Evidence map›Paper›PMID 36345008›Full record

ArticleCritical care (London, England)2022

A universal predictive and mechanistic urinary peptide signature in acute kidney injury.

Alexis Piedrafita, Justyna Siwy, Julie Klein, Amal Akkari, Ana Amaya-Garrido, Alexandre Mebazaa, Anna Belen Sanz, Benjamin Breuil, Laura Montero Herrero, Bertrand Marcheix and 13 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2022. 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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 7 institutions in 3 countries.

Alexis Piedrafita *Department of Nephrology and Organ Transplantation, University Hospital of Toulouse, and French Intensive Care Renal Network, 31000, Toulouse, France.
Justyna Siwy *Mosaiques Diagnostics GmbH, Hannover, Germany.
Julie Klein *National Institute of Health and Medical Research (INSERM), UMR 1297, Institute of Cardiovascular and Metabolic Disease, 31000, Toulouse, France.
Amal AkkariUniversité Paris-Saclay, CEA, List, 91120, Palaiseau, France.
Ana Amaya-GarridoNational Institute of Health and Medical Research (INSERM), UMR 1297, Institute of Cardiovascular and Metabolic Disease, 31000, Toulouse, France.
Alexandre MebazaaDepartment of Anesthesiology, Critical Care and Burn Unit, Hôpitaux Universitaires Saint Louis-Lariboisière, Assistance Publique-Hôpitaux de Paris, Université Paris Diderot-Paris 7, Sorbonne Paris Cité, UMR-S 942, INSERM, France, INI-CRCT, ParisNancy, France.
Anna Belen SanzSchool of Medicine, IIS-Fundación Jiménez Díaz, Autonomous University of Madrid, FRIAT and REDINREN, Madrid, Spain.
Benjamin BreuilNational Institute of Health and Medical Research (INSERM), UMR 1297, Institute of Cardiovascular and Metabolic Disease, 31000, Toulouse, France.
Laura Montero HerreroSchool of Medicine, IIS-Fundación Jiménez Díaz, Autonomous University of Madrid, FRIAT and REDINREN, Madrid, Spain.
Bertrand MarcheixUniversity Paul Sabatier, Toulouse-III, 31000, Toulouse, France.
François DepretDepartment of Anesthesiology, Critical Care and Burn Unit, Hôpitaux Universitaires Saint Louis-Lariboisière, Assistance Publique-Hôpitaux de Paris, Université Paris Diderot-Paris 7, Sorbonne Paris Cité, UMR-S 942, INSERM, France, INI-CRCT, ParisNancy, France.
Lucie FernandezNational Institute of Health and Medical Research (INSERM), UMR 1297, Institute of Cardiovascular and Metabolic Disease, 31000, Toulouse, France.
Elsa TardifDepartment of Anesthesiology and Critical Care Medicine, University Hospital of Toulouse, 31000, Toulouse, France.
Vincent MinvilleUniversity Paul Sabatier, Toulouse-III, 31000, Toulouse, France.
Melinda AlvesNational Institute of Health and Medical Research (INSERM), UMR 1297, Institute of Cardiovascular and Metabolic Disease, 31000, Toulouse, France.
Jochen MetzgerMosaiques Diagnostics GmbH, Hannover, Germany.
Kidney Attack Study Group
Julia GrossacDepartment of Anesthesiology and Critical Care Medicine, University Hospital of Toulouse, 31000, Toulouse, France.
Harald MischakMosaiques Diagnostics GmbH, Hannover, Germany.
Alberto OrtizSchool of Medicine, IIS-Fundación Jiménez Díaz, Autonomous University of Madrid, FRIAT and REDINREN, Madrid, Spain.
Stéphane GazutUniversité Paris-Saclay, CEA, List, 91120, Palaiseau, France.
Joost P Schanstra *National Institute of Health and Medical Research (INSERM), UMR 1297, Institute of Cardiovascular and Metabolic Disease, 31000, Toulouse, France. joost-peter.schanstra@inserm.fr.
Stanislas Faguer *Department of Nephrology and Organ Transplantation, University Hospital of Toulouse, and French Intensive Care Renal Network, 31000, Toulouse, France. stanislas.faguer@inserm.fr.
Université Toulouse III - Paul Sabatier · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRInserm · FRInstitut des Maladies Métaboliques et Cardiovasculaires · FRMosaiques Diagnostics and Therapeutics (Germany) · DECommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRHospital Universitario Fundación Jiménez Díaz · ES

Funding

ERA PerMed2018-JTC AC18/00 064ERA PerMed-JTC2018 01KU1907ERA PerMed-JTC2018 ANR-18-PERM-0003Fondation pour la Recherche Médicale DEQ20170336759Université Toulouse III - Paul Sabatier Ecolde Doctorale
6 · The paper itself

Abstract

backgroundThe delayed diagnosis of acute kidney injury (AKI) episodes and the lack of specificity of current single AKI biomarkers hamper its management. Urinary peptidome analysis may help to identify early molecular changes in AKI and grasp its complexity to identify potential targetable molecular pathways.

methodsIn derivation and validation cohorts totalizing 1170 major cardiac bypass surgery patients and in an external cohort of 1569 intensive care unit (ICU) patients, a peptide-based score predictive of AKI (7-day KDIGO classification) was developed, validated, and compared to the reference biomarker urinary NGAL and NephroCheck and clinical scores.

resultsA set of 204 urinary peptides derived from 48 proteins related to hemolysis, inflammation, immune cells trafficking, innate immunity, and cell growth and survival was identified and validated for the early discrimination (< 4 h) of patients according to their risk to develop AKI (OR 6.13 [3.96-9.59], p < 0.001) outperforming reference biomarkers (urinary NGAL and [IGFBP7].[TIMP2] product) and clinical scores. In an external cohort of 1569 ICU patients, performances of the signature were similar (OR 5.92 [4.73-7.45], p < 0.001), and it was also associated with the in-hospital mortality (OR 2.62 [2.05-3.38], p < 0.001).

conclusionsAn overarching AKI physiopathology-driven urinary peptide signature shows significant promise for identifying, at an early stage, patients who will progress to AKI and thus to develop tailored treatments for this frequent and life-threatening condition. Performance of the urine peptide signature is as high as or higher than that of single biomarkers but adds mechanistic information that may help to discriminate sub-phenotypes of AKI offering new therapeutic avenues.

Indexed as

Acute Kidney InjuryBiomarkersHumansLipocalin-2PeptidesPredictive Value of TestsBiomarkersLipocalin-2PeptidesAcute kidney injuryCardiac surgeryIntensive care unitPredictionUrinary peptidomics

Identifiers

PMID36345008
PMCPMC9640896
OpenAlexW4308469707

What Socratic 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 Socratic graph.