Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Dec 28;22(1):199.
doi: 10.3390/ijms22010199.

The Role of the Gut Microbiome in Liver Cirrhosis Treatment

Affiliations
Review

The Role of the Gut Microbiome in Liver Cirrhosis Treatment

Na Young Lee et al. Int J Mol Sci. .

Abstract

Liver cirrhosis is one of the most prevalent chronic liver diseases worldwide. In addition to viral hepatitis, diseases such as steatohepatitis, autoimmune hepatitis, sclerosing cholangitis and Wilson's disease can also lead to cirrhosis. Moreover, alcohol can cause cirrhosis on its own and exacerbate chronic liver disease of other causes. The treatment of cirrhosis can be divided into addressing the cause of cirrhosis and reversing liver fibrosis. To this date, there is still no clear consensus on the treatment of cirrhosis. Recently, there has been a lot of interest in potential treatments that modulate the gut microbiota and gut-liver axis for the treatment of cirrhosis. According to recent studies, modulation of the gut microbiome by probiotics ameliorates the progression of liver disease. The precise mechanism for relieving cirrhosis via gut microbial modulation has not been identified. This paper summarizes the role and effects of the gut microbiome in cirrhosis based on experimental and clinical studies on absorbable antibiotics, probiotics, prebiotics, and synbiotics. Moreover, it provides evidence of a relationship between the gut microbiome and liver fibrosis.

Keywords: gut microbiome; gut-liver axis; liver cirrhosis; liver fibrosis.

PubMed Disclaimer

Conflict of interest statement

The authors have no potential conflict of interest.

Figures

Figure 1
Figure 1
Dysbiosis and diseases. AST, aspartate aminotransferase; ALT, alanine aminotransferase; T-BIL, total bilirubin; ALB, albumin; MDA, malondialdehyde; SOD, superoxide dismutase; GSH, Glutathione; CTP, Child-Turcotte-Pugh; MELD, model for end-stage liver disease; Col, Collagen; Timp, tissue inhibitor of metallopeptidase; TGF, transforming growth factor; α-SMA, alpha-smooth muscle actin; TNF- α, tumor necrosis factor alpha; Zo-1, zonula occludenes-1; BA, bile acids; BCL-2, b-cell lymphoma 2.

References

    1. Schuppan D., Afdhal N.H. Liver cirrhosis. Lancet. 2008;371:838–851. doi: 10.1016/S0140-6736(08)60383-9. - DOI - PMC - PubMed
    1. Prinja S., Bahuguna P., Duseja A., Kaur M., Chawla Y.K. Cost of Intensive Care Treatment for Liver Disorders at Tertiary Care Level in India. Pharm. Open. 2018;2:179–190. doi: 10.1007/s41669-017-0041-4. - DOI - PMC - PubMed
    1. Lee N.Y., Yoon S.J., Han D.H., Gupta H., Youn G.S., Shin M.J., Ham Y.L., Kwak M.J., Kim B.Y., Yu J.S., et al. Lactobacillus and Pediococcus ameliorate progression of non-alcoholic fatty liver disease through modulation of the gut microbiome. Gut Microbes. 2020;11:882–899. doi: 10.1080/19490976.2020.1712984. - DOI - PMC - PubMed
    1. Duseja A., Acharya S.K., Mehta M., Chhabra S., Rana S., Das A., Dattagupta S., Dhiman R.K., Chawla Y.K. High potency multistrain probiotic improves liver histology in non-alcoholic fatty liver disease (NAFLD): A randomised, double-blind, proof of concept study. BMJ Open Gastroenterol. 2019;6:e000315. doi: 10.1136/bmjgast-2019-000315. - DOI - PMC - PubMed
    1. Bajaj J.S. Altered Microbiota in Cirrhosis and Its Relationship to the Development of Infection. Clin. Liver Dis. 2019;14:107–111. doi: 10.1002/cld.827. - DOI - PMC - PubMed