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

微生物群 医学 炎症性肠病 粪便 基因组 胃肠病学 肠道微生物群 钙蛋白酶 肠道菌群 溃疡性结肠炎 内科学 失调 病例对照研究 疾病 免疫学 微生物学 生物信息学 生物 基因 生物化学
作者
Min Heo,Young Soo Park,Hyuk Yoon,Nam-Eun Kim,Kangjin Kim,Cheol Min Shin,Na Young Kim,Dong Ho Lee
出处
期刊:Gut and Liver [Korean Association for the Study of the Liver]
卷期号:17 (1): 108-118 被引量:4
标识
DOI:10.5009/gnl220081
摘要

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

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