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Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases

PURPOSE: The gut microbiota can influence several diseases through immune modulation; however, the exact role of microbes such as Clostridium difficileand the relationship between microbiota colonization and allergic diseases are not well known. This study aimed to determine the relationship between...

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Autores principales: Lee, Sun Hwa, Gong, Yun Na, Ryoo, Eell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461278/
https://www.ncbi.nlm.nih.gov/pubmed/28592977
http://dx.doi.org/10.3345/kjp.2017.60.5.145
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author Lee, Sun Hwa
Gong, Yun Na
Ryoo, Eell
author_facet Lee, Sun Hwa
Gong, Yun Na
Ryoo, Eell
author_sort Lee, Sun Hwa
collection PubMed
description PURPOSE: The gut microbiota can influence several diseases through immune modulation; however, the exact role of microbes such as Clostridium difficileand the relationship between microbiota colonization and allergic diseases are not well known. This study aimed to determine the relationship between C. difficilecolonization and/or infection (CDCI) during infancy and allergic diseases during early childhood. METHODS: Infants 1–12 months of age presenting changes in bowel habits for more than 2 weeks were enrolled in this study. After dividing them into 2 groups according to the presence and absence of C. difficile, the risk of allergic disease development during childhood was identified and compared. RESULTS: Sixty-five patients were included in this study; 22 (33.8%) were diagnosed with CDCI. No significant differences were observed in baseline characteristics between the C. difficile-positive and -negative groups except for antibiotic exposure (22.7% vs. 60.5%, P=0.004). Compared to the C. difficile-negative group, the risk of developing at least one allergic disease was higher in the C. difficile-positive group after adjusting other variables (adjusted odds ratios, 5.61; 95% confidence interval, 1.52–20.74; P=0.007). Furthermore, food allergies were more prevalent in the C. difficile-positive group (P=0.03). CONCLUSION: CDCI during infancy were associated with a higher risk of developing allergic diseases during early childhood. These results suggest that CDCI during infancy might reflect the reduced diversity of the intestinal microbiota, which is associated with an increased risk of allergic sensitization. To identify the underlying mechanism, further investigation and a larger cohort study will be needed.
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spelling pubmed-54612782017-06-07 Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases Lee, Sun Hwa Gong, Yun Na Ryoo, Eell Korean J Pediatr Original Article PURPOSE: The gut microbiota can influence several diseases through immune modulation; however, the exact role of microbes such as Clostridium difficileand the relationship between microbiota colonization and allergic diseases are not well known. This study aimed to determine the relationship between C. difficilecolonization and/or infection (CDCI) during infancy and allergic diseases during early childhood. METHODS: Infants 1–12 months of age presenting changes in bowel habits for more than 2 weeks were enrolled in this study. After dividing them into 2 groups according to the presence and absence of C. difficile, the risk of allergic disease development during childhood was identified and compared. RESULTS: Sixty-five patients were included in this study; 22 (33.8%) were diagnosed with CDCI. No significant differences were observed in baseline characteristics between the C. difficile-positive and -negative groups except for antibiotic exposure (22.7% vs. 60.5%, P=0.004). Compared to the C. difficile-negative group, the risk of developing at least one allergic disease was higher in the C. difficile-positive group after adjusting other variables (adjusted odds ratios, 5.61; 95% confidence interval, 1.52–20.74; P=0.007). Furthermore, food allergies were more prevalent in the C. difficile-positive group (P=0.03). CONCLUSION: CDCI during infancy were associated with a higher risk of developing allergic diseases during early childhood. These results suggest that CDCI during infancy might reflect the reduced diversity of the intestinal microbiota, which is associated with an increased risk of allergic sensitization. To identify the underlying mechanism, further investigation and a larger cohort study will be needed. The Korean Pediatric Society 2017-05 2017-05-31 /pmc/articles/PMC5461278/ /pubmed/28592977 http://dx.doi.org/10.3345/kjp.2017.60.5.145 Text en Copyright © 2017 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Sun Hwa
Gong, Yun Na
Ryoo, Eell
Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases
title Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases
title_full Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases
title_fullStr Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases
title_full_unstemmed Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases
title_short Clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases
title_sort clostridium difficile colonization and/or infection during infancy and the risk of childhood allergic diseases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461278/
https://www.ncbi.nlm.nih.gov/pubmed/28592977
http://dx.doi.org/10.3345/kjp.2017.60.5.145
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