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Gut microbiome pattern in adolescents with functional gastrointestinal disease
BACKGROUND: Functional gastrointestinal disease (FGID) has a worldwide prevalence of 10–45%, and is one of the most common causes of recurrent abdominal pain in children. FGID is characterized with abdominal discomfort and changes in bowel movement. Alteration in gut microbiota is associated with FG...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
King Faisal Specialist Hospital and Research Centre
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602920/ https://www.ncbi.nlm.nih.gov/pubmed/31304222 http://dx.doi.org/10.1016/j.ijpam.2019.01.005 |
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author | Nafarin, Andrew R. Hegar, Badriul Sjakti, Hikari A. Vandenplas, Yvan |
author_facet | Nafarin, Andrew R. Hegar, Badriul Sjakti, Hikari A. Vandenplas, Yvan |
author_sort | Nafarin, Andrew R. |
collection | PubMed |
description | BACKGROUND: Functional gastrointestinal disease (FGID) has a worldwide prevalence of 10–45%, and is one of the most common causes of recurrent abdominal pain in children. FGID is characterized with abdominal discomfort and changes in bowel movement. Alteration in gut microbiota is associated with FGID, but data are limited, and there are no data from Indonesia. METHODS: A case–control study was conducted in 22 FGID children and 28 healthy subjects aged 13–18 years at the junior high school and senior high school in Central Jakarta. FGID was diagnosed using Rome IV criteria. Age, sex, and level of education were recorded. Stool samples were collected and investigated for Bifidobacterium spp. and Enterobacteriaceae. RESULTS: Most of the FGID subjects were females (17/22), with a median age of 16 years. The median values of Bifidobacterium spp. were 138.95 (range: 0.2–22,735.8) CFU/gram for the FGID subjects and 232.5 (range: 1.9–38,985.6) CFU/gram in healthy subjects, which showed no statistically significant difference (P = .49). The median values of Enterobacteriaceae were 58.9 (range: 2.5–9577.8) CFU/gram in FGID subjects and 85 (range: 12.1–3139.4) CFU/gram in healthy subjects, which showed no statistically significant difference (P = .94). Our findings indicate that the gut microbiome of adolescents with FGIDs is characterized by a huge variability in levels of Bifidobacterium spp. and Enterobacteriaceae. CONCLUSION: Because of the wide range detected in the number of Bifidobacterium spp. and Enterobacteriaceae in FGID and healthy subjects, no statistically significant difference was observed. More studies in larger groups of selected patients may be needed. |
format | Online Article Text |
id | pubmed-6602920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | King Faisal Specialist Hospital and Research Centre |
record_format | MEDLINE/PubMed |
spelling | pubmed-66029202019-07-12 Gut microbiome pattern in adolescents with functional gastrointestinal disease Nafarin, Andrew R. Hegar, Badriul Sjakti, Hikari A. Vandenplas, Yvan Int J Pediatr Adolesc Med Original Research Article BACKGROUND: Functional gastrointestinal disease (FGID) has a worldwide prevalence of 10–45%, and is one of the most common causes of recurrent abdominal pain in children. FGID is characterized with abdominal discomfort and changes in bowel movement. Alteration in gut microbiota is associated with FGID, but data are limited, and there are no data from Indonesia. METHODS: A case–control study was conducted in 22 FGID children and 28 healthy subjects aged 13–18 years at the junior high school and senior high school in Central Jakarta. FGID was diagnosed using Rome IV criteria. Age, sex, and level of education were recorded. Stool samples were collected and investigated for Bifidobacterium spp. and Enterobacteriaceae. RESULTS: Most of the FGID subjects were females (17/22), with a median age of 16 years. The median values of Bifidobacterium spp. were 138.95 (range: 0.2–22,735.8) CFU/gram for the FGID subjects and 232.5 (range: 1.9–38,985.6) CFU/gram in healthy subjects, which showed no statistically significant difference (P = .49). The median values of Enterobacteriaceae were 58.9 (range: 2.5–9577.8) CFU/gram in FGID subjects and 85 (range: 12.1–3139.4) CFU/gram in healthy subjects, which showed no statistically significant difference (P = .94). Our findings indicate that the gut microbiome of adolescents with FGIDs is characterized by a huge variability in levels of Bifidobacterium spp. and Enterobacteriaceae. CONCLUSION: Because of the wide range detected in the number of Bifidobacterium spp. and Enterobacteriaceae in FGID and healthy subjects, no statistically significant difference was observed. More studies in larger groups of selected patients may be needed. King Faisal Specialist Hospital and Research Centre 2019-03 2019-02-02 /pmc/articles/PMC6602920/ /pubmed/31304222 http://dx.doi.org/10.1016/j.ijpam.2019.01.005 Text en © 2019 Publishing services provided by Elsevier B.V. on behalf of King Faisal Specialist Hospital & Research Centre (General Organization), Saudi Arabia. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Article Nafarin, Andrew R. Hegar, Badriul Sjakti, Hikari A. Vandenplas, Yvan Gut microbiome pattern in adolescents with functional gastrointestinal disease |
title | Gut microbiome pattern in adolescents with functional gastrointestinal disease |
title_full | Gut microbiome pattern in adolescents with functional gastrointestinal disease |
title_fullStr | Gut microbiome pattern in adolescents with functional gastrointestinal disease |
title_full_unstemmed | Gut microbiome pattern in adolescents with functional gastrointestinal disease |
title_short | Gut microbiome pattern in adolescents with functional gastrointestinal disease |
title_sort | gut microbiome pattern in adolescents with functional gastrointestinal disease |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602920/ https://www.ncbi.nlm.nih.gov/pubmed/31304222 http://dx.doi.org/10.1016/j.ijpam.2019.01.005 |
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