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失代偿期肝硬化患者肠道微生物群、真菌微生物群和代谢物的特征及相互作用

The signatures and crosstalk of gut microbiome, mycobiome, and metabolites in decompensated cirrhotic patients.

作者信息

Li Yangjie, Liu Danping, He Yanglan, Zhang Zeming, Zeng Ajuan, Fan Chunlei, Lyu Lingna, He Zilong, Ding Huiguo

机构信息

Department of Gastroenterology and Hepatology, Laboratory for Clinical Medicine, Beijing You'an Hospital Affiliated to Capital Medical University, Beijing, China.

School of Engineering Medicine, Beihang University, Beijing, China.

出版信息

Front Microbiol. 2024 Aug 21;15:1443182. doi: 10.3389/fmicb.2024.1443182. eCollection 2024.

Abstract

BACKGROUND

Numerous studies have confirmed that gut microbiota plays a crucial role in the progression of cirrhosis. However, the contribution of gut fungi in cirrhosis is often overlooked due to the relatively low abundance.

METHODS

We employed 16S ribosomal RNA sequencing, internal transcribed spacer sequencing, and untargeted metabolomics techniques to investigate the composition and interaction of gut bacteria, fungi, and metabolites in cirrhotic patients.

RESULTS

Cirrhotic patients exhibited significant differences in the diversity and composition of gut microbiota and their metabolites in cirrhotic patients compared to healthy individuals. Increase in pathogenic microbial genera and a decrease in beneficial microbial genera including bacteria and fungi were observed. Various clinical indexes were closely connected with these increased metabolites, bacteria, fungi. Additionally, endoscopic treatment was found to impact the gut microbiota and metabolites in cirrhotic patients, although it did not significantly alter the gut ecology. Finally, we constructed a cirrhosis diagnostic model based on different features (bacteria, fungi, metabolites, clinical indexes) with an AUC of 0.938.

CONCLUSION

Our findings revealed the characteristics of gut microbial composition and their intricate internal crosstalk in cirrhotic patients, providing cutting-edge explorations of potential roles of gut microbes in cirrhosis.

摘要

背景

众多研究已证实肠道微生物群在肝硬化进展中起关键作用。然而,由于肠道真菌丰度相对较低,其在肝硬化中的作用常被忽视。

方法

我们采用16S核糖体RNA测序、内转录间隔区测序和非靶向代谢组学技术,研究肝硬化患者肠道细菌、真菌和代谢产物的组成及相互作用。

结果

与健康个体相比,肝硬化患者肠道微生物群及其代谢产物的多样性和组成存在显著差异。观察到致病微生物属增加,包括细菌和真菌在内的有益微生物属减少。各种临床指标与这些增加的代谢产物、细菌、真菌密切相关。此外,发现内镜治疗会影响肝硬化患者的肠道微生物群和代谢产物,尽管它并未显著改变肠道生态。最后,我们基于不同特征(细菌、真菌、代谢产物、临床指标)构建了一个肝硬化诊断模型,其曲线下面积为0.938。

结论

我们的研究结果揭示了肝硬化患者肠道微生物组成的特征及其复杂的内部相互作用,为肠道微生物在肝硬化中的潜在作用提供了前沿探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83c3/11372394/a28a7bb43564/fmicb-15-1443182-g0001.jpg

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