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Serial changes in selected serum constituents in low birth weight infants on peripheral parenteral nutrition with

Insights

High zinc supplementation is crucial for preterm infants receiving parenteral nutrition, helping maintain normal serum zinc levels. Other nutrient levels showed declines, indicating potential deficiencies despite supplementation.

Area of Science:

  • Neonatal nutrition
  • Trace element metabolism
  • Parenteral nutrition

Background:

  • Infants with very low birth weight (VLBW) often require parenteral nutrition (PN).
  • Long-term PN can lead to deficiencies in essential trace elements like zinc and copper.
  • Monitoring specific biomarkers is vital for assessing nutritional status in VLBW infants.

Purpose of the Study:

  • To investigate the impact of varying zinc and copper supplementation doses on nutrient levels in VLBW infants receiving PN.
  • To determine optimal zinc and copper supplementation strategies for preventing deficiencies.

Main Methods:

  • Randomized controlled trial involving 105 VLBW infants (<2000 g) receiving PN for ≥3 weeks.
  • Weekly monitoring of serum zinc, copper, retinol-binding protein, prealbumin, alkaline phosphatase, and aspartate transaminase.
  • Comparison of nutrient and protein biomarker concentrations across different zinc and copper supplementation groups.

Main Results:

  • Mean serum zinc, retinol-binding protein, and prealbumin levels significantly decreased over time.
  • Alkaline phosphatase levels significantly increased over the study period.
  • Only the highest zinc supplement group maintained serum zinc within the normal range at 7 weeks.
  • No significant differences in protein or enzyme levels were observed between different zinc or copper dose groups.

Conclusions:

  • Higher zinc supplementation is necessary to maintain adequate serum zinc concentrations in VLBW infants on PN.
  • Current copper supplementation strategies may not significantly alter serum copper or ceruloplasmin levels.
  • Further research is needed to optimize trace element and protein biomarker management in VLBW infants.

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