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Source and Quality of Enteral Nutrition Influences Oxidative Stress in Preterm Infants: A Prospective Cohort Study
Gerhard Fusch1,2, Souvik Mitra2, Heinrich Topp1
1Division of Neonatology and Pediatric Intensive Care, Department of Pediatrics, University of Greifswald, Greifswald, Germany.
Insights
Enteral nutrition source impacts oxidative stress in preterm infants. Formula feeding showed higher 8-oxodG levels, a marker of DNA damage, compared to breast milk or mixed feeding.
Area of Science:
- Neonatal Medicine
- Biochemistry
- Pediatric Nutrition
Background:
- Preterm infants face oxidative stress from neonatal intensive care.
- 8-Oxo-2'-deoxyguanosine (8-oxodG) is a marker for DNA damage due to oxidative stress.
- Investigating nutritional impacts on oxidative stress is crucial for preterm infant health.
Purpose of the Study:
- To assess how enteral nutrition (EN) quality and source affect renal 8-oxodG excretion in preterm infants.
- To determine if iron supplementation influences oxidative stress markers.
- To explore potential mechanisms behind observed nutritional effects.
Main Methods:
- Collected spontaneous urine samples from 33 preterm infants (postnatal days 26-31).
- Infants received either breast milk (BM), formula (FM), or a BM/FM mix.
- Measured 8-oxodG levels using high-performance liquid chromatography-electrochemical detection (HPLC-EC); iron supplementation was initiated on day 28.
Main Results:
- The 8-oxodG/creatinine ratio was significantly higher in infants fed FM compared to BM/FM mix or BM alone (P < 0.0001).
- Iron supplementation showed no significant effect on 8-oxodG excretion (P = 0.547).
- Significant interindividual variation in 8-oxodG excretion was observed, but levels were similar within twin pairs.
Conclusions:
- The quality and source of enteral nutrition appear to influence oxidative stress in preterm infants.
- The exact pathophysiological mechanisms require further investigation.
- Factors beyond iron supplementation, potentially cow's milk protein-induced inflammation, may contribute to oxidative stress.
Background:
Preterm infants are at risk of oxidative stress from neonatal intensive care interventions. 8-Oxo-2'-deoxyguanosine (8-oxodG), generated by oxygen radical attack on DNA, is a potential marker of oxidative stress. The aim of the present study was to investigate the impact of quality and source of enteral nutrition (EN) on renal excretion of 8-oxodG in preterm infants.
Methods:
Spontaneous urine samples were collected on postnatal days 26-31 in 33 preterm infants. Infants were fed either breast milk (BM), formula (FM), or BM/FM mixtures. Daily iron (Fe) supplementation was started day 28 ± 1 postnatally. 8-oxodG was determined by highperformance liquid chromatography-electrochemical detection (HPLC-EC).
Results:
The 8-oxodG/creatinine ratio was significantly higher in infants fed FM vs FM/BM (38.7 ± 28.7 vs 16.7 ± 12.2 nmol 8-oxodG/mmol creatinine, P < 0.0001) or BM (11.6 ± 10.4 nmol 8-oxodG/mmol creatinine, P < 0.0001). There was no significant effect of Fe supplementation (P = 0.547). 8-OxodG excretion showed significant interindividual variation but was similar within pairs of twins.
Conclusion:
Quality and source of EN seem to influence oxidative stress in preterm infants. The underlying pathophysiological mechanism is unclear and needs further investigation. It may be speculated that other mechanisms than Fe supplementation contribute to oxidative stress, such as cow's milk protein-mediated up-regulation of the intestinal inflammatory cascade.
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