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Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study

Fecal volatile organic compounds (VOC) reflect human and gut microbiota metabolic pathways and their interaction. VOC behold potential as non-invasive preclinical diagnostic biomarkers in various diseases, e.g., necrotizing enterocolitis and late onset sepsis. There is a need for standardization and...

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Autores principales: Deianova, Nancy, el Manouni el Hassani, Sofia, Niemarkt, Hendrik J., Cossey, Veerle, van Kaam, Anton H., Jenken, Floor, van Weissenbruch, Mirjam M., Doedes, Esmee M., Baelde, Kyra, Menezes, Renee, Benninga, Marc A., de Jonge, Wouter J., de Boer, Nanne K., de Meij, Tim G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277672/
https://www.ncbi.nlm.nih.gov/pubmed/32403393
http://dx.doi.org/10.3390/bios10050050
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author Deianova, Nancy
el Manouni el Hassani, Sofia
Niemarkt, Hendrik J.
Cossey, Veerle
van Kaam, Anton H.
Jenken, Floor
van Weissenbruch, Mirjam M.
Doedes, Esmee M.
Baelde, Kyra
Menezes, Renee
Benninga, Marc A.
de Jonge, Wouter J.
de Boer, Nanne K.
de Meij, Tim G.
author_facet Deianova, Nancy
el Manouni el Hassani, Sofia
Niemarkt, Hendrik J.
Cossey, Veerle
van Kaam, Anton H.
Jenken, Floor
van Weissenbruch, Mirjam M.
Doedes, Esmee M.
Baelde, Kyra
Menezes, Renee
Benninga, Marc A.
de Jonge, Wouter J.
de Boer, Nanne K.
de Meij, Tim G.
author_sort Deianova, Nancy
collection PubMed
description Fecal volatile organic compounds (VOC) reflect human and gut microbiota metabolic pathways and their interaction. VOC behold potential as non-invasive preclinical diagnostic biomarkers in various diseases, e.g., necrotizing enterocolitis and late onset sepsis. There is a need for standardization and assessment of the influence of clinical and environmental factors on the VOC outcome before this technique can be applied in clinical practice. The aim of this study was to investigate the influence of gestational age (GA) and mode of delivery on the fecal VOC pattern in preterm infants born below 30 weeks of gestation. Longitudinal fecal samples, collected on days 7, 14, and 21 postnatally, were analyzed by an electronic nose device (Cyranose 320(®)). In total, 58 preterm infants were included (29 infants born at GA 24–26 weeks vs. 29 at 27–29 completed weeks, 24 vaginally born vs. 34 via C-section). No differences were identified at any predefined time point in terms of GA and delivery mode (p > 0.05). We, therefore, concluded that correction for these factors in this population is not warranted when performing fecal VOC analysis in the first three weeks of life.
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spelling pubmed-72776722020-06-12 Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study Deianova, Nancy el Manouni el Hassani, Sofia Niemarkt, Hendrik J. Cossey, Veerle van Kaam, Anton H. Jenken, Floor van Weissenbruch, Mirjam M. Doedes, Esmee M. Baelde, Kyra Menezes, Renee Benninga, Marc A. de Jonge, Wouter J. de Boer, Nanne K. de Meij, Tim G. Biosensors (Basel) Article Fecal volatile organic compounds (VOC) reflect human and gut microbiota metabolic pathways and their interaction. VOC behold potential as non-invasive preclinical diagnostic biomarkers in various diseases, e.g., necrotizing enterocolitis and late onset sepsis. There is a need for standardization and assessment of the influence of clinical and environmental factors on the VOC outcome before this technique can be applied in clinical practice. The aim of this study was to investigate the influence of gestational age (GA) and mode of delivery on the fecal VOC pattern in preterm infants born below 30 weeks of gestation. Longitudinal fecal samples, collected on days 7, 14, and 21 postnatally, were analyzed by an electronic nose device (Cyranose 320(®)). In total, 58 preterm infants were included (29 infants born at GA 24–26 weeks vs. 29 at 27–29 completed weeks, 24 vaginally born vs. 34 via C-section). No differences were identified at any predefined time point in terms of GA and delivery mode (p > 0.05). We, therefore, concluded that correction for these factors in this population is not warranted when performing fecal VOC analysis in the first three weeks of life. MDPI 2020-05-11 /pmc/articles/PMC7277672/ /pubmed/32403393 http://dx.doi.org/10.3390/bios10050050 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Deianova, Nancy
el Manouni el Hassani, Sofia
Niemarkt, Hendrik J.
Cossey, Veerle
van Kaam, Anton H.
Jenken, Floor
van Weissenbruch, Mirjam M.
Doedes, Esmee M.
Baelde, Kyra
Menezes, Renee
Benninga, Marc A.
de Jonge, Wouter J.
de Boer, Nanne K.
de Meij, Tim G.
Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study
title Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study
title_full Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study
title_fullStr Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study
title_full_unstemmed Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study
title_short Fecal Volatile Organic Compound Profiles are Not Influenced by Gestational Age and Mode of Delivery: A Longitudinal Multicenter Cohort Study
title_sort fecal volatile organic compound profiles are not influenced by gestational age and mode of delivery: a longitudinal multicenter cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277672/
https://www.ncbi.nlm.nih.gov/pubmed/32403393
http://dx.doi.org/10.3390/bios10050050
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