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Pre- and perinatal exposures associated with developing pediatric-onset immune-mediated inflammatory disease: A
Anne Lærke Spangmose1, Marianne Hørby Jørgensen2, Christian Jakobsen3
1The Fertility Department, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Insights
Maternal immune-mediated inflammatory diseases (IMID) and Cesarean section delivery increase the risk of pediatric-onset IMID (pIMID) in children. While plural pregnancies may lower pIMID risk, these findings highlight potential interventions for prevention.
Area of Science:
- Pediatric immunology
- Epidemiology
- Genetics
Background:
- Pediatric-onset immune-mediated inflammatory diseases (pIMID) represent a significant health concern with complex etiologies.
- Identifying pre- and perinatal risk factors is crucial for early intervention and prevention strategies.
Purpose of the Study:
- To investigate pre- and perinatal risk factors associated with the development of pediatric-onset immune-mediated inflammatory diseases (pIMID).
Main Methods:
- A nationwide Danish cohort study included 1,350,353 children born between 1994 and 2014.
- Data on pre- and perinatal exposures were linked from national registries.
- Cox proportional hazards models were used to estimate risk, with pIMID diagnosis before age 18 as the primary outcome.
Main Results:
- A total of 2,728 children were diagnosed with pIMID.
- Maternal preconception immune-mediated inflammatory disease (IMID) significantly increased pIMID risk (HR: 3.5).
- Cesarean section delivery (HR: 1.2), female sex (HR: 1.5), and plural pregnancies (HR: 0.7) were also associated with pIMID risk.
Conclusions:
- While genetic factors contribute significantly to pIMID, modifiable risk factors like Cesarean section warrant clinical attention.
- Healthcare providers should consider these risk factors when managing pregnant women with IMID and high-risk populations.
Objectives:
We aimed to identify pre- and perinatal risk factors for developing pediatric-onset immune-mediated inflammatory (pIMID).
Methods:
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).
Results:
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]).
Conclusions:
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.
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