基于深度学习的组织学自身免疫性肝炎评估模型:AI(H).

IF 3.4 3区 医学 Q1 PATHOLOGY
Virchows Archiv Pub Date : 2024-12-01 Epub Date: 2024-06-15 DOI:10.1007/s00428-024-03841-5
Caner Ercan, Kattayoun Kordy, Anna Knuuttila, Xiaofei Zhou, Darshan Kumar, Ville Koponen, Peter Mesenbrink, Serenella Eppenberger-Castori, Parisa Amini, Marcos C Pedrosa, Luigi M Terracciano
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引用次数: 0

摘要

自身免疫性肝炎(AIH)的组织学评估具有挑战性。作为这些挑战的可能结果之一,对自身免疫性肝炎的非经典特征(如胆管损伤)的研究仍然不足。我们的目标是开发一种深度学习工具(用于自身免疫性肝炎的人工智能[AI(H)]),它能分析肝脏活检组织,并直接从常规病理切片中提供可重复、可量化和可解释的结果。Aiforia 人工智能(AI)平台共使用了 123 份治疗前肝脏活检样本、巴塞尔大学医院病理研究所档案中确诊为 AIH 的全切片图像来训练多个卷积神经网络模型。根据病理学家的手动注释,在独立测试集切片上对人工智能模型的性能进行了评估。在苏木精和伊红染色的切片上,人工智能模型在组织检测、肝脏显微解剖、坏死炎症特征、胆管损伤检测和门静脉炎症检测方面的准确率(正确预测比率)分别为 99.4%、88.0%、83.9%、81.7% 和 79.2%。此外,免疫细胞模型对不同免疫细胞(淋巴细胞、浆细胞、巨噬细胞、嗜酸性粒细胞和中性粒细胞)的检测和分类准确率为 72.4%。在天狼星红染色切片上,组织检测、肝脏微解剖和纤维化检测的准确率分别为 99.4%、94.0% 和 87.6%。此外,在 81 例 AIH(68.6%)病例中,AI(H)显示出胆管损伤。研究发现,人工智能模型在预测 AIH 活检样本的各种形态成分方面准确高效。对活检切片的计算分析提供了 AIH 景观中免疫细胞的详细空间和密度数据,而人工计数却很难做到这一点。人工智能(H)有助于提高 AIH 活检评估的可重复性,并为 AIH 组织学带来新的描述性和定量方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A deep-learning-based model for assessment of autoimmune hepatitis from histology: AI(H).

A deep-learning-based model for assessment of autoimmune hepatitis from histology: AI(H).

Histological assessment of autoimmune hepatitis (AIH) is challenging. As one of the possible results of these challenges, nonclassical features such as bile-duct injury stays understudied in AIH. We aim to develop a deep learning tool (artificial intelligence for autoimmune hepatitis [AI(H)]) that analyzes the liver biopsies and provides reproducible, quantifiable, and interpretable results directly from routine pathology slides. A total of 123 pre-treatment liver biopsies, whole-slide images with confirmed AIH diagnosis from the archives of the Institute of Pathology at University Hospital Basel, were used to train several convolutional neural network models in the Aiforia artificial intelligence (AI) platform. The performance of AI models was evaluated on independent test set slides against pathologist's manual annotations. The AI models were 99.4%, 88.0%, 83.9%, 81.7%, and 79.2% accurate (ratios of correct predictions) for tissue detection, liver microanatomy, necroinflammation features, bile duct damage detection, and portal inflammation detection, respectively, on hematoxylin and eosin-stained slides. Additionally, the immune cells model could detect and classify different immune cells (lymphocyte, plasma cell, macrophage, eosinophil, and neutrophil) with 72.4% accuracy. On Sirius red-stained slides, the test accuracies were 99.4%, 94.0%, and 87.6% for tissue detection, liver microanatomy, and fibrosis detection, respectively. Additionally, AI(H) showed bile duct injury in 81 AIH cases (68.6%). The AI models were found to be accurate and efficient in predicting various morphological components of AIH biopsies. The computational analysis of biopsy slides provides detailed spatial and density data of immune cells in AIH landscape, which is difficult by manual counting. AI(H) can aid in improving the reproducibility of AIH biopsy assessment and bring new descriptive and quantitative aspects to AIH histology.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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