FXR-dependent modulation of the human small intestinal microbiome by the bile acid derivative obeticholic acid
Open accessAbstract
Background & Aims: Intestinal bacteria can modify the composition of bile acids and bile acids, which are regulated by the farnesoid X receptor (FXR), affect the survival and growth of gut bacteria. We studied the effects of obeticholic acid (OCA), a bile acid analog and FXR agonist, on the intestinal microbiomes of humans and mice. Methods: We performed a phase 1 study in 24 healthy volunteers given OCA (5 mg, 10 mg, or 25 mg per day, for 17 days). Fecal and plasma specimens were collected at baseline (day 0) and on days 17 (end of dosing) and 37 (end of study). The fecal specimens were analyzed by shotgun metagenomic sequencing. A Uniref90 high stringency genomic analysis was used to assign specific genes to the taxonomic signature of bacteria whose abundance was associated with OCA. Male C57BL/6 mice were gavaged daily with water, vehicle, or OCA (10 mg/kg) for 2 weeks. Small intestine luminal contents were collected by flushing with saline and fecal pellets were collected at baseline and day 14. Mouse samples were analyzed by 16S tagged sequencing. Culture experiments were performed to determine taxonomic-specific effects of bile acids and OCA on bacterial growth. Results: Suppression of endogenous bile acid synthesis by OCA in subjects led to a reversible induction of Gram-positive bacteria that are found in the small intestine and are components of diet and the oral microbiota. We found that bile acids reduced proliferation of these bacteria in minimum inhibitory concentration assays. In these organisms, there was an increase in the representation of microbial genomic pathways involved in DNA synthesis and amino acid metabolism with OCA treatment of subjects. Consistent with these findings, mice fed OCA had reduced endogenous bile acid levels and an increased proportion of Firmicutes, specifically in the small intestine, compared to mice fed water or vehicle. Conclusions: In studying the effects of OCA in humans and mice, we found evidence for interactions between bile acids and features of the small intestinal microbiome. These findings indicate that FXR activation alters the intestinal microbiota and could provide opportunities for microbiome biomarker discovery or new approaches to engineering the human microbiome. Clinical trial information: ClinicalTrials.gov no: NCT01933503.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
There is an important bidirectional relationship between intestinal microbiota and bile acids.
“In recent years, it has been found that there is an important bidirectional relationship between intestinal microbiota and bile acids.”
From The role of gut dysbiosis in Parkinson’s disease: mechanistic insights and therapeutic options (2021) · cites this paper as [204]
Bile acids and FXR ligands alter intestinal microbiota, which may add to their therapeutic effects in both cholestatic and fatty liver diseases.
“Conversely, BAs and FXR ligands alter intestinal microbiota which may add to their therapeutic effects in both entities.53 56”
From Novel therapeutic targets for cholestatic and fatty liver disease (2022) · cites this paper as [56]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482 · see citing works
Trimmomatic: a flexible trimmer for Illumina sequence data
Bolger, A. M., Lohse, M., & Usadel, B. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu170 · Cited by 65,548 · see citing works
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400 · see citing works
QIIME allows analysis of high-throughput community sequencing data
Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887 · see citing works
Self-citationSearch and clustering orders of magnitude faster than BLAST
Edgar, R. C. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq461 · Cited by 20,617 · see citing works
Changes of Intestinal Functions in Liver Cirrhosis
Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820 · see citing works
Caspi, R., Billington, R., Ferrer, L., Foerster, H., Fulcher, C. A., Keseler, I. M., Kothari, A., Krummenacker, M., Latendresse, M., Mueller, L. A., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1164 · Cited by 3,395 · see citing works
Personalized nutrition by prediction of glycemic responses
Zeevi, D., Korem, T., Zmora, N., Israeli, D., Rothschild, D., Weinberger, A., Ben-Yacov, O., Lador, D., Avnit-Sagi, T., Lotan-Pompan, M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.11.001 · Cited by 2,929 · see citing works
