使用组织病理学成像预测儿童克罗恩病的深度学习

Anahita H. Sharma, Burke W. Lawlor, Jason Y. Wang, Y. Sharma, S. Sengupta, P. Fernandes, Fatima Zulqarnain, Eve May, S. Syed, Donald E. Brown
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引用次数: 0

摘要

目前诊断克罗恩病的黄金标准是由训练有素的医生对组织进行活检检查。然而,只有在选择合适的活检部位和高质量的图像时,内窥镜图像和组织学特征才明显[1]。因此,为了防止延误诊断或随着时间的推移而重新分类,需要额外的工具来加强病理学家的诊断。最近的研究已经展示了深度学习在开发数字组织学图像的全幻灯片分类方面的成功应用。在这项研究中,我们利用卷积神经网络开发了一种用于预测克罗恩病的斑块级图像分类模型。本研究获得了两家不同医院的数据:INOVA和辛辛那提儿童医院医学中心(CCHMC)。当在同一数据集上训练和验证时,我们的INOVA和CCHMC模型的验证准确率分别为84.6%和93.9%。然而,当对来自一个站点的数据进行训练并对来自另一个站点的数据进行测试时,这些模型的表现很差。为了研究这个问题,我们建立了一个额外的斑块级模型,该模型能够以99%的准确率预测活检的医院来源。这些结果表明存在通过机器学习模型可以检测到的特定地点的人工制品。我们使用颜色归一化、图像裁剪和其他转换减少了这些伪影的影响,将站点预测精度降低到74%。因此,我们建议进一步研究不同部位活检差异的原因,这样可以开发出可推广的组织病理学深度学习模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep Learning for Predicting Pediatric Crohn's Disease Using Histopathological Imaging
The current gold standard for Crohn's disease diagnosis involves the examination of biopsied tissue by a trained physician. However, endoscopic images and histological features are only evident when the appropriate biopsy site is chosen and the image is of high quality [1]. Thus, to prevent delayed diagnoses or reclassifications over time, additional tools to reinforce pathologists' diagnoses are necessary. Recent studies have showcased successful applications of deep learning for developing whole-slide classifications of digital histology images. In this study, we developed a patch-level image classification model for prediction of Crohn's disease using a convolutional neural network. This study obtained data from two different hospitals: INOVA and Cincinnati Children's Hospital Medical Center (CCHMC). When trained and validated on the same data set, our INOVA and CCHMC models achieved validation accuracies of 84.6 % and 93.9 %, respectively. However, the models performed poorly when trained on data from one site and tested on data from the other site. To investigate this issue, we built an additional patch-level model that was able to predict hospital source of the biopsy with 99 % accuracy. These results suggest the presence of site-specific artifacts which are detectable by machine learning models. We reduced the effects of these artifacts using color-normalization, image cropping, and other transformations, lowering site-predictive accuracy to 74%. Therefore, we suggest further works investigate reasons for inter-site biopsy differences such that site-generalizable, histopathological deep learning models can be developed.
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