Early IL-1 Inhibition in Still's Disease: A Window of Opportunity for Improving Outcomes.

IF 2.8 Q2 RHEUMATOLOGY
Sara Bindoli, Cristina Cadore, Irina Guidea, Andrea Doria, Roberta Ramonda, Paolo Sfriso
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Abstract

Objective: Still's disease is a complex, multisystemic disorder requiring prompt diagnosis and treatment. This study provides a general assessment of a Still's disease cohort aiming to evaluate the efficacy of early intervention with interleukin-1 inhibitors (IL-1i) in achieving clinical inactive disease (CID) and reducing glucocorticoid use in patients with Still's disease.

Methods: We retrospectively analyzed 42 adult patients diagnosed with Still's disease after 2010 and treated with IL-1i. Patients were categorized as early treated (IL-1i started before six months from symptom onset) or late treated (IL-1i started after 6 months). CID achievement, glucocorticoid use, flares, and imaging findings were assessed. The chi-square test was employed as a statistical test, and P < 0.05 was considered significant. GraphPad Prism 8 was used for statistical analysis.

Results: The median time from symptom onset to IL-1i introduction was six months (interquartile range: 2-19). Overall, 55% of patients achieved CID at six months. Early treated patients showed a trend toward higher proportion of CID achievement compared to that of late-treated patients (67% vs 38%; P = 0.17). A meta-analysis including our cohort and two other observational studies showed that early treatment was associated with an odds ratio of 6.73 (95% confidence interval: 2.31-19.64) in comparison to late treatment. All our patients initially received glucocorticoids, with 48% of those achieving CID able to discontinue glucocorticoids within six months. Ten major flares were observed, with 62% occurring after IL-1i suspension or spacing. At baseline, F-fluorodeoxyglucose positron emission tomography (PET)-computed tomography (CT) or magnetic resonance (MR) scans revealed hypermetabolic areas primarily in the bone marrow, spleen, and lymph nodes. After IL-1i introduction, these hypermetabolic regions generally showed a reduction in activity.

Conclusions: Early introduction of IL-1i in patients with Still's disease may lead to higher rates of CID achievement and glucocorticoid discontinuation. PET-CT/MR imaging may be valuable in assessing disease activity and guiding treatment decisions. These findings support the concept of a "window of opportunity" in Still's disease management, emphasizing the importance of prompt diagnosis and treatment initiation.

斯蒂尔氏病早期IL-1抑制:改善预后的机会之窗
目的:斯蒂尔氏病是一种复杂的多系统疾病,需要及时诊断和治疗。本研究对斯蒂尔氏病队列进行了总体评估,旨在评估白细胞介素-1抑制剂(IL-1i)早期干预在斯蒂尔氏病患者实现临床非活动性疾病(CID)和减少糖皮质激素使用方面的疗效。方法:回顾性分析2010年以后诊断为斯蒂尔氏病并应用IL-1i治疗的42例成人患者。患者被分为早期治疗(IL-1i在症状出现6个月前开始)或晚期治疗(IL-1i在6个月后开始)。评估CID成绩、糖皮质激素使用、耀斑和影像学表现。统计学检验采用卡方检验,P < 0.05。使用GraphPad Prism 8进行统计分析。结果:从症状出现到IL-1i引入的中位时间为6个月(四分位数范围:2-19)。总体而言,55%的患者在6个月时达到CID。早期治疗的患者比晚期治疗的患者有更高的CID实现比例的趋势(67% vs 38%; P = 0.17)。包括我们的队列和另外两项观察性研究在内的荟萃分析显示,与晚期治疗相比,早期治疗的优势比为6.73(95%可信区间:2.31-19.64)。所有患者最初均接受糖皮质激素治疗,达到CID的患者中有48%能够在6个月内停用糖皮质激素。观察到10个主要耀斑,62%发生在IL-1i暂停或间隔后。基线时,氟脱氧葡萄糖正电子发射断层扫描(PET)、计算机断层扫描(CT)或磁共振(MR)扫描显示高代谢区域主要在骨髓、脾脏和淋巴结。IL-1i引入后,这些高代谢区域的活性普遍降低。结论:斯蒂尔氏病患者早期引入IL-1i可能导致更高的CID发生率和糖皮质激素停药率。PET-CT/MR成像在评估疾病活动性和指导治疗决策方面可能有价值。这些发现支持斯蒂尔氏病管理中“机会之窗”的概念,强调了及时诊断和开始治疗的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
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