Alterations of the human gut microbiome in liver cirrhosis
Qin, N., Yang, F., Li, A., Prifti, E., Chen, Y., Shao, L., Guo, J., Le Chatelier, E., Yao, J., Wu, L., et al. (2014) · Nature · doi:10.1038/nature13568 · Cited by 2,177 · see citing works
Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota
MetaHIT consortium, Forslund, K., Hildebrand, F., Nielsen, T., Falony, G., Le Chatelier, E., Sunagawa, S., Prifti, E., Vieira-Silva, S., Gudmundsdottir, V., et al. (2015) · Nature · doi:10.1038/nature15766 · Cited by 2,116 · see citing works
Blundell, J. E., Baker, J. L., Boyland, E. J., Blaak, E. E., Charzewska, J., Henauw, S. D., Frühbeck, G., González‐Gross, M., Hebebrand, J., Holm, L., et al. (2017) · Obesity Facts · doi:10.1159/000455952 · Cited by 1,980 · see citing works
Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile
Buffie, C. G., Bucci, V., Stein, R. R., McKenney, P. T., Ling, L., Gobourne, A., No, D., Liu, H., Kinnebrew, M., Viale, A., et al. (2015) · Nature · doi:10.1038/nature13828 · Cited by 1,872 · see citing works
The interaction between bacteria and bile
Begley, M., Gahan, C. G. M., & Hill, C. (2004) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2004.09.003 · Cited by 1,793 · see citing works
Metagenomic microbial community profiling using unique clade-specific marker genes
Segata, N., Waldron, L., Ballarini, A., Narasimhan, V., Jousson, O., & Huttenhower, C. (2012) · Nature Methods · doi:10.1038/nmeth.2066 · Cited by 1,776 · see citing works
Topographical Continuity of Bacterial Populations in the Healthy Human Respiratory Tract
Charlson, E. S., Bittinger, K., Haas, A. R., Fitzgerald, A. S., Frank, I., Yadav, A., Bushman, F. D., & Collman, R. G. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201104-0655oc · Cited by 1,144 · see citing works
Self-citationLoomba, R., Seguritan, V., Li, W., Long, T., Klitgord, N., Bhatt, A., Dulai, P. S., Caussy, C., Bettencourt, R., Highlander, S. K., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.04.001 · Cited by 1,123 · see citing works
Metabolic Reconstruction for Metagenomic Data and Its Application to the Human Microbiome
Abubucker, S., Segata, N., Goll, J. B., Schubert, A. M., Izard, J., Cantarel, B. L., Rodriguez-Mueller, B., Zucker, J., Thiagarajan, M., Henrissat, B., et al. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002358 · Cited by 1,050 · see citing works
Bile Acid Is a Host Factor That Regulates the Composition of the Cecal Microbiota in Rats
Islam, K. B. M. S., Fukiya, S., Hagio, M., Fujii, N., Ishizuka, S., Ooka, T., Ogura, Y., Hayashi, T., & Yokota, A. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.046 · Cited by 918 · see citing works
Lewis, J. D., Chen, E. Z., Baldassano, R. N., Otley, A. R., Griffiths, A. M., Lee, D., Bittinger, K., Bailey, A., Friedman, E. S., Hoffmann, C., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.09.008 · Cited by 823 · see citing works
Self-citationFate, activity, and impact of ingested bacteria within the human gut microbiota
Derrien, M., & van Hylckama Vlieg, J. E. T. (2015) · Trends in Microbiology · doi:10.1016/j.tim.2015.03.002 · Cited by 605 · see citing works
Hirschfield, G. M., Mason, A., Luketic, V., Lindor, K., Gordon, S. C., Mayo, M., Kowdley, K. V., Vincent, C., Bodhenheimer, H. C., Parés, A., et al. (2015) · Gastroenterology · doi:10.1053/j.gastro.2014.12.005 · Cited by 576 · see citing works
Self-citationHe, G., Shankar, R. A., Chzhan, M., Samouilov, A., Kuppusamy, P., & Zweier, J. L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.8.4586 · Cited by 383 · see citing works
Transposases are the most abundant, most ubiquitous genes in nature
Aziz, R. K., Breitbart, M., & Edwards, R. A. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq140 · Cited by 326 · see citing works
Verbeke, L., Farre, R., Verbinnen, B., Covens, K., Vanuytsel, T., Verhaegen, J., Komuta, M., Roskams, T., Chatterjee, S., Annaert, P., et al. (2015) · The American Journal of Pathology · doi:10.1016/j.ajpath.2014.10.009 · Cited by 225 · see citing works
A role for bacterial urease in gut dysbiosis and Crohn’s disease
Ni, J., Shen, T. D., Chen, E. Z., Bittinger, K. L., Bailey, A., Roggiani, M., Sirota‐Madi, A., Friedman, E. S., Chau, L., Lin, A. C., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aah6888 · Cited by 217 · see citing works
