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Original Research Communication |
1 From Indiana University, Indianapolis (BBP and JAL); Yale University, New Haven, CT (RAE); Emory University, Atlanta (BJS); the Research Triangle Institute, Research Triangle Park, NC (MAK); the National Institute of Child Health and Human Development, Bethesda, MD (LLW); the Women and Infants Hospital, Providence, RI (WO); the University of New Mexico, Albuquerque (L-AP); the University of Miami (CRB); the University of Alabama, Birmingham (WAC); the University of Cincinnati (EFD); Case Western Reserve University, Cleveland (AAF); the University of Tennessee, Memphis (SBK); the University of Texas Southwestern Medical Center, Dallas (ARL); Wayne State University, Detroit (SS); Stanford University, Stanford, CA (DKS); and the University of Texas at Houston (JET).
Background: Glutamine is one of the most abundant amino acids in both plasma and human milk and may be conditionally essential in premature infants. However, glutamine is not provided by standard intravenous amino acid solutions.
Objective: We assessed the effect of parenteral glutamine supplementation on plasma amino acid concentrations in extremely low-birth-weight infants receiving parenteral nutrition (PN).
Design: A total of 141 infants with birth weights of 4011000 g were randomly assigned to receive a standard intravenous amino acid solution that did not contain glutamine or an isonitrogenous amino acid solution with 20% of the total amino acids as glutamine. Blood samples were obtained just before initiation of study PN and again after the infants had received study PN (mean intake: 2.3 ± 1.0 g amino acids · kg-1 · d-1) for
10 d.
Results: Infants randomly assigned to receive glutamine had mean plasma glutamine concentrations that increased significantly and were
30% higher than those in the control group in response to PN (425 ± 182 and 332 ± 148 µmol/L for the glutamine and control groups, respectively). There was no significant difference between the 2 groups in the relative change in plasma glutamate concentration between the baseline and PN samples. In both groups, there were significant decreases in plasma phenylalanine and tyrosine between the baseline and PN samples; the decrease in tyrosine was greater in the group that received glutamine.
Conclusions: In extremely low-birth-weight infants, parenteral glutamine supplementation can increase plasma glutamine concentrations without apparent biochemical risk. Currently available amino acid solutions are likely to be suboptimal in their supply of phenylalanine, tyrosine, or both for these infants.
Key Words: Glutamine phenylalanine tyrosine extremely low-birth-weight premature infants low-birth-weight infants parenteral nutrition neonatology neonatal care
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