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Published on: November 24, 2020
Early life lipid profile and metabolic programming in very young children
K P J Wijnands1, S A Obermann-Borst1, R P M Steegers-Theunissen2
1Department of Obstetrics and Gynecology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Insights
Childhood cholesterol levels are linked to epigenetic changes in tumor necrosis factor-alpha (TNFα) and leptin (LEP) genes, potentially influencing long-term cardiovascular disease risk.
Area of Science:
- Epigenetics
- Metabolic Programming
- Cardiovascular Health
Background:
- Early life lipid profiles may cause lasting epigenetic alterations.
- Metabolic programming in infancy can impact future health.
- Investigating early lipid-epigenetic links is crucial for developmental origins of health and disease (DOHaD).
Purpose of the Study:
- To examine associations between serum lipids in young children and DNA methylation of TNFα and LEP.
- To determine if maternal lipid profiles influence child DNA methylation.
Main Methods:
- Analysis of serum lipid profiles and whole blood DNA methylation in 120 children at 17 months.
- Utilized linear mixed models to assess exposure-specific differences.
- Adjusted for covariates including gestational age, birth weight, sex, breastfeeding, and education.
Main Results:
- Childhood total cholesterol correlated with reduced TNFα methylation.
- HDL-cholesterol in children was associated with decreased methylation of both TNFα and LEP.
- Maternal HDL-cholesterol showed an association with decreased child TNFα methylation.
Conclusions:
- Childhood lipid levels are associated with epigenetic changes, supporting the DOHaD hypothesis.
- These epigenetic modifications may influence future cardiovascular disease susceptibility.
- Early life lipid-epigenetic interactions are key factors in metabolic programming.
Background And Aims:
Lipid derangements during early postnatal life may induce stable epigenetic changes and alter metabolic programming. We investigated associations between serum lipid profiles in very young children and DNA methylation of tumor necrosis factor-alpha (TNFα) and leptin (LEP). Secondly, we explored if the maternal serum lipid profile modifies DNA methylation in the child.
Methods And Results:
In 120 healthy children at 17 months of age, DNA methylation of TNFα and LEP was measured in DNA derived from whole blood. Linear mixed models were used to calculate exposure-specific differences and associations. Total cholesterol in children was associated with decreased methylation of TNFα (-5.8%, p = 0.036), and HDL-cholesterol was associated with decreased methylation of both TNFα (-6.9%, p = 0.013) and LEP (-3.4%, p = 0.021). Additional adjustment for gestational age at birth, birth weight, sex, breastfeeding and educational level attenuated the effects, TNFα (-6.1%, p = 0.058) and LEP (-3.1%, p = 0.041). In mothers, HDL-cholesterol only was associated with decreased methylation of TNFα in the child (-8.7%, p = 0.001).
Conclusion:
Our data support the developmental origin of health and disease hypothesis by showing that total cholesterol and HDL-cholesterol levels in very young children are associated with epigenetic metabolic programming, which may affect their vulnerability for developing cardiovascular diseases in later life.
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