综合临床因素预测系统性红斑狼疮(SLE)成功的糖皮质激素停药:来自一项多中心回顾性队列研究的结果。

IF 5.1 2区 医学 Q1 RHEUMATOLOGY
Spyridon Katechis, Sofia Pitsigavdaki, Myrto Nikoloudaki, Ettore Silvagni, Argyro Repa, Antonio Marangoni, Irini Flouri, Nestor Avgoustidis, Konstantinos Parperis, Marcello Govoni, Prodromos Sidiropoulos, Dimitrios T Boumpas, Antonis Fanouriakis, George Bertsias, Alessandra Bortoluzzi
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引用次数: 0

摘要

目的:糖皮质激素(GC)减量和停药以减少损害是欧洲风湿病协会联盟(EULAR) SLE建议的一个关键方面。然而,无复发GC停止的最佳策略仍然不明确。我们描述了临床预测因素及其对停止GC治疗的SLE患者的综合影响。方法:回顾性队列研究324例活动性SLE患者(PGA≥1.5和/或SLEDAI-2K≥6),接受GC作为强化治疗的一部分(中位随访60个月)。生存和广义线性模型估计SELENA-SLEDAI耀斑风险及其预测因子。结果:220例(67.9%)患者停用了GCs, 1年总体和严重耀斑风险分别为50%和25%(风险比:1.48;总体耀斑95% CI: 1.12 ~ 1.96;人力资源:1.52;95% CI: 1.03 - 2.25(与未退药者相比)。在缓解期(DORIS)或狼疮低疾病活动状态(LLDAS;不包括缓解)(严重耀斑的HR: 0.23;0.12 ~ 0.43和0.30;分别为0.18至0.50),目标指数每增加一个月,就会提供进一步的保护。羟氯喹预防总发病(HR: 0.37;0.26 ~ 0.53)和重度耀斑(HR: 0.33;0.21至0.52),而霉酚酸酯和硫唑嘌呤则可减少总体的急性发作。强的松从7.5 mg/天逐渐减少到0 mg/天,6个月后可改善严重无耀斑结局(HR: 0.57;0.37 ~ 0.90)。随机生存森林鉴定出DORIS/LLDAS、羟氯喹的使用和缓慢的GC逐渐减少是最重要的预测因子,它们的共存分别使总体和严重的闪光减少了~25倍和~50倍。这种组合降低了伤害(IRR: 0.31;0.08 ~ 0.84),不引起耀斑(IRR: 0.52;95% CI: 0.18 ~ 1.16)。结论:疾病活动性低或无活动性,缓慢的逐渐减少和羟氯喹的使用可最大限度地降低耀斑的风险,促进GC停止- SLE的主要目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combination of clinical factors predicts successful glucocorticoid withdrawal in systemic lupus erythematosus (SLE): results from a multicentre, retrospective cohort study.

Objective: Glucocorticoid (GC) tapering and withdrawal to reduce damage represents a key aspect of the European Alliance of Associations for Rheumatology (EULAR) SLE recommendations. However, optimal strategies for relapse-free GC cessation remain ill-defined. We characterised clinical predictors and their combined effect on flares in patients with SLE who discontinued GC.

Methods: Retrospective cohort of 324 patients with active SLE (PGA ≥1.5 and/or SLEDAI-2K ≥6) who received GC as part of treatment intensification (median follow-up 60 months). Survival and generalised linear models estimated SELENA-SLEDAI flare risks and their predictors.

Results: GCs were discontinued in 220 (67.9%) patients with 1-year risks for overall and severe flares of 50% and 25%, respectively (HR: 1.48; 95% CI: 1.12 to 1.96 for overall flares; HR: 1.52; 95% CI: 1.03 to 2.25 for severe flares, compared with non-withdrawers). Flare risk was lowered when GCs were ceased during remission (DORIS) or Lupus Low Disease Activity State (LLDAS; excluding remission) (HR for severe flares: 0.23; 0.12 to 0.43 and 0.30; 0.18 to 0.50, respectively), with each additional month in targets providing further protection. Hydroxychloroquine prevented total (HR: 0.37; 0.26 to 0.53) and severe flares (HR: 0.33; 0.21 to 0.52), while mycophenolate and azathioprine reduced overall flares. Prednisone tapering from 7.5 mg/day to 0 over >6 months improved severe flare-free outcome (HR: 0.57; 0.37 to 0.90). Random survival forests identified DORIS/LLDAS, hydroxychloroquine use and slow GC tapering as top predictors, whose coexistence reduced overall and severe flares by ~25 fold and ~50 fold, respectively. This combination reduced damage (IRR: 0.31; 0.08 to 0.84) without inducing flares (IRR: 0.52; 95% CI: 0.18 to 1.16) compared with GC non-withdrawers.

Conclusion: Low or absent disease activity, slow tapering and hydroxychloroquine use minimise the risk of flares, facilitating GC discontinuation-a major goal in SLE.

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来源期刊
RMD Open
RMD Open RHEUMATOLOGY-
CiteScore
7.30
自引率
6.50%
发文量
205
审稿时长
14 weeks
期刊介绍: RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.
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