Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/29232
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dc.contributor.authorKoelmeyer R.en
dc.contributor.authorNim H.T.en
dc.contributor.authorNikpour M.en
dc.contributor.authorSun Y.B.en
dc.contributor.authorKao A.en
dc.contributor.authorGuenther O.en
dc.contributor.authorMorand E.en
dc.contributor.authorHoi A.en
dc.date.accessioned2021-05-14T09:52:11Zen
dc.date.available2021-05-14T09:52:11Zen
dc.date.copyright2020en
dc.date.created20200610en
dc.date.issued2020-06-10en
dc.identifier.citationLupus Science and Medicine. 7 (1) (no pagination), 2020. Article Number: e000372. Date of Publication: 27 May 2020.en
dc.identifier.issn2053-8790 (electronic)en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/29232en
dc.description.abstractObjective Disease severity in SLE is an important concept related to disease activity, treatment burden and prognosis. We set out to evaluate if high disease activity status (HDAS), based on ever attainment of a Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) disease activity score of >=10, is an indicator for disease severity in SLE. Methods Using prospectively collected data, we assessed the association of HDAS with sociodemographic and disease characteristics and adverse clinical outcomes using logistic regression or generalised estimating equations. Results Of 286 patients with SLE, who were observed for a median (range) of 5.1 years (1-10.8 years), 43.7% experienced HDAS at least once during the observational period. Autoantibody positivity, particularly anti-dsDNA and anti-Sm positivity, were associated with increased likelihood of HDAS. Age >=45 years at diagnosis was associated with reduced likelihood of HDAS (p=0.002). Patients with HDAS had higher Physician Global Assessment score (>1: OR 8.1, p<0.001) and were more likely to meet criteria for flare (mild/moderate flare: OR 4.4, p<0.001; severe flare: OR 17.2, p<0.001) at the time of experiencing HDAS. They were also more likely to have overall higher disease activity, as defined by time-adjusted mean SLEDAI-2K score in the highest quartile (OR 11.7, 95% CI 5.1 to 26.6; p>0.001), higher corticosteroid exposure (corticosteroid dose in highest quartile: OR 7.7, 95% CI 3.9 to 15.3; p<0.001) and damage accrual (OR 2.3, 95% CI 1.3 to 3.9; p=0.003) when compared with non-HDAS patients. Conclusions HDAS is associated with more severe disease, as measured by higher disease activity across time, corticosteroid exposure and damage accrual. The occurrence of HDAS may be a useful prognostic marker in the management of SLE.Copyright © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.en
dc.languageenen
dc.languageEnglishen
dc.publisherBMJ Publishing Group (E-mail: subscriptions@bmjgroup.com)en
dc.relation.ispartofLupus Science and Medicine-
dc.subject.meshSLEDAI-
dc.subject.meshsocial status-
dc.subject.meshsystemic lupus erythematosus-
dc.subject.meshautoantibody-
dc.subject.meshazathioprine-
dc.subject.meshbeta2 glycoprotein 1 antibody-
dc.subject.meshcardiolipin antibody-
dc.subject.meshcorticosteroid-
dc.subject.meshcyclophosphamide-
dc.subject.meshdouble stranded DNA antibody-
dc.subject.meshhydroxychloroquine-
dc.subject.meshLa antibody-
dc.subject.meshleflunomide-
dc.subject.meshlupus anticoagulant-
dc.subject.meshmercaptopurine-
dc.subject.meshmethotrexate-
dc.subject.meshmycophenolic acid-
dc.subject.meshneutrophil cytoplasmic antibody-
dc.subject.meshphospholipid antibody-
dc.subject.meshprednisolone-
dc.subject.meshrheumatoid factor-
dc.subject.meshribonucleoprotein antibody-
dc.subject.meshSm antibody-
dc.subject.meshhigh disease activity status-
dc.subject.meshcorticosteroid therapy-
dc.subject.meshdisease activity-
dc.subject.meshdisease activity score-
dc.subject.meshphysician-
dc.titleHigh disease activity status suggests more severe disease and damage accrual in systemic lupus erythematosus.en
dc.typeArticleen
dc.identifier.affiliationRheumatology-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1136/lupus-2019-000372-
dc.publisher.placeUnited Kingdomen
dc.identifier.source631909149en
dc.identifier.institution(Koelmeyer, Morand, Hoi) Monash Centre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, VIC, Australia (Nim) Faculty of Information Technology, Monash University, Clayton, VIC, Australia (Nikpour) Department of Medicine, University of Melbourne, Fitzroy, VIC, Australia (Nikpour) Rheumatology, St Vincent Hospital Melbourne, Fitzroy, VIC, Australia (Sun, Guenther) Global Evidence and Value Development, Merck Healthcare KGaA, Darmstadt, Germany (Kao) Global Clinical Development, EMD Serono Research and Development Institute, Darmstadt, Germany (Morand, Hoi) Department of Rheumatology, Monash Health, Clayton, VIC, Australiaen
dc.description.addressA. Hoi, Monash Centre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, VIC, Australia. E-mail: alberta.hoi@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2020 Elsevier B.V., All rights reserved.en
dc.subect.keywordsautoimmune diseases disease activity systemic lupus erythematosusen
dc.identifier.authoremailHoi A.; alberta.hoi@monash.eduen
dc.description.grantOrganization: *GlaxoSmithKline* Organization No: 100004330 Country: United Kingdom Organization: *Merck KGaA* Organization No: 100009945 Country: Germany Organization: *UCB* Organization No: 100011110 Country: Belgiumen
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptRheumatology-
crisitem.author.deptCentre for Inflammatory Diseases at Monash Health-
crisitem.author.deptRheumatology-
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