Self-citationReview: Mechanisms of How the Intestinal Microbiota Alters the Effects of Drugs and Bile Acids
Klaassen, C. D., & Cui, J. Y. (2015) · Drug Metabolism and Disposition · doi:10.1124/dmd.115.065698 · Cited by 208 · see citing works
Northfield, T. C., & McColl, I. (1973) · Gut · doi:10.1136/gut.14.7.513 · Cited by 207 · see citing works
Wang, S., Martins, R., Sullivan, M. C., Friedman, E. S., Misic, A. M., El‐Fahmawi, A., Martinis, E. C. P. D., O’Brien, K. M., Chen, Y., Bradley, C. W., et al. (2019) · Microbiome · doi:10.1186/s40168-019-0740-4 · Cited by 200 · see citing works
Self-citationBouhnik, Y., Alain, S., Attar, A., Flourié, B., Raskine, L., Sanson-Le Pors, M. J., & Rambaud, J.-C. (1999) · American Journal of Gastroenterology · doi:10.1111/j.1572-0241.1999.01016.x · Cited by 199 · see citing works
Gälman, C., Arvidsson, I., Angelin, B., & Rudling, M. (2003) · Journal of Lipid Research · doi:10.1194/jlr.d200043-jlr200 · Cited by 194 · see citing works
Engineering the gut microbiota to treat hyperammonemia
Shen, T. D., Albenberg, L. G., Bittinger, K. L., Chehoud, C., Chen, Y., Judge-Golden, C. P., Chau, L., Ni, J., Sheng, M., Lin, A. C., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci79214 · Cited by 182 · see citing works
Self-citationÚbeda, M., Lario, M., Muñoz, L., Borrero, M.-J., Rodríguez-Serrano, M., Sánchez-Díaz, A.-M., del Campo, R., Lledó, L., Pastor, Ó., García-Bermejo, L., et al. (2016) · Journal of Hepatology · doi:10.1016/j.jhep.2015.12.010 · Cited by 178 · see citing works
Diversity of human small intestinal Streptococcus and Veillonella populations
van den Bogert, B., Erkuş, O., Boekhorst, J., de Goffau, M. C., Smid, E. J., Zoetendal, E. G., & Kleerebezem, M. (2013) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12127 · Cited by 172 · see citing works
Microcins in Enterobacteriaceae: Peptide Antimicrobials in the Eco-Active Intestinal Chemosphere
Baquero, F., Lanza, V. F., Baquero, M.-R., del Campo, R., & Bravo-Vázquez, D. A. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02261 · Cited by 169 · see citing works
Role of bile acids in the gut-liver axis
Schneider, K. M., Albers, S., & Trautwein, C. (2018) · Journal of Hepatology · doi:10.1016/j.jhep.2017.11.025 · Cited by 129 · see citing works
FXR Agonists as Therapeutic Agents for Non-alcoholic Fatty Liver Disease
Carr, R. M., & Reid, A. E. (2015) · Current Atherosclerosis Reports · doi:10.1007/s11883-015-0500-2 · Cited by 123 · see citing works
Self-citationThe nonfermentable dietary fiber hydroxypropyl methylcellulose modulates intestinal microbiota
Cox, L. M., Cho, I., Young, S. A., Anderson, W. H. K., Waters, B. J., Hung, S., Gao, Z., Mahana, D., Bihan, M., Alekseyenko, A. V., et al. (2012) · The FASEB Journal · doi:10.1096/fj.12-219477 · Cited by 121 · see citing works
Gut-liver axis signaling in portal hypertension
Simbrunner, B., Mandorfer, M., Trauner, M., & Reiberger, T. (2019) · World Journal of Gastroenterology · doi:10.3748/wjg.v25.i39.5897 · Cited by 113 · see citing works
Barber, G. E., Yajnik, V., Khalili, H., Giallourakis, C. C., Garber, J. J., Xavier, R. J., & Ananthakrishnan, A. N. (2016) · The American Journal of Gastroenterology · doi:10.1038/ajg.2016.408 · Cited by 95 · see citing works
Laboratory Diagnosis of Infectious Diseases: Essentials of Diagnostic Microbiology
Engelkirk, P. G., & Duben-Engelkirk, J. L. (2007) · Medical Entomology and Zoology · Cited by 65 · see citing works
Shen, T. D., Pyrsopoulos, N., & Rustgi, V. K. (2018) · Liver Transplantation · doi:10.1002/lt.25008 · Cited by 43 · see citing works
Self-citationZhang, Y., LaCerte, C., Kansra, S., Jackson, J. P., Brouwer, K. R., & Edwards, J. E. (2017) · Pharmacology Research & Perspectives · doi:10.1002/prp2.368 · Cited by 35 · see citing works
Self-citationFlach, J., van der Waal, M. B., Kardinaal, A. F. M., Schloesser, J. E. L., Ruijschop, R. M. A. J., & Claassen, E. (2018) · Cogent Food & Agriculture · doi:10.1080/23311932.2018.1452839 · Cited by 34 · see citing works
Sookoian, S. C., & Pirola, C. J. (2019) · HepatoBiliary Surgery and Nutrition · doi:10.21037/hbsn.2019.02.04 · Cited by 5 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Gut microbiota-derived bile acids in intestinal immunity, inflammation, and tumorigenesis
Cai, J., Sun, L., & Gonzalez, F. J. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.02.004 · Cited by 869 · see citing works
Gut-liver axis: Pathophysiological concepts and clinical implications
