Division of Rheumatology, The Hospital for Sick Children, Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.
Department of Pediatric Rheumatology, Hacettepe University, Ankara, Turkey.
Ann Rheum Dis. 2018 May;77(5):728-735. doi: 10.1136/annrheumdis-2017-212403. Epub 2018 Jan 9.
The association between mutations in , encoding the NF-kB regulatory protein A20, and a new autoinflammatory disease has recently been recognised. This study aims at describing the clinical phenotypes and disease course of patients with A20 haploinsufficiency (HA20).
Data for all cases from the initial publication, and additional cases identified through collaborations since, were collected using standardised data collection forms.
A total of 16 patients (13 female) from seven families with a genetic diagnosis of HA20 were included. The disease commonly manifested in early childhood (range: first week of life to 29 years of age). The main clinical symptoms were recurrent oral, genital and/or gastrointestinal ulcers (16/16), musculoskeletal (9/16) and gastrointestinal complaints (9/16), cutaneous lesions (8/16), episodic fever (7/16), and recurrent infections (7/16). Clinical phenotypes varied considerably, even within families. Relapsing-remitting disease course was most common, and one patient died. Laboratory abnormalities included elevated acute-phase reactants and fluctuating presence of various autoantibodies such as antinuclear antibodies (4/10 patients tested) and anti-dsDNA (2/5). Tissue biopsy of different sites revealed non-specific chronic inflammation (6/12 patients tested), findings consistent with class V lupus nephritis in one patient, and pustules and normal results in two patients each. All patients were treated: 4/16 received colchicine and 12/16 various immunosuppressive agents. Cytokine inhibitors effectively suppressed systemic inflammation in 7/9 patients.
Early-onset recurrent oral, genital and/or gastrointestinal ulcers are the hallmark feature of HA20. Frequency and intensity of other clinical manifestations varied highly. Treatment regimens should be based on disease severity, and cytokine inhibitors are often required to control relapses.
最近,人们已经认识到 NF-kB 调节蛋白 A20 编码基因 中的突变与一种新的自身炎症性疾病有关。本研究旨在描述 A20 功能不全(HA20)患者的临床表型和疾病过程。
使用标准化数据收集表收集了最初发表的所有病例的数据,以及通过合作自那时以来确定的其他病例的数据。
共纳入 7 个家系的 16 例(13 例女性)遗传性 HA20 患者。疾病通常在儿童早期发作(发病年龄范围:出生后第一周至 29 岁)。主要临床症状为反复口腔、生殖器和/或胃肠道溃疡(16/16)、肌肉骨骼(9/16)和胃肠道不适(9/16)、皮肤损伤(8/16)、间歇性发热(7/16)和反复感染(7/16)。即使在同一家庭内,临床表型也存在较大差异。最常见的疾病过程是复发缓解型,有 1 例患者死亡。实验室异常包括急性期反应物升高和各种自身抗体(如抗核抗体(4/10 例患者检测)和抗 dsDNA(2/5 例))的波动存在。不同部位的组织活检显示非特异性慢性炎症(6/12 例患者检测),1 例患者符合 V 型狼疮肾炎,2 例患者各有脓疱和正常结果。所有患者均接受了治疗:16 例患者中有 4 例接受秋水仙碱治疗,12 例患者中有 12 例接受了各种免疫抑制剂治疗。细胞因子抑制剂有效地抑制了 7/9 例患者的全身炎症。
早发性反复口腔、生殖器和/或胃肠道溃疡是 HA20 的主要特征。其他临床表现的频率和强度差异很大。治疗方案应根据疾病严重程度制定,通常需要细胞因子抑制剂来控制复发。