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Published on: January 27, 2019
Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics
N B M M Rutten1, D M W Gorissen2, A Eck3
1Department of Pediatric Pulmonology and Allergology, Wilhelmina Children's Hospital, University Medical Centre, Utrecht, the Netherlands; Department of Pediatrics, St Antonius Hospital, Nieuwegein, the Netherlands.
Insights
Probiotic supplementation in infancy had minor, short-term effects on infant gut microbiota composition and diversity. Long-term analysis revealed no lasting differences, with age being the primary driver of microbiota development.
Area of Science:
- Microbiology
- Immunology
- Pediatrics
Background:
- Early childhood gut microbiota imbalance is linked to immune-mediated disorders like allergies.
- Probiotic supplementation in infancy aims to prevent infant allergies but has shown variable success.
- Long-term effects of neonatal probiotic use on microbiota composition remain largely unknown.
Purpose of the Study:
- To assess the long-term impact of probiotic supplementation on gut microbiota composition and diversity in high-risk infants.
- To analyze microbiota development from birth to six years of age in infants receiving probiotics or placebo.
- To investigate the relationship between microbiota changes, probiotic intervention, and atopic disease development.
Main Methods:
- A double-blind, randomized, placebo-controlled trial involving probiotic (Ecologic® Panda) or placebo administration.
- Pregnant women received probiotics in late pregnancy, and offspring received them during the first year of life.
- Stool samples were collected from 99 children over six years, with bacterial profiling via IS-pro.
Main Results:
- Probiotic strains were detected and showed higher abundance during supplementation in the probiotic group.
- Minor, short-term differences in microbiota composition were observed between probiotic and placebo groups.
- Gut microbiota development continued between two and six years, progressing towards an adult-like state.
Conclusions:
- Perinatal probiotic supplementation had minimal, transient effects on infant gut microbiota.
- No long-lasting differences in microbiota composition were identified between groups.
- Age-driven microbiota development is a significant factor, overriding intervention effects over time.
Introduction:
Imbalance of the human gut microbiota in early childhood is suggested as a risk factor for immune-mediated disorders such as allergies. With the objective to modulate the intestinal microbiota, probiotic supplementation during infancy has been used for prevention of allergic diseases in infants, with variable success. However, not much is known about the long-term consequences of neonatal use of probiotics on the microbiota composition. The aim of this study was to assess the composition and microbial diversity in stool samples of infants at high-risk for atopic disease, from birth onwards to six years of age, who were treated with probiotics or placebo during the first year of life.
Methods:
In a double-blind, randomized, placebo-controlled trial, a probiotic mixture consisting of B. bifidum W23, B. lactis W52 and Lc. Lactis W58 (Ecologic® Panda) was administered to pregnant women during the last 6 weeks of pregnancy and to their offspring during the first year of life. During follow-up, faecal samples were collected from 99 children over a 6-year period with the following time points: first week, second week, first month, three months, first year, eighteen months, two years and six years. Bacterial profiling was performed by IS-pro. Differences in bacterial abundance and diversity were assessed by conventional statistics.
Results:
The presence of the supplemented probiotic strains in faecal samples was confirmed, and the probiotic strains had a higher abundance and prevalence in the probiotic group during supplementation. Only minor and short term differences in composition of microbiota were found between the probiotic and placebo group and between children with or without atopy. The diversity of Bacteroidetes was significantly higher after two weeks in the placebo group, and at the age of two years atopic children had a significantly higher Proteobacteria diversity (p < 0.05). Gut microbiota development continued between two and six years, whereby microbiota composition at phylum level evolved more and more towards an adult-like configuration.
Conclusion:
Perinatal supplementation with Ecologic® Panda, to children at high-risk for atopic disease, had minor effects on gut microbiota composition during the supplementation period. No long lasting differences were identified. Regardless of intervention or atopic disease status, children had a shared microbiota development over time determined by age that continued to develop between two and six years.
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