Modulation of the fecal bile acid profile by gut microbiota in cirrhosis

被引:800
作者
Kakiyama, Genta [1 ,2 ]
Pandak, William M. [1 ,2 ]
Gillevet, Patrick M. [5 ]
Hylemon, Phillip B. [2 ,3 ]
Heuman, Douglas M. [1 ,2 ]
Daita, Kalyani [2 ,3 ]
Takei, Hajime [6 ]
Muto, Akina [6 ]
Nittono, Hiroshi [6 ]
Ridlon, Jason M. [2 ,3 ]
White, Melanie B. [1 ,2 ]
Noble, Nicole A. [1 ,2 ]
Monteith, Pamela [1 ,2 ]
Fuchs, Michael [1 ,2 ]
Thacker, Leroy R. [2 ,4 ]
Sikaroodi, Masoumeh [5 ]
Bajaj, Jasmohan S. [1 ,2 ]
机构
[1] Virginia Commonwealth Univ, Div Gastroenterol Hepatol & Nutr, Richmond, VA 23249 USA
[2] McGuire VA Med Ctr, Richmond, VA 23249 USA
[3] Virginia Commonwealth Univ, Dept Microbiol, Richmond, VA 23249 USA
[4] Virginia Commonwealth Univ, Dept Biostat, Richmond, VA 23249 USA
[5] George Mason Univ, Microbiome Anal Ctr, Manassas, VA USA
[6] Junshin Clin Bile Acid Inst, Meguro Ku, Tokyo, Japan
关键词
Gut microbiota; Complications of cirrhosis; Bile acid dehydroxylation; Dysbiosis; Rifaximin; Pathogenesis; HEPATIC-ENCEPHALOPATHY; DIARRHEA; METABOLISM; COGNITION;
D O I
10.1016/j.jhep.2013.01.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background & Aims: The 7 alpha-dehydroxylation of primary bile acids (BAs), chenodeoxycholic (CDCA) and cholic acid (CA) into the secondary BAs, lithocholic (LCA) and deoxycholic acid (DCA), is a key function of the gut microbiota. We aimed at studying the linkage between fecal BAs and gut microbiota in cirrhosis since this could help understand cirrhosis progression. Methods: Fecal microbiota were analyzed by culture-independent multitagged-pyrosequencing, fecal BAs using HPLC and serum BAs using LC-MS in controls, early (Child A) and advanced cirrhotics (Child B/C). A subgroup of early cirrhotics underwent BA and microbiota analysis before/after eight weeks of rifaximin. Results: Cross-sectional: 47 cirrhotics (24 advanced) and 14 controls were included. In feces, advanced cirrhotics had the lowest total, secondary, secondary/primary BA ratios, and the highest primary BAs compared to early cirrhotics and controls. Secondary fecal BAs were detectable in all controls but in a significantly lower proportion of cirrhotics (p <0.002). Serum primary BAs were higher in advanced cirrhotics compared to the rest. Cirrhotics, compared to controls, had a higher Enterobacteriaceae (potentially pathogenic) but lower Lachonospiraceae, Ruminococcaceae and Blautia (7 alpha-dehydroxylating bacteria) abundance. CDCA was positively correlated with Enterobacteriaceae (r = 0.57, p <0.008) while Ruminococcaceae were positively correlated with DCA (r = 0.4, p <0.05). A positive correlation between Ruminococcaceae and DCA/CA (r = 0.82, p <0.012) and Blautia with LCA/CDCA (r = 0.61, p <0.03) was also seen. Prospective study: post-rifaximin, six early cirrhotics had reduction in Veillonellaceae and in secondary/primary BA ratios. Conclusions: Cirrhosis, especially advanced disease, is associated with a decreased conversion of primary to secondary fecal BAs, which is linked to abundance of key gut microbiome taxa. (c) 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:949 / 955
页数:7
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