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Microbial changes in stool, saliva, serum, and urine before and after anti-TNF-alpha therapy in patients with inflammatory bowel diseases

Cited 9 time in Web of Science Cited 11 time in Scopus
Authors

Park, Yong Eun; Moon, Hye Su; Yong, Dongeun; Seo, Hochan; Yang, Jinho; Shin, Tae-Seop; Kim, Yoon-Keun; Kim, Jin Ran; Lee, Yoo Na; Kim, Young-Ho; Kim, Joo Sung; Cheon, Jae Hee

Issue Date
2022-04
Publisher
Nature Publishing Group
Citation
Scientific Reports, Vol.12 No.1, p. 6359
Abstract
Inflammatory bowel diseases (IBD), including Crohn's disease and ulcerative colitis, are chronic immune-mediated intestinal inflammatory disorders associated with microbial dysbiosis at multiple sites, particularly the gut. Anti-tumor necrosis factor-alpha (TNF-alpha) agents are important treatments for IBD. We investigated whether microbiome changes at multiple sites can predict the effectiveness of such treatment in IBD. Stool, saliva, serum, and urine biosamples were collected from 19 IBD patients before (V1) and 3 months after (V2) anti-TNF-alpha treatment, and 19 healthy subjects (control). Microbiota analysis was performed using extracellular vesicles (EVs; all four sample types) and next-generation sequencing (NGS; stool and saliva). The stool, using NGS analysis, was the only sample type in which alpha-diversity differed significantly between the IBD and control groups at V1 and V2. Relative to non-responders, responders to anti-TNF-alpha treatment had significantly higher levels of Firmicutes (phylum), Clostridia (class), and Ruminococcaceae (family) in V1 stool, and Prevotella in V1 saliva. Non-responders had significantly higher V2 serum and urine levels of Lachnospiraceae than responders. Finally, Acidovorax caeni was detected in all V1 sample types in responders, but was not detected in non-responders. Microbiome changes at multiple sites may predict the effectiveness of anti-TNF-alpha treatment in IBD, warranting further research.
ISSN
2045-2322
URI
https://hdl.handle.net/10371/184766
DOI
https://doi.org/10.1038/s41598-022-10450-2
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