The microbiota and the gut-liver axis in primary sclerosing cholangitis

被引:32
|
作者
Hov, Johannes R. [1 ,2 ,3 ,4 ]
Karlsen, Tom H. [1 ,2 ,3 ,4 ]
机构
[1] Oslo Univ Hosp, Norwegian PSC Res Ctr, Oslo, Norway
[2] Oslo Univ Hosp, Sect Gastroenterol, Div Surg Inflammatory Dis & Transplantat, Oslo, Norway
[3] Oslo Univ Hosp, Res Inst Internal Med, Div Surg Inflammatory Dis & Transplantat, Oslo, Norway
[4] Univ Oslo, Fac Med, Inst Clin Med, Oslo, Norway
关键词
INFLAMMATORY-BOWEL-DISEASE; GENOME-WIDE ASSOCIATION; ABNORMAL INTESTINAL PERMEABILITY; MUCOSA-ASSOCIATED MICROBIOTA; ACTIVE ULCERATIVE-COLITIS; PRIMARY BILIARY-CIRRHOSIS; BILE-ACID METABOLISM; TUBULIN ISOTYPE 5; FECAL MICROBIOTA; ORAL VANCOMYCIN;
D O I
10.1038/s41575-022-00690-y
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Primary sclerosing cholangitis (PSC) is closely associated with inflammatory bowel disease (IBD) and potentially provides unique insights into the gut-liver axis. This Review explores these links and provides an overview of the gut microbiome in PSC, including PSC-IBD, exploring related hypotheses of disease mechanisms. Primary sclerosing cholangitis (PSC) offers unique opportunities to explore the gut-liver axis owing to the close association between liver disease and colonic inflammation. It is well established that the gut microbiota in people with PSC differs from that of healthy individuals, but details of the microbial factors that demarcate PSC from inflammatory bowel disease (IBD) without PSC are poorly understood. In this Review, we aim to provide an overview of the latest literature on the gut microbiome in PSC and PSC with IBD, critically examining hypotheses on how microorganisms could contribute to the pathogenesis of PSC. A particular emphasis will be put on pathogenic features of the gut microbiota that might explain the occurrence of bile duct inflammation and liver disease in the context of IBD, and we postulate the potential existence of a specific yet unknown factor related to the gut-liver axis as causative in PSC. Available data are scrutinized in the perspective of therapeutic approaches related to the gut-liver axis.
引用
收藏
页码:135 / 154
页数:20
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