<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Boers M</submitter><funding>European Commission</funding><pagination>925-936</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9209692</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>81(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Low-dose glucocorticoid (GC) therapy is widely used in rheumatoid arthritis (RA) but the balance of benefit and harm is still unclear.&lt;h4>Methods&lt;/h4>The GLORIA (Glucocorticoid LOw-dose in RheumatoId Arthritis) pragmatic double-blind randomised trial compared 2 years of prednisolone, 5 mg/day, to placebo in patients aged 65+ with active RA. We allowed all cotreatments except long-term open label GC and minimised exclusion criteria, tailored to seniors. Benefit outcomes included disease activity (disease activity score; DAS28, coprimary) and joint damage (Sharp/van der Heijde, secondary). The other coprimary outcome was harm, expressed as the proportion of patients with ≥1 adverse event (AE) of special interest. Such events comprised serious events, GC-specific events and</pubmed_abstract><journal>Annals of the rheumatic diseases</journal><pubmed_title>Low dose, add-on prednisolone in patients with rheumatoid arthritis aged 65+: the pragmatic randomised, double-blind placebo-controlled GLORIA trial.</pubmed_title><pmcid>PMC9209692</pmcid><funding_grant_id>Horizon 2020: 634886</funding_grant_id><pubmed_authors>Allaart CF</pubmed_authors><pubmed_authors>Pinto R</pubmed_authors><pubmed_authors>Celano A</pubmed_authors><pubmed_authors>Richards P</pubmed_authors><pubmed_authors>Buttgereit F</pubmed_authors><pubmed_authors>Costa J</pubmed_authors><pubmed_authors>Raterman HG</pubmed_authors><pubmed_authors>Corduta P</pubmed_authors><pubmed_authors>Manger S</pubmed_authors><pubmed_authors>Klausch LT</pubmed_authors><pubmed_authors>Bos R</pubmed_authors><pubmed_authors>Ruiterman Y</pubmed_authors><pubmed_authors>Cutolo M</pubmed_authors><pubmed_authors>Middelink LM</pubmed_authors><pubmed_authors>Molenaar E</pubmed_authors><pubmed_authors>van Laar JM</pubmed_authors><pubmed_authors>Frazao Mateus E</pubmed_authors><pubmed_authors>Boonen A</pubmed_authors><pubmed_authors>Klaasen R</pubmed_authors><pubmed_authors>Marsman AF</pubmed_authors><pubmed_authors>Doerwald L</pubmed_authors><pubmed_authors>Codreanu C</pubmed_authors><pubmed_authors>Sieburg M</pubmed_authors><pubmed_authors>van der Heijde D</pubmed_authors><pubmed_authors>Griep EN</pubmed_authors><pubmed_authors>Masaryk P</pubmed_authors><pubmed_authors>Dekker V</pubmed_authors><pubmed_authors>Constantinescu O</pubmed_authors><pubmed_authors>GLORIA Trial consortium</pubmed_authors><pubmed_authors>Silva I</pubmed_authors><pubmed_authors>Spoorenberg J</pubmed_authors><pubmed_authors>Jacobs J</pubmed_authors><pubmed_authors>Smulders YM</pubmed_authors><pubmed_authors>Kok MR</pubmed_authors><pubmed_authors>Mendes G</pubmed_authors><pubmed_authors>Baudoin P</pubmed_authors><pubmed_authors>van den Bulk N</pubmed_authors><pubmed_authors>Elling-Audersch C</pubmed_authors><pubmed_authors>Micaelo M</pubmed_authors><pubmed_authors>Schilder AM</pubmed_authors><pubmed_authors>Aanerud GJ</pubmed_authors><pubmed_authors>Christensen R</pubmed_authors><pubmed_authors>Boers M</pubmed_authors><pubmed_authors>Szekanecz Z</pubmed_authors><pubmed_authors>Bijlsma J</pubmed_authors><pubmed_authors>Nurmohamed MT</pubmed_authors><pubmed_authors>Tas SW</pubmed_authors><pubmed_authors>Paolino S</pubmed_authors><pubmed_authors>Opris-Belinski D</pubmed_authors><pubmed_authors>Borucki D</pubmed_authors><pubmed_authors>Rusthoven C</pubmed_authors><pubmed_authors>Prinsen K</pubmed_authors><pubmed_authors>Scholte-Voshaar M</pubmed_authors><pubmed_authors>Saavedra MJ</pubmed_authors><pubmed_authors>Redol J</pubmed_authors><pubmed_authors>Jansen T</pubmed_authors><pubmed_authors>Lems WF</pubmed_authors><pubmed_authors>Ralston SH</pubmed_authors><pubmed_authors>Bakkers M</pubmed_authors><pubmed_authors>Prothmann U</pubmed_authors><pubmed_authors>Hartman L</pubmed_authors><pubmed_authors>Da Silva JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low dose, add-on prednisolone in patients with rheumatoid arthritis aged 65+: the pragmatic randomised, double-blind placebo-controlled GLORIA trial.</name><description>&lt;h4>Background&lt;/h4>Low-dose glucocorticoid (GC) therapy is widely used in rheumatoid arthritis (RA) but the balance of benefit and harm is still unclear.&lt;h4>Methods&lt;/h4>The GLORIA (Glucocorticoid LOw-dose in RheumatoId Arthritis) pragmatic double-blind randomised trial compared 2 years of prednisolone, 5 mg/day, to placebo in patients aged 65+ with active RA. We allowed all cotreatments except long-term open label GC and minimised exclusion criteria, tailored to seniors. Benefit outcomes included disease activity (disease activity score; DAS28, coprimary) and joint damage (Sharp/van der Heijde, secondary). The other coprimary outcome was harm, expressed as the proportion of patients with ≥1 adverse event (AE) of special interest. Such events comprised serious events, GC-specific events and</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2026-06-08T06:49:44.106Z</modification><creation>2026-06-08T03:14:11.416Z</creation></dates><accession>S-EPMC9209692</accession><cross_references><pubmed>35641125</pubmed><doi>10.1136/annrheumdis-2021-221957</doi></cross_references></HashMap>