JOURNAL OF HEPATOLOGY | 卷:60 |
Altered profile of human gut microbiome is associated with cirrhosis and its complications | |
Article | |
Bajaj, Jasmohan S.1,2  Heuman, Douglas M.1,2  Hylemon, Phillip B.2,3  Sanyal, Arun J.1,2  White, Melanie B.1,2  Monteith, Pamela1,2  Noble, Nicole A.1,2  Unser, Ariel B.1,2  Daita, Kalyani2,3  Fisher, Andmorgan R.4  Sikaroodi, Masoumeh4  Gillevet, Patrick M.4  | |
[1] Virginia Commonwealth Univ, Div Gastroenterol Hepatol & Nutr, Richmond, VA 23284 USA | |
[2] McGuire VA Med Ctr, Richmond, VA USA | |
[3] Virginia Commonwealth Univ, Dept Microbiol, Richmond, VA USA | |
[4] George Mason Univ, Microbiome Anal Ctr, Manassas, VA USA | |
关键词: Microbiota; Hepatic encephalopathy; Decompensation; Infections; Acute-on-chronic liver failure; Endotoxin; MELD score; Cirrhosis dysbiosis ratio; | |
DOI : 10.1016/j.jhep.2013.12.019 | |
来源: Elsevier | |
【 摘 要 】
Background & Aims: The gut microbiome is altered in cirrhosis; however its evolution with disease progression is only partly understood. We aimed to study changes in the microbiome over cirrhosis severity, its stability over time and its longitudinal alterations with decompensation. Methods: Controls and age-matched cirrhotics (compensated/decompensated/hospitalized) were included. Their stool micro-biota was quantified using multi-tagged pyrosequencing. The ratio of autochthonous to non-autochthonous taxa was calculated as the cirrhosis dysbiosis ratio (CDR); a low number indicating dysbiosis. Firstly, the microbiome was compared between controls and cirrhotic sub-groups. Secondly, for stability assessment, stool collected twice within 6 months in compensated outpatients was analyzed. Thirdly, changes after decompensation were assessed using (a) longitudinal comparison in patients before/after hepatic encephalopathy development (HE), (b) longitudinal cohort of hospitalized infected cirrhotics MELD-matched to uninfected cirrhotics followed for 30 days. Results: 244 subjects [219 cirrhotics (121 compensated outpatients, 54 decompensated outpatients, 44 inpatients) and 25 age-matched controls] were included. CDR was highest in controls (2.05) followed by compensated (0.89), decompensated (0.66), and inpatients (0.32, p < 0.0001) and negatively correlated with endotoxin. Microbiota and CDR remained unchanged in stable outpatient cirrhotics (0.91 vs. 0.86, p = 0.45). In patients studied before/after HE development, dysbiosis occurred post-HE (CDR: 1.2 to 0.42, p = 0.03). In the longitudinal matched-cohort, microbiota were significantly different between infected/uninfected cirrhotics at baseline and a low CDR was associated with death and organ failures within 30 days. Conclusions: Progressive changes in the gut microbiome accompany cirrhosis and become more severe in the setting of decompensation. The cirrhosis dysbiosis ratio may be a useful quantitative index to describe microbiome alterations accompanying cirrhosis progression. (c) 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
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