基于机器学习的小儿溃疡性结肠炎治疗反应诊断组织病理学预测

Xiaoxuan Liu, Thomas Walters, Iram Siddiqui, Oscar Lopez-Nunez, Surya Prasath, Lee A Denson, PROTECT consortium, Jasbir Dhaliwal
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摘要

背景与目的:我们曾报道过与小儿溃疡性结肠炎(UC)预后相关的临床特征。在此,我们建立了一个组织病理学模型,用于预测单用美沙拉秦治疗后的无皮质类固醇缓解(CSFR)。方法分别对 292 名和 113 名小儿 UC 患者的训练组和验证组的治疗前直肠活检切片进行数字化处理。整张切片图像(WSI)经过预处理。使用包括纹理、颜色、直方图和细胞核在内的 250 个组学特征训练了 13 个机器学习 (ML) 模型。特征的重要性由吉尼指数决定,分类器使用最重要的特征进行再训练。结果来自 292 名训练组患者(男性:53%;年龄:13 岁(IQR:11-15);CSFR:41%)的 187571 个信息斑块在 13 个 ML 分类器上进行了训练。最佳模型是随机森林(RF)。确定并训练了 18 个最佳组学特征,相应的 WSI AUROC 为 0.89 (95%CI:0.71, 0.96),CSFR 的准确率为 90%。在一个由 113 名患者组成的独立真实世界数据集上重新训练了特征,模型的 WSI AUROC 为 0.85(95%CI:0.75, 0.95),准确率为 85%。结论诊断时获得的常规组织病理学包含与 UC 治疗反应和疾病潜在机制相关的组织学特征。
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Machine Learning-Based Prediction of Pediatric Ulcerative Colitis Treatment Response using Diagnostic Histopathology
Background and Aims: We previously reported clinical features associated with outcomes in pediatric ulcerative colitis (UC). Here we developed a histopathology model to predict corticosteroid-free remission (CSFR) on mesalamine therapy alone. Methods: Pre-treatment rectal biopsy slides were digitized in training and validation groups of 292 and 113 pediatric UC patients, respectively. Whole slide images (WSI) underwent pre-processing. Thirteen machine learning (ML) models were trained using 250 histomic features including texture, color, histogram, and nuclei. Feature importance was determined by the Gini index with the classifier re-trained using the top features. Results: 187571 informative patches from 292 training group patients (Male:53%; Age:13y (IQR:11-15); CSFR:41%) were trained on 13 ML classifiers. The best model was random forest (RF). Eighteen optimal histomic features were identified and trained, and the corresponding WSI AUROC was 0.89 (95%CI:0.71, 0.96), accuracy of 90% for CSFR. Features were re-trained on an independent real-world dataset of 113 patients and the model WSI AUROC was 0.85 (95%CI:0.75, 0.95), accuracy of 85%. Conclusion: Routine histopathology obtained at diagnosis contains histomic features associated with both UC treatment responses and underlying mechanisms of disease.
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