ERA-HDHL cofunded call “Biomarkers for Nutrition and Health” (BioNH 2016)

Biomarkers for Infant Fat Mass Development and Nutrition.
BioFN
2017-11-01
2020-10-30
Albert Koulman
Partner Organization Partner Country

1. Overall project description


1.1 Summary

Childhood obesity is a rapidly growing problem in many countries across the world. Weight loss programs have limited effects and prevention is our only hope to stem this new epidemic. Development in the early life period has lifelong consequences. Early visceral fat mass development, in particular, is thought to have long-term effects on later body fat mass and fat distribution, and thus metabolic health.


Accurate measurements of fat mass development in healthy infants requires time, skilled personnel and specialized equipment, hence limiting implementation in routine neonatal care and research. Our hypothesis remains that the differences in fat mass development are associated with differences in lipid metabolism, which are driven by diet and gut microbiome activity in response to diet. We currently found a range of lipids that show a strong association with body composition at different ages (3m, 12m and 24m).


We proposed that changes in infancy diet results in major changes in the infancy microbiome leading to altered metabolism of macronutrients, especially of lipids. Data on genetically caused differences in breastmilk oligosaccharides are strongly suggesting that the effect of the gut microbiome on lipid metabolism is occurring higher up in the intestinal tract than can be assessed by faecal microbiome analysis. Lipid ratio’s that reflect desaturase and elongase activity are predictive of growth and weight gain. We are therefore rapidly covering our aims:


The aims of this project were to:


1) Develop biomarkers for body fat distribution at 2 years of life;


A series of candidate biomarkers is currently under investigation and will be further validated.


2) Develop lipid-based biomarkers at an early age to predict body fat distribution at 2 years of age;


Especially


3) Develop predictive biomarkers for later childhood (5-10 years) body composition (lean vs. fat) and


adipose tissue distribution (subcutaneous vs. visceral);


4) Quantify the dietary effect on lipid metabolism, gut microbiome metabolism and fat distribution usingdata from infants that receive both breast milk and formula (mixed feeding).


Existing detailed anthropometric and food intake data of healthy term infants from the Sophia-Pluto cohort will be combined with extensive lipidomic profiling and data from the BBSRC-DRINC project. These results will be feed into a custom-designed integrative systems biology analyses which has been established. This allows the consortium to identify, substantiate and confirm biomarkers for fat distribution in this translational project that aims to provide new tools to help to prevent childhood obesity


1.2 Highlights

Our work aims to develop biomarkers of body composition in babies and to predict childhood obestity. We are very excited about our current results, but we do not want release any details until we have been able to validate these findings. 


4. Impact


4.1 List of publications

AuthorsTitleYear, Issue, PPDoiPdf

4.2 Presentation of the project

Target groupAuthorsMeans of communicationHyperlinkPdf
ScientistsKoulman & Snowden, Cognition, leptin levels and modifications of lipid metabolism 60 years after gestational famine exposure, BMSS, Cambridge 2018oral
General publicKoulman et al., Fortune telling molecules Greenman Festival (Aug 2018)Hands on activity
General publicKoulman et al, Fortune telling molecules, Peterborough science fair (Sept 2018)Hands on activity
School childreb Koulman et al, Fortune telling molecules, Ely and Cambrihge High schools, Jun 2019

4.3 List of submitted patents and other outputs

Patent licencePartners involvedYearInternational eu or national patentCommentPdf

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