Tilg, H., Adolph, T. E., & Trauner, M. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.09.017 · Cited by 843 · see citing works
Targher, G., Byrne, C. D., & Tilg, H. (2020) · Gut · doi:10.1136/gutjnl-2020-320622 · Cited by 848 · see citing works
The gut–liver axis and gut microbiota in health and liver disease
Hsu, C. L., & Schnabl, B. (2023) · Nature Reviews Microbiology · doi:10.1038/s41579-023-00904-3 · Cited by 737 · see citing works
Molecular physiology of bile acid signaling in health, disease, and aging
Perino, A., Demagny, H., Velazquez-Villegas, L., & Schoonjans, K. (2021) · Physiological Reviews · doi:10.1152/physrev.00049.2019 · Cited by 481 · see citing works
Bile acids as modulators of gut microbiota composition and function
Larabi, A. B., Masson, H. L. P., & Bäumler, A. J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2172671 · Cited by 420 · see citing works
Kastl, A., Terry, N. A., Wu, G. D., & Albenberg, L. G. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2019.07.006 · Cited by 359 · see citing works
Self-citationRole of the Gut Microbiota and Its Metabolites in Tumorigenesis or Development of Colorectal Cancer
Qu, R., Zhang, Y., Ma, Y., Zhou, X., Sun, L., Jiang, C., Zhang, Z., & Fu, W. (2023) · Advanced Science · doi:10.1002/advs.202205563 · Cited by 303 · see citing works
Discovery of farnesoid X receptor and its role in bile acid metabolism
Chiang, J. Y. L., & Ferrell, J. M. (2022) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2022.111618 · Cited by 298 · see citing works
The role of gut dysbiosis in Parkinson’s disease: mechanistic insights and therapeutic options
Wang, Q., Luo, Y., Ray Chaudhuri, K., Reynolds, R., Tan, E.-K., & Pettersson, S. (2021) · Brain · doi:10.1093/brain/awab156 · Cited by 281 · see citing works
Mullish, B. H., McDonald, J. A. K., Pechlivanis, A., Allegretti, J. R., Kao, D., Barker, G. F., Kapila, D., Petrof, E. O., Joyce, S. A., Gahan, C. G. M., et al. (2019) · Gut · doi:10.1136/gutjnl-2018-317842 · Cited by 268 · see citing works
Microbiota and Fatty Liver Disease—the Known, the Unknown, and the Future
Lang, S., & Schnabl, B. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.07.007 · Cited by 234 · see citing works
Novel therapeutic targets for cholestatic and fatty liver disease
Trauner, M., & Fuchs, C. D. (2022) · Gut · doi:10.1136/gutjnl-2021-324305 · Cited by 204 · see citing works
Wang, S., Martins, R., Sullivan, M. C., Friedman, E. S., Misic, A. M., El‐Fahmawi, A., Martinis, E. C. P. D., O’Brien, K. M., Chen, Y., Bradley, C. W., et al. (2019) · Microbiome · doi:10.1186/s40168-019-0740-4 · Cited by 200 · see citing works
Self-citationFXR agonists in NASH treatment
Adorini, L., & Trauner, M. (2023) · Journal of Hepatology · doi:10.1016/j.jhep.2023.07.034 · Cited by 197 · see citing works
Self-citationMicrocins in Enterobacteriaceae: Peptide Antimicrobials in the Eco-Active Intestinal Chemosphere
Baquero, F., Lanza, V. F., Baquero, M.-R., del Campo, R., & Bravo-Vázquez, D. A. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02261 · Cited by 169 · see citing works
Targeting the gut-liver-immune axis to treat cirrhosis
Tranah, T. H., Edwards, L. A., Schnabl, B., & Shawcross, D. L. (2020) · Gut · doi:10.1136/gutjnl-2020-320786 · Cited by 161 · see citing works
Effect of different bile acids on the intestine through enterohepatic circulation based on FXR
Xiang, J., Zhang, Z., Xie, H., Zhang, C., Bai, Y., Cao, H., Che, Q., Guo, J., & Su, Z. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1949095 · Cited by 142 · see citing works
Intestinal dysbiosis in nonalcoholic fatty liver disease (NAFLD): focusing on the gut–liver axis
Han, H. L., Jiang, Y., Wang, M., Melaku, M., Liu, L., Zhao, Y. M., Everaert, N., Yi, B., & Zhang, H. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1966738 · Cited by 132 · see citing works
Understanding bile acid signaling in diabetes: From pathophysiology to therapeutic targets
Ferrell, J. M., & Chiang, J. Y. L. (2019) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2019.0043 · Cited by 139 · see citing works
Promises of microbiome-based therapies
Bajaj, J. S., Ng, S. C., & Schnabl, B. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2021.12.003 · Cited by 119 · see citing works
The microbiota and the gut–liver axis in primary sclerosing cholangitis
Hov, J. R., & Karlsen, T. H. (2022) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-022-00690-y · Cited by 121 · see citing works
NAFLD and Atherosclerosis: Two Sides of the Same Dysmetabolic Coin?
