Low-protein formulas with alpha-lactalbumin-enriched or glycomacropeptide-reduced whey: effects on growth, nutrient intake and protein metabolism during early infancyShow others and affiliations
2023 (English)In: Nutrients, E-ISSN 2072-6643, Vol. 15, no 4, article id 1010
Article in journal (Refereed) Published
Abstract [en]
Protein intake is higher in formula-fed than in breast-fed infants during infancy, which may lead to an increased risk of being overweight. Applying alpha-lactalbumin (α-lac)-enriched whey or casein glycomacropeptide (CGMP)-reduced whey to infant formula may enable further reduction of formula protein by improving the amino acid profile. Growth, nutrient intake, and protein metabolites were evaluated in a randomized, prospective, double-blinded intervention trial where term infants received standard formula (SF:2.2 g protein/100 kcal; n = 83) or low-protein formulas with α-lac-enriched whey (α-lac-EW;1.75 g protein/100 kcal; n = 82) or CGMP-reduced whey (CGMP-RW;1.76 g protein/100 kcal; n = 80) from 2 to 6 months. Breast-fed infants (BF; n = 83) served as reference. Except between 4 and 6 months, when weight gain did not differ between α-lac-EW and BF (p = 0.16), weight gain was higher in all formula groups compared to BF. Blood urea nitrogen did not differ between low-protein formula groups and BF during intervention, but was lower than in SF. Essential amino acids were similar or higher in α-lac-EW and CGMP-RW compared to BF. Conclusion: Low-protein formulas enriched with α-lac-enriched or CGMP-reduced whey supports adequate growth, with more similar weight gain in α-lac-enriched formula group and BF, and with metabolic profiles closer to that of BF infants.
Place, publisher, year, edition, pages
MDPI, 2023. Vol. 15, no 4, article id 1010
Keywords [en]
alpha-lactalbumin, amino acids, CGMP, energetic efficiency, infant formula, infant growth, low protein, obesity, protein metabolism, protein quality
National Category
Nutrition and Dietetics
Identifiers
URN: urn:nbn:se:umu:diva-205491DOI: 10.3390/nu15041010ISI: 000940985900001PubMedID: 36839368Scopus ID: 2-s2.0-85148898752OAI: oai:DiVA.org:umu-205491DiVA, id: diva2:1743225
2023-03-142023-03-142025-02-11Bibliographically approved