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CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia

BACKGROUND: The carbohydrate antigen 125 (CA125) was proven as a robust biomarker for risk stratification in adults with heart failure. This is the first study analyzing CA125 in a cohort of infants with congenital diaphragmatic hernia (CDH). METHODS: Sixty-eight infants with CDH, treated at the Uni...

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Autores principales: Schroeder, Lukas, Pugnaloni, Flaminia, Dolscheid-Pommerich, Ramona, Geipel, Annegret, Berg, Christoph, Holdenrieder, Stefan, Mueller, Andreas, Kipfmueller, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988682/
https://www.ncbi.nlm.nih.gov/pubmed/35705629
http://dx.doi.org/10.1038/s41390-022-02130-8
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author Schroeder, Lukas
Pugnaloni, Flaminia
Dolscheid-Pommerich, Ramona
Geipel, Annegret
Berg, Christoph
Holdenrieder, Stefan
Mueller, Andreas
Kipfmueller, Florian
author_facet Schroeder, Lukas
Pugnaloni, Flaminia
Dolscheid-Pommerich, Ramona
Geipel, Annegret
Berg, Christoph
Holdenrieder, Stefan
Mueller, Andreas
Kipfmueller, Florian
author_sort Schroeder, Lukas
collection PubMed
description BACKGROUND: The carbohydrate antigen 125 (CA125) was proven as a robust biomarker for risk stratification in adults with heart failure. This is the first study analyzing CA125 in a cohort of infants with congenital diaphragmatic hernia (CDH). METHODS: Sixty-eight infants with CDH, treated at the University Children’s Hospital Bonn (Germany), between January 2018 and February 2021, were prospectively enrolled for analysis. CA125 values were measured at the following timepoints: 6,12, 24, 48 h, and during ECMO daily from day 1 to day 7. RESULTS: In infants not surviving to discharge, CA125 values were significantly higher at day 1 (6, 12, and 24 h). Infants with subsequent need for ECMO presented significantly higher CA125 values at 12 h of life. During ECMO, CA125 values measured at day 1 were significantly higher in infants not surviving to discharge. In the ROC analysis, a CA125 value of ≥10 U/ml was calculated as optimal cut-off for the prediction of ECMO and in-hospital mortality. CA125 values correlated significantly with the severity of PH and ventricular dysfunction. CONCLUSIONS: CA125 values correlate significantly with echocardiographic markers of PH and ventricular dysfunction and correlate significantly with parameters of disease severity (need for ECMO, mortality). IMPACT: CA125 was proven as robust cardiac biomarker in adult cohorts. Information about the utility as a biomarker in neonatal cohorts is lacking. This is the first study analyzing CA125 as a cardiac biomarker in a cohort of infants with congenital diaphragmatic hernia (CDH). CA125 correlates significantly with markers of echocardiographic assessment (PH and ventricular dysfunction) in infants with CDH and helps to identify infants at high risk for ECMO and in-hospital mortality. The results underline the need for the inclusion of cardiac biomarkers in the clinical routine in neonates at risk for cardiopulmonary failure.
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spelling pubmed-99886822023-03-08 CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia Schroeder, Lukas Pugnaloni, Flaminia Dolscheid-Pommerich, Ramona Geipel, Annegret Berg, Christoph Holdenrieder, Stefan Mueller, Andreas Kipfmueller, Florian Pediatr Res Clinical Research Article BACKGROUND: The carbohydrate antigen 125 (CA125) was proven as a robust biomarker for risk stratification in adults with heart failure. This is the first study analyzing CA125 in a cohort of infants with congenital diaphragmatic hernia (CDH). METHODS: Sixty-eight infants with CDH, treated at the University Children’s Hospital Bonn (Germany), between January 2018 and February 2021, were prospectively enrolled for analysis. CA125 values were measured at the following timepoints: 6,12, 24, 48 h, and during ECMO daily from day 1 to day 7. RESULTS: In infants not surviving to discharge, CA125 values were significantly higher at day 1 (6, 12, and 24 h). Infants with subsequent need for ECMO presented significantly higher CA125 values at 12 h of life. During ECMO, CA125 values measured at day 1 were significantly higher in infants not surviving to discharge. In the ROC analysis, a CA125 value of ≥10 U/ml was calculated as optimal cut-off for the prediction of ECMO and in-hospital mortality. CA125 values correlated significantly with the severity of PH and ventricular dysfunction. CONCLUSIONS: CA125 values correlate significantly with echocardiographic markers of PH and ventricular dysfunction and correlate significantly with parameters of disease severity (need for ECMO, mortality). IMPACT: CA125 was proven as robust cardiac biomarker in adult cohorts. Information about the utility as a biomarker in neonatal cohorts is lacking. This is the first study analyzing CA125 as a cardiac biomarker in a cohort of infants with congenital diaphragmatic hernia (CDH). CA125 correlates significantly with markers of echocardiographic assessment (PH and ventricular dysfunction) in infants with CDH and helps to identify infants at high risk for ECMO and in-hospital mortality. The results underline the need for the inclusion of cardiac biomarkers in the clinical routine in neonates at risk for cardiopulmonary failure. Nature Publishing Group US 2022-06-15 2023 /pmc/articles/PMC9988682/ /pubmed/35705629 http://dx.doi.org/10.1038/s41390-022-02130-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Research Article
Schroeder, Lukas
Pugnaloni, Flaminia
Dolscheid-Pommerich, Ramona
Geipel, Annegret
Berg, Christoph
Holdenrieder, Stefan
Mueller, Andreas
Kipfmueller, Florian
CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia
title CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia
title_full CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia
title_fullStr CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia
title_full_unstemmed CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia
title_short CA125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia
title_sort ca125: a novel cardiac biomarker for infants with congenital diaphragmatic hernia
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988682/
https://www.ncbi.nlm.nih.gov/pubmed/35705629
http://dx.doi.org/10.1038/s41390-022-02130-8
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