Evaluation of the Novel Sepsis Biomarker Host-Derived Delta-like Canonical Notch Ligand 1-A Secondary Analysis of 405 Patients Suffering from Inflammatory or Infectious Diseases.

DLL-1 DLL1 Delta-like Canonical Notch Ligand 1 biomarker diagnostics sepsis systemic infection

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
23 May 2023
Historique:
received: 04 04 2023
revised: 09 05 2023
accepted: 18 05 2023
medline: 12 6 2023
pubmed: 10 6 2023
entrez: 10 6 2023
Statut: epublish

Résumé

Sepsis is defined as organ failure caused by dysregulated host response to infection. While early antibiotic treatment in patients with acute infection is essential, treating non-infectious patients must be avoided. Current guidelines recommend procalcitonin (PCT) to guide discontinuation of antibiotic treatment. For initiation of therapy, there is currently no recommended biomarker. In this study, we evaluated Host-Derived Delta-like Canonical Notch Ligand 1 (DLL1), a monocyte membrane ligand that has shown promising results in differentiating infectious from non-infectious critically ill patients. Soluble DLL1 levels were measured in plasma samples of six different cohorts. The six cohorts comprise two cohorts with non-infectious inflammatory auto-immune diseases (Hidradenitis Suppurativa, Inflammatory Bowel Disease), one cohort of bacterial skin infection, and three cohorts of suspected systemic infection or sepsis. In total, soluble DLL1 plasma levels of 405 patients were analyzed. Patients were divided into three groups: inflammatory disease, infection, and sepsis (defined according to the Sepsis-3 definition), followed by the evaluation of its diagnostic performance via Area Under the Receiver Operating Characteristics (AUROC) analyses. Patients of the sepsis group showed significantly elevated plasma DLL1 levels compared to patients with uncomplicated infections and sterile inflammation. However, patients with infections had significantly higher DLL1 levels than patients with inflammatory diseases. Diagnostic performance was evaluated and showed better performance for DLL1 for the recognition of sepsis (AUC: 0.823; CI 0.731-0.914) than C-reactive protein (AUC 0.758; CI 0.658-0.857), PCT (AUC 0.593; CI 0.474-0.711) and White Blood Cell count (AUC 0.577; CI 0.46-0.694). DLL1 demonstrated promising results for diagnosing sepsis and was able to differentiate sepsis from other infectious and inflammatory diseases.

Identifiants

pubmed: 37298115
pii: ijms24119164
doi: 10.3390/ijms24119164
pmc: PMC10252395
pii:
doi:

Substances chimiques

Ligands 0
Calcitonin 9007-12-9
Biomarkers 0
Procalcitonin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

Markus A. Weigand holds patent EP/25.10.17/EPA17198330 Delta like ligand for diagnosing severe infections and is co-founder of the Delta Theragnostics GmbH. All other authors declare no conflict of interest.

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Auteurs

Tobias Hölle (T)

Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.

Patrick Rehn (P)

Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.

Konstantinos Leventogiannis (K)

4th Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Antigone Kotsaki (A)

4th Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Theodora Kanni (T)

4th Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Nikolaos Antonakos (N)

4th Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Christos Psarrakis (C)

4th Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Georgia Damoraki (G)

4th Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Judith Schenz (J)

Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.

Felix C F Schmitt (FCF)

Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.

Florian Uhle (F)

Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.

Markus A Weigand (MA)

Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.

Evangelos J Giamarellos-Bourboulis (EJ)

4th Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.

Maximilian Dietrich (M)

Department of Anesthesiology, Heidelberg University Hospital, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.

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Classifications MeSH