Related Experiment Video
Updated: May 8, 2026

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Neuroactive metabolites and bile acids are altered in extremely premature infants with brain injury
Manuel Pristner1, Daniel Wasinger1, David Seki2
1Department of Food Chemistry and Toxicology, University of Vienna, 1090 Vienna, Austria.
Insights
The gut microbiome influences brain injury in premature infants. Researchers identified specific metabolic signatures, including bile acid conjugates, linked to brain injury in these vulnerable infants.
Area of Science:
- Neonatal neuroscience
- Microbiome research
- Metabolomics
Background:
- Gut microbiome alterations are linked to neurophysiological changes in premature infants with brain injury.
- The precise mechanisms and metabolic signatures remain unclear.
Purpose of the Study:
- To investigate fecal and plasma metabolome profiles associated with neonatal brain injury in extremely premature infants.
- To identify specific metabolic signatures and their link to the gut microbiome.
Main Methods:
- Untargeted and targeted liquid chromatography-high-resolution mass spectrometry (LC-MS) on fecal and plasma samples from 51 infants.
- Integration of metabolomics data with 16S rRNA gene sequencing, cytokine, growth factor, and T cell profiles.
Main Results:
- Early differentiation in neuroactive metabolites was observed between infants with and without brain injury.
- Bacterially derived bile acid amino acid conjugates were detected in plasma and feces.
Conclusions:
- Metabolite profiles, particularly bile acid conjugates, offer insights into early-life brain injury in extremely premature infants.
- Gut microbiome-derived metabolites may play a role in neonatal brain development and injury.
Abstract:
The gut microbiome is associated with pathological neurophysiological evolvement in extremely premature infants suffering from brain injury. The exact underlying mechanism and its associated metabolic signatures in infants are not fully understood. To decipher metabolite profiles linked to neonatal brain injury, we investigate the fecal and plasma metabolome of samples obtained from a cohort of 51 extremely premature infants at several time points, using liquid chromatography (LC)-high-resolution mass spectrometry (MS)-based untargeted metabolomics and LC-MS/MS-based targeted analysis for investigating bile acids and amidated bile acid conjugates. The data are integrated with 16S rRNA gene amplicon gut microbiome profiles as well as patient cytokine, growth factor, and T cell profiles. We find an early onset of differentiation in neuroactive metabolites between infants with and without brain injury. We detect several bacterially derived bile acid amino acid conjugates in plasma and feces. These results provide insights into the early-life metabolome of extremely premature infants.
More Related Videos
07:36Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats
Published on: November 20, 2015
05:52Early Pathological and Magnetic Resonance Detection of Cerebral Injury Using a Rat Model of Neonatal Hypoxic Ischemic Encephalopathy
Published on: October 28, 2022
Related Concept Videos
Hepatic Drug Excretion: Influencing Factors
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Gut-Brain Axis
Hepatic Encephalopathy