Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25036
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dc.contributor.authorOwen, Claire E-
dc.contributor.authorMcMaster, Christopher-
dc.contributor.authorLiew, David F L-
dc.contributor.authorLeung, Jessica L Y-
dc.contributor.authorScott, Andrew M-
dc.contributor.authorBuchanan, Russell R C-
dc.date2020-10-12-
dc.date.accessioned2020-10-15T03:15:15Z-
dc.date.available2020-10-15T03:15:15Z-
dc.date.issued2021-01-
dc.identifier.citationInternational Journal of Rheumatic Diseases 2021; 24(1): 56-62en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25036-
dc.description.abstractNeutrophil to lymphocyte ratio (NLR) and platelet to lymphocyte ratio (PLR) correlate with disease activity in several rheumatic diseases; however, their utility in polymyalgia rheumatica (PMR) remains unclear. This study evaluated their relationship with disease activity and glucocorticoid resistance in PMR. Data for disease activity (PMR-AS) and full blood examination was obtained from a prospective observational cohort comprising newly diagnosed, steroid-naïve PMR patients treated with low-dose glucocorticoid therapy. Glucocorticoid resistance was defined as non-response to prednisolone 15 mg/d or initial response followed by flare (PMR-AS ≥ 9.35 or ∆ ≥6.6) upon weaning to 5 mg/d. Univariable Bayesian linear regression analysis of the relationship between PMR-AS (baseline and mean) and NLR and PLR was performed. Predictors of glucocorticoid resistance were identified using a multivariable outcome model, with variables derived from Bayesian model selection. Of the 32 included patients, 16 (50%) fulfilled the primary outcome measure of glucocorticoid resistance. These participants were older, typically female, and had higher baseline C-reactive protein than their glucocorticoid-responsive counterparts. A statistically significant relationship was identified between PMR-AS and both NLR (odds ratio [OR] 28.1; 95% CI 1.6-54.7) and PLR (OR 40.6; 95% CI 10.1-71.4) at baseline, with PLR also found to correlate with disease activity during follow-up (OR 15.6; 95% CI 2.7-28.2). Baseline NLR proved a statistically significant predictor of glucocorticoid-resistant PMR (OR 14.01; 95% CI 1.49-278.06). Baseline NLR can predict glucocorticoid resistance in newly diagnosed PMR patients. Both NLR and PLR may be reliable biomarkers of disease activity in PMR.en
dc.language.isoeng-
dc.subjectglucocorticoidsen
dc.subjectlymphocytesen
dc.subjectneutrophilsen
dc.subjectpolymyalgia rheumaticaen
dc.subjectprognosisen
dc.titleNeutrophil to lymphocyte ratio predicts glucocorticoid resistance in polymyalgia rheumatica.en
dc.typeJournal Articleen
dc.identifier.journaltitleInternational Journal of Rheumatic Diseasesen
dc.identifier.affiliationRheumatologyen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Parkville, VIC, Australiaen
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Heidelberg, VIC, Australiaen
dc.identifier.doi10.1111/1756-185X.14000en
dc.type.contentTexten
dc.identifier.orcid0000-0002-2694-5411en
dc.identifier.orcid0000-0001-8451-8883en
dc.identifier.orcid0000-0002-3834-2706en
dc.identifier.pubmedid33043616-
local.name.researcherBuchanan, Russell R C
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptRheumatology-
crisitem.author.deptClinical Pharmacology and Therapeutics-
crisitem.author.deptRheumatology-
crisitem.author.deptClinical Pharmacology and Therapeutics-
crisitem.author.deptRheumatology-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptRheumatology-
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