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dc.date.accessioned2020-03-26T19:22:27Z
dc.date.available2020-03-26T19:22:27Z
dc.date.created2019-09-03T16:33:46Z
dc.date.issued2019
dc.identifier.citationHokstad, Ingrid Deyab, Gia Fagerland, Morten Lyberg, Torstein Hjeltnes, Gunnbjørg Førre, Øystein Thorleiv Agewall, Stefan Mollnes, Tom Eirik Hollan, Ivana . Tumor necrosis factor inhibitors are associated with reduced complement activation in spondylarthropathies: An observational study. PLOS ONE. 2019, 14(7), 1-16
dc.identifier.urihttp://hdl.handle.net/10852/74231
dc.description.abstractBackground The complement system is involved in pathogenesis of cardiovascular disease, and might play a role in accelerated atherogenesis in spondylarthropathies (SpA). Hence, we examined complement activation in SpA, and its relationship to antirheumatic treatment, inflammatory and cardiovascular markers. Methods From PSARA, a prospective observational study, we examined 51 SpA patients (31 psoriatic arthritis (PsA), and 20 ankylosing spondylitis (AS)), starting tumor necrosis factor (TNF) inhibitor alone (n = 25), combined with methotrexate (MTX) (n = 10), or MTX monotherapy (n = 16). Complement activation was determined by the soluble terminal complement complex (sC5b-9), inflammation by erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP), and endothelial function by finger plethysmography (Endopat) at baseline, after 6 weeks and 6 months of treatment. Results SpA patients had sC5b-9 levels at (PsA) or above (AS) the upper limit of the estimated reference range. Median sC5b-9 levels decreased significantly from baseline to 6 weeks, with no significant difference between the AS and PsA group. Notably, a significant reduction in sC5b-9 was observed after administration of TNF inhibitor ± MTX, whereas no significant changes were observed in patients treated with MTX alone. Between 6 weeks and 6 months, sC5b-9 remained stable across all subgroups. Reduction in sC5b-9 was independently related to decreased ESR and CRP, and to increased high density cholesterol and total cholesterol. Reduction in sC5b-9 from baseline to 6 weeks was associated with improved EF in age and gender adjusted analyses. Conclusion TNF-inhibition, but not MTX monotherapy, led to rapid and sustained reduction of complement activation in SpA. Thus, the observed decrease in cardiovascular morbidity in patients treated with TNF-inhibitors might be partly due to its beneficial effect on complement. Trial registration Clinical Trials (NCT00902005), retrospectively registered on the 14th of May 2009.
dc.description.abstractTumor necrosis factor inhibitors are associated with reduced complement activation in spondylarthropathies: An observational study
dc.languageEN
dc.publisherPLOS
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleTumor necrosis factor inhibitors are associated with reduced complement activation in spondylarthropathies: An observational study
dc.typeJournal article
dc.creator.authorHokstad, Ingrid
dc.creator.authorDeyab, Gia
dc.creator.authorFagerland, Morten
dc.creator.authorLyberg, Torstein
dc.creator.authorHjeltnes, Gunnbjørg
dc.creator.authorFørre, Øystein Thorleiv
dc.creator.authorAgewall, Stefan
dc.creator.authorMollnes, Tom Eirik
dc.creator.authorHollan, Ivana
cristin.unitcode185,53,11,21
cristin.unitnameAvdeling for klinisk service
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1721155
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLOS ONE&rft.volume=14&rft.spage=1&rft.date=2019
dc.identifier.jtitlePLOS ONE
dc.identifier.volume14
dc.identifier.issue7
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0220079
dc.identifier.urnURN:NBN:no-77331
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1932-6203
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/74231/2/Hokstad%2Bet%2Bal.pdf
dc.type.versionPublishedVersion
cristin.articleide0220079
dc.relation.projectNFR/223255


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