Department of Pediatrics, Division of Pediatric Rheumatology, Behcet and Autoinflammatory Disease Center, Western University, London, Ontario, Canada.
Department of Pediatric Rheumatology, Sanliurfa Mehmet Akif Inan Training and Research Hospital, Sanliurfa, Sanliurfa, Turkey.
Ann Rheum Dis. 2022 Jul;81(7):907-921. doi: 10.1136/annrheumdis-2021-221801. Epub 2022 May 27.
The interleukin-1 (IL-1) mediated systemic autoinflammatory diseases, including the cryopyrin-associated periodic syndromes (CAPS), tumour necrosis factor receptor-associated periodic syndrome (TRAPS), mevalonate kinase deficiency (MKD) and deficiency of the IL-1 receptor antagonist (DIRA), belong to a group of rare immunodysregulatory diseases that primarily present in early childhood with variable multiorgan involvement. When untreated, patients with severe clinical phenotypes have a poor prognosis, and diagnosis and management of these patients can be challenging. However, approved treatments targeting the proinflammatory cytokine IL-1 have been life changing and have significantly improved patient outcomes.
To establish evidence-based recommendations for diagnosis, treatment and monitoring of patients with IL-1 mediated autoinflammatory diseases to standardise their management.
A multinational, multidisciplinary task force consisting of physician experts, including rheumatologists, patients or caregivers and allied healthcare professionals, was established. Evidence synthesis, including systematic literature review and expert consensus (Delphi) via surveys, was conducted. Consensus methodology was used to formulate and vote on statements to guide optimal patient care.
The task force devised five overarching principles, 14 statements related to diagnosis, 10 on therapy, and nine focused on long-term monitoring that were evidence and/or consensus-based for patients with IL-1 mediated diseases. An outline was developed for disease-specific monitoring of inflammation-induced organ damage progression and reported treatments of CAPS, TRAPS, MKD and DIRA.
The 2021 EULAR/American College of Rheumatology points to consider represent state-of-the-art knowledge based on published data and expert opinion to guide diagnostic evaluation, treatment and monitoring of patients with CAPS, TRAPS, MKD and DIRA, and to standardise and improve care, quality of life and disease outcomes.
白细胞介素-1(IL-1)介导的自身炎症性疾病,包括 Cryopyrin 相关周期性综合征(CAPS)、肿瘤坏死因子受体相关周期性综合征(TRAPS)、甲羟戊酸激酶缺乏症(MKD)和 IL-1 受体拮抗剂缺乏症(DIRA),属于一组罕见的免疫调节疾病,主要在儿童早期发病,多器官受累。未经治疗,严重临床表型的患者预后较差,这些患者的诊断和管理具有挑战性。然而,针对促炎细胞因子 IL-1 的已批准治疗方法改变了生活,并显著改善了患者的预后。
制定基于证据的 IL-1 介导的自身炎症性疾病患者诊断、治疗和监测建议,以规范其管理。
成立了一个由医师专家(包括风湿病学家)、患者或护理人员以及相关医疗保健专业人员组成的多学科、多国家任务组。进行了证据综合,包括系统文献回顾和通过调查进行的专家共识(德尔菲法)。共识方法用于制定和投票表决指导最佳患者护理的陈述。
该工作组制定了五项总体原则、14 项与诊断相关的陈述、10 项与治疗相关的陈述和 9 项侧重于长期监测的陈述,这些陈述基于 IL-1 介导疾病的证据和/或共识。制定了疾病特异性监测炎症诱导的器官损伤进展和报告的 CAPS、TRAPS、MKD 和 DIRA 治疗方法的大纲。
2021 年 EULAR/美国风湿病学会的考虑因素代表了基于已发表数据和专家意见的最先进知识,用于指导 CAPS、TRAPS、MKD 和 DIRA 患者的诊断评估、治疗和监测,并标准化和改善护理、生活质量和疾病结局。