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微生物群在预测克罗恩病纤维性狭窄中的突出作用。

Prominence of Microbiota to Predict Fibrous Stenosis in Crohn's Disease.

作者信息

Yang Xue, Pan Yan, Gao Cai-Ping, Li Hang, Zhang Ying-Hui, Huang Chun-Li, Cao Lu, Xiao Shi-Yu, Zhou Zhou

机构信息

Department of Gastroenterology, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, People's Republic of China.

出版信息

J Inflamm Res. 2025 Feb 5;18:1413-1423. doi: 10.2147/JIR.S480473. eCollection 2025.

Abstract

PURPOSE

Intestinal fibrous stenosis due to Crohn's disease (CD) is highly prevalent. Although several clinical risk factors for fibrous stenosis have been identified, such as perianal fistulizing disease, small bowel disease location, and deep mucosal ulceration, predicting fibrous stenosis remains challenging. The intestinal microbiota plays a crucial role in the development and progression of CD. However, its role in intestinal fibrous stenosis is poorly understood. Leveraging a single-center cross-sectional study, we aimed to investigate the role of fecal microbiota in CD-associated fibrous stenosis.

METHODS

Using metagenomic analysis, we examined the differences in fecal microbiota between CD patients with intestinal fibrous stenosis and those without stenosis. We identified specific microbiota and assessed their predictive accuracy for intestinal fibrous stenosis. Additionally, we explored functional differences in intestinal microbiota between the two groups.

RESULTS

: Our investigation of fecal samples revealed no significant differences in the gut microbiota structure between patients with fibrous stenosis and those without stenosis in CD. However, taxonomically, we found 70 taxa with significantly different abundance (p < 0.05) between the two groups. Furthermore, LEfSe analysis indicated that and could predict intestinal fibrous stenosis while and could predict CD without stenosis. Functional analysis revealed differential enrichment in five metabolic pathways at the KEGG pathway level in CD patients with fibrous stenosis, including sphingolipid metabolism, lipoic acid metabolism, and biosynthesis of neomycin, kanamycin and gentamicin. In the eggNOG database, we observed differences in four functional categories between the two groups, encompassing cellular process, signaling, and metabolism.

CONCLUSION

Fecal microbiota significantly impacted intestinal fibrous stenosis in CD. Although there were no significant differences in alpha and beta diversities, fibrous stenosis was associated with changes in microbiota composition and function, suggesting the potential of fecal microbiota in predicting CD-associated fibrous stenosis.

摘要

目的

克罗恩病(CD)所致的肠道纤维性狭窄极为常见。尽管已确定了一些纤维性狭窄的临床风险因素,如肛周瘘管病、小肠疾病部位和深部黏膜溃疡,但预测纤维性狭窄仍然具有挑战性。肠道微生物群在CD的发生和发展中起着至关重要的作用。然而,其在肠道纤维性狭窄中的作用却知之甚少。利用一项单中心横断面研究,我们旨在探讨粪便微生物群在CD相关纤维性狭窄中的作用。

方法

我们采用宏基因组分析,研究了患有肠道纤维性狭窄的CD患者与无狭窄的CD患者之间粪便微生物群的差异。我们确定了特定的微生物群,并评估了它们对肠道纤维性狭窄的预测准确性。此外,我们还探讨了两组之间肠道微生物群的功能差异。

结果

我们对粪便样本的研究表明,在CD患者中,纤维性狭窄患者与无狭窄患者的肠道微生物群结构没有显著差异。然而,在分类学上,我们发现两组之间有70个分类单元的丰度存在显著差异(p<0.05)。此外,线性判别分析效应大小(LEfSe)分析表明,[具体微生物名称1]和[具体微生物名称2]可以预测肠道纤维性狭窄,而[具体微生物名称3]和[具体微生物名称4]可以预测无狭窄的CD。功能分析显示,在KEGG通路水平上,患有纤维性狭窄的CD患者在五个代谢途径中存在差异富集,包括鞘脂代谢、硫辛酸代谢以及新霉素、卡那霉素和庆大霉素的生物合成。在eggNOG数据库中,我们观察到两组之间在四个功能类别上存在差异,包括细胞过程、信号传导和代谢。

结论

粪便微生物群对CD患者的肠道纤维性狭窄有显著影响。尽管α和β多样性没有显著差异,但纤维性狭窄与微生物群组成和功能的变化有关,这表明粪便微生物群在预测CD相关纤维性狭窄方面具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e05/11807786/c722da077dbc/JIR-18-1413-g0001.jpg

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