Hestetun Sigrid V, Rudsari Hamid K, Jaholkowski Piotr, Shadrin Alexey, Haftorn Kristine L, Andersen Svend, Rygg Marite, Nordal Ellen, Frei Oleksandr, Andreassen Ole A, Selvaag Anne M, Størdal Ketil, Sanner Helga
Oslo University Hospital and University of Oslo, Oslo, Norway.
Oslo University Hospital, Oslo, Norway.
Arthritis Rheumatol. 2025 Apr;77(4):458-467. doi: 10.1002/art.43040. Epub 2024 Nov 19.
We aimed to investigate the incidence of juvenile idiopathic arthritis (JIA) in the three geographic regions of Norway and whether potential regional incidence differences are explained by environmental or genetic factors across regions.
We conducted a register-based cohort study including all Norwegian children born from 2004 to 2019, with follow-up throughout 2020. The JIA diagnosis, defined by at least two International Classification of Diseases, Tenth Revision codes for JIA, was validated against medical records. The incidence rate (IR) and hazard ratio (HR) for JIA were estimated for all Norway and for the North, Mid, and South regions. In a subsample from the Norwegian Mother, Father, and Child Cohort Study (MoBa), the genetic risk for JIA was assessed in the three regions.
After median 9.1 (range 0.3-16.0) years of follow-up, we identified 1,184 patients with JIA and 910,058 controls. The IR for JIA/100,000 person-years was 14.4 in all of Norway, 25.9 in the North region, 17.9 in the Mid region, and 12.5 in the South region. The HR (95% confidence interval [CI]) of JIA in the North region was 2.07 (1.77-2.43) and in the Mid region HR 1.43 (95% CI 1.23-1.67) compared with the South region. Adjustments for perinatal factors, socioeconomic status, and early antibiotic exposure did not change our estimates substantially. In MoBa (238 patients with JIA, 57,392 controls), the association between JIA and region of birth was no longer significant when adjusting for genetic factors.
We found a higher incidence of JIA with increasing latitude without evidence for available environmental factors explaining the observed gradient. In contrast, genetic factors modified the association, but further studies are warranted.
我们旨在调查挪威三个地理区域青少年特发性关节炎(JIA)的发病率,以及潜在的区域发病率差异是否可由各区域的环境或遗传因素来解释。
我们开展了一项基于登记的队列研究,纳入了2004年至2019年出生的所有挪威儿童,并在2020年进行了全程随访。JIA诊断依据至少两个国际疾病分类第十版JIA编码确定,并通过病历进行了验证。我们估计了全挪威以及北部、中部和南部地区JIA的发病率(IR)和风险比(HR)。在挪威母亲、父亲和儿童队列研究(MoBa)的一个子样本中,评估了三个区域JIA的遗传风险。
经过中位9.1年(范围0.3 - 16.0年)的随访,我们确定了1184例JIA患者和910058例对照。全挪威JIA的发病率/10万人年为14.4,北部地区为25.9,中部地区为17.9,南部地区为12.5。与南部地区相比,北部地区JIA的HR(95%置信区间[CI])为2.07(1.77 - 2.43),中部地区HR为1.43(95% CI 1.23 - 1.