Combined choline and DHA supplementation: a randomized controlled trial

Eur J Nutr. 2020 Mar;59(2):729-739. doi: 10.1007/s00394-019-01940-7. Epub 2019 Mar 11.

Abstract

Objective: Choline and docosahexaenoic acid (DHA) are essential nutrients for preterm infant development. They are metabolically linked via phosphatidylcholine (PC), a constitutive plasma membrane lipid and the major transport form of DHA in plasma. Plasma choline and DHA-PC concentrations rapidly decline after preterm birth. To improve preterm infant nutrition, we evaluated combined compared to exclusive choline and DHA supplementation, and standard feeding.

Design: Randomized partially blinded single-center trial.

Setting: Neonatal tertiary referral center in Tübingen, Germany.

Patients: 24 inborn preterm infants < 32 week postmenstrual age.

Interventions: Standard nutrition (control) or, additionally, enteral choline (30 mg/kg/day), DHA (60 mg/kg/day), or both for 10 days. Single enteral administration of 3.6 mg/kg [methyl-D9-] choline chloride as a tracer at 7.5 days.

Main outcome measures: Primary outcome variable was plasma choline following 7 days of supplementation. Deuterated and unlabeled choline metabolites, DHA-PC, and other PC species were secondary outcome variables.

Results: Choline supplementation increased plasma choline to near-fetal concentrations [35.4 (32.8-41.7) µmol/L vs. 17.8 (16.1-22.4) µmol/L, p < 0.01] and decreased D9-choline enrichment of PC. Single DHA treatment decreased DHA in PC relative to total lipid [66 (60-68)% vs. 78 (74-80)%; p < 0.01], which was prevented by choline. DHA alone increased DHA-PC only by 35 (26-45)%, but combined treatment by 63 (49-74)% (p < 0.001). D9-choline enrichment showed preferential synthesis of PC containing linoleic acid. PC synthesis via phosphatidylethanolamine methylation resulted in preferential synthesis of DHA-containing D3-PC, which was increased by choline supplementation.

Conclusions: 30 mg/kg/day additional choline supplementation increases plasma choline to near-fetal concentrations, dilutes the D9-choline tracer via increased precursor concentrations and improves DHA homeostasis in preterm infants.

Trial registration: clinicaltrials.gov. Identifier: NCT02509728.

Keywords: Arachidonic acid; Choline; Combined supplementation; D9-choline; Docosahexaenoic acid; LC-PUFA; Neonate; Nutrition; PEMT; Phosphatidylcholine; Phospholipid; Plasma; Preterm infant; Stable isotopes; Tandem mass spectrometry.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Biomarkers / blood
  • Choline / administration & dosage
  • Choline / blood*
  • Choline / pharmacology*
  • Dietary Supplements
  • Docosahexaenoic Acids / administration & dosage
  • Docosahexaenoic Acids / blood*
  • Docosahexaenoic Acids / pharmacology*
  • Drug Therapy, Combination / methods
  • Enteral Nutrition / methods
  • Female
  • Germany
  • Humans
  • Infant Nutritional Physiological Phenomena / drug effects*
  • Infant, Newborn
  • Infant, Premature*
  • Male

Substances

  • Biomarkers
  • Docosahexaenoic Acids
  • Choline

Associated data

  • ClinicalTrials.gov/NCT02509728