Spangmose Anne Lærke, Jørgensen Marianne Hørby, Jakobsen Christian, Wewer Vibeke, Rod Naja Hulvej, Ingels Helene, Pinborg Anja, Malham Mikkel
The Fertility Department, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Denmark.
J Autoimmun. 2023 Apr;136:103032. doi: 10.1016/j.jaut.2023.103032. Epub 2023 Mar 28.
We aimed to identify pre- and perinatal risk factors for developing pediatric-onset immune-mediated inflammatory (pIMID).
This nation-wide, cohort study included all children born in Denmark from 1994 to 2014 identified from the Danish Medical Birth registry. Individuals were followed through 2014 and cross-linked to the continuously updated national socioeconomic and healthcare registers to obtain data on pre- and perinatal exposures (maternal age, educational level, smoking, maternal IMID, parity, mode of conception and delivery, plurality, child's sex, and birth season). The primary outcome was a pIMID diagnosis (inflammatory bowel disease, autoimmune hepatitis, primary sclerosing cholangitis, juvenile idiopathic arthritis, or systemic lupus erythematosus) before 18 years of age. Risk estimates were calculated using Cox proportional hazards model and presented by hazard ratios (HR) with 95% confidence intervals (95%CI).
We included 1,350,353 children with a follow-up time of 14,158,433 person-years. Among these, 2,728 were diagnosed with a pIMID. We found a higher risk of pIMID in children born to women with a preconception IMID diagnosis (HR: 3.5 [95%CI: 2.7-4.6]), children born by Caesarean section (HR: 1.2 [95%CI: 1.0-1.3]), and among females (1.5 [95%CI: 1.4-1.6]) than among children without these characteristics. Plural pregnancies were associated with a lower risk of pIMID than single pregnancies (HR: 0.7 [95%CI: 0.6-0.9]).
Our results indicate a high genetic burden in pIMID but also identifies intervenable risk factors, such as Cesarean section. Physicians should, keep this in mind when caring for high-risk populations and pregnant women previously diagnosed with an IMID.
我们旨在确定儿童期发病的免疫介导性炎症性疾病(pIMID)的产前和围产期危险因素。
这项全国性队列研究纳入了1994年至2014年在丹麦出生的所有儿童,这些儿童来自丹麦医学出生登记处。对个体进行随访至2014年,并与不断更新的国家社会经济和医疗保健登记处进行交叉链接,以获取产前和围产期暴露数据(母亲年龄、教育水平、吸烟情况、母亲的IMID、产次、受孕和分娩方式、多胎情况、孩子性别和出生季节)。主要结局是18岁前的pIMID诊断(炎症性肠病、自身免疫性肝炎、原发性硬化性胆管炎、幼年特发性关节炎或系统性红斑狼疮)。使用Cox比例风险模型计算风险估计值,并以风险比(HR)和95%置信区间(95%CI)表示。
我们纳入了1350353名儿童,随访时间为14158433人年。其中,2728人被诊断为pIMID。我们发现,孕前被诊断为IMID的女性所生儿童患pIMID的风险更高(HR:3.5 [95%CI:为2.7 - 4.6]),剖宫产出生的儿童(HR:1.2 [95%CI:1.0 - 1.3])以及女性儿童(1.5 [95%CI:1.4 - 1.6])患pIMID的风险高于无这些特征的儿童。多胎妊娠患pIMID的风险低于单胎妊娠(HR:0.7 [95%CI:0.6 - 0.9])。
我们的结果表明pIMID存在较高的遗传负担,但也确定了可干预的危险因素,如剖宫产。医生在照顾高危人群和先前被诊断为IMID的孕妇时应牢记这一点。