The Effect of a Fish Oil and/or Probiotic Intervention from Early Pregnancy Onwards on Colostrum Immune Mediators: A Randomized, Placebo-Controlled, Double-Blinded Clinical Trial in Overweight/Obese Mothers

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6 Citeringar (Scopus)
167 Nedladdningar (Pure)

Sammanfattning

Scope: Modifying the composition of colostrum by external factors may provide opportunities to improve the infant's health. Here, we evaluated how fish oil and/or probiotics supplementation modify concentrations of colostrum immune mediators and their associations with perinatal clinical factors on mothers with overweight/obesity. Methods and results: Pregnant women were randomized in a double-blind manner into four intervention groups, and the supplements were consumed daily from early pregnancy onwards. Colostrum samples were collected from 187 mothers, and 16 immune mediators were measured using bead-based immunoassays. Interventions modified colostrum composition; the fish oil+probiotics group had higher concentrations of IL-12p70 than probiotics+placebo and higher FMS-like tyrosine kinase 3 ligand (FLT-3L) than fish oil+placebo and probiotics+placebo (one-way analysis of variance, post-hoc Tukey's test). Although the fish oil+probiotics group had higher levels of IFNα2 compared to the fish oil+placebo group, these differences were not statistically significant after correction for multiple testing. Multivariate linear model revealed significant associations between several immune mediators and the perinatal use of medication. Conclusion: Fish oil/probiotics intervention exerted a minor effect on concentrations of colostrum immune mediators. However, medication during the perinatal period modulated the immune mediators. These changes in colostrum's composition may contribute to immune system development in the infant.

OriginalspråkEngelska
Artikelnummer2200446
Antal sidor12
TidskriftMolecular Nutrition and Food Research
Volym67
Nummer15
DOI
StatusPublicerad - aug. 2023
MoE-publikationstypA1 Tidskriftsartikel-refererad

Finansiering

The clinical trial was supported by the State Research Funding for university-level health research in the Turku University Hospital Expert Responsibility Area, Finland, Academy of Finland (#258606), Finland, the Diabetes Research Foundation, Finland. The funding for breast milk analyses and reporting were provided by the Juho Vainio Foundation, Finland. Support for Diana Toivola by Academy of Finland 332582, Finland, and InFLAMES Flagship Programme of the Academy of Finland (337531), Finland and State Research Funding are acknowledged. These funding sources had no role in the design, execution, analyses, interpretation of the data, or decision to submit these results. The clinical trial was supported by the State Research Funding for university‐level health research in the Turku University Hospital Expert Responsibility Area, Finland, Academy of Finland (#258606), Finland, the Diabetes Research Foundation, Finland. The funding for breast milk analyses and reporting were provided by the Juho Vainio Foundation, Finland. Support for Diana Toivola by Academy of Finland 332582, Finland, and InFLAMES Flagship Programme of the Academy of Finland (337531), Finland and State Research Funding are acknowledged. These funding sources had no role in the design, execution, analyses, interpretation of the data, or decision to submit these results.

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