Docosahexaenoic acid-rich algae oil supplementation on breast milk fatty acid profile of mothers who delivered prematurely: a randomized clinical trial

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作者
Hélène Fougère
Jean-François Bilodeau
Pascal M. Lavoie
Ibrahim Mohamed
Iwona Rudkowska
Etienne Pronovost
David Simonyan
Line Berthiaume
Mireille Guillot
Bruno Piedboeuf
Pierre Julien
Isabelle Marc
机构
[1] CHU de Québec-Université Laval,Department of Pediatrics
[2] Université Laval,Department of Medicine, Faculty of Medicine
[3] CHU de Québec-Université Laval,Endocrinology and Nephrology Research Axis
[4] University of British Columbia,Department of Pediatrics
[5] University of Montreal,Departments of Pediatrics and Nutrition, CHU Sainte
[6] Université Laval,Justine
[7] CHU de Québec-Université Laval,Department of Kinesiology
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Preterm infants are deficient in long-chain polyunsaturated fatty acids, especially docosahexaenoic acid (DHA), a fatty acid (FA) associated with an increase in bronchopulmonary dysplasia (BPD). In two previous randomized control trials, DHA supplementation did not reduce the risk of BPD. We examined the breast milk FA profile, collected 14 days after birth, of mothers who delivered before 29 weeks of gestation and who were supplemented with DHA-rich algae oil or a placebo within 72 h after birth as part of the MOBYDIck trial. Milk FA were analyzed by gas chromatography. The total amount of FA (mg/mL) was similar in both groups but the supplementation increased DHA (expressed as % of total FA, mean ± SD, treatment vs placebo, 0.95 ± 0.44% vs 0.34 ± 0.20%; P < 0.0001), n-6 docosapentaenoic acid (DPA) (0.275 ± 0.14% vs 0.04 ± 0.04%; P < 0.0001) and eicosapentaenoic acid (0.08 ± 0.08% vs 0.07 ± 0.07%; P < 0.0001) while decreasing n-3 DPA (0.16 ± 0.05% vs 0.17 ± 0.06%; P < 0.05). Supplementation changed the ratio of DHA to arachidonic acid (1.76 ± 1.55% vs 0.60 ± 0.31%; P < 0.0001) and n-6 to n-3 FA (0.21 ± 0.06% vs 0.17 ± 0.04%; P < 0.0001). DHA-rich algae supplementation successfully increased the DHA content of breast milk but also included secondary changes that are closely involved with inflammation and may contribute to changing clinical outcomes.
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