Supplementation of Infant Formula with Bovine Milk Fat Globule Membranes
- PMID: 28298277
- PMCID: PMC5347108
- DOI: 10.3945/an.116.014142
Supplementation of Infant Formula with Bovine Milk Fat Globule Membranes
Abstract
Studies have shown that supplementation of infant formula with bovine milk fat globule membranes (MFGMs) may substantially narrow the gap in health outcomes between formula-fed and breastfed infants. In one study, consumption of a formula supplemented with a lipid-rich MFGM concentrate between 2 and 6 mo of age improved cognitive performance at 24 wk of age. In another study, a formula supplemented with a protein-rich MFGM concentrate given between 2 and 6 mo of age improved cognitive performance at 12 mo of age, decreased infectious morbidity until 6 mo of age, and yielded serum cholesterol concentrations closer to those of breastfed infants. A third study that assessed the safety of supplementing infant formula with a lipid-rich or a protein-rich MFGM concentrate found a noninferior weight gain for both groups compared with a nonsupplemented formula. In this study, there was an increased risk of eczema in the protein-rich group, but no serious adverse events. Infant formulas with supplemental MFGMs have been launched on the market in several countries. However, the evidence base must still be considered quite limited. Based on 3 randomized controlled trials that are not comparable, the intervention seems safe, but there is not enough evidence for a general recommendation on which MFGM fraction to use and at what concentration as formula supplement for a given outcome.
Keywords: MFGM; cholesterol; cognition; infant formula; infection; neurodevelopment; otitis.
© 2017 American Society for Nutrition.
Conflict of interest statement
Author disclosures: Hero and Semper partly financed a study conducted by the authors and referred to in the text, but had no influence on the study design; collection, analysis, or interpretation of data; writing of the report; or decision to submit the paper for publication. N Timby has participated as a clinical investigator or speaker for Hero, Semper, and Hipp; M Domellöf has participated as clinical investigator or speaker for Hero, Semper, Baxter, Nutricia, Nestlé, and Nestlé Nutrition Institute; B Lönnerdal has participated as a clinical investigator, advisory board member, consultant, or speaker for Mead Johnson Nutrition, Arla Foods, Semper, Hero, Albion, Valio, Humana, Biostime, Hipp, Nestlé, and Nestlé Nutrition Institute; and O Hernell has participated as a clinical investigator, advisory board member, consultant, or speaker for Swedish Orphan Biovitrum, Mead Johnson Nutrition, Arla Foods, Hero, Semper, Hipp, and Valio.
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