Hügle Boris, Hinze Claas, Lainka Elke, Fischer Nadine, Haas Johannes-Peter
German Center for Pediatric and Adolescent Rheumatology, Gehfeldstrasse 24, 82467 Garmisch-Partenkirchen, Germany.
German Center for Pediatric and Adolescent Rheumatology, Gehfeldstrasse 24, 82467 Garmisch-Partenkirchen, Germany ; Department of Pediatric Rheumatology and Immunology, University Children's Hospital Münster, Münster, Germany.
Pediatr Rheumatol Online J. 2014 Jul 16;12:28. doi: 10.1186/1546-0096-12-28. eCollection 2014.
Systemic juvenile idiopathic arthritis (sJIA) is commonly considered an autoinflammatory disease. However, sJIA patients may develop aggressive arthritis without systemic inflammation later in the disease, resembling an autoimmune phenotype similar to other subtypes of JIA. The objective of this study was to determine whether antinuclear antibodies (ANA) and rheumatoid factor (RF) will develop in patients with sJIA over the course of the disease.
A single center sample of sJIA patients with follow-up of more than one year was obtained. A retrospective chart survey was used to extract demographic and clinical data as well as presence and titers of ANA and RF at diagnosis and during follow-up. 32 patients were included in the study, with a median age of 4.2 years and median follow-up of 6.0 years. 8/32 patients had ANA titers ≥ 1:80 at diagnosis, with 22/32 patients showing rising ANA titers with titers ≥ 1:80 at last follow-up (p =0.001). 10/32 patients had a positive RF at least once during follow-up, compared to 0/32 at diagnosis (p = 0.001). In 5/10 patients, positive RF was documented at least twice, more than twelve weeks apart. Patients treated with TNF antagonists were not significantly more likely to develop positive ANA titers (p = 0.425) or positive RF (p = 0.703).
Patients with sJIA developed increased ANA titers and positive RF over the course of the disease, independent of treatment with TNF antagonists. This might point towards an autoimmune, rather than an autoinflammatory phenotype later in the course of sJIA.
全身型幼年特发性关节炎(sJIA)通常被认为是一种自身炎症性疾病。然而,sJIA患者在疾病后期可能会出现无全身炎症的侵袭性关节炎,类似于其他幼年特发性关节炎亚型的自身免疫表型。本研究的目的是确定sJIA患者在疾病过程中是否会出现抗核抗体(ANA)和类风湿因子(RF)。
获得了一个随访时间超过一年的sJIA患者单中心样本。采用回顾性病历调查来提取人口统计学和临床数据,以及诊断时和随访期间ANA和RF的存在情况及滴度。32例患者纳入研究,中位年龄4.2岁,中位随访时间6.0年。8/32例患者在诊断时ANA滴度≥1:80,22/32例患者在最后一次随访时ANA滴度上升至≥1:80(p = 0.001)。10/32例患者在随访期间至少有一次RF阳性,而诊断时为0/32(p = 0.001)。在5/10例患者中,记录到RF阳性至少两次,间隔超过12周。接受肿瘤坏死因子拮抗剂治疗的患者出现ANA滴度阳性(p = 0.425)或RF阳性(p = 0.703)的可能性并无显著增加。
sJIA患者在疾病过程中ANA滴度升高且RF阳性,这与是否接受肿瘤坏死因子拮抗剂治疗无关。这可能表明在sJIA病程后期存在自身免疫而非自身炎症表型。