Identification and validation of biomarkers of persistent acute kidney injury: the RUBY study.

Biomarkers C-C motif chemokine ligand 14 (CCL14) KIM-1 (kidney injury molecule-1) NGAL (Neutrophil gelatinase-associated lipocalin) Persistent acute kidney injury Plasma cystatin C

Journal

Intensive care medicine
ISSN: 1432-1238
Titre abrégé: Intensive Care Med
Pays: United States
ID NLM: 7704851

Informations de publication

Date de publication:
05 2020
Historique:
received: 29 08 2019
accepted: 26 12 2019
pubmed: 7 2 2020
medline: 28 4 2021
entrez: 7 2 2020
Statut: ppublish

Résumé

The aim of the RUBY study was to evaluate novel candidate biomarkers to enable prediction of persistence of renal dysfunction as well as further understand potential mechanisms of kidney tissue damage and repair in acute kidney injury (AKI). The RUBY study was a multi-center international prospective observational study to identify biomarkers of the persistence of stage 3 AKI as defined by the KDIGO criteria. Patients in the intensive care unit (ICU) with moderate or severe AKI (KDIGO stage 2 or 3) were enrolled. Patients were to be enrolled within 36 h of meeting KDIGO stage 2 criteria. The primary study endpoint was the development of persistent severe AKI (KDIGO stage 3) lasting for 72 h or more (NCT01868724). 364 patients were enrolled of whom 331 (91%) were available for the primary analysis. One hundred ten (33%) of the analysis cohort met the primary endpoint of persistent stage 3 AKI. Of the biomarkers tested in this study, urinary C-C motif chemokine ligand 14 (CCL14) was the most predictive of persistent stage 3 AKI with an area under the receiver operating characteristic curve (AUC) (95% CI) of 0.83 (0.78-0.87). This AUC was significantly greater than values for other biomarkers associated with AKI including urinary KIM-1, plasma cystatin C, and urinary NGAL, none of which achieved an AUC > 0.75. Elevated urinary CCL14 predicts persistent AKI in a large heterogeneous cohort of critically ill patients with severe AKI. The discovery of CCL14 as a predictor of persistent AKI and thus, renal non-recovery, is novel and could help identify new therapeutic approaches to AKI.

Identifiants

pubmed: 32025755
doi: 10.1007/s00134-019-05919-0
pii: 10.1007/s00134-019-05919-0
pmc: PMC7210248
doi:

Substances chimiques

Biomarkers 0
Lipocalin-2 0

Banques de données

ClinicalTrials.gov
['NCT01868724']

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

943-953

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM110240
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI135964
Pays : United States

Investigateurs

Eric Hoste (E)
Azra Bihorac (A)
Ali Al-Khafaji (A)
Luis M Ortega (LM)
Marlies Ostermann (M)
Michael Haase (M)
Kai Zacharowski (K)
Richard Wunderink (R)
Michael Heung (M)
Kyle Gunnerson (K)
Matthew Lissauer (M)
Daniel Herr (D)
Wesley H Self (WH)
Jay L Koyner (JL)
Patrick M Honore (PM)
John R Prowle (JR)
Danielle Davison (D)
Antonio Artigas (A)
Michael Joannidis (M)
Rebecca Schroeder (R)
Sevag Demirjian (S)
Lui G Forni (LG)
Luke Hodgson (L)
Scott Wilber (S)
Jennifer A Frey (JA)
Ian Reilly (I)
Jing Shi (J)
J Patrick Kampf (JP)
Thomas Kwan (T)
Paul McPherson (P)
John A Kellum (JA)
Lakhmir S Chawla (LS)

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Auteurs

Eric Hoste (E)

Ghent University Hospital, Ghent University, Ghent, Belgium.

Azra Bihorac (A)

Department of Medicine, University of Florida, Gainesville, FL, USA.

Ali Al-Khafaji (A)

Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

Luis M Ortega (LM)

Allegheny General Hospital, Pittsburgh, PA, USA.

Marlies Ostermann (M)

King's College London, Guy's & St Thomas' Hospital, London, UK.

Michael Haase (M)

MVZ Diaverum Am Neuen Garten, Potsdam, Germany.
Medizinische Fakultät, Otto-Von-Guericke Universität Magdeburg, Magdeburg, Germany.

Kai Zacharowski (K)

University Hospital Frankfurt, Goethe University, Frankfurt, Germany.

Richard Wunderink (R)

Department of Medicine, Pulmonary and Critical Care Division, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Michael Heung (M)

Division of Nephrology, Department of Medicine, University of Michigan, Ann Arbor, MI, USA.

Matthew Lissauer (M)

Rutgers-Robert Wood Johnson Medical School, New Brunswick, NJ, 08901, USA.

Wesley H Self (WH)

Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.

Jay L Koyner (JL)

Section of Nephrology, Department of Medicine, University of Chicago, Chicago, IL, USA.

Patrick M Honore (PM)

University Hospital Brussels, Brussels, Belgium.

John R Prowle (JR)

Royal London Hospital, Barts Health NHS Trust, London, UK.

Michael Joannidis (M)

Division of Intensive Care and Emergency Medicine, Department of Internal Medicine, Medical University Innsbruck, Innsbruck, Austria.

Lui G Forni (LG)

Department of Clinical & Experimental Medicine, Faculty of Health Sciences, University of Surrey, Guildford, UK.

J Patrick Kampf (JP)

Astute Medical, Inc, San Diego, CA, USA.

Paul McPherson (P)

Astute Medical, Inc, San Diego, CA, USA.

John A Kellum (JA)

Department of Critical Care Medicine, Center for Critical Care Nephrology, University of Pittsburgh, Pittsburgh, PA, USA.

Lakhmir S Chawla (LS)

Department of Medicine, Veterans Affairs Medical Center, 3350 La Jolla Village Dr, San Diego, CA, 92161, USA. minkchawla@gmail.com.

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