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Birth weight, subsequent growth, and cholesterol metabolism in children 8-12 years old born preterm
M Mortaz1, M S Fewtrell, T J Cole
1Department of Nutrition and Dietetics, King's College London, London W8 7AH, UK. m.mortaz@ich.ucl.ac.uk
Insights
Birth size and growth impact cholesterol metabolism in preterm children. Smaller birth size and significant postnatal weight gain are linked to altered cholesterol absorption and synthesis later in childhood.
Area of Science:
- Pediatric Endocrinology
- Metabolic Health
- Developmental Biology
Background:
- Birth size and early growth are critical determinants of long-term health.
- Cholesterol metabolism plays a vital role in overall health and disease prevention.
- Understanding early life influences on metabolic programming is essential for pediatric health.
Purpose of the Study:
- To investigate the relationship between birth size, subsequent growth, and plasma lipid profiles in children.
- To examine how cholesterol biosynthesis (lathosterol) and absorption (campesterol) markers relate to early growth patterns.
- To determine if early life factors influence cholesterol metabolism programming in preterm children.
Main Methods:
- Studied 412 preterm children (birth weight <1850g) with recorded birth data and follow-up at 8-12 years.
- Measured plasma lipids, lipoproteins, apolipoproteins, triacylglycerol, lathosterol, and campesterol.
- Analyzed associations between birth weight for gestational age, postnatal growth, and measured metabolic markers.
Main Results:
- Birth weight for gestational age positively correlated with cholesterol absorption marker (campesterol).
- Birth weight negatively correlated with cholesterol synthesis marker (lathosterol) after adjusting for current body size.
- Postnatal weight gain (centile crossing) significantly influenced cholesterol synthesis and absorption markers, independent of birth size for some children.
Conclusions:
- Preterm children with smaller birth size for gestational age exhibit lower cholesterol absorption efficiency later in childhood.
- Accelerated postnatal growth is associated with higher endogenous cholesterol synthesis and lower absorption efficiency.
- Fetal and childhood growth trajectories appear to program cholesterol metabolism in preterm children.
Aims:
To test the hypothesis that plasma lipids, lipoproteins, and markers of cholesterol biosynthesis (lathosterol) and absorption efficiency (campesterol) in children aged 8-12 years are related to birth size and subsequent growth.
Methods:
A total of 412 girls and boys weighing less than 1850 g at birth were studied. Birth weight, gestation, and weight at 18 months were recorded and followed up at 8-12 years. Plasma total cholesterol, low density lipoprotein cholesterol, high density lipoprotein cholesterol, apolipoprotein A1, apolipoprotein B, triacylglycerol, lathosterol, and campesterol were measured.
Results:
Birth weight for gestational age was positively related to plasma campesterol, and remained so after adjusting for current body size or fatness. Birth weight was negatively related to current plasma lathosterol but only after adjusting for current body size or fatness. For both lathosterol and campesterol the significant relation with birth size adjusted for current size indicates that the change in size between these points (postnatal upward centile crossing) was influential. These relations were absent for total cholesterol, lipoproteins, apolipoproteins, and triacylglycerol.
Conclusion:
Preterm children who were smaller for gestational age at birth had lower predicted cholesterol absorption efficiency 8-12 years later. Among children of the same current size, predicted endogenous cholesterol synthesis was higher and cholesterol absorption efficiency lower in those who showed the greatest increase in weight centile between birth and follow up. This finding was not confined to children with the smallest birth weights for gestational age. We suggest that both fetal and childhood growth relate to programming of cholesterol metabolism in children born preterm.
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