Advances in Gut Microbiota of Viral Hepatitis Cirrhosis
Open accessAbstract
Although gut dysbiosis appears in 20%–75% of cirrhotic patients, there are limited data on microbiota profiles in viral hepatitis cirrhotics and its role in progression to cirrhosis. Further understanding on the relationship between gut dysbiosis and cirrhosis presents a unique opportunity in not only predicting the development of cirrhosis but also discovering new therapies. Recent advances have been made on identifying unique microbiota in viral hepatitis cirrhotics and adopting the microbiota index to predict cirrhosis. Therapeutic intervention with microbiome-modulating has been explored. Cirrhosis from viral infection has unique bacterial or fungal profiles, which include increased numbers of Prevotella, Streptococcus, Staphylococcaceae, and Enterococcus, as well as decreased Ruminococcus and Clostridium. In addition, the gut microbiota can stimulate liver immunity, effectively helping hepatitis virus clearance. In clinical settings, CDR, GDI, Basidiomycota/Ascomycota, specific POD, and so forth are efficient microbiota indexes to diagnose or prognosticate cirrhosis from viral hepatitis. FMT, probiotics, and prebiotics can restore microbial diversity in cirrhotic patients with viral hepatitis, decrease ammonia serum or endotoxemia levels, prevent complications, reduce rehospitalization rate, and improve prognosis. Cirrhotics from viral hepatitis had unique bacterial or fungal profiles, associated with specific metabolic, immune, and endocrinological statuses. Such profiles are modifiable with medical treatment. The role of gut archaea and virome, implementation of FMT, microbiota metabolites as adjuvant immunotherapy, and microbiota indexes for prognostication deserve attention.
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Progression of cirrhosis is associated with increased intestinal permeability, small intestinal bacterial overgrowth, and bacterial translocation.
“The progression of cirrhosis is associated with increased intestinal permeability, small intestinal bacterial overgrowth, and bacterial translocation.”
From Viral Infections, the Microbiome, and Probiotics (2021) · cites this paper as Wang et al., 2019
This permits microbially derived compounds to access the liver via portal circulation, stimulating production of pro-inflammatory cytokines that promote liver inflammation, fibrogenesis and ultimately cirrhosis.
“This situation permits microbially derived compounds (e.g., ethanol, acetaldehyde, lipopolysaccharide) to access the liver via the portal circulation stimulating production of pro-inflammatory cytokines that promote liver inflammation, fibrogenesis and ultimately cirrhosis (Wang et al., 2019).”
From Viral Infections, the Microbiome, and Probiotics (2021) · cites this paper as Wang et al., 2019
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References 55 · Cited by 52
- Authors
- Wang, Y., Pan, C. Q., & Xing, H.
- Affiliations
- Peking University (CN)
- NYU Langone Health (US)
- Capital Medical University (CN)
- Corresponding author
- Xing, Huichun
- Venue
- BioMed Research International
- Publisher
- Wiley
- Published
- 2019-11-22
- Volume
- 2019
- Pages
- 1-9
- ISSN
- 1110-7243 (ISSN-L)
- 2314-6133
- 2314-6141
- PMC
- PMC6893240
- OpenAlex
- W2990223293
- Cited by
- 52
- References
- 55
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 20 · 2023: 4 · 2022: 9 · 2021: 10 · 2020: 4 · 2017: 1
- FWCI
- 0.51
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- BioMed Research International (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Science and Technology Major Project of China (2018ZX10302206-003-00, XMLX201837, XXT26)
- Beijing Hospitals Authority Clinical Medicine Development of Special Funding Support (2018ZX10302206-003-00, XMLX201837, XXT26)
- Digestive Medical Coordinated Development Center of Beijing Hospitals Authority (2018ZX10302206-003-00, XMLX201837, XXT26)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- gut microbiota, viral hepatitis, liver cirrhosis, gut dysbiosis, fecal microbiota transplantation, probiotics, prebiotics, Prevotella, Streptococcus, Staphylococcaceae, Enterococcus, Ruminococcus, Clostridium, gut archaea, virome, microbiota metabolites, adjuvant immunotherapy, endotoxemia, ammonia, liver immunity, fungal microbiota
- MeSH terms
- Gastrointestinal Microbiome, Hepatitis, Humans, Liver, Liver Cirrhosis, Dysbiosis
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