Abstract

It is unknown whether a novel small-quantity lipid-based nutrient supplement (SQ-LNS) containing alpha-linolenic (ALA) and linoleic acids impacts maternal plasma lipids and fatty acid status. We measured plasma fatty acids (wt%) and lipid concentrations at 36 wk gestation and breast milk fatty acids (wt%) at 6 months postpartum in a subsample of women enrolled in a randomized controlled trial studying the effects of SQ-LNS on birth outcomes and child growth. Women≤20 wk gestation in Ghana (n=1,320) and Malawi (n=1,391) were assigned to receive daily either: 1) iron-folic acid (pregnancy); 2) multiple micronutrients (pregnancy and lactation); or 3) SQ-LNS (pregnancy and lactation). At 36 wk, plasma ALA levels were higher in those receiving SQ-LNS. SQ-LNS increased breast milk ALA in Ghana but not Malawi. There was no effect on plasma lipids or other selected fatty acids. SQ-LNS may impact plasma and breast milk ALA levels depending on the population.

Highlights

  • Adequate amounts of the essential polyunsaturated fatty acids (PUFAs) alpha-linolenic acid (ALA, omega-3) and linoleic acid (LA, omega-6) are required during pregnancy and lactation for optimal fetal and infant growth [1]

  • This was a sub-study of participants from two randomized controlled trials conducted in Malawi and Ghana as part of the International Lipid-Based Nutrient Supplements Project

  • The primary objective of these trials was to determine the effect of Small-quantity lipid-based nutrient supplements (SQ-LNS), provided during pregnancy, lactation, and early childhood, on child growth at 18 months of age, as compared with iron-folic acid (IFA) provided during pregnancy or multiple micronutrient (MMN) provided to the mother during pregnancy and the first six months postpartum

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Summary

Introduction

Adequate amounts of the essential polyunsaturated fatty acids (PUFAs) alpha-linolenic acid (ALA, omega-3) and linoleic acid (LA, omega-6) are required during pregnancy and lactation for optimal fetal and infant growth [1]. Fatty acid consumption and body stores of the mother have a direct effect on fetal and infant fatty acid status [1]. Fatty acid supplementation trials in pregnant populations have primarily focused on the long-chain fatty acid derivatives of ALA – docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) [2] – due to the accumulation of DHA in the brain and retina and the low conversion rate of ALA to DHA (approximately 9% of ALA converts to DHA in women) [3]. One trial to date, conducted in the Netherlands, has examined the effect of maternal ALA supplementation on fatty acid status during pregnancy [6]. ALA supplementation led to higher concentrations of ALA, eicosapentaenoic acid (EPA), and docosapentaenoic acid (DPA) (wt%) in maternal plasma at delivery but had no effect on DHA or AA

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