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Development of severe bronchopulmonary dysplasia is associated with alterations in fecal volatile organic compounds.
Berkhout, Daniel J C; Niemarkt, Hendrik J; Benninga, Marc A; Budding, Andries E; van Kaam, Anton H; Kramer, Boris W; Pantophlet, Charlene M; van Weissenbruch, Mirjam M; de Boer, Nanne K H; de Meij, Tim G J.
Affiliation
  • Berkhout DJC; Department of Pediatric Gastroenterology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
  • Niemarkt HJ; Neonatal Intensive Care Unit, Máxima Medical Center, Veldhoven, The Netherlands.
  • Benninga MA; Department of Pediatric Gastroenterology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
  • Budding AE; Department of Microbiology, VU University Medical Center, Amsterdam, The Netherlands.
  • van Kaam AH; Neonatal Intensive Care Unit, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
  • Kramer BW; Department of Pediatrics, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Pantophlet CM; Department of Pediatric Gastroenterology, VU University Medical Center, Amsterdam, The Netherlands.
  • van Weissenbruch MM; Neonatal Intensive Care Unit, VU University Medical Center, Amsterdam, The Netherlands.
  • de Boer NKH; Department of Gastroenterology and Hepatology, VU University Medical Center, Amsterdam, The Netherlands.
  • de Meij TGJ; Department of Pediatric Gastroenterology, VU University Medical Center, Amsterdam, The Netherlands.
Pediatr Res ; 83(2): 412-419, 2018 02.
Article in En | MEDLINE | ID: mdl-29053703
ABSTRACT
BackgroundThe aim of this study was to evaluate the potential of fecal volatile organic compounds (VOCs), obtained by means of an electronic nose device (Cyranose 320), as early non-invasive biomarker for BPD.MethodsIn this nested case-control study performed at three Neonatal Intensive Care Units, fecal samples obtained at postnatal age of 7, 14, 21, and 28 days from preterm infants with severe bronchopulmonary dysplasia (BPD) were compared with fecal VOC profiles from matched controls. Microbiota analysis was performed by means of IS-pro technique on fecal samples collected at 28 days postnatally.ResultsVOC profiles of infants developing severe BPD (n=15) could be discriminated from matched controls (n=15) at postnatal age of 14 days (area under the curve (±95% confidence interval), P-value, sensitivity, specificity; 0.72 (0.54-0.90), 0.040, 60.0%, 73.3%), 21 days (0.71 (0.52-0.90), 0.049, 66.7%, 73.3%) and 28 days (0.77 (0.59-0.96), 0.017, 69.2%, 69.2%) but not at 7 days. Intestinal microbiota did not differ between BPD subjects and controls.ConclusionFecal VOC profiles of infants developing BPD could be differentiated from controls at postnatal day 14, 21, and 28. VOC differences could not be directed to intestinal microbiota alterations but presumably reflect local and systemic metabolic and inflammatory pathways associated with BPD.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchopulmonary Dysplasia / Volatile Organic Compounds / Feces / Electronic Nose Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Newborn Language: En Journal: Pediatr Res Year: 2018 Type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchopulmonary Dysplasia / Volatile Organic Compounds / Feces / Electronic Nose Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Newborn Language: En Journal: Pediatr Res Year: 2018 Type: Article Affiliation country: Netherlands