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Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts
OBJECTIVE: To compare faecal microbial composition in patients with systemic sclerosis (SSc) from 2 independent cohorts with controls and to determine whether certain genera are associated with SSc-gastrointestinal tract (GIT) symptoms. DESIGN: Adult patients with SSc from the University of Californ...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508636/ https://www.ncbi.nlm.nih.gov/pubmed/28761687 http://dx.doi.org/10.1136/bmjgast-2017-000134 |
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author | Volkmann, Elizabeth R Hoffmann-Vold, Anna-Maria Chang, Yu-Ling Jacobs, Jonathan P Tillisch, Kirsten Mayer, Emeran A Clements, Philip J Hov, Johannes R Kummen, Martin Midtvedt, Øyvind Lagishetty, Venu Chang, Lin Labus, Jennifer S Molberg, Øyvind Braun, Jonathan |
author_facet | Volkmann, Elizabeth R Hoffmann-Vold, Anna-Maria Chang, Yu-Ling Jacobs, Jonathan P Tillisch, Kirsten Mayer, Emeran A Clements, Philip J Hov, Johannes R Kummen, Martin Midtvedt, Øyvind Lagishetty, Venu Chang, Lin Labus, Jennifer S Molberg, Øyvind Braun, Jonathan |
author_sort | Volkmann, Elizabeth R |
collection | PubMed |
description | OBJECTIVE: To compare faecal microbial composition in patients with systemic sclerosis (SSc) from 2 independent cohorts with controls and to determine whether certain genera are associated with SSc-gastrointestinal tract (GIT) symptoms. DESIGN: Adult patients with SSc from the University of California, Los Angeles (UCLA) and Oslo University Hospital (OUH) and healthy controls participated in this study (1:1:1). All participants provided stool specimens for 16S rRNA sequencing. Linear discriminant analysis effect size demonstrated genera with differential expression in SSc. Differential expression analysis for sequence count data identified specific genera associated with GIT symptoms as assessed by the GIT 2.0 questionnaire. RESULTS: The UCLA-SSc and OUH-SSc cohorts were similar in age (52.1 and 60.5 years, respectively), disease duration (median (IQR): 6.6 (2.5–16.4) and 7.0 (1.0–19.2) years, respectively), gender distribution (88% and 71%, respectively), and GIT symptoms (mean (SD) total GIT 2.0 scores of 0.7 (0.6) and 0.6 (0.5), respectively). Principal coordinate analysis illustrated significant microbial community differences between SSc and controls (UCLA: p=0.001; OUH: p=0.002). Patients with SSc had significantly lower levels of commensal genera deemed to protect against inflammation, such as Bacteroides (UCLA and OUH), Faecalibacterium (UCLA), Clostridium (OUH); and significantly higher levels of pathobiont genera, such as Fusobacterium (UCLA), compared with controls. Increased abundance of Clostridium was associated with less severe GIT symptoms in both cohorts. CONCLUSIONS: The present analysis detected specific aberrations in the lower GIT microbiota of patients with SSc from 2 geographically and ethnically distinct cohorts. These findings suggest that GIT dysbiosis may be a pathological feature of the SSc disease state. |
format | Online Article Text |
id | pubmed-5508636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55086362017-07-31 Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts Volkmann, Elizabeth R Hoffmann-Vold, Anna-Maria Chang, Yu-Ling Jacobs, Jonathan P Tillisch, Kirsten Mayer, Emeran A Clements, Philip J Hov, Johannes R Kummen, Martin Midtvedt, Øyvind Lagishetty, Venu Chang, Lin Labus, Jennifer S Molberg, Øyvind Braun, Jonathan BMJ Open Gastroenterol Intestinal Microflora OBJECTIVE: To compare faecal microbial composition in patients with systemic sclerosis (SSc) from 2 independent cohorts with controls and to determine whether certain genera are associated with SSc-gastrointestinal tract (GIT) symptoms. DESIGN: Adult patients with SSc from the University of California, Los Angeles (UCLA) and Oslo University Hospital (OUH) and healthy controls participated in this study (1:1:1). All participants provided stool specimens for 16S rRNA sequencing. Linear discriminant analysis effect size demonstrated genera with differential expression in SSc. Differential expression analysis for sequence count data identified specific genera associated with GIT symptoms as assessed by the GIT 2.0 questionnaire. RESULTS: The UCLA-SSc and OUH-SSc cohorts were similar in age (52.1 and 60.5 years, respectively), disease duration (median (IQR): 6.6 (2.5–16.4) and 7.0 (1.0–19.2) years, respectively), gender distribution (88% and 71%, respectively), and GIT symptoms (mean (SD) total GIT 2.0 scores of 0.7 (0.6) and 0.6 (0.5), respectively). Principal coordinate analysis illustrated significant microbial community differences between SSc and controls (UCLA: p=0.001; OUH: p=0.002). Patients with SSc had significantly lower levels of commensal genera deemed to protect against inflammation, such as Bacteroides (UCLA and OUH), Faecalibacterium (UCLA), Clostridium (OUH); and significantly higher levels of pathobiont genera, such as Fusobacterium (UCLA), compared with controls. Increased abundance of Clostridium was associated with less severe GIT symptoms in both cohorts. CONCLUSIONS: The present analysis detected specific aberrations in the lower GIT microbiota of patients with SSc from 2 geographically and ethnically distinct cohorts. These findings suggest that GIT dysbiosis may be a pathological feature of the SSc disease state. BMJ Publishing Group 2017-04-01 /pmc/articles/PMC5508636/ /pubmed/28761687 http://dx.doi.org/10.1136/bmjgast-2017-000134 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Intestinal Microflora Volkmann, Elizabeth R Hoffmann-Vold, Anna-Maria Chang, Yu-Ling Jacobs, Jonathan P Tillisch, Kirsten Mayer, Emeran A Clements, Philip J Hov, Johannes R Kummen, Martin Midtvedt, Øyvind Lagishetty, Venu Chang, Lin Labus, Jennifer S Molberg, Øyvind Braun, Jonathan Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts |
title | Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts |
title_full | Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts |
title_fullStr | Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts |
title_full_unstemmed | Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts |
title_short | Systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts |
title_sort | systemic sclerosis is associated with specific alterations in gastrointestinal microbiota in two independent cohorts |
topic | Intestinal Microflora |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508636/ https://www.ncbi.nlm.nih.gov/pubmed/28761687 http://dx.doi.org/10.1136/bmjgast-2017-000134 |
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