4.2 Article

Daily Enteral DHA Supplementation Alleviates Deficiency in Premature Infants

Journal

LIPIDS
Volume 51, Issue 4, Pages 423-433

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11745-016-4130-4

Keywords

Neonatal nutrition; Premature infants; Docosahexaenoic acid (DHA); Long chain polyunsaturated fatty acids (LCPUFA); Essential dietary lipids

Funding

  1. Sanford Health Seed Grant, a Gerber Foundation Pediatric Nutrition Grant [PN12-005-1372-3069]
  2. Sanford Research
  3. Eunice Kennedy Shriver National Institute of Child Health & Human Development of the National Institutes of Health [K08HD078504]
  4. NIH Center of Biomedical Research Excellence (COBRE) Grant [P20 GM103620-01A1]

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Docosahexaenoic acid (DHA) is an essential fatty acid (FA) important for health and neurodevelopment. Premature infants are at risk of DHA deficiency and circulating levels directly correlate with health outcomes. Most supplementation strategies have focused on increasing DHA content in mother's milk or infant formula. However, extremely premature infants may not reach full feedings for weeks and commercially available parenteral lipid emulsions do not contain preformed DHA, so blood levels decline rapidly after birth. Our objective was to develop a DHA supplementation strategy to overcome these barriers. This double-blind, randomized, controlled trial determined feasibility, tolerability and efficacy of daily enteral DHA supplementation (50 mg/day) in addition to standard nutrition for preterm infants (24-34 weeks gestational age) beginning in the first week of life. Blood FA levels were analyzed at baseline, full feedings and near discharge in DHA (n = 31) or placebo supplemented (n = 29) preterm infants. Term peers (n = 30) were analyzed for comparison. Preterm infants had lower baseline DHA levels (p < 0.0001). Those receiving DHA had a progressive increase in circulating DHA over time (from 3.33 to 4.09 wt% or 2.88 to 3.55 mol%, p < 0.0001) while placebo-supplemented infants receiving standard neonatal nutrition) had no increase over time (from 3.35 to 3.32 wt% or 2.91 to 2.87 mol%). Although levels increased with additional DHA supplementation, preterm infants still had lower blood DHA levels than term peers (4.97 wt% or 4.31 mol%) at discharge (p = 0.0002). No differences in adverse events were observed between the groups. Overall, daily enteral DHA supplementation is feasible and alleviates deficiency in premature infants.

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