Evidence mapPaperPMID 38310171Full record

ArticleScientific reports2024

AI models for automated segmentation of engineered polycystic kidney tubules.

Simone Monaco, Nicole Bussola, Sara Buttò, Diego Sona, Flavio Giobergia, Giuseppe Jurman, Christodoulos Xinaris, Daniele Apiletti

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
3.3field-weighted citation impact, top 9% of its field
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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Reactive Oxygen Species in Cystic Kidney Disease.Antioxidants (Basel, Switzerland) · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Simone MonacoDAUIN, Politecnico di Torino, 10129, Turin, Italy.
Nicole BussolaFondazione Bruno Kessler, 38123, Trento, Italy.
Sara ButtòIstituto di Ricerche Farmacologiche Mario Negri - IRCCS, 24126, Bergamo, Italy.
Diego SonaFondazione Bruno Kessler, 38123, Trento, Italy.
Flavio GiobergiaDAUIN, Politecnico di Torino, 10129, Turin, Italy.
Giuseppe JurmanFondazione Bruno Kessler, 38123, Trento, Italy.
Christodoulos XinarisIstituto di Ricerche Farmacologiche Mario Negri - IRCCS, 24126, Bergamo, Italy. christodoulos.xinaris@marionegri.it.
Daniele ApilettiDAUIN, Politecnico di Torino, 10129, Turin, Italy. daniele.apiletti@polito.it.
Polytechnic University of Turin · ITFondazione Bruno Kessler · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITMario Negri Institute for Pharmacological Research · ITUniversity of Trento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is a monogenic, rare disease, characterized by the formation of multiple cysts that grow out of the renal tubules. Despite intensive attempts to develop new drugs or repurpose existing ones, there is currently no definitive cure for ADPKD. This is primarily due to the complex and variable pathogenesis of the disease and the lack of models that can faithfully reproduce the human phenotype. Therefore, the development of models that allow automated detection of cysts' growth directly on human kidney tissue is a crucial step in the search for efficient therapeutic solutions. Artificial Intelligence methods, and deep learning algorithms in particular, can provide powerful and effective solutions to such tasks, and indeed various architectures have been proposed in the literature in recent years. Here, we comparatively review state-of-the-art deep learning segmentation models, using as a testbed a set of sequential RGB immunofluorescence images from 4 in vitro experiments with 32 engineered polycystic kidney tubules. To gain a deeper understanding of the detection process, we implemented both pixel-wise and cyst-wise performance metrics to evaluate the algorithms. Overall, two models stand out as the best performing, namely UNet++ and UACANet: the latter uses a self-attention mechanism introducing some explainability aspects that can be further exploited in future developments, thus making it the most promising algorithm to build upon towards a more refined cyst-detection platform. UACANet model achieves a cyst-wise Intersection over Union of 0.83, 0.91 for Recall, and 0.92 for Precision when applied to detect large-size cysts. On all-size cysts, UACANet averages at 0.624 pixel-wise Intersection over Union. The code to reproduce all results is freely available in a public GitHub repository.

Indexed as

CystsPolycystic Kidney, Autosomal DominantArtificial IntelligenceHumansKidneyKidney Tubules

Identifiers

PMID38310171
PMCPMC11289110
OpenAlexW4391509849

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.