Stols‐Gonçalves, D., Hovingh, G. K., Nieuwdorp, M., & Holleboom, A. G. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.08.008 · Cited by 118 · see citing works
Schnabl, B., Damman, C. J., & Carr, R. M. (2025) · Journal of Clinical Investigation · doi:10.1172/jci186423 · Cited by 126 · see citing works
Self-citationGut-liver axis signaling in portal hypertension
Simbrunner, B., Mandorfer, M., Trauner, M., & Reiberger, T. (2019) · World Journal of Gastroenterology · doi:10.3748/wjg.v25.i39.5897 · Cited by 113 · see citing works
Bile acid modulators for the treatment of nonalcoholic steatohepatitis (NASH)
Fiorucci, S., Biagioli, M., Sepe, V., Zampella, A., & Distrutti, E. (2020) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2020.1763302 · Cited by 99 · see citing works
Littmann, E. R., Lee, J., Denny, J. E., Alam, Z., Maslanka, J. R., Zarin, I., Matsuda, R., Carter, R. A., Sušac, B., Saffern, M., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20793-x · Cited by 92 · see citing works
Self-citationFu, T., Huan, T., Rahman, G., Zhi, H., Xu, Z. Z., Oh, T. G., Guo, J. P., Coulter, S., Tripathi, A., Martino, C., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112997 · Cited by 90 · see citing works
Bile Acids, Their Receptors, and the Gut Microbiota
Poland, J. C., & Flynn, C. R. (2021) · Physiology · doi:10.1152/physiol.00028.2020 · Cited by 85 · see citing works
Jin, P., Duan, X., Huang, Z., Dong, Y., Zhu, J., Guo, H., Tian, H., Zou, C., & Xie, K. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02270-3 · Cited by 86 · see citing works
Farnesoid X Receptor, Bile Acid Metabolism, and Gut Microbiota
Mori, H., Svegliati‐Baroni, G., Marzioni, M., Nicola, F. D., Santori, P., Maroni, L., Abenavoli, L., & Scarpellini, E. (2022) · Metabolites · doi:10.3390/metabo12070647 · Cited by 80 · see citing works
Novel approaches in IBD therapy: targeting the gut microbiota-bile acid axis
Pan, Y., Zhang, H., Li, M., He, T., Guo, S., Zhu, L., Tan, J., & Wang, B. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2356284 · Cited by 78 · see citing works
Li, B., Zhang, J., Chen, Y., Wang, Q., Li, Y., Wang, R., Wei, Y., You, Z., Li, Y., Miao, Q., et al. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1946366 · Cited by 74 · see citing works
Self-citationCarino, A., Biagioli, M., Marchianò, S., Fiorucci, C., Zampella, A., Monti, M. C., Scarpelli, P. T., Ricci, P., Distrutti, E., & Fiorucci, S. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2019.07.006 · Cited by 68 · see citing works
Bile Salt Hydrolase-Competent Probiotics in the Management of IBD: Unlocking the “Bile Acid Code”
Gadaleta, R. M., Cariello, M., Crudele, L., & Moschetta, A. (2022) · Nutrients · doi:10.3390/nu14153212 · Cited by 67 · see citing works
Nuclear Receptors Regulate Intestinal Inflammation in the Context of IBD
Klepsch, V., Moschen, A. R., Tilg, H., Baier, G., & Hermann‐Kleiter, N. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01070 · Cited by 63 · see citing works
The contribution of bile acid metabolism to the pathogenesis of Clostridioides difficile infection
Mullish, B. H., & Allegretti, J. R. (2021) · Therapeutic Advances in Gastroenterology · doi:10.1177/17562848211017725 · Cited by 58 · see citing works
Zhao, M., Jiafeng, Z., Yang, H., Ouyang, Z., Lv, C., Geng, Z., & Zhao, J. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118182 · Cited by 62 · see citing works
Targeting nonalcoholic fatty liver disease via gut microbiome-centered therapies
Koning, M., Herrema, H., Nieuwdorp, M., & Meijnikman, A. S. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2226922 · Cited by 56 · see citing works
