Enrichment of Formula in Probiotics or Prebiotics and Risk of Infection and Allergic Diseases up to Age 5.5 Years in the Nationwide Etude Longitudinale Française depuis l'Enfance (ELFE) Cohort.


Journal

The Journal of nutrition
ISSN: 1541-6100
Titre abrégé: J Nutr
Pays: United States
ID NLM: 0404243

Informations de publication

Date de publication:
04 2022
Historique:
received: 07 10 2021
revised: 02 12 2021
accepted: 13 01 2022
medline: 28 3 2023
entrez: 26 3 2023
pubmed: 27 3 2023
Statut: ppublish

Résumé

An increasing number of infant and follow-on formulas are enriched with probiotics and/or prebiotics; however, evidence for health effects of such enrichment in early childhood remains inconclusive. The present study aimed to assess whether the consumption of formula enriched with probiotics or prebiotics was associated with the risk of infection and allergic diseases in early childhood. Analyses involved data for 8389 formula-fed children from the Etude Longitudinale Française depuis l'Enfance (ELFE) cohort. Enrichment of the formula with probiotics or prebiotics that was consumed from the age of 2-10 mo was identified by the formula ingredient list. Lower respiratory tract infection (LRTI), upper respiratory tract infection (URTI), gastrointestinal infection, wheezing, asthma, food allergy, and itchy rash were prospectively reported by parents up to the age of 5.5 y. Adjusted logistic regression models were used to assess associations between the consumption of enriched formula and risk of infection and allergic diseases. Aged 2 mo, more than half of formula-fed infants consumed the probiotic-enriched formula and only 1 in 10 consumed the prebiotic-enriched formula. Consumption of the Bifidobacterium lactis-enriched formula at 2 mo was associated with a lower risk of LRTI [OR (95% CI) = 0.84 (0.73-0.96)]. Consumption of the Bifidobacterium breve-enriched formula up to 6 mo was associated with a higher risk of LRTI [OR (95% CI) = 1.75 (1.29-2.38)] and asthma [OR (95% CI) = 1.95 (1.28-2.97)], whereas its consumption from 6 to 10 mo was associated with a lower risk of LRTI [OR (95% CI) = 0.64 (0.48-0.86)] and asthma [OR (95% CI) = 0.59 (0.40-0.88)]. Moreover, the consumption of Streptococcus thermophilus from 6 to 10 mo was associated with a higher risk of asthma [OR (95% CI) = 1.84 (1.29-2.63)]. No significant association was found for gastrointestinal infection, food allergy, and itchy rash. Overall, the consumption of prebiotic-enriched formula was not significantly associated with infection and allergy risk. Associations between the consumption of probiotic-enriched formula and risk of respiratory symptoms differ according to the strain considered and consumption period. Further well-designed studies are needed to confirm these results.

Sections du résumé

BACKGROUND
An increasing number of infant and follow-on formulas are enriched with probiotics and/or prebiotics; however, evidence for health effects of such enrichment in early childhood remains inconclusive.
OBJECTIVES
The present study aimed to assess whether the consumption of formula enriched with probiotics or prebiotics was associated with the risk of infection and allergic diseases in early childhood.
METHODS
Analyses involved data for 8389 formula-fed children from the Etude Longitudinale Française depuis l'Enfance (ELFE) cohort. Enrichment of the formula with probiotics or prebiotics that was consumed from the age of 2-10 mo was identified by the formula ingredient list. Lower respiratory tract infection (LRTI), upper respiratory tract infection (URTI), gastrointestinal infection, wheezing, asthma, food allergy, and itchy rash were prospectively reported by parents up to the age of 5.5 y. Adjusted logistic regression models were used to assess associations between the consumption of enriched formula and risk of infection and allergic diseases.
RESULTS
Aged 2 mo, more than half of formula-fed infants consumed the probiotic-enriched formula and only 1 in 10 consumed the prebiotic-enriched formula. Consumption of the Bifidobacterium lactis-enriched formula at 2 mo was associated with a lower risk of LRTI [OR (95% CI) = 0.84 (0.73-0.96)]. Consumption of the Bifidobacterium breve-enriched formula up to 6 mo was associated with a higher risk of LRTI [OR (95% CI) = 1.75 (1.29-2.38)] and asthma [OR (95% CI) = 1.95 (1.28-2.97)], whereas its consumption from 6 to 10 mo was associated with a lower risk of LRTI [OR (95% CI) = 0.64 (0.48-0.86)] and asthma [OR (95% CI) = 0.59 (0.40-0.88)]. Moreover, the consumption of Streptococcus thermophilus from 6 to 10 mo was associated with a higher risk of asthma [OR (95% CI) = 1.84 (1.29-2.63)]. No significant association was found for gastrointestinal infection, food allergy, and itchy rash. Overall, the consumption of prebiotic-enriched formula was not significantly associated with infection and allergy risk.
CONCLUSIONS
Associations between the consumption of probiotic-enriched formula and risk of respiratory symptoms differ according to the strain considered and consumption period. Further well-designed studies are needed to confirm these results.

Identifiants

pubmed: 36967171
pii: S0022-3166(23)10564-5
doi: 10.1093/jn/nxac013
pii:
doi:

Substances chimiques

Prebiotics 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1138-1148

Informations de copyright

Copyright © 2022 American Society for Nutrition.

Auteurs

Moufidath Adjibade (M)

Université de Paris, Centre de Recherche en Epidémiologie et StatistiqueS (CRESS), Inserm, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France.

Camille Davisse-Paturet (C)

Université de Paris, Centre de Recherche en Epidémiologie et StatistiqueS (CRESS), Inserm, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France.

Amandine Divaret-Chauveau (A)

EA3450, Université de Lorraine, Vandoeuvre-lès-Nancy, France; Unité d'allergologie pédiatrique, Hôpital d'Enfants, Centre Hospitalier Régional et Universitaire (CHRU) de Nancy, Vandoeuvre-lès-Nancy, France.

Karine Adel-Patient (K)

Université Paris-Saclay, Commissariat à l'Energie Atomique et aux Energies Alternatives, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement, Département Médicaments et Technologies pour la Santé (CEA, INRAE, DMTS), Gif-sur-Yvette, France.

Chantal Raherison (C)

Bordeaux University, Inserm, Bordeaux Population Health Research Center, Team Epidémiologie des cancers et expositions environnementales (EPICENE), Unité Mixte de Recherche (UMR), Bordeaux, France.

Marie-Noëlle Dufourg (MN)

Unité mixte Institut National de la Santé et de la Recherche Médicale-Institut National de la Santé et de la Recherche Médicale-Etablissement Français du Sang (Inserm-Ined-EFS) Etude Longitudinale Française depuis l'Enfance (ELFE), Institut National d'Etudes Démographiques (INED), Paris, France.

Sandrine Lioret (S)

Université de Paris, Centre de Recherche en Epidémiologie et StatistiqueS (CRESS), Inserm, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France.

Marie-Aline Charles (MA)

Université de Paris, Centre de Recherche en Epidémiologie et StatistiqueS (CRESS), Inserm, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France; Unité mixte Institut National de la Santé et de la Recherche Médicale-Institut National de la Santé et de la Recherche Médicale-Etablissement Français du Sang (Inserm-Ined-EFS) Etude Longitudinale Française depuis l'Enfance (ELFE), Institut National d'Etudes Démographiques (INED), Paris, France.

Blandine de Lauzon-Guillain (B)

Université de Paris, Centre de Recherche en Epidémiologie et StatistiqueS (CRESS), Inserm, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France. Electronic address: blandine.delauzon@inserm.fr.

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