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Impact of Extensively Hydrolyzed Infant Formula on Circulating Lipids During Early Life
Santosh Lamichhane1, Heli Siljander2,3, Marja Salonen3
1Turku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, Finland.
Insights
Extensively hydrolyzed infant formula (HF) alters infant serum lipid profiles, including sphingomyelins and triacylglycerols, compared to conventional formula (RF). These changes may influence gut health and long-term metabolic outcomes.
Area of Science:
- Infant nutrition
- Metabolomics
- Gastroenterology
Background:
- Infant formula (IF) composition impacts infant gut microbiome, intestinal function, and immunity.
- The effect of IF on infant circulating lipid profiles remains poorly understood.
- This study investigates the impact of extensively hydrolyzed IF (HF) versus conventional formula (RF) on infant serum lipidome.
Purpose of the Study:
- To compare the serum lipidome of infants fed HF versus RF.
- To associate changes in circulatory lipids with gastrointestinal biomarkers, including intestinal permeability.
Main Methods:
- Randomized, double-blind controlled nutritional intervention study (n=73).
- Mass spectrometry-based lipidomics analyzed serum lipids at 3, 9, and 12 months.
- Measured growth, lactulose mannitol (LM) ratio, fecal calprotectin, and fecal beta-defensin.
Main Results:
- Higher sphingomyelin concentrations in the HF group compared to RF.
- Elevated triacylglycerols (TGs) in HF at 3 months, downregulated by 9-12 months.
- Lower LM ratio in the HF group at 9 months, with altered associations between lipids and LM ratio.
Conclusions:
- HF intervention significantly alters the circulating lipidome in infants.
- Changes in lipid profiles may be linked to gut health and potentially to conditions like T1D.
Background:
Current evidence suggests that the composition of infant formula (IF) affects the gut microbiome, intestinal function, and immune responses during infancy. However, the impact of IF on circulating lipid profiles in infants is still poorly understood. The objectives of this study were to (1) investigate how extensively hydrolyzed IF impacts serum lipidome compared to conventional formula and (2) to associate changes in circulatory lipids with gastrointestinal biomarkers including intestinal permeability.
Methods:
In a randomized, double-blind controlled nutritional intervention study (n = 73), we applied mass spectrometry-based lipidomics to analyze serum lipids in infants who were fed extensively hydrolyzed formula (HF) or conventional, regular formula (RF). Serum samples were collected at 3, 9, and 12 months of age. Child's growth (weight and length) and intestinal functional markers, including lactulose mannitol (LM) ratio, fecal calprotectin, and fecal beta-defensin, were also measured at given time points. At 3 months of age, stool samples were analyzed by shotgun metagenomics.
Results:
Concentrations of sphingomyelins were higher in the HF group as compared to the RF group. Triacylglycerols (TGs) containing saturated and monounsaturated fatty acyl chains were found in higher levels in the HF group at 3 months, but downregulated at 9 and 12 months of age. LM ratio was lower in the HF group at 9 months of age. In the RF group, the LM ratio was positively associated with ether-linked lipids. Such an association was, however, not observed in the HF group.
Conclusion:
Our study suggests that HF intervention changes the circulating lipidome, including those lipids previously found to be associated with progression to islet autoimmunity or overt T1D.
Clinical Trial Registration:
[Clinicaltrials.gov], identifier [NCT01735123].
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