Juvenile idiopathic arthritis in relation to perinatal and maternal characteristics: a case control study
Samantha W Bell1,2,3, Susan Shenoi4, J Lee Nelson5
1Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA, USA. Samantha.Bell@ucsf.edu.
Insights
Greater maternal parity was linked to a reduced risk of juvenile idiopathic arthritis (JIA), while prematurity and prior fetal loss were associated with increased JIA risk. These findings suggest potential links to the hygiene and microchimerism hypotheses in autoimmune disease development.
Area of Science:
- Rheumatology
- Epidemiology
- Immunology
Background:
- Limited data exists on maternal and early childhood exposures linked to juvenile idiopathic arthritis (JIA) risk.
- Previous studies suggest potential roles for prematurity, number of siblings, and infections in JIA development.
- This study investigates JIA in relation to infant and maternal characteristics as potential markers for exposures relevant to autoimmune disease pathways like the hygiene hypothesis and microchimerism.
Purpose of the Study:
- To explore associations between maternal and early life factors and the risk of juvenile idiopathic arthritis (JIA).
- To examine these associations across different International League of Associations for Rheumatology (ILAR) JIA categories.
- To evaluate potential links to the hygiene hypothesis and microchimerism in autoimmune disease occurrence.
Main Methods:
- A case-control study involving 1,234 JIA cases and 5,993 matched controls.
- Exposure data sourced from Washington State birth certificates.
- Multivariable logistic regression analysis to calculate adjusted odds ratios (OR) and 95% confidence intervals (CI).
Main Results:
- Increased maternal parity correlated with a decreased JIA risk (OR 0.32 for persistent oligoarticular JIA).
- Prior fetal loss was associated with an increased JIA risk (excluding oligoarticular JIA).
- Prematurity showed increased risk for enthesitis-related arthritis (OR 1.9) and rheumatoid factor-positive polyarticular JIA (OR 2.2).
Conclusions:
- Selected maternal factors demonstrate associations with JIA risk, varying by JIA subtype.
- Reduced JIA risk with higher maternal parity aligns with hygiene and microchimerism hypotheses.
- Further research incorporating biomarkers is needed to clarify these associations and underlying mechanisms.
Background:
Existing data on associations between maternal and early childhood exposures and juvenile idiopathic arthritis (JIA) risk is scant and inconsistent with previous studies showing potential role for prematurity, number of siblings and infections. We explored JIA and International League of Associations for Rheumatology (ILAR) JIA categories in relation to selected infant (birthweight, size-for-gestational-age, gestational age), and maternal (parity, delivery type, prior fetal loss) characteristics that may be markers for exposures related to two pathways (hygiene hypothesis, microchimerism) potentially associated with autoimmune disorder occurrence.
Methods:
A case-control analysis with 1,234 JIA cases and 5,993 birth year-matched controls was conducted. Exposure information was obtained from WA state birth certificates. Multivariable logistic regression was used to estimate adjusted odds ratios (OR) and 95% confidence intervals (CI) for associations with maternal and early life exposures for JIA and JIA categories.
Results:
Greater maternal parity was associated with a decreased OR for JIA (most marked for persistent oligoarticular JIA, OR 0.32, 95% CI 0.15; 0.71, p for trend = 0.0001). Prior fetal loss (except for oligoarticular JIA) was associated with an increased OR for JIA. Prematurity was associated with increased risk of enthesitis related arthritis (OR 1.9, 95% CI: 1.3-2.9) and rheumatoid factor positive polyarticular JIA (OR 2.2, 95% CI: 1.0-4.8).
Conclusions:
We observed associations of selected maternal factors with JIA, some of which varied across JIA categories. The findings of decreased ORs for JIA in relation to greater maternal parity may be consistent with the hygiene and microchimerism hypotheses. Future studies with biomarkers relevant to these hypotheses will help elucidate any associations.
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