Research progress on the relationship between bile acid metabolism and type 2 diabetes mellitus
Hou, Y., Zhai, X., Wang, X., Wu, Y., Wang, H., Qin, Y., Han, J., & Meng, Y. (2023) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-023-01207-6 · Cited by 58 · see citing works
Zazueta, A., Valenzuela-Pérez, L., Ortiz‐López, N., Pinto-León, A., Torres, V., Guiñez, D., Aliaga, N., Merino, P., Sandoval, A., Covarrubías, N., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084387 · Cited by 54 · see citing works
Yao, Y., Li, X., Xu, B., Luo, L., Guo, Q., Wang, X., Sun, L., Zhang, Z., & Li, P. (2022) · Cell Communication and Signaling · doi:10.1186/s12964-022-00890-8 · Cited by 50 · see citing works
Xiang, D., Yang, J., Liu, L., Yu, H., Gong, X., & Liu, D. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115606 · Cited by 50 · see citing works
Gut microbiota and their metabolites in the progression of non-alcoholic fatty liver disease
Zhou, J., Tripathi, M., Sinha, R. A., Singh, B. K., & Yen, P. M. (2021) · Hepatoma Research · doi:10.20517/2394-5079.2020.134 · Cited by 47 · see citing works
Kastl, A., Zong, W., Gershuni, V. M., Friedman, E. S., Tanes, C., Boateng, A., Mitchell, W. J., O’Connor, K., Bittinger, K. L., Terry, N. A., et al. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2083417 · Cited by 46 · see citing works
Self-citationEthanol-induced changes to the gut microbiome compromise the intestinal homeostasis: a review
Sosnowski, K., & Przybyłkowski, A. M. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2393272 · Cited by 48 · see citing works
Review of the Relationships Between Human Gut Microbiome, Diet, and Obesity
Patloka, O., Komprda, T., & Franke, G. (2024) · Nutrients · doi:10.3390/nu16233996 · Cited by 45 · see citing works
Crosstalk between Gut Microbiota and Bile Acids in Cholestatic Liver Disease
Shi, Q., Yuan, X., Zeng, Y., Wang, J., Zhang, Y., Chen, X., & Li, L. (2023) · Nutrients · doi:10.3390/nu15102411 · Cited by 41 · see citing works
The Influence of the Microbiome on NAFLD and NASH
Albhaisi, S. A. M., & Bajaj, J. S. (2021) · Clinical Liver Disease · doi:10.1002/cld.1010 · Cited by 40 · see citing works
Bile Acids: Key Regulators and Novel Treatment Targets for Type 2 Diabetes
Wu, Y., Zhou, A., Tang, L., Lei, Y., Tang, B., & Zhang, L. (2020) · Journal of Diabetes Research · doi:10.1155/2020/6138438 · Cited by 38 · see citing works
Obeticholic Acid and Other Farnesoid-X-Receptor (FXR) Agonists in the Treatment of Liver Disorders
Fiorucci, S., Urbani, G., Distrutti, E., & Biagioli, M. (2025) · Pharmaceuticals · doi:10.3390/ph18091424 · Cited by 41 · see citing works
The Role of the Intestinal Microbiota in Nonalcoholic Steatohepatitis
Xiang, H., Sun, D., Liu, X., She, Z., & Chen, Y. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.812610 · Cited by 37 · see citing works
Regulating bile acids signaling for NAFLD: molecular insights and novel therapeutic interventions
Wei, M., Tu, W., & Huang, G. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1341938 · Cited by 37 · see citing works
Intestinal barrier in chronic gut and liver diseases: Pathogenesis and therapeutic targets
Zhang, Y., Liu, Y., Liang, X., Wen, Y., Zhao, J., He, Y., Xie, Q., & Xie, C. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.08.028 · Cited by 37 · see citing works
Bile acid and its bidirectional interactions with gut microbiota: a review
He, S., Li, L., Yao, Y., Su, J., Lei, S., Zhang, Y., & Zeng, H. (2023) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2023.2262020 · Cited by 35 · see citing works
Targeting Nuclear Receptors for Cancer Therapy: Premises, Promises, and Challenges.
