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Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema

BACKGROUND: Studies have suggested that selective microbial targets prevail in the fecal microbiota of infants with eczema. This study evaluated the composition of fecal microbiota of infants who developed eczema in the first 5 years of life and compared these with those of healthy controls. FINDING...

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Autores principales: Yap, Gaik Chin, Loo, Evelyn Xiu Ling, Aw, Marion, Lu, Qingshu, Shek, Lynette Pei-Chi, Lee, Bee Wah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994565/
https://www.ncbi.nlm.nih.gov/pubmed/24650346
http://dx.doi.org/10.1186/1756-0500-7-166
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author Yap, Gaik Chin
Loo, Evelyn Xiu Ling
Aw, Marion
Lu, Qingshu
Shek, Lynette Pei-Chi
Lee, Bee Wah
author_facet Yap, Gaik Chin
Loo, Evelyn Xiu Ling
Aw, Marion
Lu, Qingshu
Shek, Lynette Pei-Chi
Lee, Bee Wah
author_sort Yap, Gaik Chin
collection PubMed
description BACKGROUND: Studies have suggested that selective microbial targets prevail in the fecal microbiota of infants with eczema. This study evaluated the composition of fecal microbiota of infants who developed eczema in the first 5 years of life and compared these with those of healthy controls. FINDINGS: Children who developed eczema in the first 2 years, those with eczema at 5 years of age and healthy controls were selected from the placebo arm of a birth cohort of at-risk infants participating in a randomized double-blind trial on the protective effects of supplemental probiotics in early life on allergic outcomes. Molecular evaluation of fecal microbiota were conducted using Fluorescence In Situ Hybridization-Flow Cytometry (FISH-FC) for fecal samples collected. Longitudinal analysis of fecal microbiota composition at three days, one and three months and one year of life revealed higher abundance of Enterobacteriaceae [coefficient (B): 1.081, 95% CI: 0.229-1.933, adj p = 0.014] and Clostridium perfringens [coefficient (B): 0.521, 95% CI: 0.556-0.988, adj p = 0.03] in those who developed eczema in the first 2 years life. In those with eczema at 5 years of age, a lower abundance of Bifidobacterium was observed [coefficient (B): -27.635, 95% CI: -50.040 - -5.231, adj p = 0.018]. CONCLUSIONS: The differences in infant fecal microbiota observed in eczema subjects in this study support the notion that relative abundance of selective microbial targets may contribute to the subsequent development of eczema in childhood.
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spelling pubmed-39945652014-04-23 Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema Yap, Gaik Chin Loo, Evelyn Xiu Ling Aw, Marion Lu, Qingshu Shek, Lynette Pei-Chi Lee, Bee Wah BMC Res Notes Short Report BACKGROUND: Studies have suggested that selective microbial targets prevail in the fecal microbiota of infants with eczema. This study evaluated the composition of fecal microbiota of infants who developed eczema in the first 5 years of life and compared these with those of healthy controls. FINDINGS: Children who developed eczema in the first 2 years, those with eczema at 5 years of age and healthy controls were selected from the placebo arm of a birth cohort of at-risk infants participating in a randomized double-blind trial on the protective effects of supplemental probiotics in early life on allergic outcomes. Molecular evaluation of fecal microbiota were conducted using Fluorescence In Situ Hybridization-Flow Cytometry (FISH-FC) for fecal samples collected. Longitudinal analysis of fecal microbiota composition at three days, one and three months and one year of life revealed higher abundance of Enterobacteriaceae [coefficient (B): 1.081, 95% CI: 0.229-1.933, adj p = 0.014] and Clostridium perfringens [coefficient (B): 0.521, 95% CI: 0.556-0.988, adj p = 0.03] in those who developed eczema in the first 2 years life. In those with eczema at 5 years of age, a lower abundance of Bifidobacterium was observed [coefficient (B): -27.635, 95% CI: -50.040 - -5.231, adj p = 0.018]. CONCLUSIONS: The differences in infant fecal microbiota observed in eczema subjects in this study support the notion that relative abundance of selective microbial targets may contribute to the subsequent development of eczema in childhood. BioMed Central 2014-03-20 /pmc/articles/PMC3994565/ /pubmed/24650346 http://dx.doi.org/10.1186/1756-0500-7-166 Text en Copyright © 2014 Yap et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), 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
Yap, Gaik Chin
Loo, Evelyn Xiu Ling
Aw, Marion
Lu, Qingshu
Shek, Lynette Pei-Chi
Lee, Bee Wah
Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema
title Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema
title_full Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema
title_fullStr Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema
title_full_unstemmed Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema
title_short Molecular analysis of infant fecal microbiota in an Asian at-risk cohort–correlates with infant and childhood eczema
title_sort molecular analysis of infant fecal microbiota in an asian at-risk cohort–correlates with infant and childhood eczema
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994565/
https://www.ncbi.nlm.nih.gov/pubmed/24650346
http://dx.doi.org/10.1186/1756-0500-7-166
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