Automated Computational Detection of Interstitial Fibrosis, Tubular Atrophy, and Glomerulosclerosis.

convolutional neural network diabetes eGFR glomerulosclerosis interstitial fibrosis machine learning prognostication transplant tubular atrophy whole slide segmentation

Journal

Journal of the American Society of Nephrology : JASN
ISSN: 1533-3450
Titre abrégé: J Am Soc Nephrol
Pays: United States
ID NLM: 9013836

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 13 05 2020
accepted: 14 12 2020
pubmed: 25 2 2021
medline: 25 2 2021
entrez: 24 2 2021
Statut: ppublish

Résumé

Interstitial fibrosis, tubular atrophy (IFTA), and glomerulosclerosis are indicators of irrecoverable kidney injury. Modern machine learning (ML) tools have enabled robust, automated identification of image structures that can be comparable with analysis by human experts. ML algorithms were developed and tested for the ability to replicate the detection and quantification of IFTA and glomerulosclerosis that renal pathologists perform. A renal pathologist annotated renal biopsy specimens from 116 whole-slide images (WSIs) for IFTA and glomerulosclerosis. A total of 79 WSIs were used for training different configurations of a convolutional neural network (CNN), and 17 and 20 WSIs were used as internal and external testing cases, respectively. The best model was compared against the input of four renal pathologists on 20 new testing slides. Further, for 87 testing biopsy specimens, IFTA and glomerulosclerosis measurements made by pathologists and the CNN were correlated to patient outcome using classic statistical tools. The best average performance across all image classes came from a DeepLab version 2 network trained at 40× magnification. IFTA and glomerulosclerosis percentages derived from this CNN achieved high levels of agreement with four renal pathologists. The pathologist- and CNN-based analyses of IFTA and glomerulosclerosis showed statistically significant and equivalent correlation with all patient-outcome variables. ML algorithms can be trained to replicate the IFTA and glomerulosclerosis assessment performed by renal pathologists. This suggests computational methods may be able to provide a standardized approach to evaluate the extent of chronic kidney injury in situations in which renal-pathologist time is restricted or unavailable.

Sections du résumé

BACKGROUND BACKGROUND
Interstitial fibrosis, tubular atrophy (IFTA), and glomerulosclerosis are indicators of irrecoverable kidney injury. Modern machine learning (ML) tools have enabled robust, automated identification of image structures that can be comparable with analysis by human experts. ML algorithms were developed and tested for the ability to replicate the detection and quantification of IFTA and glomerulosclerosis that renal pathologists perform.
METHODS METHODS
A renal pathologist annotated renal biopsy specimens from 116 whole-slide images (WSIs) for IFTA and glomerulosclerosis. A total of 79 WSIs were used for training different configurations of a convolutional neural network (CNN), and 17 and 20 WSIs were used as internal and external testing cases, respectively. The best model was compared against the input of four renal pathologists on 20 new testing slides. Further, for 87 testing biopsy specimens, IFTA and glomerulosclerosis measurements made by pathologists and the CNN were correlated to patient outcome using classic statistical tools.
RESULTS RESULTS
The best average performance across all image classes came from a DeepLab version 2 network trained at 40× magnification. IFTA and glomerulosclerosis percentages derived from this CNN achieved high levels of agreement with four renal pathologists. The pathologist- and CNN-based analyses of IFTA and glomerulosclerosis showed statistically significant and equivalent correlation with all patient-outcome variables.
CONCLUSIONS CONCLUSIONS
ML algorithms can be trained to replicate the IFTA and glomerulosclerosis assessment performed by renal pathologists. This suggests computational methods may be able to provide a standardized approach to evaluate the extent of chronic kidney injury in situations in which renal-pathologist time is restricted or unavailable.

Identifiants

pubmed: 33622976
pii: 00001751-202104000-00011
doi: 10.1681/ASN.2020050652
pmc: PMC8017538
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

837-850

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK093770
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK114485
Pays : United States
Organisme : NIDDK NIH HHS
ID : U2C DK114886
Pays : United States
Organisme : NIH HHS
ID : S10 OD024973
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK056942
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 by the American Society of Nephrology.

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Auteurs

Brandon Ginley (B)

Departments of Pathology and Anatomical Sciences, University at Buffalo - The State University of New York, Buffalo, New York.

Kuang-Yu Jen (KY)

Department of Pathology and Laboratory Medicine, University of California at Davis, Sacramento, California.

Seung Seok Han (SS)

Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

Luís Rodrigues (L)

University Clinic of Nephrology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Nephrology Unit, Coimbra Hospital and University Center, Coimbra, Portugal.

Sanjay Jain (S)

Division of Nephrology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.

Agnes B Fogo (AB)

Departments of Pathology, Microbiology, and Immunology, and Medicine, Vanderbilt University, Nashville, Tennessee.

Jonathan Zuckerman (J)

Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Vighnesh Walavalkar (V)

Department of Pathology, University of California at San Francisco, San Francisco, California.

Jeffrey C Miecznikowski (JC)

Department of Biostatistics, University at Buffalo - The State University of New York, Buffalo, New York.

Yumeng Wen (Y)

Division of Nephrology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Felicia Yen (F)

Department of Pathology and Laboratory Medicine, University of California at Davis, Sacramento, California.

Donghwan Yun (D)

Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

Kyung Chul Moon (KC)

Department of Pathology, Seoul National University College of Medicine, Seoul, Korea.

Avi Rosenberg (A)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Chirag Parikh (C)

Division of Nephrology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Pinaki Sarder (P)

Departments of Pathology and Anatomical Sciences, University at Buffalo - The State University of New York, Buffalo, New York.
Department of Biomedical Engineering, University at Buffalo - The State University of New York, Buffalo, New York.

Classifications MeSH