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Human Milk Oligosaccharides Modulate Fecal Microbiota and Are Safe for Use in Children With Overweight: A Randomized Controlled Trial.
Fonvig, Cilius Esmann; Amundsen, Ingvild Dybdrodt; Vigsnæs, Louise Kristine; Sørensen, Nikolaj; Frithioff-Bøjsøe, Christine; Christiansen, Michael; Hedley, Paula Louise; Holm, Louise Aas; McConnell, Bruce; Holm, Jens-Christian.
Afiliação
  • Fonvig CE; The Children's Obesity Clinic, Accredited European Centre for Obesity Management, Department of Pediatrics, Copenhagen University Hospital Holbaek, Holbaek.
  • Amundsen ID; The Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, University of Copenhagen, Copenhagen.
  • Vigsnæs LK; Department of Pediatrics, Kolding Hospital a part of Lillebælt Hospital, Kolding.
  • Sørensen N; DSM, Hoersholm.
  • Frithioff-Bøjsøe C; DSM, Hoersholm.
  • Christiansen M; Clinical Microbiomics.
  • Hedley PL; The Children's Obesity Clinic, Accredited European Centre for Obesity Management, Department of Pediatrics, Copenhagen University Hospital Holbaek, Holbaek.
  • Holm LA; The Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, University of Copenhagen, Copenhagen.
  • McConnell B; Department for Congenital Disorders, Danish National Biobank and Biomarkers, Statens Serum Institut.
  • Holm JC; Department of Biomedical Sciences.
J Pediatr Gastroenterol Nutr ; 73(3): 408-414, 2021 09 01.
Article em En | MEDLINE | ID: mdl-34139746
ABSTRACT

OBJECTIVES:

Human milk oligosaccharides (HMOs) impact the intestinal microbiota by increasing beneficial bacteria in infants and adults, and are safe and well tolerated in these age groups. Effects on intestinal microbiota, safety, and digestive tolerance in children have not been, however, assessed. The aims of this trial were to evaluate if HMOs are able to specifically modulate the intestinal microbiota in children, and to assess safety and digestive tolerance.

METHODS:

In this randomized, double-blinded, placebo-controlled trial, 75 children with overweight (including obesity) ages 6 to 12 years were randomized to receive 2'-fucosyllactose (2'FL), a mix of 2'FL and lacto-N-neotetraose (Mix), or a glucose placebo orally administrated once per day for 8 weeks.

RESULTS:

The relative abundance of bifidobacteria increased significantly after 4 (P < 0.001) and 8 (P = 0.025) weeks of intervention in the 2'FL-group and after 4 weeks (P = 0.033) in the Mix-group, whereas no change was observed in the placebo group. Compared with placebo, the 2'FL-group had a significant increase in bifidobacteria abundance after 4 weeks (P < 0.001) and 8 weeks (P = 0.010) and the Mix-group showed a tendency to increased bifidobacteria abundance after 4 (P = 0.071) and 8 weeks (P = 0.071). Bifidobacterium adolescentis drove the bifidogenic effect in the 2 groups. Biochemical markers indicated no safety concerns, and the products did not induce digestive tolerance issues as assessed by Gastrointestinal Symptoms Rating Scale and Bristol Stool Form Scale.

CONCLUSIONS:

Both 2'FL and the Mix beneficially modulate intestinal microbiota by increasing bifidobacteria. Furthermore, supplementation with either 2'FL alone or a Mix is safe and well tolerated in children.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbiota / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbiota / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2021 Tipo de documento: Article