Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patients

AbstractBackground The analytical renal pathology system (ARPS) based on convolutional neural networks has been used successfully in native IgA nephropathy (IgAN) patients. Considering the similarity of pathologic features, we aim to evaluate the performance of the ARPS in allograft IgAN patients an...

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Main Authors: Xumeng Liu, Huiwen Fang, Dongmei Liang, Qunjuan Lei, Jiaping Wang, Feng Xu, Shaoshan Liang, Dandan Liang, Fan Yang, Heng Li, Jianghua Chen, Yuan Ni, Guotong Xie, Caihong Zeng
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Renal Failure
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/0886022X.2024.2322043
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author Xumeng Liu
Huiwen Fang
Dongmei Liang
Qunjuan Lei
Jiaping Wang
Feng Xu
Shaoshan Liang
Dandan Liang
Fan Yang
Heng Li
Jianghua Chen
Yuan Ni
Guotong Xie
Caihong Zeng
author_facet Xumeng Liu
Huiwen Fang
Dongmei Liang
Qunjuan Lei
Jiaping Wang
Feng Xu
Shaoshan Liang
Dandan Liang
Fan Yang
Heng Li
Jianghua Chen
Yuan Ni
Guotong Xie
Caihong Zeng
author_sort Xumeng Liu
collection DOAJ
description AbstractBackground The analytical renal pathology system (ARPS) based on convolutional neural networks has been used successfully in native IgA nephropathy (IgAN) patients. Considering the similarity of pathologic features, we aim to evaluate the performance of the ARPS in allograft IgAN patients and broaden its implementation.Methods Biopsy-proven allograft IgAN patients from two different centers were enrolled for internal and external validation. We implemented the ARPS to identify glomerular lesions and intrinsic glomerular cells, and then evaluated its performance. Consistency between the ARPS and pathologists was assessed using intraclass correlation coefficients. The association of digital pathological features with clinical and pathological data was measured. Kaplan-Meier survival curve and cox proportional hazards model were applied to investigate prognosis prediction.Results A total of 56 biopsy-proven allograft IgAN patients from the internal center and 17 biopsy-proven allograft IgAN patients from the external center were enrolled in this study. The ARPS was successfully applied to identify the glomerular lesions (F1-score, 0.696–0.959) and quantify intrinsic glomerular cells (F1-score, 0.888–0.968) in allograft IgAN patients rapidly and precisely. Furthermore, the mesangial hypercellularity score was positively correlated with all mesangial metrics provided by ARPS [Spearman’s correlation coefficient (r), 0.439–0.472, and all p values < 0.001]. Besides, a higher allograft survival was noticed among patients in the high-level groups of the maximum and ratio of endothelial cells, as well as the maximum and density of podocytes.Conclusion We propose that the ARPS could be implemented in future clinical practice with outstanding capability.
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spelling doaj.art-2bf9974e0cdb4fc4be17b35f130ba8a22024-03-01T06:29:40ZengTaylor & Francis GroupRenal Failure0886-022X1525-60492024-12-0146110.1080/0886022X.2024.2322043Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patientsXumeng Liu0Huiwen Fang1Dongmei Liang2Qunjuan Lei3Jiaping Wang4Feng Xu5Shaoshan Liang6Dandan Liang7Fan Yang8Heng Li9Jianghua Chen10Yuan Ni11Guotong Xie12Caihong Zeng13National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaPing An Healthcare Technology, Shanghai, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaKidney Disease Center, First Affiliated Hospital, College of Medicine, Zhejiang University, Zhejiang, ChinaKidney Disease Center, First Affiliated Hospital, College of Medicine, Zhejiang University, Zhejiang, ChinaPing An Healthcare Technology, Shanghai, ChinaPing An Healthcare Technology, Shanghai, ChinaNational Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, ChinaAbstractBackground The analytical renal pathology system (ARPS) based on convolutional neural networks has been used successfully in native IgA nephropathy (IgAN) patients. Considering the similarity of pathologic features, we aim to evaluate the performance of the ARPS in allograft IgAN patients and broaden its implementation.Methods Biopsy-proven allograft IgAN patients from two different centers were enrolled for internal and external validation. We implemented the ARPS to identify glomerular lesions and intrinsic glomerular cells, and then evaluated its performance. Consistency between the ARPS and pathologists was assessed using intraclass correlation coefficients. The association of digital pathological features with clinical and pathological data was measured. Kaplan-Meier survival curve and cox proportional hazards model were applied to investigate prognosis prediction.Results A total of 56 biopsy-proven allograft IgAN patients from the internal center and 17 biopsy-proven allograft IgAN patients from the external center were enrolled in this study. The ARPS was successfully applied to identify the glomerular lesions (F1-score, 0.696–0.959) and quantify intrinsic glomerular cells (F1-score, 0.888–0.968) in allograft IgAN patients rapidly and precisely. Furthermore, the mesangial hypercellularity score was positively correlated with all mesangial metrics provided by ARPS [Spearman’s correlation coefficient (r), 0.439–0.472, and all p values < 0.001]. Besides, a higher allograft survival was noticed among patients in the high-level groups of the maximum and ratio of endothelial cells, as well as the maximum and density of podocytes.Conclusion We propose that the ARPS could be implemented in future clinical practice with outstanding capability.https://www.tandfonline.com/doi/10.1080/0886022X.2024.2322043Deep learningallograft IgANglomerular lesionintrinsic glomerular celloutcome
spellingShingle Xumeng Liu
Huiwen Fang
Dongmei Liang
Qunjuan Lei
Jiaping Wang
Feng Xu
Shaoshan Liang
Dandan Liang
Fan Yang
Heng Li
Jianghua Chen
Yuan Ni
Guotong Xie
Caihong Zeng
Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patients
Renal Failure
Deep learning
allograft IgAN
glomerular lesion
intrinsic glomerular cell
outcome
title Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patients
title_full Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patients
title_fullStr Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patients
title_full_unstemmed Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patients
title_short Advancing the application of the analytical renal pathology system in allograft IgA nephropathy patients
title_sort advancing the application of the analytical renal pathology system in allograft iga nephropathy patients
topic Deep learning
allograft IgAN
glomerular lesion
intrinsic glomerular cell
outcome
url https://www.tandfonline.com/doi/10.1080/0886022X.2024.2322043
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