Randomized Controlled Trial of Early Docosahexaenoic Acid and Arachidonic Acid Enteral Supplementation in Very Low

Brandy L Frost1, Aloka L Patel2, Daniel T Robinson3

  • 1Department of Pediatrics, NorthShore University HealthSystem, Evanston, IL; Department of Pediatrics, University of Chicago Pritzker School of Medicine, Chicago, IL.

The Journal of Pediatrics
|December 28, 2020
PubMed

Insights

Supplementing very low birth weight infants with long-chain polyunsaturated fatty acids (LCPUFA) supports higher blood docosahexaenoic acid (DHA) levels. A higher dose of LCPUFA (360 mg) is needed to maintain and increase arachidonic acid (ARA) and DHA levels.

Area of Science:

  • Neonatal nutrition
  • Biochemistry
  • Pediatric research

Background:

  • Very low birth weight infants have unique nutritional needs.
  • Long-chain polyunsaturated fatty acids (LCPUFA) are crucial for infant development.
  • Assessing the impact of LCPUFA supplementation in this vulnerable population is important.

Purpose of the Study:

  • To evaluate the feasibility of administering a concentrated emulsified LCPUFA supplement to very low birth weight infants.
  • To measure blood LCPUFA concentrations at 2 and 8 weeks of supplementation.
  • To determine optimal LCPUFA dosing for neonatal nutrition.

Main Methods:

  • Prospective, randomized, double-blind, placebo-controlled trial.
  • Infants received either LCPUFA-120, LCPUFA-360, or sunflower oil (placebo) for 8 weeks.
  • Whole blood LCPUFA levels (DHA and ARA) were measured at baseline, 2, and 8 weeks.

Main Results:

  • At 2 weeks, significant differences in blood DHA and ARA changes from baseline were observed across groups (P < .003).
  • The LCPUFA-360 group showed increases in DHA and ARA, while the placebo group showed decreases.
  • Significant differences in DHA and ARA changes persisted at 8 weeks (P < .02).

Conclusions:

  • Enteral LCPUFA supplementation is feasible and supports increased blood DHA by 2 weeks.
  • Supplementation with 360 mg/kg/day of combined DHA and ARA is likely necessary to prevent declines and promote increases in blood LCPUFA concentrations.
  • Optimized LCPUFA intake is critical for very low birth weight infants during early life.
Abstract