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Apelin-13 as a Potential Biomarker in Critical Illness

Background: The adrenocortical system and copeptin as prognostic markers were intensively investigated in critical illness. The potential predictive power of apelin-13 as a biomarker is largely unknown. We aimed to investigate the prognostic role of apelin-13 in relation to free cortisol, aldosteron...

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Autores principales: Gergics, Marin, Pham-Dobor, Gréta, Kurdi, Csilla, Montskó, Gergely, Mihályi, Krisztina, Bánfai, Gábor, Kanizsai, Péter, Kőszegi, Tamás, Mezősi, Emese, Bajnok, László
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381233/
https://www.ncbi.nlm.nih.gov/pubmed/37510916
http://dx.doi.org/10.3390/jcm12144801
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author Gergics, Marin
Pham-Dobor, Gréta
Kurdi, Csilla
Montskó, Gergely
Mihályi, Krisztina
Bánfai, Gábor
Kanizsai, Péter
Kőszegi, Tamás
Mezősi, Emese
Bajnok, László
author_facet Gergics, Marin
Pham-Dobor, Gréta
Kurdi, Csilla
Montskó, Gergely
Mihályi, Krisztina
Bánfai, Gábor
Kanizsai, Péter
Kőszegi, Tamás
Mezősi, Emese
Bajnok, László
author_sort Gergics, Marin
collection PubMed
description Background: The adrenocortical system and copeptin as prognostic markers were intensively investigated in critical illness. The potential predictive power of apelin-13 as a biomarker is largely unknown. We aimed to investigate the prognostic role of apelin-13 in relation to free cortisol, aldosterone, CRH, and copeptin in critically ill patients. Methods: In this prospective observational study, 124 critically ill patients (64 men, 60 women, median age: 70 (59–78) years) were consecutively enrolled at the time of admission. All routinely available clinical and laboratory parameters were evaluated and correlated to hormonal changes. Results: Serum apelin-13 was 1161 (617–2967) pg/mL in non-survivors vs. 2477 (800–3531) pg/mL in survivors (p = 0.054). The concentrations of apelin-13 and CRH had strong positive correlations (r = 0.685, p < 0.001) and were significantly higher in surviving non-septic patients (Apelin-13 (pg/mL): 2286 (790–3330) vs. 818 (574–2732) p < 0.05; CRH (pg/mL) 201 (84–317) vs. 89 (74–233) p < 0.05). Apelin-13 and free cortisol were independent determinants of survival in the multivariate Cox regression analysis, while copeptin, CRH, or aldosterone were not. Conclusions: Beyond free cortisol, serum apelin-13 may also help refine prognostic predictions in the early phase of critical illness, especially in non-septic patients.
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spelling pubmed-103812332023-07-29 Apelin-13 as a Potential Biomarker in Critical Illness Gergics, Marin Pham-Dobor, Gréta Kurdi, Csilla Montskó, Gergely Mihályi, Krisztina Bánfai, Gábor Kanizsai, Péter Kőszegi, Tamás Mezősi, Emese Bajnok, László J Clin Med Article Background: The adrenocortical system and copeptin as prognostic markers were intensively investigated in critical illness. The potential predictive power of apelin-13 as a biomarker is largely unknown. We aimed to investigate the prognostic role of apelin-13 in relation to free cortisol, aldosterone, CRH, and copeptin in critically ill patients. Methods: In this prospective observational study, 124 critically ill patients (64 men, 60 women, median age: 70 (59–78) years) were consecutively enrolled at the time of admission. All routinely available clinical and laboratory parameters were evaluated and correlated to hormonal changes. Results: Serum apelin-13 was 1161 (617–2967) pg/mL in non-survivors vs. 2477 (800–3531) pg/mL in survivors (p = 0.054). The concentrations of apelin-13 and CRH had strong positive correlations (r = 0.685, p < 0.001) and were significantly higher in surviving non-septic patients (Apelin-13 (pg/mL): 2286 (790–3330) vs. 818 (574–2732) p < 0.05; CRH (pg/mL) 201 (84–317) vs. 89 (74–233) p < 0.05). Apelin-13 and free cortisol were independent determinants of survival in the multivariate Cox regression analysis, while copeptin, CRH, or aldosterone were not. Conclusions: Beyond free cortisol, serum apelin-13 may also help refine prognostic predictions in the early phase of critical illness, especially in non-septic patients. MDPI 2023-07-20 /pmc/articles/PMC10381233/ /pubmed/37510916 http://dx.doi.org/10.3390/jcm12144801 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gergics, Marin
Pham-Dobor, Gréta
Kurdi, Csilla
Montskó, Gergely
Mihályi, Krisztina
Bánfai, Gábor
Kanizsai, Péter
Kőszegi, Tamás
Mezősi, Emese
Bajnok, László
Apelin-13 as a Potential Biomarker in Critical Illness
title Apelin-13 as a Potential Biomarker in Critical Illness
title_full Apelin-13 as a Potential Biomarker in Critical Illness
title_fullStr Apelin-13 as a Potential Biomarker in Critical Illness
title_full_unstemmed Apelin-13 as a Potential Biomarker in Critical Illness
title_short Apelin-13 as a Potential Biomarker in Critical Illness
title_sort apelin-13 as a potential biomarker in critical illness
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381233/
https://www.ncbi.nlm.nih.gov/pubmed/37510916
http://dx.doi.org/10.3390/jcm12144801
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