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Abstract Number: 2679

Early-Life Nutrition and Gene-Environment Interactions Influencing Juvenile Idiopathic Arthritis Risk: Results from a Pregnancy Cohort

Vilde Øverlien Dåstøl1, Ida Henriette Caspersen2, Kristine Løkås Haftorn3, Sigrid Hestetun4, Siri Eldevik Håberg5, Karen H. Costenbader6, Marin Strøm7, Sjurdur Frodi Olsen8, Anne Lise Brantsæter9, Ketil Størdal10 and Helga Sanner1, 1Oslo University Hospital, Oslo, Norway, 2Norwegian Institute of Public Health, Centre for Fertility and Health/Oslo University Hospital, Oslo, Norway, 3Oslo University Hospital, Department of Rheumatology, Oslo, Norway, 4Oslo University Hospital, Department of Rheumatology/University of Oslo, Oslo, Norway, 5Norwegian Institute of Public Health, Centre for Fertility and Health/University of Bergen, Oslo, Norway, 6Harvard Medical School and Brigham and Women's Hospital, Boston, MA, 7Statens Serum Institut, Department of Epidemiology Research, Copenhagen, Denmark, 8Statens Serum Institut,Biobank, congenital disorders, and vaccines preparedness/Harvard T.H. Chan School of Public Health, Copenhagen, Denmark, 9Norwegian Institute of Public Health, Department of Food Safety and Centre for Sustainable Diets, Oslo, Norway, 10Oslo University Hospital, Department of Pediatric and Adolescent Medicine/University of Oslo, Oslo, Norway

Meeting: ACR Convergence 2025

Keywords: Epidemiology, genetics, Juvenile idiopathic arthritis, nutrition, Pediatric rheumatology

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Session Information

Date: Wednesday, October 29, 2025

Title: Abstracts: Pediatric Rheumatology – Clinical III (2675–2680)

Session Type: Abstract Session

Session Time: 12:30PM-12:45PM

Background/Purpose: Early-life nutrition may influence the risk of immune-mediated diseases like juvenile idiopathic arthritis (JIA). The benefits of breastfeeding are well established, but findings related to JIA have been inconsistent and mainly based on small case-control studies (1). Early introduction of solid food may promote immune tolerance (2), which could reduce the risk of immune-mediated diseases like JIA, but this has not been studied. We aimed to investigate the association between breastfeeding duration, age at introduction of solid food, and risk of JIA in a large population-based pregnancy cohort, including possible gene-environment interactions.

Methods: We used The Norwegian Mother, Father, and Child Cohort Study (MoBa), a cohort that recruited pregnant women from 1999-2008, with data from >114 000 mother-infant pairs. A JIA case was, as previously validated (3), defined as having at least two ICD-10 codes (M08/M09) by linking the cohort to the Norwegian Patient Registry. At 6 months post-partum, mothers completed a questionnaire reporting infant feeding practices. Full breastfeeding was defined as receiving only breast milk without any formula or solid food. We categorized breastfeeding and age at solid food introduction as: < 4 months, 4–5 months (reference), and ≥6 months.We used multivariable logistic regression and estimated odds ratios (aORs) adjusted for: maternal history of inflammatory rheumatic disease, age, education, BMI, parity, mode of delivery, preterm birth and gestational smoking. Umbilical cord blood sampling at birth allowed genotyping of a subsample of the children. We calculated polygenic risk scores (PRSs) using summary statistics from a large genome-wide association study (GWAS) to estimate the children’s genetic risk of JIA (4). By using these PRSs, we assessed gene-environment interactions.

Results: Our final analytical sample included 239 infants who later developed JIA and 71,761 infants who did not, with genotyping data on 169 cases and 39,488 non-cases. The risk of JIA was non-significantly higher in those with a full breastfeeding duration ≥6 months (aOR 1.39, 95% CI 0.98-1.99) (Table 1). We identified interactions between genetic susceptibility to JIA and both short (< 4 months) and prolonged (≥6 months) breastfeeding (p = 0.02 and 0.04). Additionally, delayed introduction of solid food (≥6 months) was associated with an increased risk of JIA (aOR 1.48, 95% CI 1.09-2.00) (Table 1), with no evidence of gene-environment interaction.

Conclusion: Our findings suggest that later introduction of solid food is associated with an increased risk of JIA, supporting the hypothesis that earlier dietary exposures may promote immune tolerance. Additionally, we observed interactions between genetic susceptibility to JIA and breastfeeding duration, indicating that genetic predisposition may modify the association between breastfeeding and disease risk, which warrants further investigation.References:1) Clarke SLN, et al. Rheumatology (Oxford). 2022;61(2)2) Skjerven HO, et al. Lancet. 2022 Jun 25;399(10344)3) Hestetun SV, et al. Arthritis Rheumatol. 2025 Apr;77(4)4) López-Isac E, et al. Ann Rheum Dis. 2021;80(3)

Supporting image 1Table 1. Results of Analyses of Breastfeeding duration and Age at Introduction of Solid Food, and Child Risk of Developing JIA in the MoBa Cohort


Disclosures: V. Dåstøl: None; I. Caspersen: None; K. Haftorn: None; S. Hestetun: None; S. Håberg: None; K. Costenbader: AbbVie, 2, 5, Bain, 2, 5, Biogen, 2, 5, Brigham & Women’s Hospital, 3, GSK, 2, 5; M. Strøm: None; S. Olsen: None; A. Brantsæter: None; K. Størdal: None; H. Sanner: None.

To cite this abstract in AMA style:

Dåstøl V, Caspersen I, Haftorn K, Hestetun S, Håberg S, Costenbader K, Strøm M, Olsen S, Brantsæter A, Størdal K, Sanner H. Early-Life Nutrition and Gene-Environment Interactions Influencing Juvenile Idiopathic Arthritis Risk: Results from a Pregnancy Cohort [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/early-life-nutrition-and-gene-environment-interactions-influencing-juvenile-idiopathic-arthritis-risk-results-from-a-pregnancy-cohort/. Accessed .
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