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Published on: March 13, 2014
Association between polyunsaturated fatty acid intake and plasma oxylipin profiles in preterm infants: A
Hiroki Suganuma1, Naho Ikeda2, Natsuki Ohkawa2
1Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan.
Insights
Dietary polyunsaturated fatty acids (PUFAs) impact oxylipin profiles in preterm infants. Higher intake of arachidonic acid (AA) and docosahexaenoic acid (DHA) correlated with lower levels of their derived oxylipins.
Area of Science:
- Biochemistry
- Neonatal Nutrition
- Lipid Metabolism
Background:
- Oxylipins are bioactive lipid mediators derived from polyunsaturated fatty acids (PUFAs).
- PUFAs are essential for infant development, obtained through breast milk or formula.
- Preterm infants have unique nutritional needs and altered metabolic pathways.
Purpose of the Study:
- To characterize the oxylipin profile in preterm infants receiving enteral PUFA feeding.
- To investigate the relationship between dietary PUFA intake and plasma oxylipin levels in this population.
Main Methods:
- Quantified weekly PUFA intake (breast milk and formula) in 27 preterm infants (30-34 weeks gestation) over 4 weeks.
- Measured plasma oxylipin levels on postnatal days 7, 14, 21, and 28 using ultra-high-performance liquid chromatography-mass spectrometry.
- Analyzed associations between PUFA intake and oxylipins using marginal structural models with inverse probability weighting.
Main Results:
- Dynamic changes in weekly PUFA intake were observed, with linoleic acid (LA) and alpha-linolenic acid (ALA) peaking at week 2.
- Arachidonic acid (AA) and docosahexaenoic acid (DHA) levels showed steady and sharp increases, respectively.
- AA- and DHA-derived oxylipins exhibited significant inverse correlations with their respective intakes, despite minimal magnitude of change.
Conclusions:
- Dietary PUFA composition influences the oxylipin profile in preterm infants.
- Negative correlations between AA/DHA intake and their derived oxylipins suggest a regulatory mechanism.
- Findings highlight the importance of tailored PUFA nutrition in preterm neonates.
Objective:
Oxylipins, synthesized through the oxidation of polyunsaturated fatty acids (PUFAs), are bioactive downstream lipid mediators that play crucial roles in proinflammatory responses and potential cytotoxicity. Infants received PUFAs from breast milk or formula. This study aimed to describe the oxylipin profile of preterm infants receiving enteral PUFA feeding.
Methods:
Twenty-seven preterm infants born at 30-34 weeks of gestation were included. Weekly PUFA intake from breast milk and formula was quantified for 4 weeks, and plasma oxylipin levels were measured on postnatal days 7, 14, 21, and 28 using ultrahigh-performance liquid chromatography mass spectroscopy. Associations between PUFA intake and oxylipins were analyzed using marginal structural models with inverse probability weighting.
Results:
Weekly PUFA intake exhibited dynamic changes, with ω-6 linoleic acid (LA) and alpha-linolenic acid (ALA) peaking at Week 2, arachidonic acid (AA) increasing steadily, eicosapentaenoic acid (EPA) rising gradually, and docosahexaenoic acid (DHA) increasing sharply before plateauing. LA-derived oxylipins remained relatively stable, with nominal positive associations that lost significance after multiple testing correction. AA-derived oxylipins several hydroxy-eicosatetraenoic acids exhibited strong inverse correlations with AA intake, maintaining significance after false discovery rate adjustment. DHA-derived oxylipins, including 19,20- epoxy docosapentaenoic acid and several hydroxy-docosahexaenoic acids, consistently demonstrated inverse associations with DHA intake, with all retaining significance postadjustment.
Conclusion:
This study demonstrates that the composition of dietary PUFA intake from enteral feeding can influence the oxylipin profile in preterm infants. Negative correlations were identified between AA- and DHA-derived oxylipins and their respective intakes, although the magnitude of change was notably minimal.
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