Evidence map›Paper›PMID 38370429›Full record

ArticleClinical kidney journal2024

Recognition of intraglomerular histological features with deep learning in protocol transplant biopsies and their association with kidney function and prognosis.

Imane Farhat, Elise Maréchal, Doris Calmo, Manon Ansart, Michel Paindavoine, Patrick Bard, Georges Tarris, Didier Ducloux, Sophie Adrian Felix, Laurent Martin and 6 more

Erratum issuedAbstract read
In one paragraph

Article in Clinical kidney journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Imane FarhatDepartment of Nephrology, CHU Dijon, Dijon, France.
Elise MaréchalDepartment of Nephrology, CHU Dijon, Dijon, France.
Doris CalmoDepartment of Nephrology, CHU Besançon, Besançon, France.
Manon AnsartLEAD-CNRS, UMR 5022, Université de Bourgogne, Dijon, France.
Michel PaindavoineLEAD-CNRS, UMR 5022, Université de Bourgogne, Dijon, France.
Patrick BardLEAD-CNRS, UMR 5022, Université de Bourgogne, Dijon, France.
Georges TarrisDepartment of Pathology, CHU Dijon, Dijon, France.
Didier DuclouxDepartment of Nephrology, CHU Besançon, Besançon, France.
Sophie Adrian FelixDepartment of Pathology, CHU Besançon, Besançon 25000, France.
Laurent MartinDepartment of Pathology, CHU Dijon, Dijon, France.
Claire TinelDepartment of Nephrology, CHU Dijon, Dijon, France.
Jean-Baptiste GibierDepartment of Pathology, CHU Lille, Lille, France.
Mathilde Funes de la VegaDepartment of Pathology, CHU Dijon, Dijon, France.
Jean-Michel RebibouDepartment of Nephrology, CHU Dijon, Dijon, France.
Jamal BamoulidDepartment of Nephrology, CHU Besançon, Besançon, France.
Mathieu LegendreDepartment of Nephrology, CHU Dijon, Dijon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Banff Classification may not adequately address protocol transplant biopsies categorized as normal in patients experiencing unexplained graft function deterioration. This study seeks to employ convolutional neural networks to automate the segmentation of glomerular cells and capillaries and assess their correlation with transplant function. Methods: A total of 215 patients were categorized into three groups. In the Training cohort, glomerular cells and capillaries from 37 patients were manually annotated to train the networks. The Test cohort (24 patients) compared manual annotations vs automated predictions, while the Application cohort (154 protocol transplant biopsies) examined predicted factors in relation to kidney function and prognosis. Results: In the Test cohort, the networks recognized histological structures with Precision, Recall, F-score and Intersection Over Union exceeding 0.92, 0.85, 0.89 and 0.74, respectively. Univariate analysis revealed associations between the estimated glomerular filtration rate (eGFR) at biopsy and relative endothelial area (r = 0.19, Conclusion: This study automated the measurement of intraglomerular cells and capillaries. Our results suggest that the precise segmentation of endothelial and epithelial cells may serve as a potential future marker for the risk of graft loss.

Indexed as

artificial intelligencedeep learningglomeruluskidney pathologytransplant biopsies

Identifiers

PMID38370429
PMCPMC10873504

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.