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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
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.
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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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