Evidence map›Paper›PMID 39790049›Full record

ReviewProteomics2025

The Omics-Driven Machine Learning Path to Cost-Effective Precision Medicine in Chronic Kidney Disease.

Marta B Lopes, Roberta Coletti, Flore Duranton, Griet Glorieux, Mayra Alejandra Jaimes Campos, Julie Klein, Matthias Ley, Paul Perco, Alexia Sampri, Aviad Tur-Sinai

Abstract readReview
In one paragraph

Review in Proteomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

10 authors.

Marta B LopesCenter for Mathematics and Applications (NOVA Math), NOVA School of Science and Technology (NOVA FCT), Caparica, Portugal.ORCID 0000-0002-4135-1857
Roberta ColettiCenter for Mathematics and Applications (NOVA Math), NOVA School of Science and Technology (NOVA FCT), Caparica, Portugal.
Flore DurantonRD-Néphrologie, Montpellier, France.ORCID 0000-0003-3202-0551
Griet GlorieuxDepartment of Internal Medicine and Pediatrics, Nephrology Unit, Ghent University Hospital, Gent, Belgium.
Mayra Alejandra Jaimes CamposDepartment of Biomarker Research, Mosaiques Diagnostics GmbH, Hannover, Germany.
Julie KleinInstitut National de la Santé et de la Recherche Médicale (INSERM), Institute of Cardiovascular and Metabolic Disease, Toulouse, France.
Matthias LeyDelta4 GmbH, Vienna, Austria.
Paul PercoDelta4 GmbH, Vienna, Austria.ORCID 0000-0003-2087-5691
Alexia SampriDepartment of Public Health and Primary Care, British Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge, Cambridge, UK.
Aviad Tur-SinaiSchool of Public Health, University of Haifa, Haifa, Israel.

Funding

European Cooperation in Science and Technology CA21165Fundação para a Ciência e a Tecnologia CEECINST/00042/2021Fundação para a Ciência e a Tecnologia UIDB/00297/2020Fundação para a Ciência e a Tecnologia UIDB/00667/2020Fundação para a Ciência e a Tecnologia UIDP/00297/2020Fundação para a Ciência e a Tecnologia UIDP/00667/2020Horizon Europe Marie Skłodowska-Curie Action Doctoral NetworkÖsterreichische Forschungsförderungsgesellschaft 911422Wellcome TrustWellcome Trust HDRUK2023.0028
6 · The paper itself

Abstract

Chronic kidney disease (CKD) poses a significant and growing global health challenge, making early detection and slowing disease progression essential for improving patient outcomes. Traditional diagnostic methods such as glomerular filtration rate and proteinuria are insufficient to capture the complexity of CKD. In contrast, omics technologies have shed light on the molecular mechanisms of CKD, helping to identify biomarkers for disease assessment and management. Artificial intelligence (AI) and machine learning (ML) could transform CKD care, enabling biomarker discovery for early diagnosis and risk prediction, and personalized treatment. By integrating multi-omics datasets, AI can provide real-time, patient-specific insights, improve decision support, and optimize cost efficiency by early detection and avoidance of unnecessary treatments. Multidisciplinary collaborations and sophisticated ML methods are essential to advance diagnostic and therapeutic strategies in CKD. This review presents a comprehensive overview of the pipeline for translating CKD omics data into personalized treatment, covering recent advances in omics research, the role of ML in CKD, and the critical need for clinical validation of AI-driven discoveries to ensure their efficacy, relevance, and cost-effectiveness in patient care.

Indexed as

Machine LearningPrecision MedicineProteomicsRenal Insufficiency, ChronicBiomarkersCost-Benefit AnalysisGenomicsHumansBiomarkersartificial intelligencechronic kidney diseasecost‐effectivenessmachine learningmulti‐omics

Identifiers

PMID39790049
PMCPMC12205302

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.