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乙肝病毒相关肝病不同阶段的健康个体和患者肠道微生物群的多样性与组成

Diversity and composition of gut microbiota in healthy individuals and patients at different stages of hepatitis B virus-related liver disease.

作者信息

Lin Meng-Ju, Su Tung-Hung, Chen Chieh-Chang, Wu Wei-Kai, Hsu Shih-Jer, Tseng Tai-Chung, Liao Sih-Han, Hong Chun-Ming, Yang Hung-Chih, Liu Chun-Jen, Wu Ming-Shiang, Kao Jia-Horng

机构信息

School of Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.

Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, 1 Chang-Te Street, Taipei, 10048, Taiwan.

出版信息

Gut Pathog. 2023 May 22;15(1):24. doi: 10.1186/s13099-023-00549-w.

Abstract

BACKGROUND

Hepatitis B virus (HBV) causes chronic hepatitis B (CHB), liver cirrhosis, and hepatocellular carcinoma. The evolution of human gut microbiota during the progression of HBV-related liver diseases remains unclear. Therefore, we prospectively enrolled patients with HBV-related liver diseases and healthy individuals. Through 16S ribosomal RNA amplicon sequencing, we characterized the gut microbiota of the participants and predicted the functions of microbial communities.

RESULTS

We analyzed the gut microbiota of 56 healthy controls and 106 patients with HBV-related liver disease [14 with resolved HBV infection, 58 with CHB, and 34 with advanced liver disease (15 with liver cirrhosis and 19 with hepatocellular carcinoma)]. Patients with HBV-related liver disease exhibited a higher degree of bacterial richness (all P < 0.05) than did healthy controls. Beta diversity analyses revealed a distinct clustering pattern between healthy controls and patients with HBV-related liver disease (all P < 0.05). The composition of bacteria (from the phylum level to the genus level) varied across the stages of liver disease. Linear discriminant analysis effect size revealed multiple taxa that differ significantly in abundance between healthy controls and patients with HBV-related liver disease; however, fewer differences were observed among patients with resolved HBV infection, those with CHB, and those with advanced liver disease. The ratio of Firmicutes to Bacteroidetes was increased in all three patient groups compared with the ratio in healthy controls (all P < 0.001). The analysis of the sequencing data by using PICRUSt2 revealed the changes in microbial functions with disease progression.

CONCLUSIONS

The diversity and composition of gut microbiota appear to vary significantly between healthy controls and patients at different stages of HBV-related liver disease. The understanding of gut microbiota may provide novel therapeutic options in these patients.

摘要

背景

乙型肝炎病毒(HBV)可导致慢性乙型肝炎(CHB)、肝硬化和肝细胞癌。HBV相关肝病进展过程中人类肠道微生物群的演变仍不清楚。因此,我们前瞻性地纳入了HBV相关肝病患者和健康个体。通过16S核糖体RNA扩增子测序,我们对参与者的肠道微生物群进行了表征,并预测了微生物群落的功能。

结果

我们分析了56名健康对照者和106名HBV相关肝病患者的肠道微生物群[14名HBV感染已缓解者、58名CHB患者和34名晚期肝病患者(15名肝硬化患者和19名肝细胞癌患者)]。HBV相关肝病患者的细菌丰富度高于健康对照者(所有P < 0.05)。β多样性分析显示健康对照者和HBV相关肝病患者之间存在明显的聚类模式(所有P < 0.05)。细菌组成(从门水平到属水平)在肝病的不同阶段有所不同。线性判别分析效应大小显示,健康对照者和HBV相关肝病患者之间有多个分类群的丰度存在显著差异;然而,在HBV感染已缓解者、CHB患者和晚期肝病患者之间观察到的差异较少。与健康对照者相比,所有三组患者的厚壁菌门与拟杆菌门的比例均升高(所有P < 0.001)。使用PICRUSt2对测序数据进行分析,揭示了微生物功能随疾病进展的变化。

结论

健康对照者与HBV相关肝病不同阶段患者的肠道微生物群多样性和组成似乎存在显著差异。对肠道微生物群的了解可能为这些患者提供新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dac/10201741/70951ef1cb17/13099_2023_549_Fig1_HTML.jpg

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