Circulating dipeptidyl peptidase-3 at admission is associated with circulatory failure, acute kidney injury and death in severely ill burn patients.


Journal

Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902

Informations de publication

Date de publication:
22 04 2020
Historique:
received: 20 02 2020
accepted: 13 04 2020
entrez: 24 4 2020
pubmed: 24 4 2020
medline: 1 12 2020
Statut: epublish

Résumé

Dipeptidyl peptidase-3 (DPP3) is a metallopeptidase which cleaves bioactive peptides, notably angiotensin II, and is involved in inflammation regulation. DPP3 has been proposed to be a myocardial depressant factor and to be involved in circulatory failure in acute illnesses, possibly due to angiotensin II cleavage. In this study, we evaluated the association between plasmatic DPP3 level and outcome (mortality and hemodynamic failure) in severely ill burn patients. In this biomarker analysis of a prospective cohort study, we included severely ill adult burn patients in two tertiary burn intensive care units. DPP3 was measured at admission (DPP3 One hundred and eleven consecutive patients were enrolled. The median age was 48 (32.5-63) years, with a median total body surface area burned of 35% (25-53.5) and Abbreviated Burn Severity Index (ABSI) of 8 (7-11). Ninety-day mortality was 32%. The median DPP3 Plasma DPP3 concentration at admission was associated with an increased risk of death, circulatory failure, and AKI in severely burned patients. Whether DPP3 plasma levels could identify patients who would respond to alternative hemodynamic support strategies, such as intravenous angiotensin II, should be explored.

Sections du résumé

BACKGROUND
Dipeptidyl peptidase-3 (DPP3) is a metallopeptidase which cleaves bioactive peptides, notably angiotensin II, and is involved in inflammation regulation. DPP3 has been proposed to be a myocardial depressant factor and to be involved in circulatory failure in acute illnesses, possibly due to angiotensin II cleavage. In this study, we evaluated the association between plasmatic DPP3 level and outcome (mortality and hemodynamic failure) in severely ill burn patients.
METHODS
In this biomarker analysis of a prospective cohort study, we included severely ill adult burn patients in two tertiary burn intensive care units. DPP3 was measured at admission (DPP3
RESULTS
One hundred and eleven consecutive patients were enrolled. The median age was 48 (32.5-63) years, with a median total body surface area burned of 35% (25-53.5) and Abbreviated Burn Severity Index (ABSI) of 8 (7-11). Ninety-day mortality was 32%. The median DPP3
CONCLUSIONS
Plasma DPP3 concentration at admission was associated with an increased risk of death, circulatory failure, and AKI in severely burned patients. Whether DPP3 plasma levels could identify patients who would respond to alternative hemodynamic support strategies, such as intravenous angiotensin II, should be explored.

Identifiants

pubmed: 32321571
doi: 10.1186/s13054-020-02888-5
pii: 10.1186/s13054-020-02888-5
pmc: PMC7178561
doi:

Substances chimiques

Dipeptidyl-Peptidases and Tripeptidyl-Peptidases EC 3.4.14.-
DPP3 protein, human EC 3.4.14.4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

168

Subventions

Organisme : Union des Blessés de la Face et de la Tête
ID : 2012
Pays : International

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Auteurs

François Dépret (F)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.
University Paris Diderot, Paris, France.
UMR INSERM 942, Institut National de la Santé et de la Recherche Médicale (INSERM), F-CRIN INICRCT network, Paris, France.

Juliette Amzallag (J)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Adrien Pollina (A)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Laure Fayolle-Pivot (L)

Department of Anesthesiology and Critical Care, Burn Center Pierre Colson, Hospices Civils de Lyon, Edouard Herriot Hospital, Lyon, France.

Maxime Coutrot (M)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.
University Paris Diderot, Paris, France.

Maïté Chaussard (M)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Karine Santos (K)

4TEEN4 Pharmaceuticals GmbH, Hennigsdorf, Germany.

Oliver Hartmann (O)

4TEEN4 Pharmaceuticals GmbH, Hennigsdorf, Germany.

Marion Jully (M)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Alexandre Fratani (A)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Haikel Oueslati (H)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Alexandru Cupaciu (A)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Mourad Benyamina (M)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.
University Paris Diderot, Paris, France.

Lucie Guillemet (L)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.

Benjamin Deniau (B)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.
University Paris Diderot, Paris, France.
UMR INSERM 942, Institut National de la Santé et de la Recherche Médicale (INSERM), F-CRIN INICRCT network, Paris, France.

Alexandre Mebazaa (A)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.
University Paris Diderot, Paris, France.
UMR INSERM 942, Institut National de la Santé et de la Recherche Médicale (INSERM), F-CRIN INICRCT network, Paris, France.

Etienne Gayat (E)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France.
University Paris Diderot, Paris, France.
UMR INSERM 942, Institut National de la Santé et de la Recherche Médicale (INSERM), F-CRIN INICRCT network, Paris, France.

Boris Farny (B)

Department of Anesthesiology and Critical Care, Burn Center Pierre Colson, Hospices Civils de Lyon, Edouard Herriot Hospital, Lyon, France.
EA 7426 Pathophysiology of Injury-induced Immunosuppression, University of Lyon1-Hospices Civils de Lyon-bioMérieux, Hôpital Edouard Herriot, Lyon, France.

Julien Textoris (J)

Department of Anesthesiology and Critical Care, Burn Center Pierre Colson, Hospices Civils de Lyon, Edouard Herriot Hospital, Lyon, France.
EA 7426 Pathophysiology of Injury-induced Immunosuppression, University of Lyon1-Hospices Civils de Lyon-bioMérieux, Hôpital Edouard Herriot, Lyon, France.

Matthieu Legrand (M)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, GH St-Louis-Lariboisière, Paris, France. matthieu.legrand@ucsf.edu.
University Paris Diderot, Paris, France. matthieu.legrand@ucsf.edu.
UMR INSERM 942, Institut National de la Santé et de la Recherche Médicale (INSERM), F-CRIN INICRCT network, Paris, France. matthieu.legrand@ucsf.edu.
Department of Anesthesia and Perioperative Care, UCSF Medical Center, University of California, 500 Parnassus Avenue MUE416, Box 0648, San Francisco, CA, 94143, USA. matthieu.legrand@ucsf.edu.

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