Microbiota, cirrhosis, and the emerging oral-gut-liver axis
Cirrhosis is a prevalent cause of morbidity and mortality, especially for those at an advanced decompensated stage. Cirrhosis development and progression involves several important interorgan communications, and recently, the gut microbiome has been implicated in pathophysiology of the disease. Dysb...
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description | Cirrhosis is a prevalent cause of morbidity and mortality, especially for those at an advanced decompensated stage. Cirrhosis development and progression involves several important interorgan communications, and recently, the gut microbiome has been implicated in pathophysiology of the disease. Dysbiosis, defined as a pathological change in the microbiome, has a variable effect on the compensated versus decompensated stage of cirrhosis. Adverse microbial changes, both in composition and function, can act at several levels within the gut (stool and mucosal) and have also been described in the blood and oral cavity. While dysbiosis in the oral cavity could be a source of systemic inflammation, current cirrhosis treatment modalities are targeted toward the gut-liver axis and do not address the oral microbiome. As interventions designed to modulate oral dysbiosis may delay progression of cirrhosis, a better understanding of this process is of the utmost importance. The concept of oral microbiota dysbiosis in cirrhosis is relatively new; therefore, this review will highlight the emerging role of the oral-gut-liver axis and introduce perspectives for future research. |
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Cirrhosis development and progression involves several important interorgan communications, and recently, the gut microbiome has been implicated in pathophysiology of the disease. Dysbiosis, defined as a pathological change in the microbiome, has a variable effect on the compensated versus decompensated stage of cirrhosis. Adverse microbial changes, both in composition and function, can act at several levels within the gut (stool and mucosal) and have also been described in the blood and oral cavity. While dysbiosis in the oral cavity could be a source of systemic inflammation, current cirrhosis treatment modalities are targeted toward the gut-liver axis and do not address the oral microbiome. As interventions designed to modulate oral dysbiosis may delay progression of cirrhosis, a better understanding of this process is of the utmost importance. 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Cirrhosis development and progression involves several important interorgan communications, and recently, the gut microbiome has been implicated in pathophysiology of the disease. Dysbiosis, defined as a pathological change in the microbiome, has a variable effect on the compensated versus decompensated stage of cirrhosis. Adverse microbial changes, both in composition and function, can act at several levels within the gut (stool and mucosal) and have also been described in the blood and oral cavity. While dysbiosis in the oral cavity could be a source of systemic inflammation, current cirrhosis treatment modalities are targeted toward the gut-liver axis and do not address the oral microbiome. As interventions designed to modulate oral dysbiosis may delay progression of cirrhosis, a better understanding of this process is of the utmost importance. The concept of oral microbiota dysbiosis in cirrhosis is relatively new; therefore, this review will highlight the emerging role of the oral-gut-liver axis and introduce perspectives for future research.</description><subject>Dysbiosis - microbiology</subject><subject>Gastrointestinal Microbiome</subject><subject>Humans</subject><subject>Inflammation - microbiology</subject><subject>Liver - microbiology</subject><subject>Liver Cirrhosis - microbiology</subject><subject>Liver Cirrhosis - physiopathology</subject><subject>Microbiota</subject><subject>Mouth Mucosa - microbiology</subject><subject>Review</subject><issn>2379-3708</issn><issn>2379-3708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkF1LwzAUhoMobsz9AG-kl17YmaRpPhAEGX7BxBu9DmmbtBltM5Nu6L83ujnm1Tmc8573vDwAnCM4Q4jh62VpZ7YPtm6GmSAE0SMwxhkTacYgPz7oR2AawhJCiBjBMOenYIS5YJwJMQY3L7b0rrBuUFdJab1vXLDhKlF9lQyNTnSnfW37OnFetWm9HtLWbrRP1KcNZ-DEqDbo6a5OwPvD_dv8KV28Pj7P7xZpSWg-pArBklYkQ8ZopU2RKa4IN1AJEgPlomII50ZVpkIa04wXUFFcUMYhJgzGyQTcbn1X66LTVan7IYaRK2875b-kU1b-3_S2kbXbyJwTxDmKBpc7A-8-1joMsrOh1G2reu3WQaKYhCJKchGlaCuNVELw2uzfICh_uMvIXe64y1_u8ebiMN_-4o9y9g0gZoH_</recordid><startdate>20171005</startdate><enddate>20171005</enddate><creator>Acharya, Chathur</creator><creator>Sahingur, Sinem Esra</creator><creator>Bajaj, Jasmohan S</creator><general>American Society for Clinical Investigation</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6089-637X</orcidid></search><sort><creationdate>20171005</creationdate><title>Microbiota, cirrhosis, and the emerging oral-gut-liver axis</title><author>Acharya, Chathur ; Sahingur, Sinem Esra ; Bajaj, Jasmohan S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-a10c6d431ffeaefb3a8a48f0a9474259d7125fadfd1e2638b0a62b67802470263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Dysbiosis - microbiology</topic><topic>Gastrointestinal Microbiome</topic><topic>Humans</topic><topic>Inflammation - microbiology</topic><topic>Liver - microbiology</topic><topic>Liver Cirrhosis - microbiology</topic><topic>Liver Cirrhosis - physiopathology</topic><topic>Microbiota</topic><topic>Mouth Mucosa - microbiology</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Acharya, Chathur</creatorcontrib><creatorcontrib>Sahingur, Sinem Esra</creatorcontrib><creatorcontrib>Bajaj, Jasmohan S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JCI insight</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Acharya, Chathur</au><au>Sahingur, Sinem Esra</au><au>Bajaj, Jasmohan S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microbiota, cirrhosis, and the emerging oral-gut-liver axis</atitle><jtitle>JCI insight</jtitle><addtitle>JCI Insight</addtitle><date>2017-10-05</date><risdate>2017</risdate><volume>2</volume><issue>19</issue><issn>2379-3708</issn><eissn>2379-3708</eissn><abstract>Cirrhosis is a prevalent cause of morbidity and mortality, especially for those at an advanced decompensated stage. Cirrhosis development and progression involves several important interorgan communications, and recently, the gut microbiome has been implicated in pathophysiology of the disease. Dysbiosis, defined as a pathological change in the microbiome, has a variable effect on the compensated versus decompensated stage of cirrhosis. Adverse microbial changes, both in composition and function, can act at several levels within the gut (stool and mucosal) and have also been described in the blood and oral cavity. While dysbiosis in the oral cavity could be a source of systemic inflammation, current cirrhosis treatment modalities are targeted toward the gut-liver axis and do not address the oral microbiome. As interventions designed to modulate oral dysbiosis may delay progression of cirrhosis, a better understanding of this process is of the utmost importance. 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subjects | Dysbiosis - microbiology Gastrointestinal Microbiome Humans Inflammation - microbiology Liver - microbiology Liver Cirrhosis - microbiology Liver Cirrhosis - physiopathology Microbiota Mouth Mucosa - microbiology Review |
title | Microbiota, cirrhosis, and the emerging oral-gut-liver axis |
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