Evidence map›Paper›PMID 39990883›Full record

ArticleKidney international reports2025

Explainability of a Deep Learning-Based Classification Model for Antineutrophil Cytoplasmic Autoantibody-Associated Glomerulonephritis.

Maria A C Wester Trejo, Maryam Sadeghi, Shivam Singh, Naghmeh Mahmoodian, Samir Sharifli, Zdenka Hruskova, Vladimír Tesař, Xavier Puéchal, Jan Anthonie Bruijn, Georg Göbel and 2 more

Abstract read
In one paragraph

Article in Kidney international reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Maria A C Wester TrejoDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Maryam SadeghiDepartment of Medical Statistics, Informatics and Health Economics, Medical University of Innsbruck, Innsbruck, Austria.
Shivam SinghDepartment of Medical Statistics, Informatics and Health Economics, Medical University of Innsbruck, Innsbruck, Austria.
Naghmeh MahmoodianFaculty of Computer Science, Otto von Guericke University, Magdeburg, Germany.
Samir SharifliDepartment of Internal Medicine IV, Nephrology and Hypertension, Medical University of Innsbruck, Innsbruck, Austria.
Zdenka HruskovaDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Vladimír TesařDepartment of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czechia.
Xavier PuéchalDepartment of Internal Medicine, Hôpital Cochin, AP-HP, Paris, France.
Jan Anthonie BruijnDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Georg GöbelDepartment of Medical Statistics, Informatics and Health Economics, Medical University of Innsbruck, Innsbruck, Austria.
Ingeborg M BajemaDepartment of Pathology and Medical Biology, University Medical Center Groningen, Groningen, The Netherlands.
Andreas KronbichlerDepartment of Internal Medicine IV, Nephrology and Hypertension, Medical University of Innsbruck, Innsbruck, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The histopathological classification for antineutrophil cytoplasmic autoantibody (ANCA)-associated glomerulonephritis (ANCA-GN) is a well-established tool to reflect the variety of patterns and severity of lesions that can occur in kidney biopsies. It was demonstrated previously that deep learning (DL) approaches can aid in identifying histopathological classes of kidney diseases; for example, of diabetic kidney disease. These models can potentially be used as decision support tools for kidney pathologists. Although they reach high prediction accuracies, their "black box" structure makes them nontransparent. Explainable (X) artificial intelligence (AI) techniques can be used to make the AI model decisions accessible for human experts. We have developed a DL-based model, which detects and classifies the glomerular lesions according to the Berden classification. Methods: Kidney biopsy slides of 80 patients with ANCA-GN from 3 European centers, who underwent a diagnostic kidney biopsy between 1991 and 2011, were included. We also investigated the explainability of our model using Gradient-weighted Class Activation Mapping (Grad-CAM) heatmaps. These maps were analyzed by pathologists to compare the decision-making criteria of humans and the DL model and assess the impact of different training settings. Results: The DL model shows a prediction accuracy of 93% for classifying lesions. The heatmaps from our trained DL models showed that the most predictive areas in the image correlated well with the areas deemed to be important by the pathologist. Conclusion: We present the first DL-based computational pipeline for classifying ANCA-GN kidney biopsies as per the Berden classification. XAI techniques helped us to make the decision-making criteria of the DL accessible for renal pathologists, potentially improving clinical decision-making.

Indexed as

ANCAartificial intelligencehistopathologymachine learningvasculitis

Identifiers

PMID39990883
PMCPMC11843110

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.