Systemic juvenile idiopathic arthritis and adult-onset Still's disease are the same disease: evidence from systematic reviews and meta-analyses informing the 2023 EULAR/PReS recommendations for the diagnosis and management of Still's disease.

IF 20.3 1区 医学 Q1 RHEUMATOLOGY Annals of the Rheumatic Diseases Pub Date : 2024-11-14 DOI:10.1136/ard-2024-225853
Arianna De Matteis, Sara Bindoli, Fabrizio De Benedetti, Loreto Carmona, Bruno Fautrel, Stéphane Mitrovic
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Abstract

Objectives: To analyse the similarity in clinical manifestations and laboratory findings between systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still's disease (AOSD).

Methods: Three systematic reviews (SR) were performed. One included cohort studies comparing sJIA versus AOSD that described clinical and biological manifestations with at least 20 patients in each group (SR1). The second identified studies of biomarkers in both diseases and their diagnostic performance (SR2). The last focused on diagnostic biomarkers for macrophage activation syndrome (MAS, SR3). Medline (PubMed), Embase and Cochrane Library were systematically searched. The risk of bias was assessed with an adapted form of the Hoy scale for prevalence studies in SR1 and the Quality Assessment of Diagnostic Accuracy Studies-2 in SR2 and SR3. We performed meta-analyses of proportions for the qualitative descriptors.

Results: Eight studies were included in SR1 (n=1010 participants), 33 in SR2 and 10 in SR3. The pooled prevalence of clinical manifestations did not differ between sJIA and AOSD, except for myalgia, sore throat and weight loss, which were more frequent in AOSD than sJIA because they are likely ascertained incompletely in sJIA, especially in young children. Except for AA amyloidosis, more frequent in sJIA than AOSD, the prevalence of complications did not differ, nor did the prevalence of biological findings. Ferritin, S100 proteins and interleukin-18 (IL-18) were the most frequently used diagnostic biomarkers, with similar diagnostic performance. For MAS diagnosis, novel biomarkers such as IL-18, C-X-C motif ligand 9, adenosine deaminase 2 activity and activated T cells seemed promising.

Conclusion: Our results argue for a continuum between sJIA and AOSD.

Prospero registration number: CRD42022374240 and CRD42024534021.

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系统性幼年特发性关节炎和成人型斯蒂尔病是同一种疾病:系统回顾和荟萃分析的证据为 2023 年 EULAR/PReS 关于斯蒂尔病诊断和管理的建议提供了参考。
目的分析全身性幼年特发性关节炎(sJIA)与成人型斯蒂尔病(AOSD)在临床表现和实验室检查结果上的相似性:方法:进行了三项系统综述(SR)。其中一篇纳入了比较 sJIA 与 AOSD 的队列研究,这些研究描述了每组至少 20 名患者的临床和生物学表现(SR1)。第二项研究确定了这两种疾病的生物标志物及其诊断性能(SR2)。最后一项研究侧重于巨噬细胞活化综合征(MAS,SR3)的诊断生物标志物。对 Medline (PubMed)、Embase 和 Cochrane 图书馆进行了系统检索。在 SR1 中,我们采用了针对流行病学研究的 Hoy 量表的改编形式来评估偏倚风险;在 SR2 和 SR3 中,我们采用了诊断准确性研究质量评估-2。我们对定性描述的比例进行了荟萃分析:SR1纳入了8项研究(n=1010名参与者),SR2纳入了33项研究,SR3纳入了10项研究。除了肌痛、咽喉痛和体重减轻外,sJIA 和 AOSD 的临床表现的总体流行率没有差异,AOSD 比 sJIA 更常出现肌痛、咽喉痛和体重减轻,因为这些症状在 sJIA 中可能无法完全确定,尤其是在幼儿中。除了 AA 淀粉样变性在 sJIA 中的发病率高于 AOSD 外,其他并发症的发病率和生物学结果的发病率均无差异。铁蛋白、S100 蛋白和白细胞介素-18(IL-18)是最常用的诊断生物标志物,诊断效果相似。对于 MAS 诊断,新型生物标记物,如 IL-18、C-X-C 矩阵配体 9、腺苷脱氨酶 2 活性和活化 T 细胞似乎很有希望:结论:我们的研究结果表明,sJIA 和 AOSD 之间存在连续性:Prospero 注册号:CRD42022374240 和 CRD42024534021。
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来源期刊
Annals of the Rheumatic Diseases
Annals of the Rheumatic Diseases 医学-风湿病学
CiteScore
35.00
自引率
9.90%
发文量
3728
审稿时长
1.4 months
期刊介绍: Annals of the Rheumatic Diseases (ARD) is an international peer-reviewed journal covering all aspects of rheumatology, which includes the full spectrum of musculoskeletal conditions, arthritic disease, and connective tissue disorders. ARD publishes basic, clinical, and translational scientific research, including the most important recommendations for the management of various conditions.
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