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Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Early Postnatal Metabolic Profile in Neonates With Different Birth Weight Status: A Pilot Study
Serdar Beken1, Saygin Abali2, Neslihan Yildirim Saral3
1Department of Pediatrics, Section of Neonatology, School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey.
Insights
Newborns with abnormal intrauterine growth show distinct metabolomic profiles, particularly in amino acids and carnitine levels. These early metabolic differences in small for gestational age (SGA) and large for gestational age (LGA) infants may predict future health risks.
Area of Science:
- Metabolomics
- Neonatal Medicine
- Endocrinology
Background:
- Intrauterine growth restriction (IUGR) and excessive fetal growth are linked to metabolic disorders.
- Amino acid and carnitine/acylcarnitine profiles are crucial for energy metabolism in fetuses and newborns.
Purpose of the Study:
- To investigate the association between intrauterine growth status and early postnatal metabolomic profiles.
- To identify specific metabolic differences in infants small for gestational age (SGA) and large for gestational age (LGA).
Main Methods:
- A retrospective cohort study of 361 newborns categorized as SGA, appropriate for gestational age (AGA), or LGA.
- Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to analyze amino acid and carnitine/acylcarnitine profiles.
Main Results:
- LGA infants showed higher glutamic acid and lower ornithine, alanine, and glycine levels compared to AGA.
- SGA infants exhibited higher alanine and glycine levels, along with altered carnitine and acylcarnitine species (e.g., higher total carnitine, C0, C2, C4, C5, C10:1, C18:1, C18:2, C14-OH, C18:2-OH; lower C3, C6-DC).
- LGA infants had higher C3 and C5:1 levels and lower C18:2 and C16:1-OH levels. Correlations were found between metabolites and ponderal index.
Conclusions:
- Significant metabolomic differences exist in newborns with abnormal intrauterine growth, reflecting altered energy metabolism.
- These early metabolic signatures in SGA and LGA infants may indicate a predisposition to future metabolic disturbances.
Abstract:
Introduction: Restricted or enhanced intrauterine growth is associated with elevated risks of early and late metabolic problems in humans. Metabolomics based on amino acid and carnitine/acylcarnitine profile may have a role in fetal and early postnatal energy metabolism. In this study, the relationship between intrauterine growth status and early metabolomics profile was evaluated. Materials and Methods: A single-center retrospective cohort study was conducted. Three hundred and sixty-one newborn infants were enrolled into the study, and they were grouped according to their birth weight percentile as small for gestational age (SGA, n = 69), appropriate for gestational age (AGA, n = 168), and large for gestational age (LGA, n = 124) infants. In all infants, amino acid and carnitine/acylcarnitine profiles with liquid chromatography-tandem mass spectrometry (LC-MS/MS) were recorded and compared between groups. Results: LGA infants had higher levels of glutamic acid and lower levels of ornithine, alanine, and glycine (p < 0.05) when compared with AGA infants. SGA infants had higher levels of alanine and glycine levels when compared with AGA and LGA infants. Total carnitine, C0, C2, C4, C5, C10:1, C18:1, C18:2, C14-OH, and C18:2-OH levels were significantly higher and C3 and C6-DC levels were lower in SGA infants (p < 0.05). LGA infants had higher C3 and C5:1 levels and lower C18:2 and C16:1-OH levels (p < 0.05). There were positive correlations between free carnitine and phenylalanine, arginine, methionine, alanine, and glycine levels (p < 0.05). Also, a positive correlation between ponderal index and C3, C5-DC, C14, and C14:1 and a negative correlation between ponderal index and ornithine, alanine, glycine, C16:1-OH, and C18:2 were shown. Conclusion: We demonstrated differences in metabolomics possibly reflecting the energy metabolism in newborn infants with intrauterine growth problems in the early postnatal period. These differences might be the footprints of metabolic disturbances in future adulthood.
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