Comparative Analysis of Fecal Microbiota Composition Between Rheumatoid Arthritis and Osteoarthritis Patients

The aim of this study was to investigate differences between the gut microbiota composition in patients with rheumatoid arthritis (RA) and those with osteoarthritis (OA). Stool samples from nine RA patients and nine OA patients were collected, and DNA was extracted. The gut microbiome was assessed u...

Full description

Saved in:
Bibliographic Details
Published inGenes Vol. 10; no. 10; p. 748
Main Authors Lee, Jin-Young, Mannaa, Mohamed, Kim, Yunkyung, Kim, Jehun, Kim, Geun-Tae, Seo, Young-Su
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 25.09.2019
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The aim of this study was to investigate differences between the gut microbiota composition in patients with rheumatoid arthritis (RA) and those with osteoarthritis (OA). Stool samples from nine RA patients and nine OA patients were collected, and DNA was extracted. The gut microbiome was assessed using 16S rRNA gene amplicon sequencing. The structures and differences in the gut microbiome between RA and OA were analyzed. The analysis of diversity revealed no differences in the complexity of samples. The RA group had a lower Bacteroidetes: Firmicutes ratio than did the OA group. Lactobacilli and , particularly , were more abundant in the RA than in the OA group, although these differences were not statistically significant. The relative abundance of Bacteroides and was lower in the RA group. At the species level, the abundance of certain bacterial species was significantly lower in the RA group, such as . The microbial properties of the gut differed between RA and OA patients, and the RA dysbiosis revealed results similar to those of other autoimmune diseases, suggesting that a specific gut microbiota pattern is related to autoimmunity.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
These authors contributed equally to this work.
ISSN:2073-4425
2073-4425
DOI:10.3390/genes10100748