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Lipid metabolism is associated with developmental epigenetic programming.

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Maternal metabolites, like fatty acids and histidine, are stable during pregnancy and link to infant DNA methylation. This suggests lipids influence fetal epigenetic programming, potentially affecting lifelong health.

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Area of Science:

  • Reproductive biology
  • Metabolomics
  • Epigenetics

Background:

  • Maternal diet and metabolism significantly influence fetal development.
  • Epigenetic reprogramming is a key mechanism for fetal adaptation to in utero environments.
  • Understanding the maternal-fetal metabolic-epigenetic link is crucial for developmental health.

Purpose of the Study:

  • To investigate the association between maternal metabolite levels and infant DNA methylation.
  • To determine if specific maternal metabolites correlate with global and gene-specific DNA methylation in newborns.
  • To explore the stability and correlation of maternal metabolites throughout pregnancy.

Main Methods:

  • Analysis of a clinical birth cohort of 40 mother-infant dyads.
  • Targeted metabolomics on maternal plasma (1st trimester and delivery) and infant cord blood plasma.
  • Quantitative DNA methylation analysis in maternal and infant plasma samples.

Main Results:

  • Very long chain fatty acids, medium chain acylcarnitines, and histidine were stable in maternal plasma and correlated across maternal and infant samples.
  • These metabolites were among the top maternal factors associated with infant DNA methylation.
  • Global DNA methylation showed high correlation across maternal and infant samples.

Conclusions:

  • Circulating maternal lipids and certain metabolites are tightly controlled and associated with infant DNA methylation patterns.
  • Maternal metabolic profiles may play a role in developmental epigenetic programming.
  • Further research is needed to establish a causal relationship between maternal plasma lipids and infant epigenetic programming.