Abstract

PurposeCholine is an essential nutrient for fetal and infant growth and development. Parenteral nutrition used in neonatal care lack free choline but contain small amounts of lipid-bound choline in the form of phosphatidylcholine (PC). Here, we examined the longitudinal development of serum free choline and metabolically related compounds betaine and methionine in extremely preterm infants and how the concentrations were affected by the proportion of parenteral fluids the infants received during the first 28 postnatal days (PNDs).MethodsThis prospective study included 87 infants born at gestational age (GA) < 28 weeks. Infant serum samples were collected PND 1, 7, 14, and 28, and at postmenstrual age (PMA) 32, 36, and 40 weeks. The serum concentrations of free choline, betaine, and methionine were determined by 1H NMR spectroscopy.ResultsThe median (25th–75th percentile) serum concentrations of free choline, betaine, and methionine were 33.7 (26.2–41.2), 71.2 (53.2–100.8), and 25.6 (16.4–35.3) µM, respectively, at PND 1. The choline concentration decreased rapidly between PND one and PND seven [18.4 (14.1–26.4) µM], and then increased over the next 90 days, though never reaching PND one levels. There was a negative correlation between a high intake of parenteral fluids and serum-free choline.ConclusionCirculating free choline in extremely preterm infants is negatively affected by the proportion of parenteral fluids administered.Trial registrationClinicalTrials.gov Identifier NCT02760472, April 29, 2016, retrospectively registered.

Highlights

  • Choline is an essential nutrient for humans and plays crucial roles in fetal and infant development

  • We demonstrate in a cohort of extremely preterm infants that the free serum concentration of choline decreases as parenteral fluids are increased

  • The concentration of free serum choline the first day of life was similar in this cohort as to what has been reported for free plasma choline levels in preterm infants [10, 22]

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Summary

Introduction

Choline is an essential nutrient for humans and plays crucial roles in fetal and infant development. Choline is a principal component in the biosynthesis of structural and signaling phospholipids, including sphingomyelins, phosphatidylcholines (PC) and lyso-PC [1]. Choline may form an ester with acetic acid to produce the neurotransmitter acetylcholine [5]. PC, and thereby choline, can be synthesized endogenously through sequential methylation of the head-group of phosphatidylethanolamine (PE) in the hepatic PE-N-methyltransferase (PEMT) pathway [6]. This pathway is not sufficient to meet the body’s requirement for choline and it must

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