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Intestinal microbiota composition after antibiotic treatment in early life: the INCA study

BACKGROUND: The acquisition and development of infant gut microbiota can be influenced by numerous factors, of which early antibiotic treatment is an important one. However, studies on the effects of antibiotic treatment in early life on clinical outcomes and establishment and development of the gut...

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Autores principales: Rutten, N. B. M. M., Rijkers, G. T., Meijssen, C. B., Crijns, C. E., Oudshoorn, J. H., van der Ent, C. K., Vlieger, A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673740/
https://www.ncbi.nlm.nih.gov/pubmed/26645894
http://dx.doi.org/10.1186/s12887-015-0519-0
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author Rutten, N. B. M. M.
Rijkers, G. T.
Meijssen, C. B.
Crijns, C. E.
Oudshoorn, J. H.
van der Ent, C. K.
Vlieger, A. M.
author_facet Rutten, N. B. M. M.
Rijkers, G. T.
Meijssen, C. B.
Crijns, C. E.
Oudshoorn, J. H.
van der Ent, C. K.
Vlieger, A. M.
author_sort Rutten, N. B. M. M.
collection PubMed
description BACKGROUND: The acquisition and development of infant gut microbiota can be influenced by numerous factors, of which early antibiotic treatment is an important one. However, studies on the effects of antibiotic treatment in early life on clinical outcomes and establishment and development of the gut microbiota of term infants are limited. Disturbed microbiota composition is hypothesized to be an underlying mechanism of an aberrant development of the immune system. This study aims to investigate the potential clinical and microbial consequences of empiric antibiotic use in early life. METHODS/DESIGN: 450 term born infants, of whom 150 are exposed to antibiotic treatment in early life and 300 are not (control group), are included in this observational cohort study with a one-year follow-up. Clinical outcomes, including coughing, wheezing, fever >38 °C, runny nose, glue ear, rash, diarrhea and >3 crying hours a day, are recorded daily by parents and examined by previously defined doctor’s diagnosis. A blood sample is taken at closure to investigate the infant’s vaccination response and sensitization for food and inhalant allergens. Fecal samples are obtained at eight time points during the first year of life. Potential differences in microbial profiles of infants treated with antibiotics versus healthy controls will be determined by use of 16S-23S rRNA gene analysis (IS-pro). Microbiota composition will be described by means of abundance, diversity and (dis)similarity. Diversity is calculated using the Shannon index. Dissimilarities between samples are calculated as the cosine distance between each pair of samples and analyzed with principal coordinate analysis. Clinical variables and possible associations are assessed by appropriate statistics. DISCUSSION: Both clinical quantitative and qualitative microbial effects of antibiotic treatment in early life may be demonstrated. These findings can be important, since there is evidence that manipulation of the infant microbiota by using pre- or probiotics can restore the ecological balance of the microbiota and may mitigate potential negative effects on the developing immune system, when use of antibiotics cannot be avoided. TRIAL REGISTRATION: ClinicalTrials.gov NCT02536560. Registered 28 August 2015.
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spelling pubmed-46737402015-12-10 Intestinal microbiota composition after antibiotic treatment in early life: the INCA study Rutten, N. B. M. M. Rijkers, G. T. Meijssen, C. B. Crijns, C. E. Oudshoorn, J. H. van der Ent, C. K. Vlieger, A. M. BMC Pediatr Study Protocol BACKGROUND: The acquisition and development of infant gut microbiota can be influenced by numerous factors, of which early antibiotic treatment is an important one. However, studies on the effects of antibiotic treatment in early life on clinical outcomes and establishment and development of the gut microbiota of term infants are limited. Disturbed microbiota composition is hypothesized to be an underlying mechanism of an aberrant development of the immune system. This study aims to investigate the potential clinical and microbial consequences of empiric antibiotic use in early life. METHODS/DESIGN: 450 term born infants, of whom 150 are exposed to antibiotic treatment in early life and 300 are not (control group), are included in this observational cohort study with a one-year follow-up. Clinical outcomes, including coughing, wheezing, fever >38 °C, runny nose, glue ear, rash, diarrhea and >3 crying hours a day, are recorded daily by parents and examined by previously defined doctor’s diagnosis. A blood sample is taken at closure to investigate the infant’s vaccination response and sensitization for food and inhalant allergens. Fecal samples are obtained at eight time points during the first year of life. Potential differences in microbial profiles of infants treated with antibiotics versus healthy controls will be determined by use of 16S-23S rRNA gene analysis (IS-pro). Microbiota composition will be described by means of abundance, diversity and (dis)similarity. Diversity is calculated using the Shannon index. Dissimilarities between samples are calculated as the cosine distance between each pair of samples and analyzed with principal coordinate analysis. Clinical variables and possible associations are assessed by appropriate statistics. DISCUSSION: Both clinical quantitative and qualitative microbial effects of antibiotic treatment in early life may be demonstrated. These findings can be important, since there is evidence that manipulation of the infant microbiota by using pre- or probiotics can restore the ecological balance of the microbiota and may mitigate potential negative effects on the developing immune system, when use of antibiotics cannot be avoided. TRIAL REGISTRATION: ClinicalTrials.gov NCT02536560. Registered 28 August 2015. BioMed Central 2015-12-09 /pmc/articles/PMC4673740/ /pubmed/26645894 http://dx.doi.org/10.1186/s12887-015-0519-0 Text en © Rutten et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Study Protocol
Rutten, N. B. M. M.
Rijkers, G. T.
Meijssen, C. B.
Crijns, C. E.
Oudshoorn, J. H.
van der Ent, C. K.
Vlieger, A. M.
Intestinal microbiota composition after antibiotic treatment in early life: the INCA study
title Intestinal microbiota composition after antibiotic treatment in early life: the INCA study
title_full Intestinal microbiota composition after antibiotic treatment in early life: the INCA study
title_fullStr Intestinal microbiota composition after antibiotic treatment in early life: the INCA study
title_full_unstemmed Intestinal microbiota composition after antibiotic treatment in early life: the INCA study
title_short Intestinal microbiota composition after antibiotic treatment in early life: the INCA study
title_sort intestinal microbiota composition after antibiotic treatment in early life: the inca study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673740/
https://www.ncbi.nlm.nih.gov/pubmed/26645894
http://dx.doi.org/10.1186/s12887-015-0519-0
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