Yang, Z.-N., Gimple, R., Zhou, N.-X., Zhao, L.-J., Gustafsson, J., & Zhou, S.-T. (2020) · Trends in Cancer · doi:10.1016/j.trecan.2020.11.007 · Cited by 33 · see citing works
Immunomodulation by foods and microbes: Unravelling the molecular tango
Forde, B. M., Yao, L., Shaha, R., Murphy, S., Lunjani, N., & O’Mahony, L. (2022) · Allergy · doi:10.1111/all.15455 · Cited by 35 · see citing works
Wu, L. M., Han, Y., Zheng, Z., Zhu, S., Chen, J., Yao, Y., Yue, S., Teufel, A., Weng, H., Li, L., et al. (2021) · Nutrients · doi:10.3390/nu13030940 · Cited by 34 · see citing works
Disruption of intestinal oxygen balance in acute colitis alters the gut microbiome
Zong, W., Friedman, E. S., Allu, S., Firrman, J., Tu, V., Daniel, S. G., Bittinger, K. L., Liu, L., Vinogradov, S. A., & Wu, G. D. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2361493 · Cited by 33 · see citing works
Self-citationFecal microbiome and bile acid metabolome in adult short bowel syndrome
Boutte, H. J., Chen, J., Wylie, T. N., Wylie, K. M., Xie, Y., Geisman, M., Prabu, A., Gazit, V., Tarr, P. I., Levin, M. S., et al. (2022) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00091.2021 · Cited by 33 · see citing works
Carr, R. M., Li, Y., Chau, L., Friedman, E. S., Lee, J., Adorini, L., Erickson, M., Zaru, L., Shringarpure, R., MacConell, L., et al. (2023) · Hepatology · doi:10.1097/hep.0000000000000474 · Cited by 34 · see citing works
Self-citationBile Acid Receptor Therapeutics Effects on Chronic Liver Diseases
Meadows, V., Kennedy, L. L., Kundu, D., Alpini, G. D., & Francis, H. (2020) · Frontiers in Medicine · doi:10.3389/fmed.2020.00015 · Cited by 31 · see citing works
Mouzaki, M., & Loomba, R. S. (2019) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756284819858470 · Cited by 31 · see citing works
Role of Farnesoid X Receptor in the Pathogenesis of Respiratory Diseases
Wu, J., Chen, J., & Chen, J. (2020) · Canadian Respiratory Journal · doi:10.1155/2020/9137251 · Cited by 31 · see citing works
Guo, Z., He, K., Pang, K., Yang, D., Lyu, C., Xu, H., & Wu, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084321 · Cited by 29 · see citing works
Potential of Intestine-Selective FXR Modulation for Treatment of Metabolic Disease
van Zutphen, T., Bertolini, A., de Vries, H. D., Bloks, V. W., de Boer, J. F., Jonker, J. W., & Kuipers, F. (2019) · Handbook of experimental pharmacology · doi:10.1007/164_2019_233 · Cited by 30 · see citing works
Xiong, F., Zheng, Z., Xiao, L., Su, C., Chen, J., Gu, X., Tang, J., Zhao, Y., Luo, H., & Zha, L. (2021) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202100067 · Cited by 29 · see citing works
Nuclear Receptors in the Pathogenesis and Management of Inflammatory Bowel Disease
Ning, L., Lou, X., Zhang, F., & Xu, G. (2019) · Mediators of Inflammation · doi:10.1155/2019/2624941 · Cited by 27 · see citing works
Retroperfusion studies of the aqueous outflow system. Part 2: Studies in human eyes.
Ethier, C. R., Coloma, F. M., de Kater, A. W., & Allingham, R. R. (1995) · PubMed · Cited by 28 · see citing works
Intestine-specific FXR agonists as potential therapeutic agents for colorectal cancer
Yin, Y., Wang, M., Gu, W., & Chen, L. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114430 · Cited by 27 · see citing works
Emerging roles of bile acids in control of intestinal functions
Yang, J., Palmiotti, A., & Kuipers, F. (2020) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000709 · Cited by 26 · see citing works
The Gut‒Liver Axis in Liver Disease: Molecular Mechanisms and Therapeutic Targets
Chen, Z., Liao, S., Wu, S., Chen, S., Tang, Q., Zhou, L., Li, X., Hu, H., Xu, J., Zhang, A., et al. (2025) · MedComm · doi:10.1002/mco2.70458 · Cited by 27 · see citing works
Zeng, Z., Zhou, Y., Xu, Y., Wang, S., Wang, B., Zeng, Z., Wang, Q., Ye, X., Lu, J., Yue, M., et al. (2022) · Food & Function · doi:10.1039/d1fo03170h · Cited by 24 · see citing works
Bile acid–gut microbiota crosstalk in irritable bowel syndrome
Gu, Y., Li, L., Yang, M., Liu, T., Song, X., Qin, X., Xu, X. J., Liu, J., Wang, B., & Cao, H. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2022.2058353 · Cited by 26 · see citing works
Said, I., Ahad, H., & Said, A. (2022) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v14.i5.947 · Cited by 24 · see citing works
Jiang, J., Zhang, H., Hussain, M., Abdullah, Feng, F., Guan, R., & Zhong, H. (2025) · Biology · doi:10.3390/biology14070802 · Cited by 26 · see citing works
Self-citationSecondary bile acids as immune and metabolic mediators
Fiorucci, S., Biagioli, M., Marchianò, S., Zampella, A., & Distrutti, E. (2026) · Trends in Immunology · doi:10.1016/j.it.2025.12.008 · Cited by 23 · see citing works
Nonalcoholic fatty liver disease and the gut microbiome: Are bacteria responsible for fatty liver?
