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Monitoring circulating dipeptidyl peptidase 3 (DPP3) predicts improvement of organ failure and survival in sepsis: a prospective observational multinational study

Authors :
Alice Blet
Benjamin Deniau
Karine Santos
Dirk P. T. van Lier
Feriel Azibani
Xavier Wittebole
Benjamin G. Chousterman
Etienne Gayat
Oliver Hartmann
Joachim Struck
Andreas Bergmann
Massimo Antonelli
Albertus Beishuizen
Jean-Michel Constantin
Charles Damoisel
Nicolas Deye
Salvatore Di Somma
Thierry Dugernier
Bruno François
Stephane Gaudry
Vincent Huberlant
Jean-Baptiste Lascarrou
Gernot Marx
Emmanuelle Mercier
Haikel Oueslati
Peter Pickkers
Romain Sonneville
Matthieu Legrand
Pierre-François Laterre
Alexandre Mebazaa
AdrenOSS-1 Study Investigators
Source :
Critical Care, Vol 25, Iss 1, Pp 1-10 (2021)
Publication Year :
2021
Publisher :
BMC, 2021.

Abstract

Abstract Background Dipeptidyl peptidase 3 (DPP3) is a cytosolic enzyme involved in the degradation of various cardiovascular and endorphin mediators. High levels of circulating DPP3 (cDPP3) indicate a high risk of organ dysfunction and mortality in cardiogenic shock patients. Methods The aim was to assess relationships between cDPP3 during the initial intensive care unit (ICU) stay and short-term outcome in the AdrenOSS-1, a prospective observational multinational study in twenty-four ICU centers in five countries. AdrenOSS-1 included 585 patients admitted to the ICU with severe sepsis or septic shock. The primary outcome was 28-day mortality. Secondary outcomes included organ failure as defined by the Sequential Organ Failure Assessment (SOFA) score, organ support with focus on vasopressor/inotropic use and need for renal replacement therapy. cDPP3 levels were measured upon admission and 24 h later. Results Median [IQR] cDPP3 concentration upon admission was 26.5 [16.2–40.4] ng/mL. Initial SOFA score was 7 [5–10], and 28-day mortality was 22%. We found marked associations between cDPP3 upon ICU admission and 28-day mortality (unadjusted standardized HR 1.8 [CI 1.6–2.1]; adjusted HR 1.5 [CI 1.3–1.8]) and between cDPP3 levels and change in renal and liver SOFA score (p = 0.0077 and 0.0009, respectively). The higher the initial cDPP3 was, the greater the need for organ support and vasopressors upon admission; the longer the need for vasopressor(s), mechanical ventilation or RRT and the higher the need for fluid load (all p 40.4 ng/mL upon admission, a decrease in cDPP3 below 40.4 ng/mL after 24 h was associated with an improvement of organ function at 48 h and better 28-day outcome. By contrast, persistently elevated cDPP3 at 24 h was associated with worsening organ function and high 28-day mortality. Conclusions Admission levels and rapid changes in cDPP3 predict outcome during sepsis. Trial Registration ClinicalTrials.gov, NCT02393781. Registered on March 19, 2015.

Details

Language :
English
ISSN :
13648535
Volume :
25
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Critical Care
Publication Type :
Academic Journal
Accession number :
edsdoj.00497743bbc542e38c17b2eb90d320e0
Document Type :
article
Full Text :
https://doi.org/10.1186/s13054-021-03471-2