Influence of long-chain polyunsaturated fatty acid formula feeds on vitamin E status in preterm infants
- PMID: 14639802
- DOI: 10.1024/0300-9831.73.5.377
Influence of long-chain polyunsaturated fatty acid formula feeds on vitamin E status in preterm infants
Abstract
It has been recommended to supplement formulas for preterm infants with n-3 and n-6 long-chain polyunsaturated fatty acids (LCP) to improve growth, visual acuity, and neurodevelopmental performance. However, large amounts of LCP may increase lipid peroxidation and oxidative stress in preterm infants. We investigated if, under high supplementation of natural tocopherols, LCP addition to formula can be performed safely without causing tocopherol depletion in cell membranes. Thirty-one healthy preterm infants with gestational ages from 28 to 32 weeks were evaluated in a prospective, randomized study from birth to day 42. Nine infants received an n-3 and n-6 LCP-enriched formula (A), eleven infants a standard formula (B), and eleven infants breast milk (control group). Alpha- and gamma-tocopherol extracts were added to both formulas, amounting to five times the value in breast milk (2.3 mg/dL in both formulas versus 0.45 mg/dL in breast milk). Erythrocyte arachidonic acid (AA) and docosahexaenoic acid (DHA) in the phosphatidylethanolamine fraction were similar in the three groups over the study period, whereas a significant reduction of erythrocyte AA and DHA could be detected in the phosphatidylcholine fraction in all three groups from day 14 onwards, when compared to respective cord blood values, with lowest values in the standard formula group. Amazingly, levels of alpha- and gamma-tocopherol were higher in plasma, erythrocytes, platelets, monocytes, and polymorphonuclear leukocytes with LCP supplementation as compared to standard formula and breast milk from day 7 onwards, whereas in buccal mucosal cells, this was not the case until day 42. Gammatocopherol uptake in the LCP-supplemented group was also significantly higher in all cell fractions studied from day 7 onwards. We therefore hypothesize that the LCP supplementation used in formula A improves tocopherol solubility and stability in biological membranes. Under high-dose vitamin E addition to n-3 and n-6 LCP-supplemented formula, no evidence for tocopherol depletion and furthermore, high accumulation of tocopherols, can be detected in healthy preterm infants.
Similar articles
-
Fatty acid profiles, antioxidant status, and growth of preterm infants fed diets without or with long-chain polyunsaturated fatty acids. A randomized clinical trial.Eur J Nutr. 2003 Oct;42(5):243-53. doi: 10.1007/s00394-003-0418-2. Eur J Nutr. 2003. PMID: 14569405 Clinical Trial.
-
Docosahexaenoic and arachidonic acid content of serum and red blood cell membrane phospholipids of preterm infants fed breast milk, standard formula or formula supplemented with n-3 and n-6 long-chain polyunsaturated fatty acids.Eur J Pediatr. 1996 May;155(5):410-6. doi: 10.1007/BF01955275. Eur J Pediatr. 1996. PMID: 8741041
-
Influence of long chain unsaturated fatty acids in formula feeds on lipid peroxidation and antioxidants in preterm infants.Pediatr Res. 1996 Nov;40(5):680-6. doi: 10.1203/00006450-199611000-00006. Pediatr Res. 1996. PMID: 8910932 Clinical Trial.
-
Dietary PUFA for preterm and term infants: review of clinical studies.Crit Rev Food Sci Nutr. 2005;45(3):205-29. doi: 10.1080/10408690590956378. Crit Rev Food Sci Nutr. 2005. PMID: 16048149 Review.
-
Role of long-chain polyunsaturated fatty acids in the first year of life.J Pediatr Gastroenterol Nutr. 2008 Nov;47 Suppl 2:S41-4. doi: 10.1097/01.mpg.0000338811.52062.b2. J Pediatr Gastroenterol Nutr. 2008. PMID: 18931599 Review.
Cited by
-
Omega-3 LCPUFA supplement: a nutritional strategy to prevent maternal and neonatal oxidative stress.Matern Child Nutr. 2017 Apr;13(2):e12300. doi: 10.1111/mcn.12300. Epub 2016 Apr 13. Matern Child Nutr. 2017. PMID: 27072591 Free PMC article. Clinical Trial.
-
Polyunsaturated fatty acid supplementation in infancy for the prevention of allergy.Cochrane Database Syst Rev. 2016 Oct 28;10(10):CD010112. doi: 10.1002/14651858.CD010112.pub2. Cochrane Database Syst Rev. 2016. PMID: 27788565 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical