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Is there any association between gut microbiota and type 1 diabetes? A systematic review

INTRODUCTION: Type 1 diabetes (T1D) is the second most common autoimmune disease among children. There is evidence suggesting that dysbiosis of some gut colonizing bacteria are associated with the pathogenesis of T1D. However, these studies are still controversial and a systematic review was conduct...

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Autores principales: Jamshidi, Parnian, Hasanzadeh, Saba, Tahvildari, Azin, Farsi, Yeganeh, Arbabi, Mahta, Mota, João Felipe, Sechi, Leonardo A., Nasiri, Mohammad Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791003/
https://www.ncbi.nlm.nih.gov/pubmed/31636716
http://dx.doi.org/10.1186/s13099-019-0332-7
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author Jamshidi, Parnian
Hasanzadeh, Saba
Tahvildari, Azin
Farsi, Yeganeh
Arbabi, Mahta
Mota, João Felipe
Sechi, Leonardo A.
Nasiri, Mohammad Javad
author_facet Jamshidi, Parnian
Hasanzadeh, Saba
Tahvildari, Azin
Farsi, Yeganeh
Arbabi, Mahta
Mota, João Felipe
Sechi, Leonardo A.
Nasiri, Mohammad Javad
author_sort Jamshidi, Parnian
collection PubMed
description INTRODUCTION: Type 1 diabetes (T1D) is the second most common autoimmune disease among children. There is evidence suggesting that dysbiosis of some gut colonizing bacteria are associated with the pathogenesis of T1D. However, these studies are still controversial and a systematic review was conducted to evaluate the association between gut microbiota and T1D. METHODS: A systematic search was carried out in Medline (Via Pubmed) and Embase from January 2000 to January 2019 for all original cross-sectional, cohort, case–control or nested case–control studies investigating the association between gut microbiota and T1D. RESULTS: Of 568 articles identified, 26 studies met the inclusion criteria. The total population study of these articles consists of 2600 children (under 18 years old) and 189 adults. Among the included studies, 24 articles confirmed the association between gut microbiota dysbiosis and T1D. The most common bacterial alterations in T1D patients included Bacteroides spp., Streptococcus spp., Clostridium spp., Bifidobacterium spp., Prevotella spp., Staphylococcus spp., Blautia spp., Faecalibacterium spp., Roseburia spp., and Lactobacillus spp. CONCLUSION: Our study showed a significant association between alterations in intestinal microbial composition and T1D; however, in some articles, it is not clear which one happens first. Investigation of altered gut microbiota can help in the early detection of T1D before seropositivity. Targeted microbiome modulation can be a novel potential therapeutic strategy.
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spelling pubmed-67910032019-10-21 Is there any association between gut microbiota and type 1 diabetes? A systematic review Jamshidi, Parnian Hasanzadeh, Saba Tahvildari, Azin Farsi, Yeganeh Arbabi, Mahta Mota, João Felipe Sechi, Leonardo A. Nasiri, Mohammad Javad Gut Pathog Review INTRODUCTION: Type 1 diabetes (T1D) is the second most common autoimmune disease among children. There is evidence suggesting that dysbiosis of some gut colonizing bacteria are associated with the pathogenesis of T1D. However, these studies are still controversial and a systematic review was conducted to evaluate the association between gut microbiota and T1D. METHODS: A systematic search was carried out in Medline (Via Pubmed) and Embase from January 2000 to January 2019 for all original cross-sectional, cohort, case–control or nested case–control studies investigating the association between gut microbiota and T1D. RESULTS: Of 568 articles identified, 26 studies met the inclusion criteria. The total population study of these articles consists of 2600 children (under 18 years old) and 189 adults. Among the included studies, 24 articles confirmed the association between gut microbiota dysbiosis and T1D. The most common bacterial alterations in T1D patients included Bacteroides spp., Streptococcus spp., Clostridium spp., Bifidobacterium spp., Prevotella spp., Staphylococcus spp., Blautia spp., Faecalibacterium spp., Roseburia spp., and Lactobacillus spp. CONCLUSION: Our study showed a significant association between alterations in intestinal microbial composition and T1D; however, in some articles, it is not clear which one happens first. Investigation of altered gut microbiota can help in the early detection of T1D before seropositivity. Targeted microbiome modulation can be a novel potential therapeutic strategy. BioMed Central 2019-10-14 /pmc/articles/PMC6791003/ /pubmed/31636716 http://dx.doi.org/10.1186/s13099-019-0332-7 Text en © The Author(s) 2019 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 Review
Jamshidi, Parnian
Hasanzadeh, Saba
Tahvildari, Azin
Farsi, Yeganeh
Arbabi, Mahta
Mota, João Felipe
Sechi, Leonardo A.
Nasiri, Mohammad Javad
Is there any association between gut microbiota and type 1 diabetes? A systematic review
title Is there any association between gut microbiota and type 1 diabetes? A systematic review
title_full Is there any association between gut microbiota and type 1 diabetes? A systematic review
title_fullStr Is there any association between gut microbiota and type 1 diabetes? A systematic review
title_full_unstemmed Is there any association between gut microbiota and type 1 diabetes? A systematic review
title_short Is there any association between gut microbiota and type 1 diabetes? A systematic review
title_sort is there any association between gut microbiota and type 1 diabetes? a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791003/
https://www.ncbi.nlm.nih.gov/pubmed/31636716
http://dx.doi.org/10.1186/s13099-019-0332-7
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