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Endothelial Cell Phenotypes Demonstrate Different Metabolic Patterns and Predict Mortality in Trauma Patients

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dc.contributor.author Henriksen, Hanne H.
dc.contributor.author Marín de Mas, Igor
dc.contributor.author Nielsen, Lars K.
dc.contributor.author Krocker, Joseph
dc.contributor.author Stensballe, Jakob
dc.contributor.author Karvelsson, Sigurður T.
dc.contributor.author Secher, Niels H.
dc.contributor.author Rolfsson, Óttar
dc.contributor.author Wade, Charles E.
dc.contributor.author Johansson, Pär I.
dc.date.accessioned 2023-08-22T01:04:47Z
dc.date.available 2023-08-22T01:04:47Z
dc.date.issued 2023-01-23
dc.identifier.citation Henriksen , H H , Marín de Mas , I , Nielsen , L K , Krocker , J , Stensballe , J , Karvelsson , S T , Secher , N H , Rolfsson , Ó , Wade , C E & Johansson , P I 2023 , ' Endothelial Cell Phenotypes Demonstrate Different Metabolic Patterns and Predict Mortality in Trauma Patients ' , International Journal of Molecular Sciences , vol. 24 , no. 3 , 2257 . https://doi.org/10.3390/ijms24032257
dc.identifier.issn 1661-6596
dc.identifier.other 155768870
dc.identifier.other 1d347b31-0244-4f06-abcf-70eeaca6b9f1
dc.identifier.other 85147890500
dc.identifier.other 36768579
dc.identifier.other unpaywall: 10.3390/ijms24032257
dc.identifier.uri https://hdl.handle.net/20.500.11815/4445
dc.description Funding Information: HHH has been supported by a PhD-scholarship from Rigshospitalet, Denmark, and would like to thank The Candys Foundation for the grant (2018-279). IMdM and LKN were supported by The Novo Nordisk Foundation (NNF Grant numbers: NNF20CC0035580; NNF14OC0009473; and NNF20SA0066621). Publisher Copyright: © 2023 by the authors.
dc.description.abstract In trauma patients, shock-induced endotheliopathy (SHINE) is associated with a poor prognosis. We have previously identified four metabolic phenotypes in a small cohort of trauma patients (N = 20) and displayed the intracellular metabolic profile of the endothelial cell by integrating quantified plasma metabolomic profiles into a genome-scale metabolic model (iEC-GEM). A retrospective observational study of 99 trauma patients admitted to a Level 1 Trauma Center. Mass spectrometry was conducted on admission samples of plasma metabolites. Quantified metabolites were analyzed by computational network analysis of the iEC-GEM. Four plasma metabolic phenotypes (A–D) were identified, of which phenotype D was associated with an increased injury severity score (p < 0.001); 90% (91.6%) of the patients who died within 72 h possessed this phenotype. The inferred EC metabolic patterns were found to be different between phenotype A and D. Phenotype D was unable to maintain adequate redox homeostasis. We confirm that trauma patients presented four metabolic phenotypes at admission. Phenotype D was associated with increased mortality. Different EC metabolic patterns were identified between phenotypes A and D, and the inability to maintain adequate redox balance may be linked to the high mortality.
dc.format.extent 2172912
dc.format.extent
dc.language.iso en
dc.relation.ispartofseries International Journal of Molecular Sciences; 24(3)
dc.rights info:eu-repo/semantics/openAccess
dc.subject endotheliopathy
dc.subject genome-scale metabolic model
dc.subject metabolomics
dc.subject systems biology
dc.subject trauma
dc.subject tricarboxylic acid cycle
dc.subject Shock
dc.subject Metabolomics
dc.subject Phenotype
dc.subject Prospective Studies
dc.subject Endothelial Cells
dc.subject Humans
dc.subject Molecular Biology
dc.subject Spectroscopy
dc.subject Catalysis
dc.subject Inorganic Chemistry
dc.subject Computer Science Applications
dc.subject Physical and Theoretical Chemistry
dc.subject Organic Chemistry
dc.title Endothelial Cell Phenotypes Demonstrate Different Metabolic Patterns and Predict Mortality in Trauma Patients
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.3390/ijms24032257
dc.relation.url http://www.scopus.com/inward/record.url?scp=85147890500&partnerID=8YFLogxK
dc.contributor.department Faculty of Medicine


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