Microbiota, cirrhosis, and the emerging oral-gut-liver axis

被引:230
作者
Acharya, Chathur [1 ,2 ]
Sahingur, Sinem Esra [3 ]
Bajaj, Jasmohan S. [1 ,2 ]
机构
[1] Virginia Commonwealth Univ, Dept Gastroenterol & Hepatol, Richmond, VA USA
[2] McGuire VA Med Ctr, 1201 Broad Rock Blvd, Richmond, VA 23249 USA
[3] Virginia Commonwealth Univ, Dept Periodont, Richmond, VA USA
关键词
SYSTEMS BIOLOGY ANALYSIS; SECONDARY BILE-ACIDS; UNITED-STATES; HEPATIC-ENCEPHALOPATHY; OBETICHOLIC ACID; INTESTINAL MICROBIOTA; COLONIC INFLAMMATION; AMERICAN ASSOCIATION; PERIODONTAL-DISEASE; PRACTICE GUIDELINE;
D O I
10.1172/jci.insight.94416
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
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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页数:11
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