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Human milk enhances antioxidant defenses against hydroxyl radical aggression in preterm infants
Ana Ledo1, Alessandro Arduini, Miguel A Asensi
1Division of Neonatology, Hospital Universitario Materno Infantil La Fe, Valencia, Spain.
Insights
Preterm infants experience oxidative stress, but feeding them human milk helps reduce harmful byproducts. Human milk offers partial protection against this stress compared to preterm formula.
Area of Science:
- Neonatal physiology
- Biochemistry
- Pediatric nutrition
Background:
- Preterm infants have underdeveloped antioxidant systems, increasing susceptibility to oxidative stress.
- Hydroxyl radicals, potent reactive oxygen species, lack direct measurement methods but their activity can be inferred from DNA and phenylalanine oxidation byproducts.
- Human milk exhibits a higher antioxidant capacity than infant formula.
Purpose of the Study:
- To investigate whether feeding human milk to preterm infants can mitigate oxidative stress.
- To compare the levels of oxidative stress markers in preterm infants fed human milk versus preterm formula.
Main Methods:
- A cohort of stable preterm infants was divided into two groups: exclusively fed human milk (HM) or preterm formula (PTF).
- Urine samples were analyzed for 8-hydroxy-2'-deoxyguanosine (8-oxodG)/2'-deoxyguanosine (2dG) ratio and ortho-tyrosine (o-Tyr)/Phe ratio using HPLC-tandem mass spectrometry.
- Healthy term newborns served as controls.
Main Results:
- Both preterm groups showed higher metabolite elimination than controls.
- The PTF group had significantly higher urinary 8-oxodG/2dG and o-Tyr/Phe ratios compared to the HM group.
- A correlation between 8-oxodG/2dG and o-Tyr/Phe ratios was observed, influenced by gestational age and birth weight.
Conclusions:
- Prematurity is linked to ongoing oxidative stress.
- Human milk consumption provides partial protection against oxidative stress in preterm infants.
Background:
Preterm infants endowed with an immature antioxidant defense system are prone to oxidative stress. Hydroxyl radicals are very aggressive reactive oxygen species that lack specific antioxidants. These radicals cannot be measured directly, but oxidation byproducts of DNA or phenylalanine in urine are reliable markers of their activity. Human milk has a higher antioxidant capacity than formula.
Objective:
We hypothesized that oxidative stress associated with prematurity could be diminished by feeding human milk.
Design:
We recruited a cohort of stable preterm infants who lacked perinatal conditions associated with oxidative stress; were not receiving prooxidant or antioxidant drugs, vitamins, or minerals before recruitment; and were fed exclusively human milk (HM group) or preterm formula (PTF group). Collected urine was analyzed for oxidative bases of DNA [8-hydroxy-2'-deoxyguanosine (8-oxodG)/2'-deoxyguanosine (2dG) ratio] and oxidative derivatives of phenylalanine [ortho-tyrosine (o-Tyr)/Phe ratio] by HPLC coupled to tandem mass spectrometry. Healthy term newborn infants served as control subjects.
Results:
Both preterm groups eliminated greater amounts of metabolites than did the control group. However, the PTF group eliminated significantly (P < 0.02) higher amounts of 8-oxodG (8-oxodG/2dG ratio: 10.46 +/- 3.26) than did the HM group (8-oxodG/2dG ratio: 9.05 +/- 2.19) and significantly (P < 0.01) higher amounts of o-Tyr (o-Tyr/Phe ratio: 14.90 +/- 3.75) than did the HM group (o-Tyr/Phe ratio: 12.53 +/- 3.49). When data were lumped together independently of the type of feeding received, a significant correlation was established between the 8-oxodG/2dG and o-Tyr/Phe ratios in urine, dependent on gestational age and birth weight.
Conclusion:
Prematurity is associated with protracted oxidative stress, and human milk is partially protective.
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