Growth differentiation factor 15 and early prognosis after out-of-hospital cardiac arrest.

Biomarkers Growth differentiation factor 15 Neurologic outcome Out-of-hospital cardiac arrest Prognostication

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
17 Oct 2019
Historique:
received: 17 05 2019
accepted: 05 10 2019
entrez: 19 10 2019
pubmed: 19 10 2019
medline: 19 10 2019
Statut: epublish

Résumé

Growth differentiation factor 15 (GDF-15) is an inflammatory cytokine released in response to tissue injury. It has prognostic value in cardiovascular diseases and other acute and chronic conditions. Here, we explored the value of GDF-15 as an early predictor of neurologic outcome after an out-of-hospital cardiac arrest (OHCA). Prospective registry study of patients in coma after an OHCA, admitted in the intensive cardiac care unit from a single university center. Serum levels of GDF-15 were measured on admission. Neurologic status was evaluated according to the cerebral performance category (CPC) scale. The relationship between GDF-15 levels and poor neurologic outcome at 6 months was analyzed. Among 62 patients included, 32 (51.6%) presented poor outcome (CPC 3-5). Patients with CPC 3-5 exhibited significantly higher GDF-15 levels (median, 17.1 [IQR, 11.1-20.4] ng/mL) compared to those with CPC 1-2 (7.6 [IQR, 4.1-13.1] ng/mL; p = 0.004). Multivariable logistic regression analyses showed that age (OR, 1.09; 95% CI 1.01-1.17; p = 0.020), home setting arrest (OR, 8.07; 95% CI 1.61-40.42; p = 0.011), no bystander cardiopulmonary resuscitation (OR, 7.91; 95% CI 1.84-34.01; p = 0.005), and GDF-15 levels (OR, 3.74; 95% CI 1.32-10.60; p = 0.013) were independent predictors of poor outcome. The addition of GDF-15 in a dichotomous manner (≥ 10.8 vs. < 10.8 ng/mL) to the resulting clinical model improved discrimination; it increased the area under the curve from 0.867 to 0.917, and the associated continuous net reclassification improvement was 0.90 (95% CI 0.48-1.44), which allowed reclassification of 37.1% of patients. After an OHCA, increased GDF-15 levels were an independent, early predictor of poor neurologic outcome. Furthermore, when added to the most common clinical factors, GDF-15 improved discrimination and allowed patient reclassification.

Sections du résumé

BACKGROUND BACKGROUND
Growth differentiation factor 15 (GDF-15) is an inflammatory cytokine released in response to tissue injury. It has prognostic value in cardiovascular diseases and other acute and chronic conditions. Here, we explored the value of GDF-15 as an early predictor of neurologic outcome after an out-of-hospital cardiac arrest (OHCA).
METHODS METHODS
Prospective registry study of patients in coma after an OHCA, admitted in the intensive cardiac care unit from a single university center. Serum levels of GDF-15 were measured on admission. Neurologic status was evaluated according to the cerebral performance category (CPC) scale. The relationship between GDF-15 levels and poor neurologic outcome at 6 months was analyzed.
RESULTS RESULTS
Among 62 patients included, 32 (51.6%) presented poor outcome (CPC 3-5). Patients with CPC 3-5 exhibited significantly higher GDF-15 levels (median, 17.1 [IQR, 11.1-20.4] ng/mL) compared to those with CPC 1-2 (7.6 [IQR, 4.1-13.1] ng/mL; p = 0.004). Multivariable logistic regression analyses showed that age (OR, 1.09; 95% CI 1.01-1.17; p = 0.020), home setting arrest (OR, 8.07; 95% CI 1.61-40.42; p = 0.011), no bystander cardiopulmonary resuscitation (OR, 7.91; 95% CI 1.84-34.01; p = 0.005), and GDF-15 levels (OR, 3.74; 95% CI 1.32-10.60; p = 0.013) were independent predictors of poor outcome. The addition of GDF-15 in a dichotomous manner (≥ 10.8 vs. < 10.8 ng/mL) to the resulting clinical model improved discrimination; it increased the area under the curve from 0.867 to 0.917, and the associated continuous net reclassification improvement was 0.90 (95% CI 0.48-1.44), which allowed reclassification of 37.1% of patients.
CONCLUSIONS CONCLUSIONS
After an OHCA, increased GDF-15 levels were an independent, early predictor of poor neurologic outcome. Furthermore, when added to the most common clinical factors, GDF-15 improved discrimination and allowed patient reclassification.

Identifiants

pubmed: 31624933
doi: 10.1186/s13613-019-0593-9
pii: 10.1186/s13613-019-0593-9
pmc: PMC6797678
doi:

Types de publication

Journal Article

Langues

eng

Pagination

119

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Auteurs

Ferran Rueda (F)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.
PhD Program in Internal Medicine, Autonomous University of Barcelona, Barcelona, Spain.

Germán Cediel (G)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Cosme García-García (C)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Júlia Aranyó (J)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Marta González-Lopera (M)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

M Cruz Aranda Nevado (MC)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Judith Serra Gregori (J)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Teresa Oliveras (T)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Carlos Labata (C)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Marc Ferrer (M)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Nabil El Ouaddi (N)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain.

Antoni Bayés-Genís (A)

Heart Institute, Germans Trias i Pujol University Hospital, Carretera de Canyet s/n, Badalona, 08916, Barcelona, Spain. abayesgenis@gmail.com.
Department of Medicine, CIBERCV, Autonomous University of Barcelona, Barcelona, Spain. abayesgenis@gmail.com.

Classifications MeSH