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Cyst(e)ine requirements in enterally fed very low birth weight preterm infants
Maaike A Riedijk1, Gardi Voortman, Ron H T van Beek
1Erasmus MC-Sophia Children's Hospital, Department of Pediatrics, Division of Neonatology, Dr Molewaterplein 60, 3015 GJ, Rotterdam, The Netherlands.
Insights
Cystine is likely not essential for preterm infants fed enterally with adequate methionine. Studies show no increased need for cystine, suggesting it
Area of Science:
- Nutritional biochemistry and metabolism in neonates.
- Pediatric gastroenterology and clinical nutrition.
- Amino acid metabolism in preterm infants.
Background:
- Optimal nutrition is critical for preterm infant development.
- Amino acid requirements differ in preterm infants due to growth rates.
- Cystine may be conditionally essential for preterm infants.
Purpose of the Study:
- To determine cystine requirements in enterally fed preterm infants (<29 weeks gestational age).
- To assess cystine needs at 32 and 35 weeks postmenstrual age.
- To investigate if cystine is conditionally essential in this population.
Main Methods:
- Randomized controlled trial with 5 graded cystine diets (adequate methionine).
- Indicator amino acid oxidation technique using [1-(13)C]phenylalanine.
- 24-hour adaptation period before measurement.
Main Results:
- 47 very low birth weight preterm infants (gestational age <29 weeks) were studied.
- Increased dietary cystine did not decrease [1-(13)C]phenylalanine oxidation.
- No evidence of limited endogenous cystine synthesis was found.
Conclusions:
- Cystine is likely not conditionally essential in preterm infants >32 weeks postmenstrual age with adequate methionine.
- Estimated cystine requirement is <18 mg/kg/day in this group.
- Findings do not support the hypothesis of limited endogenous cystine synthesis.
Objective:
Optimal nutrition is of utmost importance for the preterm infant's later health and developmental outcome. Amino acid requirements for preterm infants differ from those for term and older infants, because growth rates differ. Some nonessential amino acids, however, cannot be sufficiently synthesized endogenously. Cyst(e)ine is supposed to be such a conditionally essential amino acid in preterm infants. The objective of this study was to determine, at 32 and 35 weeks' postmenstrual age, cyst(e)ine requirements in fully enterally fed very low birth weight preterm infants with gestational ages of <29 weeks.
Methods:
Infants were randomly assigned to 1 of the 5 graded cystine test diets that contained generous amounts of methionine. Cyst(e)ine requirement was determined with the indicator amino acid oxidation technique ([1-(13)C]phenylalanine) after 24-hour adaptation.
Results:
Fractional [1-(13)C]phenylalanine oxidation was established in 47 very low birth weight preterm infants (mean gestational age: 28 weeks +/- 1 week SD; birth weight: 1.07 kg +/- 0.21 kg SD). Increase in dietary cyst(e)ine intake did not result in a decrease in fractional [1-(13)C]phenylalanine oxidation.
Conclusions:
These data do not support the hypothesis that endogenous cyst(e)ine synthesis is limited in very low birth weight preterm infants with gestational ages of <29 weeks, both at 32 and 35 weeks postmenstrual age. It is safe to conclude that cyst(e)ine requirement is <18 mg/kg per day in enterally fed very low birth weight preterm infants who are older than 32 weeks' postmenstrual age and whose methionine intake is adequate. Therefore, cyst(e)ine is probably not a conditionally essential amino acid in these infants.
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