Longitudinal fecal microbiota and volatile metabolomics preceding necrotizing enterocolitis in preterm infants: a case–control study

Alterations in fecal microbiota and volatile organic compound (VOC) profiles of preterm infants have been demonstrated before onset of necrotizing enterocolitis (NEC). However, NEC-specific signatures need to be identified before potential application as predictive biomarker in clinical practice. A prospective multicenter case-control study was conducted to identify preclinical fecal microbiota and VOC profiles of infants that developed NEC. Microbiota analysis (PCR-based IS-pro technique) and VOC analysis (gas chromatography-mass spectrometry) were performed on fecal samples collected up to three days before clinical NEC onset. In 112 infants (56 NEC, 56 matched controls), sufficient number fecal samples were collected for either microbiota or VOC analysis. Prior to NEC onset, Clostridium perfringens (p = 0.023, unadjusted) was more present in infants with NEC, versus controls. VOC analysis showed a clear distinction between fecal profiles of NEC cases and controls (area under the curve = 0.82). Fourteen unique VOC features contributed to this discrimination. Fecal microbiota and VOC profiles may serve as early indicators of NEC, and allow for increased understanding of pathophysiological mechanisms of NEC, but larger validation cohorts are needed before an overarching NEC-specific predictive microbiota-based biomarker can be implemented.

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Publication Details

Journal
Scientific Reports
Published
2025-03-26
DOI
https://doi.org/10.1038/s41598-025-94692-w
Citations
2
Primary Topic
Infant Nutrition and Health
Type
article
Field-Weighted Citation Impact
2.24

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article

Longitudinal fecal microbiota and volatile metabolomics preceding necrotizing enterocolitis in preterm infants: a case–control study

Nanne K.H. de Boer, Hans Weda, Meirong Xu, Xiang Long et al.
2 citations
Scientific Reports
Infant Nutrition and Health
2.24
article

Longitudinal fecal microbiota and volatile metabolomics preceding necrotizing enterocolitis in preterm infants: a case–control study

Nanne K.H. de Boer, Hans Weda, Meirong Xu, Xiang Long, Nina M. Frerichs, Tamara M. E. Nijsen, Sofia el Manouni el Hassani, Christian V. Hulzebos, Andries E. Budding, Daniel C. Vijlbrief, Veerle Cossey, Tim G. J. de Meij, Hendrik J. Niemarkt, Carel F.W. Peeters, Daan J. C. Berkhout, Richard A. van Lingen, Boris W. W. Kramer, Willem P. de Boode, Anton H. van Kaam, Marc Alexander Benninga, Mirjam M. van Weissenbruch, Hugo Knobel, L. Wijnoltz
article en
2 citations

Abstract

Alterations in fecal microbiota and volatile organic compound (VOC) profiles of preterm infants have been demonstrated before onset of necrotizing enterocolitis (NEC). However, NEC-specific signatures need to be identified before potential application as predictive biomarker in clinical practice. A prospective multicenter case-control study was conducted to identify preclinical fecal microbiota and VOC profiles of infants that developed NEC. Microbiota analysis (PCR-based IS-pro technique) and VOC analysis (gas chromatography-mass spectrometry) were performed on fecal samples collected up to three days before clinical NEC onset. In 112 infants (56 NEC, 56 matched controls), sufficient number fecal samples were collected for either microbiota or VOC analysis. Prior to NEC onset, Clostridium perfringens (p = 0.023, unadjusted) was more present in infants with NEC, versus controls. VOC analysis showed a clear distinction between fecal profiles of NEC cases and controls (area under the curve = 0.82). Fourteen unique VOC features contributed to this discrimination. Fecal microbiota and VOC profiles may serve as early indicators of NEC, and allow for increased understanding of pathophysiological mechanisms of NEC, but larger validation cohorts are needed before an overarching NEC-specific predictive microbiota-based biomarker can be implemented.

Scientific ReportsVol. 15(1)
Radboud University Nijmegen (NL), Radboud University Medical Center (NL), Maastricht University (NL), Emma Kinderziekenhuis (NL), Eurofins (Netherlands) (NL), Radboud Institute for Molecular Life Sciences (NL), Amalia Kinderziekenhuis (NL), Philips (Netherlands) (NL), Máxima Medisch Centrum (NL), Isala (NL), Nederlands Instituut Publieke Veiligheid (NL), Amsterdam University Medical Centers (NL), Wilhelmina Children's Hospital (NL), Eindhoven University of Technology (NL), Vrije Universiteit Amsterdam (NL), Wageningen University & Research (NL), KU Leuven (BE)
Stichting Zeldzame Ziekten Fonds
Zero hunger
Openalex Percentile: Top 15%
Infant Nutrition and Health
2.24
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