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Disorders of gut microbiota in children with Tetralogy of Fallot

BACKGROUND: Gut microbiota plays an important role in cardiovascular health and disease, including congenital heart disease (CHD). Tetralogy of Fallot (TOF) is the most common form of cyanotic CHD characterized by systemic chronic hypoxia and sustained pressure overload of the right ventricle. It is...

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Autores principales: Liu, Xiang, Lu, Shaoyou, Shao, Yijia, Zhang, Duo, Tu, Jiazichao, Chen, Jimei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976677/
https://www.ncbi.nlm.nih.gov/pubmed/35378966
http://dx.doi.org/10.21037/tp-22-33
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author Liu, Xiang
Lu, Shaoyou
Shao, Yijia
Zhang, Duo
Tu, Jiazichao
Chen, Jimei
author_facet Liu, Xiang
Lu, Shaoyou
Shao, Yijia
Zhang, Duo
Tu, Jiazichao
Chen, Jimei
author_sort Liu, Xiang
collection PubMed
description BACKGROUND: Gut microbiota plays an important role in cardiovascular health and disease, including congenital heart disease (CHD). Tetralogy of Fallot (TOF) is the most common form of cyanotic CHD characterized by systemic chronic hypoxia and sustained pressure overload of the right ventricle. It is well-known that hypoxia and pressure overload can affect gut microbiota. However, the effects of TOF on the gut microbiota remain little understood. This study explored the profile of the gut microbiota in children with unrepaired TOF. METHODS: A total of 12 pediatric patients diagnosed with TOF and 9 healthy age- and gender-matched children were enrolled in this study. Fecal samples were collected from every participant and subjected to 16S rDNA gene sequencing. The raw sequencing data were processed using the Quantitative Insights Into Microbial Ecology pipeline. RESULTS: A comparison of the gut microbiota revealed that pediatric patients with TOF had developed dysbiosis as reflected by the altered taxonomic composition and impaired functional profile. A total of 14 indicative bacterial genera were identified as differential biomarkers capable of distinguishing between healthy children and TOF patients. Furthermore, functional annotations revealed that the gut microbiota in TOF patients was characterized by increased levels of inflammatory, oxidative, and immune responses, and decreased activities of adaptation, synthesis, and metabolism. CONCLUSIONS: Pediatric patients with unrepaired TOF have intestinal dysbacteriosis that is characterized by altered taxonomic composition and impaired functional profile. These findings suggested that the interplay between gut microbiota and the host may be dysregulated in patients with TOF.
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spelling pubmed-89766772022-04-03 Disorders of gut microbiota in children with Tetralogy of Fallot Liu, Xiang Lu, Shaoyou Shao, Yijia Zhang, Duo Tu, Jiazichao Chen, Jimei Transl Pediatr Original Article BACKGROUND: Gut microbiota plays an important role in cardiovascular health and disease, including congenital heart disease (CHD). Tetralogy of Fallot (TOF) is the most common form of cyanotic CHD characterized by systemic chronic hypoxia and sustained pressure overload of the right ventricle. It is well-known that hypoxia and pressure overload can affect gut microbiota. However, the effects of TOF on the gut microbiota remain little understood. This study explored the profile of the gut microbiota in children with unrepaired TOF. METHODS: A total of 12 pediatric patients diagnosed with TOF and 9 healthy age- and gender-matched children were enrolled in this study. Fecal samples were collected from every participant and subjected to 16S rDNA gene sequencing. The raw sequencing data were processed using the Quantitative Insights Into Microbial Ecology pipeline. RESULTS: A comparison of the gut microbiota revealed that pediatric patients with TOF had developed dysbiosis as reflected by the altered taxonomic composition and impaired functional profile. A total of 14 indicative bacterial genera were identified as differential biomarkers capable of distinguishing between healthy children and TOF patients. Furthermore, functional annotations revealed that the gut microbiota in TOF patients was characterized by increased levels of inflammatory, oxidative, and immune responses, and decreased activities of adaptation, synthesis, and metabolism. CONCLUSIONS: Pediatric patients with unrepaired TOF have intestinal dysbacteriosis that is characterized by altered taxonomic composition and impaired functional profile. These findings suggested that the interplay between gut microbiota and the host may be dysregulated in patients with TOF. AME Publishing Company 2022-03 /pmc/articles/PMC8976677/ /pubmed/35378966 http://dx.doi.org/10.21037/tp-22-33 Text en 2022 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Liu, Xiang
Lu, Shaoyou
Shao, Yijia
Zhang, Duo
Tu, Jiazichao
Chen, Jimei
Disorders of gut microbiota in children with Tetralogy of Fallot
title Disorders of gut microbiota in children with Tetralogy of Fallot
title_full Disorders of gut microbiota in children with Tetralogy of Fallot
title_fullStr Disorders of gut microbiota in children with Tetralogy of Fallot
title_full_unstemmed Disorders of gut microbiota in children with Tetralogy of Fallot
title_short Disorders of gut microbiota in children with Tetralogy of Fallot
title_sort disorders of gut microbiota in children with tetralogy of fallot
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976677/
https://www.ncbi.nlm.nih.gov/pubmed/35378966
http://dx.doi.org/10.21037/tp-22-33
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