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January 23, 2026Journal of Crohn s and Colitis0 citations

P1189Maternal fish intake during pregnancy is associated with reduced offspring Inflammatory Bowel Disease risk and metabolic profile alterations

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GCG CiobotaruSAS AytenOAO M R Anneberg

Key Points

  • The study aims to examine the relationship between maternal fish consumption during pregnancy and the subsequent risk of inflammatory bowel disease in offspring, along with metabolite profile alterations.
  • Analyzed maternal and offspring data from the Danish National Birth Cohort and National Patient Register.
  • Evaluated maternal fish intake using food frequency questionnaires and categorized by tertiles.
  • Followed offspring for inflammatory bowel disease diagnosis until age 18.
  • Conducted metabolite profile analysis using dried blood spots collected at birth.
  • High total fish intake was associated with a 39% reduced risk of inflammatory bowel disease compared to low intake.
  • Average fish intake correlated with a 35% reduced risk of inflammatory bowel disease.
  • Specific reductions in Crohn's disease (CD) and ulcerative colitis (UC) risk associated with lean fish and omega-3 intakes were noted.
  • Maternal fish intake correlated with changes in 64 offspring metabolites but none were linked to inflammatory bowel disease risk.

Abstract

Abstract Background This study investigated how maternal fish intake during pregnancy influences offspring’s risk for inflammatory bowel disease (IBD) Crohn’s disease (CD), Ulcerative colitis (UC), and explored associated offspring metabolite changes. Methods Maternal and offspring data were retrieved from the Danish National Birth Cohort and National Patient Register. Mother-child dyads were selected if mothers had a singleton pregnancy, responded to the food frequency questionnaire at week 25 of pregnancy, and had energy intakes between 2,500 and 25,000 kJ/day. Offspring were followed for diagnosis of IBD until age 18. Maternal intakes of total, lean and oily fish, and fish omega-3 polyunsaturated fatty acids (PUFAs) were assessed in g/day as tertiles, while fish oil supplementation was assessed as yes/no. A subset of later IBD cases was matched for sample acquisition and collection times, gestational age or birthweight, and sex, and dried blood spot cards collected at birth were used to determine the metabolite profiles in offspring. Hazard ratios (HR) for IBD with 95% confidence intervals (CI) were evaluated using Cox regression for the dietary and metabolites analyses. To identify metabolites associated with each fish group, regularised linear regression was implemented. All analyses were adjusted for pre-pregnancy body mass index, job qualification, age at birth, maternal antibiotic use, smoking, parental IBD, maternal energy intake, while metabolite analyses were additionally adjusted for gestational age, offspring gender and birth weight. Results In total, 59,430 mother-child dyads were included, with 169 offspring developing IBD (CD = 93; UC = 76). A subset of 120 mother-child dyads was included in the metabolite analysis, with 62 offspring developing IBD. The median total fish intake was 20.3 g/day, and 576 metabolites were analysed. High (HR 0.61; 95% CI 0.42- 0.89) and average (0.65; 0.45-0.94) total fish intakes were associated with reduced offspring IBD risk. Similarly, high (0.56; 0.39-0.82) and average (0.55; 0.38-0.80) lean fish and high fish omega-3 PUFAs (0.66; 0.44-0.98) were associated with reduced IBD risk. Moreover, high total (0.52; 0.30-0.89) and lean fish (0.47; 0.27-0.80) intakes were significantly associated with reduced CD when compared to low intake, while average lean fish intake was associated with reduced UC risk (0.42; 0.23-0.77). Additionally, maternal fish intake was associated with 64 offspring metabolites, including phenolic, amino acid and tryptophan metabolites, although none were associated with IBD risk in offspring. Conclusion Maternal fish intake during pregnancy was associated with reduced risk for IBD in offspring and with distinct changes in the metabolite profile at birth in the offspring. Conflict of interest: Ms. Ciobotaru, Gabriela: There are no conflicts of interest to declare. Ayten, Serife: I declare no conflicts of interest. Anneberg, Olivia Mariella Rosie: No conflicts if interest to declare. Olsen, Sjurdur Frodi: I have no conflicts of interest to declare Vinkel Hansen, Anne: Anne Vinkel Hansen discloses no conflicts of interest Bjerregaard, Anne Ahrendt: None to declare Halldorsson, Thorhallur: none Ernst, Madeleine: None declared. Ottosson, Filip: None Jess, Tine: Personal Fees: Consultancy for Ferring, Pfizer, Johnson&Johnson Brusco De Freitas, Maiara: I have no conflict of interest

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Cite This Study

Ciobotaru et al. (2026) studied this question.

synapsesocial.com/papers/69730f78c8125b09b0d1f334https://doi.org/10.1093/ecco-jcc/jjaf231.1370
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