Your browser doesn't support javascript.
loading
Potential of Gut Microbe-Derived Extracellular Vesicles to Differentiate Inflammatory Bowel Disease Patients from Healthy Controls.
Heo, Min; Park, Young Soo; Yoon, Hyuk; Kim, Nam-Eun; Kim, Kangjin; Shin, Cheol Min; Kim, Nayoung; Lee, Dong Ho.
Afiliação
  • Heo M; Interdisciplinary Program of Bioinformatics, College of Natural Sciences, Seoul National University, Seoul, Korea.
  • Park YS; Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
  • Yoon H; Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
  • Kim NE; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Kim K; Department of Public Health Science, Graduate School of Public Health, Seoul, Korea.
  • Shin CM; Institute of Health and Environment, Seoul National University, Seoul, Korea.
  • Kim N; Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
  • Lee DH; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Gut Liver ; 17(1): 108-118, 2023 01 15.
Article em En | MEDLINE | ID: mdl-36424722
ABSTRACT
Background/

Aims:

This study aimed to evaluate the potential of the stool microbiome and gut microbe-derived extracellular vesicles (EVs) to differentiate between patients with inflammatory bowel disease (IBD) and healthy controls, and to predict relapse in patients with IBD.

Methods:

Metagenomic profiling of the microbiome and bacterial EVs in stool samples of controls (n=110) and patients with IBD (n=110) was performed using 16S rRNA sequencing and then compared. Patients with IBD were divided into two enterotypes based on their microbiome, and the cumulative risk of relapse was evaluated.

Results:

There was a significant difference in the composition of the stool microbiome and gut microbe-derived EVs between patients with IBD and controls. The alpha diversity of the microbiome in patients with IBD was significantly lower than that in controls, while the beta diversity also differed significantly between the two groups. These findings were more prominent in gut microbe-derived EVs than in the stool microbiome. The survival curve tended to be different for enterotypes based on the gut microbe-derived EVs; however, this difference was not statistically significant (log-rank test, p=0.166). In the multivariable analysis, elevated fecal calprotectin (>250 mg/kg) was the only significant risk factor associated with relapse (adjusted hazard ratio, 3.147; 95% confidence interval, 1.545 to 6.408; p=0.002).

Conclusions:

Analysis of gut microbe-derived EVs is better at differentiating patients with IBD from healthy controls than stool microbiome analysis.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Vesículas Extracelulares / Microbioma Gastrointestinal Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Vesículas Extracelulares / Microbioma Gastrointestinal Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article