The Translation of Lipid Profiles to Nutritional Biomarkers in the Study of Infant Metabolism
Overview
Authors
Affiliations
Introduction: Links between early life exposures and later health outcomes may, in part, be due to in infancy. This hypothesis is supported by observed long-term benefits associated with breastfeeding, such as better cognitive development in childhood, and lower risks of obesity and high blood pressure in later life. However, the possible underlying mechanisms are expected to be complex and may be difficult to disentangle due to the lack of understanding of the metabolic processes that differentiate breastfed infants compared to those receiving just formula feed.
Objective: Our aim was to investigate the relationships between infant feeding and the lipid profiles and to validate specific lipids in separate datasets so that a small set of lipids can be used as nutritional biomarkers.
Method: We utilized a direct infusion high-resolution mass spectrometry method to analyse the lipid profiles of 3.2 mm dried blood spot samples collected at age 3 months from the Cambridge Baby Growth Study (CBGS-1), which formed the discovery cohort. For validation two sample sets were profiled: Cambridge Baby Growth Study (CBGS-2) and Pregnancy Outcome Prediction Study (POPS). Lipidomic profiles were compared between infant groups who were either exclusively breastfed, exclusively formula-fed or mixed-fed at various levels. Data analysis included supervised Random Forest method with combined classification and regression mode. Selection of lipids was based on an iterative backward elimination procedure without compromising the class error in the classification mode.
Conclusion: From this study, we were able to identify and validate three lipids: PC(35:2), SM(36:2) and SM(39:1) that can be used collectively as biomarkers for infant nutrition during early development. These biomarkers can be used to determine whether young infants (3-6 months) are breast-fed or receive formula milk.
Cusworth S, Gkoutos G, Acharjee A BMC Med Inform Decis Mak. 2024; 24(1):90.
PMID: 38549123 PMC: 10979623. DOI: 10.1186/s12911-024-02487-2.
Impact of Extensively Hydrolyzed Infant Formula on Circulating Lipids During Early Life.
Lamichhane S, Siljander H, Salonen M, Ruohtula T, Virtanen S, Ilonen J Front Nutr. 2022; 9:859627.
PMID: 35685890 PMC: 9171511. DOI: 10.3389/fnut.2022.859627.
Nixon R, Ip T, Jenkins B, Yip P, Clarke P, Ponnusamy V Nutrients. 2021; 13(12).
PMID: 34959853 PMC: 8703828. DOI: 10.3390/nu13124301.
Fetal programming of human energy homeostasis brain networks: Issues and considerations.
Rasmussen J, Thompson P, Entringer S, Buss C, Wadhwa P Obes Rev. 2021; 23(3):e13392.
PMID: 34845821 PMC: 10308600. DOI: 10.1111/obr.13392.
Metabolomics in early life and the association with body composition at age 2 years.
van Beijsterveldt I, Snowden S, Myers P, de Fluiter K, van de Heijning B, Brix S Pediatr Obes. 2021; 17(3):e12859.
PMID: 34644810 PMC: 9286420. DOI: 10.1111/ijpo.12859.