Three-month tapering and discontinuation of long- term, low-dose glucocorticoids in senior patients with rheumatoid arthritis is feasible and safe: placebo-controlled double blind tapering after the GLORIA trial

医学 泼尼松龙 类风湿性关节炎 逐渐变细 安慰剂 中止 内科学 关节炎 痹症科 外科 计算机图形学(图像) 替代医学 病理 计算机科学
作者
Abdullah Ali Hadi Almayali,Maarten Boers,Linda Hartman,Daniela Opriş-Belinski,Reinhard Bos,Marc R. Kok,José António Pereira da Silva,E. N. Griep,Ruth Klaasen,Cornelia F Allaart,Paul Baudoin,Hennie G. Raterman,Zoltán Szekanecz,Frank Buttgereit,P. Masaryk,Willem F. Lems,Yvo M. Smulders,Maurizio Cutolo,Marieke M. ter Wee
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:82 (10): 1307-1314 被引量:9
标识
DOI:10.1136/ard-2023-223977
摘要

The randomised placebo-controlled GLORIA (Glucocorticoid LOw-dose in RheumatoId Arthritis) trial evaluated the benefits and harms of prednisolone 5 mg/day added to standard care for 2 years in patients aged 65+ years with rheumatoid arthritis (RA). Here, we studied disease activity, flares and possible adrenal insufficiency after blinded withdrawal of study medication.Per protocol, patients successfully completing the 2-year trial period linearly tapered and stopped blinded study medication in 3 months. We compared changes in disease activity after taper between treatment groups (one-sided testing). Secondary outcomes (two-sided tests) comprised disease flares (DAS28 (Disease Activity Score 28 joints) increase >0.6, open-label glucocorticoids or disease-modifying antirheumatic drug (DMARD) increase/switch after week 4 of tapering) and symptoms/signs of adrenal insufficiency. In a subset of patients from 3 Dutch centres, cortisol and ACTH were measured in spot serum samples after tapering.191 patients were eligible; 36 met treatment-related flare criteria and were only included in the flare analysis. Mean (SD) DAS28 change at follow-up: 0.2 (1.0) in the prednisolone group (n=76) vs 0.0 (1.2) in placebo (n=79). Adjusted for baseline, the between-group difference in DAS28 increase was 0.16 (95% confidence limit -0.06, p=0.12). Flares occurred in 45% of prednisolone patients compared with 33% in placebo, relative risk (RR) 1.37 (95% CI 0.95 to 1.98; p=0.12). We found no evidence for adrenal insufficiency.Tapering prednisolone moderately increases disease activity to the levels of the placebo group (mean still at low disease activity levels) and numerically increases the risk of flare without evidence for adrenal insufficiency. This suggests that withdrawal of low-dose prednisolone is feasible and safe after 2 years of administration.
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