Unravelling the clinical heterogeneity of undefined recurrent fever over time in the European registries on Autoinflammation.

IF 2.8 3区 医学 Q1 PEDIATRICS Pediatric Rheumatology Pub Date : 2024-05-17 DOI:10.1186/s12969-024-00987-z
Y Vyzhga, H Wittkowski, V Hentgen, S Georgin-Lavialle, A Theodoropoulou, S Fuehner, M Jesenak, J Frenkel, E Papadopoulou-Alataki, Jordi Anton, A Nunzia Olivieri, J Brunner, J Sanchez, I Koné-Paut, S Fingerhutova, P Pillet, U Meinzer, R Khubchandani, A Jansson, J-P Haas, R Berendes, T Kallinich, G Horneff, E Lilienthal, R Papa, D Foell, E Lainka, R Caorsi, M Gattorno, M Hofer
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引用次数: 0

Abstract

Background: Systemic autoinflammatory disorders (SAIDs) represent a growing spectrum of diseases characterized by dysregulation of the innate immune system. The most common pediatric autoinflammatory fever syndrome, Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA), has well defined clinical diagnostic criteria, but there is a subset of patients who do not meet these criteria and are classified as undefined autoinflammatory diseases (uAID). This project, endorsed by PRES, supported by the EMERGE fellowship program, aimed to analyze the evolution of symptoms in recurrent fevers without molecular diagnosis in the context of undifferentiated AIDs, focusing on PFAPA and syndrome of undifferentiated recurrent fever (SURF), using data from European AID registries.

Methods: Data of patients with PFAPA, SURF and uSAID were collected from 3 registries including detailed epidemiological, demographic and clinical data, results of the genetic testing and additional laboratory investigations with retrospective application of the modified Marshall and PRINTO/Eurofever classification criteria on the cohort of PFAPA patients and preliminary SURF criteria on uSAID/SURF patients.

Results: Clinical presentation of PFAPA is variable and some patients did not fit the conventional PFAPA criteria and exhibit different symptoms. Some patients did not meet the criteria for either PFAPA or SURF, highlighting the heterogeneity within these groups. The study also explored potential overlaps between PFAPA and SURF/uAID, revealing that some patients exhibited symptoms characteristic of both conditions, emphasizing the need for more precise classification criteria.

Conclusions: Patients with recurrent fevers without molecular diagnoses represent a clinically heterogeneous group. Improved classification criteria are needed for both PFAPA and SURF/uAID to accurately identify and manage these patients, ultimately improving clinical outcomes.

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在欧洲自体发炎登记中揭示未定义的复发性发热随时间变化的临床异质性。
背景:全身性自身炎症性疾病(SAIDs)是一种以先天性免疫系统失调为特征的疾病,其范围正在不断扩大。最常见的儿科自身炎症性发热综合征,即周期性发热、阿弗他口腔炎、咽炎、腺炎(PFAPA),有明确的临床诊断标准,但也有一部分患者不符合这些标准,被归类为未定义的自身炎症性疾病(uAID)。该项目得到了PRES的认可和EMERGE奖学金计划的支持,旨在利用欧洲AID登记数据分析未分化AID中未经分子诊断的复发性发热症状的演变,重点关注PFAPA和未分化复发性发热综合征(SURF):方法:从3个登记处收集PFAPA、SURF和uSAID患者的数据,包括详细的流行病学、人口统计学和临床数据、基因检测结果和其他实验室检查,并对PFAPA患者队列回顾性应用修改后的Marshall和PRINTO/Eurofever分类标准,对uSAID/SURF患者应用初步的SURF标准:PFAPA的临床表现多种多样,一些患者不符合传统的PFAPA标准,表现出不同的症状。有些患者既不符合 PFAPA 标准,也不符合 SURF 标准,这凸显了这些群体的异质性。研究还探讨了PFAPA和SURF/uAID之间可能存在的重叠,发现一些患者表现出两种疾病的特征性症状,强调了制定更精确分类标准的必要性:结论:无分子诊断的反复发热患者是一个临床异质性群体。结论:无分子诊断的复发性发热患者是一个临床异质性群体,需要改进 PFAPA 和 SURF/uAID 的分类标准,以准确识别和管理这些患者,最终改善临床预后。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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