Evidence map›Paper›PMID 41776654›Full record

ArticleCritical care (London, England)2026

Prognosis of critically ill patients with severe acute kidney injury and high circulating dipeptidyl peptidase 3: a post hoc analysis of the AKIKI 2 trial.

Adrien Picod, Jeremy Boussier, Sarah Tubiana, Guillaume Louis, Laurent Martin Lefevre, Dimitri Titeca-Beauport, Béatrice La Combe, Sébastien Besset, Julio Badie, Guillaume Chevrel and 18 more

Abstract read
In one paragraph

Article in Critical care (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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. Review
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

28 authors.

Adrien Picod *Département de réanimation médico-chirurgicale, APHP Hôpital Avicenne, Bobigny, France.
Jeremy Boussier *Département de réanimation médico-chirurgicale, APHP Hôpital Avicenne, Bobigny, France.
Sarah TubianaCentre de ressources biologiques, APHP Hôpital Bichat, Paris, France.
Guillaume LouisRéanimation polyvalente, CHR Metz-Thionville Hôpital de Mercy, Metz, France.
Laurent Martin LefevreRéanimation polyvalente, CHR départementale La Roche Sur Yon, La Roche Sur Yon, France.
Dimitri Titeca-BeauportRéanimation médicale, CHU d'Amiens Picardie, Amiens, France.
Béatrice La CombeRéanimation, CH de Bretagne Sud, Lorient, France.
Sébastien BessetMédecine Intensive-Réanimation, APHP, Hôpital Louis Mourier, Université de Paris, Colombes, France.
Julio BadieRéanimation polyvalente, Hôpital Nord Franche-Comte CH Belfort, Belfort, France.
Guillaume ChevrelRéanimation polyvalente, CH Sud Francilien, Corbeil Essonnes, France.
Nicolas Chudeau, Réanimation médico-chirurgicale, CH du Mans, Le Mans, France.
Saber BarbarRéanimation, Hôpital Caremeau, Nimes, France.
Christophe VinsonneauRéanimation et USC, CH Bethune Beuvry - Bermont et Gauthier, Bethune, France.
Jean-Marie Forel, Réanimation médicale, Hôpital Nord, Marseille, France.
Didier TheveninRéanimation et USC, CH Dr Schaffner, Lens, France.
Guillaume LacaveRéanimation médico-chirurgicale, Hôpital André Mignot, Versailles, France.
Saad NseirMédecine Intensive-Réanimation, Hôpital R. Salengro, CHU de Lille, Lille Cedex ; Inserm U1285, Université de Lille, CNRS, UMR 8576 - UGSF , Lille, France.
Johanna OzielDépartement de réanimation médico-chirurgicale, APHP Hôpital Avicenne, Bobigny, France.
Julien MayauxPneumologie et Réanimation médicale, Hôpital Pitié Salpêtrière, Paris, France.
Kada KloucheMédecine Intensive Réanimation, Hôpital Lapeyronnie, Montpellier, France.
Jean ReignierNantes Université, CHU Nantes, Médecine Intensive Réanimation,Movement - Interactions - Performance, MIP, UR 4334, Colombes, Paris, 44000, France.
Jean-Damien RicardUniversité Paris Cité, AP-HP, Hôpital Louis Mourier, DMU ESPRIT, Service de Médecine Intensive Réanimation, Colombes ; INSERM IAME U1137, Paris, France.
Jean-Pierre QuenotDepartment of Intensive Care, François Mitterrand University Hospital, Dijon, France.
Alexandre MebazaaINSERM UMR-S 942 MASCOT - Paris - Cité University, Paris, France.
Feriel AzibaniINSERM UMR-S 942 MASCOT - Paris - Cité University, Paris, France.
Didier DreyfussMédecine Intensive-Réanimation, APHP, Hôpital Louis Mourier, Université de Paris, Colombes, France.
Stéphane Gaudry *Département de réanimation médico-chirurgicale, APHP Hôpital Avicenne, Bobigny, France.
Khalil Chaïbi *Département de réanimation médico-chirurgicale, APHP Hôpital Avicenne, Bobigny, France. Khalil.chaibi@aphp.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is a frequent and severe complication among critically ill patients. Circulating dipeptidyl peptidase 3 (cDPP3), an enzyme released upon cellular injury, has been implicated in hemodynamic instability and organ dysfunction. Its role in severe AKI remains poorly defined. We aimed to assess the prognostic significance of cDPP3 in critically ill patients with severe AKI.

methodsIn this post hoc analysis of the AKIKI 2 study, we included ICU patients with severe AKI (KDIGO stage 3) who were receiving (or had received) invasive mechanical ventilation and/or vasopressor support and had available blood samples at inclusion. Patients were stratified according to cDPP3 concentration using a predefined cutoff of 40 ng/mL. The primary outcome was 28-day mortality; secondary outcomes were organ support-free days.

resultsAmong 287 included patients, 143 (49.8%) had cDPP3 concentrations above 40 ng/mL. High cDPP3 was associated with increased 28-day mortality (hazard ratio 1.95; 95% confidence interval 1.37-2.87, p < 0.001). Furthermore, high cDPP3 was associated with fewer days alive without vasopressors (mean difference - 5.59; 95% CI - 8.29 to - 2.78, p < 0.001), invasive mechanical ventilation (mean difference - 6.23; 95% CI - 8.89 to - 3.36, p < 0.001), or renal replacement therapy (mean difference - 6.35; 95% CI - 9.14 to - 3.26, p < 0.001). After adjustment for baseline markers of severity, both the associations with 28-day mortality and organ support-free days remained significant.

conclusionsIn critically ill patients with severe AKI, a high cDPP3 concentration at diagnosis is associated with increased short-term mortality and prolonged dependence on organ support.

Indexed as

Acute Kidney InjuryDipeptidyl-Peptidases and Tripeptidyl-PeptidasesAgedBiomarkersCritical IllnessFemaleHumansIntensive Care UnitsMaleMiddle AgedPrognosisBiomarkersDipeptidyl-Peptidases and Tripeptidyl-PeptidasesDPP3 protein, humanAcute Kidney InjuryBiomarkersCirculating dipeptidyl peptidase 3Circulatory failure

Identifiers

PMID41776654
PMCPMC13141426

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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.