Growth, stool consistency and bone mineral content in healthy term infants fed sn-2-palmitate-enriched starter infant formula: A randomized, double-blind, multicentre clinical trial.


Journal

Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603

Informations de publication

Date de publication:
06 2019
Historique:
received: 10 11 2017
revised: 24 05 2018
accepted: 25 05 2018
pubmed: 16 6 2018
medline: 29 5 2020
entrez: 16 6 2018
Statut: ppublish

Résumé

Palmitate in breast milk is predominantly located in the triacylglycerol sn-2 position, while infant formulae contain palmitate predominantly in the sn-1 and sn-3 positions. During digestion, palmitate in the sn-1 and sn-3 positions is hydrolyzed to free palmitic acid that can subsequently complex with calcium to form insoluble soaps; this may partially explain why formula-fed infants have harder stools than breast-fed infants. This large (n = 488) randomized, double-blind, multicentre trial investigated whether increasing the sn-2 palmitate content of infant formula improves stool consistency and bone mineral content (measured by dual-energy x-ray absorptiometry), without affecting growth or health. From ∼1 week to 4 months of age, infants were exclusively fed one of three formulae: i) control formula (CF; 16% of total palmitate at sn-2; n = 162), (ii) experimental formula 1 (EF1; 43% of total palmitate at sn-2; n = 166) or (iii) experimental formula 2 (EF2; 51% of total palmitate at sn-2; n = 160). Intention-to-treat analysis showed softer stools in both EF groups (vs. CF) at ages 2 weeks and 1 and 2 months (p ≤ 0.01), but not 3 and 4 months. At 4 months, all groups had similar growth outcomes while bone mineral content was significantly higher in EF1 (p = 0.0012) and EF2 (p = 0.0002) compared with CF. Comparison of reported adverse events up to 12 months revealed no differences among groups. All 3 infant formulae exhibited equally good digestive tolerance. Formulae enriched in sn-2 palmitate fed in early infancy are safe, improve stool consistency (from 2 weeks to 2 months) and increase bone mineral content (at 4 months).

Sections du résumé

BACKGROUND
Palmitate in breast milk is predominantly located in the triacylglycerol sn-2 position, while infant formulae contain palmitate predominantly in the sn-1 and sn-3 positions. During digestion, palmitate in the sn-1 and sn-3 positions is hydrolyzed to free palmitic acid that can subsequently complex with calcium to form insoluble soaps; this may partially explain why formula-fed infants have harder stools than breast-fed infants.
METHODS
This large (n = 488) randomized, double-blind, multicentre trial investigated whether increasing the sn-2 palmitate content of infant formula improves stool consistency and bone mineral content (measured by dual-energy x-ray absorptiometry), without affecting growth or health. From ∼1 week to 4 months of age, infants were exclusively fed one of three formulae: i) control formula (CF; 16% of total palmitate at sn-2; n = 162), (ii) experimental formula 1 (EF1; 43% of total palmitate at sn-2; n = 166) or (iii) experimental formula 2 (EF2; 51% of total palmitate at sn-2; n = 160).
RESULTS
Intention-to-treat analysis showed softer stools in both EF groups (vs. CF) at ages 2 weeks and 1 and 2 months (p ≤ 0.01), but not 3 and 4 months. At 4 months, all groups had similar growth outcomes while bone mineral content was significantly higher in EF1 (p = 0.0012) and EF2 (p = 0.0002) compared with CF. Comparison of reported adverse events up to 12 months revealed no differences among groups. All 3 infant formulae exhibited equally good digestive tolerance.
CONCLUSIONS
Formulae enriched in sn-2 palmitate fed in early infancy are safe, improve stool consistency (from 2 weeks to 2 months) and increase bone mineral content (at 4 months).

Identifiants

pubmed: 29903473
pii: S0261-5614(18)30200-0
doi: 10.1016/j.clnu.2018.05.015
pii:
doi:

Substances chimiques

Palmitates 0

Banques de données

ClinicalTrials.gov
['NCT02332967']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1023-1030

Informations de copyright

Copyright © 2018 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

Laurent Béghin (L)

Univ. Lille, Inserm, CHU Lille, CIC 1403 - Centre d'investigation clinique, F-59000 Lille, France; Univ. Lille, Inserm, CHU Lille, U995 - LIRIC - Lille Inflammation Research International Center, F-59000 Lille, France. Electronic address: laurent.beghin@chru-lille.fr.

Xavier Marchandise (X)

Department of Nuclear Medicine, Lille University Hospital, Lille Hauts de France University, F-59000 Lille, France.

Eric Lien (E)

Department of Food Science and Human Nutrition, University of Illinois, Urbana, USA.

Myriam Bricout (M)

Ambulatory Paediatrician from the GREPA-Nord (Groupe de Recherche et d'Etudes en Pédiatrie Ambulatoire-Research and Study Group in Ambulatory Paediatrics from the North of France), French Association of Ambulatory Paediatrics, F-59000 Lille, France(1).

Jean-Paul Bernet (JP)

Ambulatory Paediatrician from the GREPA-Nord (Groupe de Recherche et d'Etudes en Pédiatrie Ambulatoire-Research and Study Group in Ambulatory Paediatrics from the North of France), French Association of Ambulatory Paediatrics, F-59000 Lille, France(1).

Jean-François Lienhardt (JF)

Ambulatory Paediatrician from the GREPA-Nord (Groupe de Recherche et d'Etudes en Pédiatrie Ambulatoire-Research and Study Group in Ambulatory Paediatrics from the North of France), French Association of Ambulatory Paediatrics, F-59000 Lille, France(1).

Françoise Jeannerot (F)

Ambulatory Paediatrician from the GREPA-Nord (Groupe de Recherche et d'Etudes en Pédiatrie Ambulatoire-Research and Study Group in Ambulatory Paediatrics from the North of France), French Association of Ambulatory Paediatrics, F-59000 Lille, France(1).

Vincent Menet (V)

Ambulatory Paediatrician from the GREPA-Nord (Groupe de Recherche et d'Etudes en Pédiatrie Ambulatoire-Research and Study Group in Ambulatory Paediatrics from the North of France), French Association of Ambulatory Paediatrics, F-59000 Lille, France(1).

Jean-Christophe Requillart (JC)

Ambulatory Paediatrician from the GREPA-Nord (Groupe de Recherche et d'Etudes en Pédiatrie Ambulatoire-Research and Study Group in Ambulatory Paediatrics from the North of France), French Association of Ambulatory Paediatrics, F-59000 Lille, France(1).

Jacques Marx (J)

Ambulatory Paediatrician from the GREPA-Nord (Groupe de Recherche et d'Etudes en Pédiatrie Ambulatoire-Research and Study Group in Ambulatory Paediatrics from the North of France), French Association of Ambulatory Paediatrics, F-59000 Lille, France(1).

Nanda De Groot (N)

Nestlé Nutrition, Nestec Ltd, Vevey, Switzerland.

Jonathan Jaeger (J)

Nestlé Research Center, Lausanne, Switzerland.

Philippe Steenhout (P)

Nestlé Health Science, Vevey, Switzerland.

Dominique Turck (D)

Univ. Lille, Inserm, CHU Lille, U995 - LIRIC - Lille Inflammation Research International Center, F-59000 Lille, France; Division of Gastroenterology, Hepatology and Nutrition, Department of Paediatrics, Jeanne de Flandre Lille University Children's Hospital and Lille University Faculty of Medicine, F-59000 Lille, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH