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本文引用的文献

1
Therapeutic Insights in Chronic Kidney Disease Progression.慢性肾脏病进展的治疗见解
Front Med (Lausanne). 2021 Feb 23;8:645187. doi: 10.3389/fmed.2021.645187. eCollection 2021.
2
Automated Computational Detection of Interstitial Fibrosis, Tubular Atrophy, and Glomerulosclerosis.间质纤维化、肾小管萎缩和肾小球硬化的自动计算检测
J Am Soc Nephrol. 2021 Apr;32(4):837-850. doi: 10.1681/ASN.2020050652. Epub 2021 Feb 23.
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Digital pathology and computational image analysis in nephropathology.数字病理学和肾脏病学中的计算图像分析。
Nat Rev Nephrol. 2020 Nov;16(11):669-685. doi: 10.1038/s41581-020-0321-6. Epub 2020 Aug 26.
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Artificial intelligence as the next step towards precision pathology.人工智能作为迈向精准病理学的下一步。
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Computational Segmentation and Classification of Diabetic Glomerulosclerosis.糖尿病肾小球硬化的计算分割与分类。
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Comprehensive Integration of Single-Cell Data.单细胞数据的综合整合。
Cell. 2019 Jun 13;177(7):1888-1902.e21. doi: 10.1016/j.cell.2019.05.031. Epub 2019 Jun 6.
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Dimensionality reduction for visualizing single-cell data using UMAP.使用UMAP进行单细胞数据可视化的降维方法。
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A 2018 Reference Guide to the Banff Classification of Renal Allograft Pathology.2018 年肾移植病理的班夫分类参考指南。
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9
Should We Always Defer Treatment of Kidney Disease When There Is Extensive Interstitial Fibrosis on Biopsy?当活检显示广泛间质纤维化时,我们是否应该始终推迟肾脏疾病的治疗?
Am J Nephrol. 2016;44(4):286-288. doi: 10.1159/000449513. Epub 2016 Sep 15.
10
Renal histologic changes and the outcome in patients with diabetic nephropathy.糖尿病肾病患者的肾脏组织学变化及预后
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全肾活检的自动化肾小管形态计量可视化

Automated Tubular Morphometric Visualization for Whole Kidney Biopsy.

作者信息

Kavthekar Neil, Ginley Brandon, Border Samuel, Lucarelli Nicholas, Jen Kuang-Yu, Sarder Pinaki

机构信息

Departments of Biomedical Engineering, University at Buffalo, the State University of New York.

Pathology & Anatomical Sciences, University at Buffalo, the State University of New York.

出版信息

Proc SPIE Int Soc Opt Eng. 2022 Feb-Mar;12039. doi: 10.1117/12.2613496. Epub 2022 Apr 4.

DOI:10.1117/12.2613496
PMID:37817876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10563114/
Abstract

One of the strongest prognostic predictors of chronic kidney disease is interstitial fibrosis and tubular atrophy (IFTA). The ultimate goal of IFTA calculation is an estimation of the functional nephritic area. However, the clinical gold standard of estimation by pathologist is imprecise, primarily due to the overwhelming number of tubules sampled in a standard kidney biopsy. Artificial intelligence algorithms could provide significant benefit in this aspect as their high-throughput could identify and quantitatively measure thousands of tubules in mere minutes. Towards this goal, we use a custom panoptic convolutional network similar to Panoptic-DeepLab to detect tubules from 87 WSIs of biopsies from native diabetic kidneys and transplant kidneys. We measure 206 features on each tubule, including commonly understood features like tubular basement membrane thickness and tubular diameter. Finally, we have developed a tool which allows a user to select a range of tubule morphometric features to be highlighted in corresponding WSIs. The tool can also highlight tubules in WSI leveraging multiple morphometric features through selection of regions-of-interest in a uniform manifold approximation and projection plot.

摘要

慢性肾脏病最强的预后预测指标之一是间质纤维化和肾小管萎缩(IFTA)。计算IFTA的最终目标是估计功能性肾实质面积。然而,病理学家进行估计的临床金标准并不精确,主要原因是在标准肾活检中采样的肾小管数量过多。人工智能算法在这方面可以提供显著的益处,因为它们的高通量能够在短短几分钟内识别并定量测量数千个肾小管。为了实现这一目标,我们使用了一个类似于全景深度实验室(Panoptic-DeepLab)的定制全景卷积网络,从87张来自原发性糖尿病肾病和移植肾活检的全切片图像(WSIs)中检测肾小管。我们在每个肾小管上测量206个特征,包括诸如肾小管基底膜厚度和肾小管直径等常见特征。最后,我们开发了一种工具,允许用户选择一系列肾小管形态计量特征,以便在相应的全切片图像中突出显示。该工具还可以通过在统一流形近似和投影图中选择感兴趣区域,利用多个形态计量特征突出显示全切片图像中的肾小管。