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dc.contributor.authorKindberg, Kristine Mørk
dc.contributor.authorBroch, Kaspar
dc.contributor.authorAndersen, Geir Øystein
dc.contributor.authorAnstensrud, Anne Kristine
dc.contributor.authorÅkra, Sissel
dc.contributor.authorWoxholt, Sindre
dc.contributor.authorTøllefsen, Ingvild Maria
dc.contributor.authorUeland, Thor
dc.contributor.authorAmundsen, Brage H.
dc.contributor.authorKløw, Nils-Einar
dc.contributor.authorHalvorsen, Bente
dc.contributor.authorDahl, Tuva Børresdatter
dc.contributor.authorHuse, Camilla
dc.contributor.authorMurphy, Sarah Louise Mikalsen
dc.contributor.authorDamås, Jan Kristian
dc.contributor.authorOpdahl, Anders
dc.contributor.authorWiseth, Rune
dc.contributor.authorGullestad, Lars
dc.contributor.authorAukrust, Pål
dc.contributor.authorSantos-Gallego, Carlos
dc.contributor.authorSeljeflot, Ingebjørg
dc.contributor.authorStokke, Mathis Korseberg
dc.contributor.authorHelseth, Ragnhild Merckoll
dc.date.accessioned2024-10-07T09:20:35Z
dc.date.available2024-10-07T09:20:35Z
dc.date.issued2024-08-15
dc.description.abstractBackground - Interleukin-6-receptor inhibition with tocilizumab improves myocardial salvage in patients with ST-segment elevation myocardial infarction (STEMI). Reduced levels of neutrophil extracellular traps (NETs), which consist of nuclear material studded with proteins released upon neutrophil activation, might contribute to this effect.<p> <p>Objectives - The purpose of this study was to evaluate the effect of tocilizumab on NETs and investigate the association between NETs and myocardial injury in patients with STEMI.<p> <p>Methods - In the ASSAIL-MI study, 199 patients with STEMI were randomized to tocilizumab or placebo during percutaneous coronary intervention. In this substudy, we analyzed blood levels of the NET markers double-stranded deoxyribonucleic acid (dsDNA), myeloperoxidase-DNA, and citrullinated histone 3 (H3Cit) at admission and after 24 hours and 3 to 7 days. In a subgroup of patients, we assessed regulation of transcripts related to the formation of NETs. We also investigated associations between NET markers and the myocardial salvage index (MSI).<p> <p>Results - All NET markers were lower in the tocilizumab group than in the placebo group at 3 to 7 days (all P < 0.04). Several NET-related pathways were downregulated in the tocilizumab group. The beneficial effect of tocilizumab on the MSI seemed to be partly dependent on reduction of NETs (structural equation modeling: 0.05, P = 0.001 [dsDNA] and 0.02, P = 0.055 [H3Cit]). Patients with NETs in the 3 lowest quartiles had higher MSI than patients in quartile 4 (β = 10.9 [95% CI: 4.0-15.0] [dsDNA] and β = 8.9 [95% CI: 2.0-15.9] [H3Cit], both P = 0.01).<p> <p>Conclusions - NETs were reduced by tocilizumab and associated with myocardial injury. The effect of tocilizumab on MSI might be mediated through reduced NETs. (ASSessing the Effect of Anti-IL-6 Treatment in Myocardial Infarction: The ASSAIL-MI Trial [ASSAIL-MI]en_US
dc.identifier.citationKindberg, Broch, Andersen, Anstensrud, Åkra, Woxholt, Tøllefsen, Ueland, Amundsen, Kløw, Halvorsen, Dahl, Huse, Murphy, Damås, Opdahl, Wiseth, Gullestad, Aukrust, Santos-Gallego, Seljeflot, Stokke, Helseth. Neutrophil Extracellular Traps in ST-Segment Elevation Myocardial Infarction: Reduced by Tocilizumab and Associated With Infarct Size. JACC: Advances. 2024;3(9)en_US
dc.identifier.cristinIDFRIDAID 2290825
dc.identifier.doi10.1016/j.jacadv.2024.101193
dc.identifier.issn2772-963X
dc.identifier.urihttps://hdl.handle.net/10037/35077
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.journalJACC: Advances
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2024 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleNeutrophil Extracellular Traps in ST-Segment Elevation Myocardial Infarction: Reduced by Tocilizumab and Associated With Infarct Sizeen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
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