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dc.date.accessioned2021-04-25T19:14:21Z
dc.date.available2021-04-25T19:14:21Z
dc.date.created2020-07-31T12:08:54Z
dc.date.issued2020
dc.identifier.citationNorvang, Vibeke Brinkmann, Gina Charlotte Hetland Yoshida, Kazuki Lillegraven, Siri Aga, Anna-Birgitte Sexton, Joseph Andrew Tedeschi, Sara K. Lyu, Houchen Norli, Ellen Sauar Uhlig, Tillmann Kvien, Tore Kristian Mjaavatten, Maria Dahl Solomon, Daniel H. Haavardsholm, Espen Andre . Achievement of Remission in Two Early Rheumatoid Arthritis Cohorts Implementing Different Treat-to-Target Strategies. Arthritis & Rheumatology. 2020, 72(7), 1072-1081
dc.identifier.urihttp://hdl.handle.net/10852/85603
dc.description.abstractObjective The objective of this study was to compare achievement of remission in 2 early rheumatoid arthritis (RA) treat‐to‐target (TTT) cohorts, a tight control cohort with a target of stringent remission in a randomized controlled trial and an observational cohort targeting a looser definition of remission in clinical practice. Methods We analyzed data from the Aiming for Remission in Rheumatoid Arthritis: a randomised trial examining the benefit of ultrasound in a Clinical Tight Control regimen (ARCTIC) trial and the Norwegian Very Early Arthritis Clinic (NOR‐VEAC) observational study. Both were Norwegian multicenter studies that included disease‐modifying antirheumatic drug (DMARD)–naive RA patients and implemented TTT. The target in the ARCTIC trial was remission defined as a Disease Activity Score (DAS) of <1.6 plus 0 swollen joints on a 44‐joint count, while the target in the NOR‐VEAC study was the less stringent remission target of a DAS28 of <2.6. We assessed achievement of the study‐specific targets and compared the odds of achieving the American College of Rheumatology(ACR)/European League Against Rheumatism (EULAR) Boolean remission during 2 years of follow‐up. Results We included 189 patients from the ARCTIC trial and 330 patients from the NOR‐VEAC study. The study‐specific target had been achieved in more than half of the patients in each cohort at 6 months, increasing to >60% at 12 and 24 months. The odds of achieving ACR/EULAR Boolean remission during follow‐up were higher in the ARCTIC trial than in the NOR‐VEAC study, with significant differences at 3 months (odds ratio 1.73 [95% confidence interval 1.03–2.89]), 12 months (odds ratio 1.97 [95% confidence interval 1.21–3.20]), and 24 months (odds ratio 1.82 [95% confidence interval 1.05–3.16]). Conclusion A majority of patients in both cohorts reached the study‐specific treatment targets. More patients in the ARCTIC trial than in the NOR‐VEAC study achieved ACR/EULAR Boolean remission during follow‐up, suggesting that targeting a more stringent definition of remission provides further potential for favorable outcomes of a TTT strategy.
dc.languageEN
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleAchievement of Remission in Two Early Rheumatoid Arthritis Cohorts Implementing Different Treat-to-Target Strategies
dc.typeJournal article
dc.creator.authorNorvang, Vibeke
dc.creator.authorBrinkmann, Gina Charlotte Hetland
dc.creator.authorYoshida, Kazuki
dc.creator.authorLillegraven, Siri
dc.creator.authorAga, Anna-Birgitte
dc.creator.authorSexton, Joseph Andrew
dc.creator.authorTedeschi, Sara K.
dc.creator.authorLyu, Houchen
dc.creator.authorNorli, Ellen Sauar
dc.creator.authorUhlig, Tillmann
dc.creator.authorKvien, Tore Kristian
dc.creator.authorMjaavatten, Maria Dahl
dc.creator.authorSolomon, Daniel H.
dc.creator.authorHaavardsholm, Espen Andre
cristin.unitcode185,52,0,0
cristin.unitnameInstitutt for helse og samfunn
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1821127
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Arthritis & Rheumatology&rft.volume=72&rft.spage=1072&rft.date=2020
dc.identifier.jtitleArthritis & Rheumatology
dc.identifier.volume72
dc.identifier.issue7
dc.identifier.startpage1072
dc.identifier.endpage1081
dc.identifier.doihttps://doi.org/10.1002/art.41232
dc.identifier.urnURN:NBN:no-88281
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2326-5191
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/85603/2/Achievement%2Bof%2BRemission%2Bin%2BTwo%2BEarly%2BRheumatoid.pdf
dc.type.versionPublishedVersion


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