dc.contributor.author
Lücht, Jana
dc.contributor.author
Seiler, Raphael
dc.contributor.author
Herre, Alexa Leona
dc.contributor.author
Brankova, Liliya
dc.contributor.author
Fritsche-Guenther, Raphaela
dc.contributor.author
Kirwan, Jennifer
dc.contributor.author
Huscher, Dörte
dc.contributor.author
Münzfeld, Hanna
dc.contributor.author
Berger, Felix
dc.contributor.author
Photiadis, Joachim
dc.contributor.author
Tong, Giang
dc.contributor.author
Schmitt, Katharina R. L.
dc.date.accessioned
2025-07-04T12:19:10Z
dc.date.available
2025-07-04T12:19:10Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/48142
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-47864
dc.description.abstract
Objective: Cold-inducible RNA binding Protein (CIRBP) has been shown to be a potent inflammatory mediator and could serve as a novel biomarker for inflammation. Systemic inflammatory response syndrome (SIRS) and capillary leak syndrome (CLS) are frequent complications after pediatric cardiac surgery increasing morbidity, therefore early diagnosis and therapy is crucial. As CIRBP serum levels have not been analyzed in a pediatric population, we conducted a clinical feasibility establishing a customized magnetic bead panel analyzing CIRBP in pediatric patients undergoing cardiac surgery.
Methods: A prospective hypothesis generating observational clinical study was conducted at the German Heart Center Berlin during a period of 9 months starting in May 2020 (DRKS00020885, https://drks.de/search/de/trial/DRKS00020885). Serum samples were obtained before the cardiac operation, upon arrival at the pediatric intensive care unit, 6 and 24 h after the operation in patients up to 18 years of age with congenital heart disease (CHD). Customized multiplex magnetic bead-based immunoassay panels were developed to analyze CIRBP, Interleukin-1β (IL-1β), Interleukin-6 (IL-6), Interleukin-8 (IL-8), Interleukin-10 (IL-10), Monocyte chemotactic protein 1 (MCP-1), Syndecan-1 (SDC-1), Thrombomodulin (TM), Vascular endothelial growth factor (VEGF-A), Angiopoietin-2 (Ang-2), and Fibroblast growth factor 23 (FGF-23) in 25 µl serum using the Luminex MagPix® system.
Results: 19 patients representing a broad range of CHD (10 male patients, median age 2 years, 9 female patients, median age 3 years) were included in the feasibility study. CIRBP was detectable in the whole patient cohort. Relative to individual baseline values, CIRBP concentrations increased 6 h after operation and returned to baseline levels over time. IL-6, IL-8, IL-10, and MCP-1 concentrations were significantly increased after operation and except for MCP-1 concentrations stayed upregulated over time. SDC-1, TM, Ang-2, as well as FGF-23 concentrations were also significantly increased, whereas VEGF-A concentration was significantly decreased after surgery.
Discussion: Using customized magnetic bead panels, we were able to detect CIRBP in a minimal serum volume (25 µl) in all enrolled patients. To our knowledge this is the first clinical study to assess CIRBP serum concentrations in a pediatric population.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
pediatric cardiology
en
dc.subject
pediatric cardiac surgery
en
dc.subject
cold inducible RNA-binding protein (CIRBP)
en
dc.subject
inflammation
en
dc.subject
endothelial dysfunction
en
dc.subject
feasibility study
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Promising results of a clinical feasibility study: CIRBP as a potential biomarker in pediatric cardiac surgery
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
1247472
dcterms.bibliographicCitation.doi
10.3389/fcvm.2024.1247472
dcterms.bibliographicCitation.journaltitle
Frontiers in Cardiovascular Medicine
dcterms.bibliographicCitation.originalpublishername
Frontiers Media SA
dcterms.bibliographicCitation.volume
11
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
38361581
dcterms.isPartOf.eissn
2297-055X