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Identification of glomerular lesions and intrinsic glomerular cells types in kidney diseases via deep learning.

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Abstract

Identification of glomerular lesions and structures is a key point for pathological diagnosis, treatment instructions and prognosis evaluation in kidney diseases. These time-consuming tasks require a more accurate and reproducible quantitative analysis method. We established derivation and validation cohorts composed of 400 Chinese patients with Immunoglobulin A nephropathy (IgAN) retrospectively. Deep convolutional neural networks and biomedical image processing algorithms were implemented to locate glomeruli, identify glomerular lesions (global and segmental glomerular sclerosis, crescent, and none of the above), identify and quantify different intrinsic glomerular cells, and assess a network-based mesangial hypercellularity score in Periodic Acid Schiff (PAS)-stained slides. Our framework achieved 93.1% average precision and 94.9% average recall for location of glomeruli, and a total Cohen’s kappa of 0.912 [95% confidence interval (CI), 0.892-0.932] for glomerular lesion classification. The evaluation of global, segmental glomerular sclerosis and crescents achieved Cohen’s kappa values of 1.0, 0.776, 0.861 and 95% CI of [1.0, 1.0], [0.727, 0.825], [0.824, 0.898], respectively. The well designed neural network can identify three kinds of intrinsic glomerular cells with 92.2% accuracy, surpassing the about 5-11% average accuracy of junior pathologists. Statistical interpretation shows that there was a significant difference (p value <0.0001) between this analytic renal pathology system (ARPS) and four junior pathologists for identifying mesangial and endothelial cells, while that for podocytes were similar, with p value = 0.0602. In addition, this study indicated that the ratio of mesangial cells, endothelial cells and podocytes within glomeruli from IgAN was 0.41:0.36:0.23. and the performance of mesangial score assessment reached a Cohen’s kappa of 0.42 and 95% CI [0.18, 0.69]. The proposed computer-aided diagnosis system has feasibility for quantitative analysis and auxiliary recognition of glomerular pathological features. This article is protected by copyright. All rights reserved.
This article is protected by copyright. All rights reserved.

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