型都是黑箱模型,对预测的驱动机制几乎没有深入的了解。在这里,我们引入了一种可解释的设计生存模型,通过眼底图像预测老年性黄斑变性(AMD)的进展。与黑盒模型相比,我们的模型不仅实现了最先进的预测性能,而且还为单个患者提供了AMD进展的局部证据稀疏图。我们的证据图忠实地反映了模型的决策过程,与广泛使用的事后显著性方法形成鲜明对比。此外,我们还表明,所识别的区域大多与已确定的临床 AMD 进展标记一致。我们相信,我们的方法可能有助于为治疗决策提供依据,并能让人们更好地了解指示疾病进展的成像生物标志物。该项目的代码见 github.com/berenslab/interpretable-deep-survival-analysis。
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