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https://ahro.austin.org.au/austinjspui/handle/1/25036
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DC Field | Value | Language |
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dc.contributor.author | Owen, Claire E | - |
dc.contributor.author | McMaster, Christopher | - |
dc.contributor.author | Liew, David F L | - |
dc.contributor.author | Leung, Jessica L Y | - |
dc.contributor.author | Scott, Andrew M | - |
dc.contributor.author | Buchanan, Russell R C | - |
dc.date | 2020-10-12 | - |
dc.date.accessioned | 2020-10-15T03:15:15Z | - |
dc.date.available | 2020-10-15T03:15:15Z | - |
dc.date.issued | 2021-01 | - |
dc.identifier.citation | International Journal of Rheumatic Diseases 2021; 24(1): 56-62 | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/25036 | - |
dc.description.abstract | Neutrophil 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.iso | eng | - |
dc.subject | glucocorticoids | en |
dc.subject | lymphocytes | en |
dc.subject | neutrophils | en |
dc.subject | polymyalgia rheumatica | en |
dc.subject | prognosis | en |
dc.title | Neutrophil to lymphocyte ratio predicts glucocorticoid resistance in polymyalgia rheumatica. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | International Journal of Rheumatic Diseases | en |
dc.identifier.affiliation | Rheumatology | en |
dc.identifier.affiliation | Department of Medicine, University of Melbourne, Parkville, VIC, Australia | en |
dc.identifier.affiliation | Molecular Imaging and Therapy | en |
dc.identifier.affiliation | Olivia Newton-John Cancer Research Institute | en |
dc.identifier.affiliation | School of Cancer Medicine, La Trobe University, Heidelberg, VIC, Australia | en |
dc.identifier.doi | 10.1111/1756-185X.14000 | en |
dc.type.content | Text | en |
dc.identifier.orcid | 0000-0002-2694-5411 | en |
dc.identifier.orcid | 0000-0001-8451-8883 | en |
dc.identifier.orcid | 0000-0002-3834-2706 | en |
dc.identifier.pubmedid | 33043616 | - |
local.name.researcher | Buchanan, Russell R C | |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | Rheumatology | - |
crisitem.author.dept | Clinical Pharmacology and Therapeutics | - |
crisitem.author.dept | Rheumatology | - |
crisitem.author.dept | Clinical Pharmacology and Therapeutics | - |
crisitem.author.dept | Rheumatology | - |
crisitem.author.dept | Molecular Imaging and Therapy | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Rheumatology | - |
Appears in Collections: | Journal articles |
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