Department of Medicine, University of California San Diego , La Jolla, CA, USA.
Department of Medicine, VA San Diego Healthcare System , San Diego, CA, USA.
Gut Microbes. 2020 Nov 9;12(1):1785251. doi: 10.1080/19490976.2020.1785251. Epub 2020 Jul 20.
Alcoholic hepatitis is the most severe form of alcohol-related liver disease. While the gut microbiome is known to play a role in disease development and progression, less is known about specific compositional changes of the gut bacterial microbiome associated with disease severity. Therefore, the aim of our study was to correlate gut microbiota features with disease severity in alcoholic hepatitis patients.
We used 16S rRNA gene sequencing on fecal samples from 74 alcoholic hepatitis patients, which were enrolled at 9 centers in Europe, the United States, and Mexico in a multi-center observational study. The relative abundance of gut bacterial taxa on genus level, as well as the microbiome diversity, was correlated to various clinical, laboratory, and histologic parameters.
We observed a negative correlation between the model for end-stage liver disease score and Shannon diversity, independent of potentially confounding factors (P = 0.046). Alcoholic hepatitis patients with more severe disease had significantly decreased relative abundances of while the relative abundance of was increased. We observed a reduction in the abundance (P = 0.048) and Shannon diversity (P = 0.018) in antibiotic-treated patients and patients receiving steroids had an increase in abundance (P = 0.005), which was both independent of potentially confounding factors.
We observed distinct changes in the gut bacterial microbiome of alcoholic hepatitis patients with more severe disease. The gut bacterial microbiome might be an attractive target to prevent and treat this deadly disease.
酒精性肝炎是最严重的酒精相关肝病。尽管肠道微生物群在疾病的发生和发展中起作用,但对与疾病严重程度相关的肠道细菌微生物群的特定组成变化了解较少。因此,我们的研究目的是将肠道微生物组特征与酒精性肝炎患者的疾病严重程度相关联。
我们使用来自欧洲、美国和墨西哥的 9 个中心的 74 名酒精性肝炎患者的粪便样本进行 16S rRNA 基因测序,这些患者在一项多中心观察性研究中被纳入。基于属水平的肠道细菌分类群的相对丰度以及微生物组多样性与各种临床、实验室和组织学参数相关联。
我们观察到终末期肝病模型评分与 Shannon 多样性之间存在负相关,独立于潜在的混杂因素(P=0.046)。疾病更严重的酒精性肝炎患者的相对丰度显著降低,而 的相对丰度增加。我们观察到抗生素治疗患者的 丰度降低(P=0.048)和 Shannon 多样性降低(P=0.018),而接受类固醇治疗的患者的 丰度增加(P=0.005),这两者均独立于潜在的混杂因素。
我们观察到疾病更严重的酒精性肝炎患者的肠道细菌微生物组发生了明显变化。肠道细菌微生物组可能是预防和治疗这种致命疾病的有吸引力的靶点。