Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2022 Jul 19;12(1):12310.
doi: 10.1038/s41598-022-16351-8.

Fecal amine metabolite analysis before onset of severe necrotizing enterocolitis in preterm infants: a prospective case-control study

Affiliations
Multicenter Study

Fecal amine metabolite analysis before onset of severe necrotizing enterocolitis in preterm infants: a prospective case-control study

N Deianova et al. Sci Rep. .

Abstract

Infants developing necrotizing enterocolitis (NEC) have a different metabolomic profile compared to controls. The potential of specific metabolomics, i.e. amino acids and amino alcohols (AAA), as early diagnostic biomarkers for NEC is largely unexplored. In this multicenter prospective case-control study, longitudinally collected fecal samples from preterm infants (born <30 weeks of gestation) from 1-3 days before diagnosis of severe NEC (Bell's stage IIIA/IIIB), were analyzed by targeted high-performance liquid chromatography (HPLC). Control samples were collected from gestational and postnatal age-matched infants. Thirty-one NEC cases (15 NEC IIIA;16 NEC IIIB) with 1:1 matched controls were included. Preclinical samples of infants with NEC were characterized by five increased essential amino acids-isoleucine, leucine, methionine, phenylalanine and valine. Lysine and ethanolamine ratios were lower prior to NEC, compared to control samples. A multivariate model was rendered based on isoleucine, lysine, ethanolamine, tryptophan and ornithine, modestly discriminating cases from controls (AUC 0.67; p < 0.001). Targeted HPLC pointed to several specific AAA alterations in samples collected 1-3 days before NEC onset, compared to controls. Whether this reflects metabolic alterations and has a role in early biomarker development for NEC, has yet to be elucidated.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Flow chart of study subject enrollment. NEC necrotizing enterocolitis.

References

    1. Schindler T, et al. Causes of death in very preterm infants cared for in neonatal intensive care units: A population-based retrospective cohort study. BMC Pediatr. 2017;17(1):59–59. doi: 10.1186/s12887-017-0810-3. - DOI - PMC - PubMed
    1. Challis P, et al. Validation of the diagnosis of necrotising enterocolitis in a Swedish population-based observational study. Acta Paediatr (Oslo, Norway: 1992) 2019;108(5):835–841. doi: 10.1111/apa.14585. - DOI - PMC - PubMed
    1. Hintz SR, et al. Neurodevelopmental and growth outcomes of extremely low birth weight infants after necrotizing enterocolitis. Pediatrics. 2005;115(3):696–703. doi: 10.1542/peds.2004-0569. - DOI - PubMed
    1. Wang H, et al. Prediction of intestinal failure from necrotizing enterocolitis following surgery: A multicenter retrospective review. Medicine. 2019;98(19):e15568–e15568. doi: 10.1097/MD.0000000000015568. - DOI - PMC - PubMed
    1. Gephart SM, et al. Necrotizing enterocolitis risk: State of the science. Adv. Neonatal Care. 2012;12:2. doi: 10.1097/ANC.0b013e318265b4bd. - DOI - PMC - PubMed

Publication types