Potential of Gut Microbe-Derived Extracellular Vesicles to Differentiate Inflammatory Bowel Disease Patients from Healthy Controls

被引:9
作者
Heo, Min [1 ]
Park, Young Soo [2 ]
Yoon, Hyuk [2 ,3 ,4 ]
Kim, Nam-Eun [5 ]
Kim, Kangjin [6 ]
Shin, Cheol Min [2 ,3 ,4 ]
Kim, Nayoung [2 ,3 ,4 ]
Lee, Dong Ho [2 ,3 ,4 ]
机构
[1] Seoul Natl Univ, Coll Nat Sci, Interdisciplinary Program Bioinformat, Seoul, South Korea
[2] Seoul Natl Univ, Dept Internal Med, Bundang Hosp, Seongnam, South Korea
[3] Seoul Natl Univ, Dept Internal Med, Coll Med, Seoul, South Korea
[4] Seoul Natl Univ, Liver Res Inst, Coll Med, Seoul, South Korea
[5] Seoul Natl Univ, Dept Publ Hlth Sci, Grad Sch Publ Hlth, Seoul, South Korea
[6] Seoul Natl Univ, Inst Hlth & Environm, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Inflammatory bowel diseases; Microbiota; Extracellular vesicles; ULCERATIVE-COLITIS; PATHOGENESIS; DYSBIOSIS; DATABASE;
D O I
10.5009/gnl220081
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:108 / 118
页数:11
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