Evidence map›Paper›PMID 40011503›Full record

ArticleScientific reports2025

Early detection of feline chronic kidney disease via 3-hydroxykynurenine and machine learning.

Ellen Vanden Broecke, Laurens Van Mulders, Ellen De Paepe, Dominique Paepe, Sylvie Daminet, Lynn Vanhaecke

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
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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

6 authors.

Ellen Vanden BroeckeFaculty of Veterinary Medicine, Department of Translational Physiology, Infectiology and Public Health, Laboratory of Integrative Metabolomics (LIMET), Ghent University, Salisburylaan 133, B-9820, Merelbeke, Belgium.
Laurens Van MuldersFaculty of Veterinary Medicine, Department of Translational Physiology, Infectiology and Public Health, Laboratory of Integrative Metabolomics (LIMET), Ghent University, Salisburylaan 133, B-9820, Merelbeke, Belgium.
Ellen De PaepeFaculty of Veterinary Medicine, Department of Translational Physiology, Infectiology and Public Health, Laboratory of Integrative Metabolomics (LIMET), Ghent University, Salisburylaan 133, B-9820, Merelbeke, Belgium.
Dominique PaepeFaculty of Veterinary Medicine, Small Animal Department, Ghent University, Salisburylaan 133, B-9820, Merelbeke, Belgium.
Sylvie DaminetFaculty of Veterinary Medicine, Small Animal Department, Ghent University, Salisburylaan 133, B-9820, Merelbeke, Belgium.
Lynn VanhaeckeFaculty of Veterinary Medicine, Department of Translational Physiology, Infectiology and Public Health, Laboratory of Integrative Metabolomics (LIMET), Ghent University, Salisburylaan 133, B-9820, Merelbeke, Belgium. Lynn.Vanhaecke@Ugent.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Feline chronic kidney disease (CKD) is one of the most frequently encountered diseases in veterinary practice, and the leading cause of mortality in cats over five years of age. While diagnosing advanced CKD is straightforward, current routine tests fail to diagnose early CKD. Therefore, this study aimed to identify early metabolic biomarkers. First, cats were retrospectively divided into two populations to conduct a case-control study, comparing the urinary and serum metabolome of healthy (n = 61) and CKD IRIS stage 2 cats (CKD2, n = 63). Subsequently, longitudinal validation was conducted in an independent population comprising healthy cats that remained healthy (n = 26) and cats that developed CKD2 (n = 22) within one year. Univariate, multivariate, and machine learning-based (ML) approaches were compared. The serum-to-urine ratio of 3-hydroxykynurenine was identified as a single biomarker candidate, yielding a high AUC (0.844) and accuracy (0.804), while linear support vector machine-based modelling employing metabolites and clinical parameters enhanced AUC (0.929) and accuracy (0.862) six months before traditional diagnosis. Furthermore, analysis of variable importance indicated consistent key serum metabolites, namely creatinine, SDMA, 2-hydroxyethanesulfonate, and aconitic acid. By enabling accurate diagnosis at least six months earlier, the highlighted metabolites may pave the way for improved diagnostics, ultimately contributing to timely disease management.

Indexed as

Cat DiseasesKynurenineMachine LearningRenal Insufficiency, ChronicAnimalsBiomarkersCase-Control StudiesCatsEarly DiagnosisFemaleMaleRetrospective Studies3-hydroxykynurenineBiomarkersKynurenineDiagnostic panelKynureninesMachine learning algorithmsMultivariate modelsRenal diseaseTargeted metabolomics

Identifiers

PMID40011503
PMCPMC11865484

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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 OpenQuestion graph.