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Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome

BACKGROUND: The composition of the intestinal microbiota seems to be an important factor in determining the clinical outcome in children with short bowel syndrome (SBS). Alterations in the microbiota may result in serious complications such as small bowel bacterial overgrowth (SBBO) and intestinal m...

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Autores principales: Engstrand Lilja, Helene, Wefer, Hugo, Nyström, Niklas, Finkel, Yigael, Engstrand, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418071/
https://www.ncbi.nlm.nih.gov/pubmed/25941569
http://dx.doi.org/10.1186/s40168-015-0084-7
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author Engstrand Lilja, Helene
Wefer, Hugo
Nyström, Niklas
Finkel, Yigael
Engstrand, Lars
author_facet Engstrand Lilja, Helene
Wefer, Hugo
Nyström, Niklas
Finkel, Yigael
Engstrand, Lars
author_sort Engstrand Lilja, Helene
collection PubMed
description BACKGROUND: The composition of the intestinal microbiota seems to be an important factor in determining the clinical outcome in children with short bowel syndrome (SBS). Alterations in the microbiota may result in serious complications such as small bowel bacterial overgrowth (SBBO) and intestinal mucosal inflammation that lead to prolonged parenteral nutrition (PN) dependency with subsequently increased risk of liver failure and sepsis. To date, there are no reported mappings of the intestinal microbiome in children with SBS. Here, we present the first report on the intestinal microbial community profile in children with SBS. FINDINGS: The study includes children diagnosed with SBS in the neonatal period. Healthy siblings served as controls. Fecal samples were collected, and microbial profiles were analyzed by using 16S rRNA gene sequencing on the Illumina MiSeq platform. We observed a pronounced microbial dysbiosis in children with SBS on PN treatment with an increased and totally dominating relative abundance of Enterobacteriacae in four out of five children compared to children with SBS weaned from PN and healthy siblings. CONCLUSIONS: The overall decreased bacterial diversity in children with SBS is consistent with intestinal microbiome mappings in inflammatory bowel diseases such as Crohn’s disease and necrotizing enterocolitis in preterm infants. Our findings indicate that intestinal dysbiosis in children with SBS is associated with prolonged PN dependency. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0084-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-44180712015-05-05 Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome Engstrand Lilja, Helene Wefer, Hugo Nyström, Niklas Finkel, Yigael Engstrand, Lars Microbiome Short Report BACKGROUND: The composition of the intestinal microbiota seems to be an important factor in determining the clinical outcome in children with short bowel syndrome (SBS). Alterations in the microbiota may result in serious complications such as small bowel bacterial overgrowth (SBBO) and intestinal mucosal inflammation that lead to prolonged parenteral nutrition (PN) dependency with subsequently increased risk of liver failure and sepsis. To date, there are no reported mappings of the intestinal microbiome in children with SBS. Here, we present the first report on the intestinal microbial community profile in children with SBS. FINDINGS: The study includes children diagnosed with SBS in the neonatal period. Healthy siblings served as controls. Fecal samples were collected, and microbial profiles were analyzed by using 16S rRNA gene sequencing on the Illumina MiSeq platform. We observed a pronounced microbial dysbiosis in children with SBS on PN treatment with an increased and totally dominating relative abundance of Enterobacteriacae in four out of five children compared to children with SBS weaned from PN and healthy siblings. CONCLUSIONS: The overall decreased bacterial diversity in children with SBS is consistent with intestinal microbiome mappings in inflammatory bowel diseases such as Crohn’s disease and necrotizing enterocolitis in preterm infants. Our findings indicate that intestinal dysbiosis in children with SBS is associated with prolonged PN dependency. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0084-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-04 /pmc/articles/PMC4418071/ /pubmed/25941569 http://dx.doi.org/10.1186/s40168-015-0084-7 Text en © Engstrand Lilja et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Engstrand Lilja, Helene
Wefer, Hugo
Nyström, Niklas
Finkel, Yigael
Engstrand, Lars
Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome
title Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome
title_full Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome
title_fullStr Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome
title_full_unstemmed Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome
title_short Intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome
title_sort intestinal dysbiosis in children with short bowel syndrome is associated with impaired outcome
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418071/
https://www.ncbi.nlm.nih.gov/pubmed/25941569
http://dx.doi.org/10.1186/s40168-015-0084-7
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