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One-step Metabolomics: Carbohydrates, Organic and Amino Acids Quantified in a Single Procedure
Published on: June 25, 2010
Urinary organic acid excretion by babies born before 33 weeks of gestation
1Clinical Biochemistry, University of Southampton, Southampton General Hospital, U.K.
Insights
This study analyzed urinary organic acids in premature infants to help diagnose metabolic disorders. New methods identified novel metabolites, aiding in understanding infant metabolic health.
Area of Science:
- Biochemistry
- Neonatal Medicine
- Metabolic Disorders
Background:
- Premature neonates require careful monitoring for metabolic health.
- Diagnosing inherited organic acid defects is crucial for early intervention.
- Standard analytical methods are available for metabolic disorder investigations.
Purpose of the Study:
- To establish a diagnostic basis for inherited organic acid defects in premature neonates.
- To characterize urinary organic acid profiles in this vulnerable population.
- To identify novel urinary metabolites in normal neonates.
Main Methods:
- Analysis of 127 random urine samples from 22 premature infants (25-32 weeks gestation).
- Sample preparation involved oximation, extraction, and derivatization to trimethylsilyl forms.
- Gas-liquid chromatography with mass spectrometry (GC-MS) was used for metabolite identification.
Main Results:
- A wide range of organic acids was detected, with significant individual variability.
- No significant ketonuria was observed.
- Three metabolites, 2,3-butanediol, 3-hydroxy-2-butanone (acetoin), and 4-hydroxy-3-methoxyphenyllactic acid, were identified in normal neonate urine for the first time.
- Increased excretion of 4-hydroxyphenyllactic acid and other phenolic acids was noted during parenteral feeding.
Conclusions:
- Urinary organic acid profiling is a valuable tool for assessing metabolic status in premature infants.
- The identified novel metabolites expand the understanding of neonatal metabolism.
- Variations in metabolite profiles highlight the influence of clinical care and gut microbiome on neonates.
Abstract:
Using analytical procedures that are widely used by laboratories investigating metabolic disorders, we investigated urinary organic acid excretion by premature neonates who were receiving the usual clinical care. Our purpose was to provide a basis for the diagnosis of inherited organic acid defects. We analyzed 127 random (untimed) urine samples collected weekly from 22 infants of 25-32 weeks of gestation (median, 28 weeks). A wide variety of organic acids was excreted. After oximation, they were extracted with ethyl acetate and diethyl ether, derivatized to trimethylsilyl forms, and analyzed by gas-liquid chromatography on a nonpolar fused silica capillary column, with mass spectrometry for identification. Profiles for individual babies varied markedly on different occasions, reflecting their metabolic status and bacterial activity in the gut. There was no significant ketonuria. Three metabolites identified for the first time in urine from normal neonates were 2,3-butanediol, 3-hydroxy-2-butanone (acetoin), and 4-hydroxy-3-methoxyphenyllactic acid. Significantly increased excretion of 4-hydroxyphenyllactic acid and other phenolic acids occurred during parenteral feeding.
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