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Published on: November 20, 2015
Choline concentrations are lower in postnatal plasma of preterm infants than in cord plasma
Wolfgang Bernhard1, Marco Raith, Rebecca Kunze
1Department of Neonatology, Faculty of Medicine, Eberhard-Karls-University, Calwer Straße 7, 72076, Tūbingen, Germany, wolfgang.bernhard@med.uni-tuebingen.de.
Insights
Preterm infants show a significant drop in plasma choline after birth, indicating undernourishment. This choline deficiency may negatively impact infant development and cognitive outcomes.
Area of Science:
- Neonatal Medicine
- Biochemistry
- Nutritional Science
Background:
- Choline is vital for fetal brain development, bile formation, and methyl group donation.
- Maternal choline supply is linked to infant cognitive outcomes.
- Reduced placental choline transfer may disrupt homeostasis in preterm infants.
Purpose of the Study:
- To compare postnatal plasma choline, betaine, and dimethylglycine (DMG) levels in preterm infants with cord and maternal blood.
- To assess the impact of postmenstrual age (PMA) on these metabolite concentrations.
Main Methods:
- Plasma samples were collected from very low-birth-weight infants (n=162) and cord blood (n=176) across a range of PMAs (24-42 weeks).
- Maternal serum (n=36) and healthy women's plasma (n=40) were also analyzed.
- Metabolite concentrations were quantified using tandem mass spectrometry.
Main Results:
- Cord plasma choline inversely correlated with PMA and was lower in female term infants.
- Postnatal choline levels in preterm infants dropped by 50% within 48 hours.
- Betaine and DMG levels showed correlations with choline across all studied groups.
Conclusions:
- Preterm infants experience significant postnatal choline depletion, suggesting undernourishment.
- This choline deficiency may contribute to adverse outcomes in preterm infants.
- Further research into choline supplementation for preterm infants is warranted.
Background:
Choline is essential to human development, particularly of the brain in the form of phosphatidylcholine, sphingomyelin and acetylcholine, for bile and lipoprotein formation, and as a methyl group donator. Choline is actively transported into the fetus, and maternal supply correlates with cognitive outcome. Interruption of placental supply may therefore impair choline homeostasis in preterm infants.
Objective:
Determination of postnatal plasma concentrations of choline and its derivatives betaine and dimethylglycine (DMG) in preterm infants compared to cord and maternal blood matched for postmenstrual age (PMA).
Design:
We collected plasma of very low-birth-weight infants undergoing neonatal intensive care (n = 162), cord plasma of term and preterm infants (n = 176, 24-42-week PMA), serum of parturients (n = 36), and plasma of healthy premenopausal women (n = 40). Target metabolites were analyzed with tandem mass spectrometry and reported as median (25th/75th percentiles).
Results:
Cord plasma choline concentration was 41.4 (31.8-51.2) µmol/L and inversely correlated with PMA. In term but not in preterm infants, cord plasma choline was lower in girls than in boys. Prenatal glucocorticoid treatment did not affect choline levels in cord plasma, whereas betaine was decreased and DMG increased. In parturients and non-pregnant women, choline concentrations were 14.1 (10.3-16.9) and 8.8 (5.7-11.2) µmol/L, respectively, whereas betaine was lowest in parturients. After delivery, preterm infant plasma choline decreased to 20.8 (16.0-27.6) µmol/L within 48 h. Betaine and DMG correlated with plasma choline in all groups.
Conclusions:
In preterm infants, plasma choline decreases to 50 % of cord plasma concentrations, reflecting choline undernourishment and postnatal metabolic adaptation, and potentially contributing to impaired outcome.
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