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Published on: October 25, 2015
Fetal metabolic influences of neonatal anthropometry and adiposity
Jean M Donnelly1, Karen L Lindsay2, Jennifer M Walsh3
1UCD Obstetrics and Gynaecology, School of Medicine and Medical Science, University College Dublin, Dublin, Ireland. jeandonnelly80@yahoo.co.uk.
Insights
Fetal leptin levels in cord blood are a key predictor of neonatal adiposity, independent of other factors. This finding may inform interventions to reduce childhood obesity risk in large for gestational age infants.
Area of Science:
- Perinatal medicine
- Neonatal health
- Endocrinology
Background:
- Large for gestational age (LGA) infants face higher risks of lifelong obesity and metabolic issues.
- Understanding neonatal adiposity predictors is crucial for developing antenatal interventions.
- This study focused on fetal metabolic factors influencing regional neonatal adiposity in women with prior LGA offspring.
Purpose of the Study:
- To identify fetal metabolic factors predicting regional neonatal adiposity.
- To analyze the association between fetal leptin and C-peptide with neonatal adiposity markers.
Main Methods:
- Analysis of data from the ROLO Kids study (derived from the ROLO trial).
- Comparison of neonatal anthropometry and skinfold measurements with cord blood leptin and C-peptide in 185 infants.
- Examination of associations between fetal metabolic factors, birthweight, anthropometry, and adiposity markers.
Main Results:
- Fetal leptin significantly correlated with birthweight, general adiposity, and various anthropometric measurements.
- Fetal leptin remained a significant predictor of neonatal adiposity after adjusting for gender, maternal BMI, gestational age, and study group.
- Fetal C-peptide was not significantly associated with neonatal adiposity in the final analysis.
Conclusions:
- Fetal leptin emerges as a critical predictor of regional neonatal adiposity.
- Further interventional studies are needed to evaluate the impact of neonatal adiposity on childhood obesity.
- Investigating interventions to reduce circulating leptin levels may be beneficial for improving neonatal adiposity.
Background:
Large for gestational age infants have an increased risk of obesity, cardiovascular and metabolic complications during life. Knowledge of the key predictive factors of neonatal adiposity is required to devise targeted antenatal interventions. Our objective was to determine the fetal metabolic factors that influence regional neonatal adiposity in a cohort of women with previous large for gestational age offspring.
Methods:
Data from the ROLO [Randomised COntrol Trial of LOw Glycaemic Index in Pregnancy] study were analysed in the ROLO Kids study. Neonatal anthropometric and skinfold measurements were compared with fetal leptin and C-peptide results from cord blood in 185 cases. Analyses were performed to examine the association between these metabolic factors and birthweight, anthropometry and markers of central and generalised adiposity.
Results:
Fetal leptin was found to correlate with birthweight, general adiposity and multiple anthropometric measurements. On multiple regression analysis, fetal leptin remained significantly associated with adiposity, independent of gender, maternal BMI, gestational age or study group assignment, while fetal C-peptide was no longer significant.
Conclusion:
Fetal leptin may be an important predictor of regional neonatal adiposity. Interventional studies are required to assess the impact of neonatal adiposity on the subsequent risk of childhood obesity and to determine whether interventions which reduce circulating leptin levels have a role to play in improving neonatal adiposity measures.
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