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Fecal Volatile Metabolomics Predict Gram-Negative Late-Onset Sepsis in Preterm Infants: A Nationwide Case-Control Study.
Frerichs, Nina M; El Manouni El Hassani, Sofia; Deianova, Nancy; van Weissenbruch, Mirjam M; van Kaam, Anton H; Vijlbrief, Daniel C; van Goudoever, Johannes B; Hulzebos, Christian V; Kramer, Boris W; d'Haens, Esther J; Cossey, Veerle; de Boode, Willem P; de Jonge, Wouter J; Wicaksono, Alfian N; Covington, James A; Benninga, Marc A; de Boer, Nanne K H; Niemarkt, Hendrik J; de Meij, Tim G J.
Affiliation
  • Frerichs NM; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.
  • El Manouni El Hassani S; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.
  • Deianova N; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.
  • van Weissenbruch MM; Department of Neonatology, Amsterdam Reproduction and Development Research Institute, Emma Children's Hospital, 1105 AZ Amsterdam, The Netherlands.
  • van Kaam AH; Department of Neonatology, Amsterdam Reproduction and Development Research Institute, Emma Children's Hospital, 1105 AZ Amsterdam, The Netherlands.
  • Vijlbrief DC; Department of Neonatology, University Medical Center Utrecht, Wilhelmina Children's Hospital, 3584 CX Utrecht, The Netherlands.
  • van Goudoever JB; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.
  • Hulzebos CV; Department of Neonatology, Beatrix Children's Hospital, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
  • Kramer BW; Department of Pediatrics, Maastricht University Medical Centre, 6229 ER Maastricht, The Netherlands.
  • d'Haens EJ; Department of Neonatology, Isala Hospital, 8025 AB Zwolle, The Netherlands.
  • Cossey V; Department of Neonatology, University Hospitals Leuven, 3000 Leuven, Belgium.
  • de Boode WP; Department of Neonatology, Radboud UMC, Amalia Children's Hospital, 6525 XZ Nijmegen, The Netherlands.
  • de Jonge WJ; Tytgat Institute for Liver and Intestinal Research, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • Wicaksono AN; School of Engineering, University of Warwick, Coventry CV4 7AL, UK.
  • Covington JA; School of Engineering, University of Warwick, Coventry CV4 7AL, UK.
  • Benninga MA; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.
  • de Boer NKH; Department of Gastroenterology and Hepatology, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, 1081 HZ Amsterdam, The Netherlands.
  • Niemarkt HJ; Department of Neonatology, Máxima Medical Center, 5504 DB Veldhoven, The Netherlands.
  • de Meij TGJ; Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The Netherlands.
Microorganisms ; 11(3)2023 Feb 24.
Article in En | MEDLINE | ID: mdl-36985146
Early detection of late-onset sepsis (LOS) in preterm infants is crucial since timely treatment initiation is a key prognostic factor. We hypothesized that fecal volatile organic compounds (VOCs), reflecting microbiota composition and function, could serve as a non-invasive biomarker for preclinical pathogen-specific LOS detection. Fecal samples and clinical data of all preterm infants (≤30 weeks' gestation) admitted at nine neonatal intensive care units in the Netherlands and Belgium were collected daily. Samples from one to three days before LOS onset were analyzed by gas chromatography-ion mobility spectrometry (GC-IMS), a technique based on pattern recognition, and gas chromatography-time of flight-mass spectrometry (GC-TOF-MS), to identify unique metabolites. Fecal VOC profiles and metabolites from infants with LOS were compared with matched controls. Samples from 121 LOS infants and 121 matched controls were analyzed using GC-IMS, and from 34 LOS infants and 34 matched controls using GC-TOF-MS. Differences in fecal VOCs were most profound one and two days preceding Escherichia coli LOS (Area Under Curve; p-value: 0.73; p = 0.02, 0.83; p < 0.002, respectively) and two and three days before gram-negative LOS (0.81; p < 0.001, 0.85; p < 0.001, respectively). GC-TOF-MS identified pathogen-specific discriminative metabolites for LOS. This study underlines the potential for VOCs as a non-invasive preclinical diagnostic LOS biomarker.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Language: En Journal: Microorganisms Year: 2023 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Language: En Journal: Microorganisms Year: 2023 Document type: Article Affiliation country: Country of publication: