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dc.contributor.authorRognes, Ingrid Nygren
dc.contributor.authorPischke, Søren Erik
dc.contributor.authorOttestad, William
dc.contributor.authorRøislien, Jo
dc.contributor.authorBerg, Jens Petter
dc.contributor.authorJohnson, Christina
dc.contributor.authorEken, Torsten
dc.contributor.authorMollnes, Tom Eirik
dc.date.accessioned2021-10-14T12:20:09Z
dc.date.available2021-10-14T12:20:09Z
dc.date.created2021-07-09T19:19:48Z
dc.date.issued2021
dc.identifier.citationMolecular medicine (Cambridge, Mass. Print). 2021, 27 (1), 1-13.en_US
dc.identifier.issn1076-1551
dc.identifier.urihttps://hdl.handle.net/11250/2823053
dc.description.abstractBackground - Complement activation is a central mechanism in systemic inflammation and remote organ dysfunction following major trauma. Data on temporal changes of complement activation early after injury is largely missing. We aimed to describe in detail the kinetics of complement activation in individual trauma patients from admission to 10 days after injury, and the association with trauma characteristics and outcome. Methods - In a prospective cohort of 136 trauma patients, plasma samples obtained with high time resolution (admission, 2, 4, 6, 8 h, and thereafter daily) were assessed for terminal complement complex (TCC). We studied individual TCC concentration curves and calculated a summary measure to obtain the accumulated TCC response 3 to 6 h after injury (TCC-AUC3–6). Correlation analyses and multivariable linear regression analyses were used to explore associations between individual patients’ admission TCC, TCC-AUC3–6, daily TCC during the intensive care unit stay, trauma characteristics, and predefined outcome measures. Results - TCC concentration curves showed great variability in temporal shapes between individuals. However, the highest values were generally seen within the first 6 h after injury, before they subsided and remained elevated throughout the intensive care unit stay. Both admission TCC and TCC-AUC3–6 correlated positively with New Injury Severity Score (Spearman’s rho, p-value 0.31, 0.0003 and 0.21, 0.02) and negatively with admission Base Excess (− 0.21, 0.02 and − 0.30, 0.001). Multivariable analyses confirmed that deranged physiology was an important predictor of complement activation. For patients without major head injury, admission TCC and TCC-AUC3–6 were negatively associated with ventilator-free days. TCC-AUC3–6 outperformed admission TCC as a predictor of Sequential Organ Failure Assessment score at day 0 and 4. Conclusions - Complement activation 3 to 6 h after injury was a better predictor of prolonged mechanical ventilation and multiple organ dysfunction syndrome than admission TCC. Our data suggest that the greatest surge of complement activation is found within the first 6 h after injury, and we argue that this time period should be in focus in the design of future experimental studies and clinical trials using complement inhibitors.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleIncreased complement activation 3 to 6 h after trauma is a predictor of prolonged mechanical ventilation and multiple organ dysfunction syndrome: a prospective observational studyen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-13en_US
dc.source.volume27en_US
dc.source.journalMolecular medicine (Cambridge, Mass. Print)en_US
dc.source.issue1en_US
dc.identifier.doi10.1186/s10020-021-00286-3
dc.identifier.cristin1921263
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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