Dong, T. S., & Jacobs, J. P. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219836739 · Cited by 22 · see citing works
Sun, Q., Xin, X., An, Z., Hu, Y., & Feng, Q. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.854879 · Cited by 20 · see citing works
Li, Y., Wang, K., Ding, J., Sun, S., Ni, Z., & Yu, C. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.954684 · Cited by 20 · see citing works
Self-citationLiu, Y., Xiao, Y., Chen, S., Tian, X., Wang, W., Wang, Y., & Cai, W. (2021) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000003135 · Cited by 20 · see citing works
Marzano, M., Fosso, B., Colliva, C., Notario, E., Passeri, D., Intranuovo, M., Gioiello, A., Adorini, L., Pesole, G., Pellicciari, R., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113380 · Cited by 20 · see citing works
Self-citationEffects of bile acid metabolism on intestinal health of livestock and poultry
Jia, H., & Dong, N. (2024) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.13969 · Cited by 19 · see citing works
Metabolic Analysis of Regionally Distinct Gut Microbial Communities Using an In Vitro Platform
Firrman, J., Liu, L., Tanes, C., Friedman, E. S., Bittinger, K. L., Daniel, S. G., den Abbeele, P. V., & Evans, B. S. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b05202 · Cited by 19 · see citing works
Self-citationChen, P., Jiang, X., Fu, J., Ou, C., Li, Y., Jia, J., & Liao, C. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1419160 · Cited by 19 · see citing works
Self-citationFarnesoid X receptor: a potential therapeutic target in multiple organs.
Zhang, C., Wang, Z., Feng, Q., Chen, W.-D., & Wang, Y.-D. (2021) · Histology and Histopathology · doi:10.14670/hh-18-301 · Cited by 16 · see citing works
Antibiotic exposure is associated with minimal gut microbiome perturbations in healthy term infants
Benitez, A., Tanes, C., Friedman, E. S., Zackular, J. P., Ford, E., Gerber, J. S., DeRusso, P. A., Kelly, A. T., Li, H., Elovitz, M. A., et al. (2025) · Microbiome · doi:10.1186/s40168-024-01999-3 · Cited by 18 · see citing works
Self-citationSecretory IgM regulates gut microbiota homeostasis and metabolism
Ding, Y., Fernández-Montero, Á., Mani, A., Casadei, E., Miyazawa, R., Zhou, C., Chaumont, L., Posavi, M., Cole, S. D., Shibasaki, Y., et al. (2025) · Nature Microbiology · doi:10.1038/s41564-025-02013-8 · Cited by 17 · see citing works
Lin, X., Zhu, X., Xin, Y., Zhang, P., Xiao, Y., He, T., & Guo, H. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202200595 · Cited by 17 · see citing works
Mo, Q., Deng, X., Zhou, Z., & Yin, L. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104777 · Cited by 18 · see citing works
Wu, Y., Wang, Z., Zhao, Z., Song, X., Miao, M., & Zhang, X. (2023) · Diabetes Obesity and Metabolism · doi:10.1111/dom.15104 · Cited by 17 · see citing works
Mao, J., Wei, Y., Ni, Z., Zhang, J., Zhu, J., & Wang, H. (2025) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-025-01169-x · Cited by 15 · see citing works
Wang, L. J., Sun, J., Chen, S., Sun, Y., Zheng, Y., & Feng, J. C. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2024.1490929 · Cited by 18 · see citing works
Zhang, C., Gan, Y., Lv, J.-W., Qin, M.-Q., Hu, W., Liu, Z.-B., Ma, L., Song, B., Li, J., Jiang, W., et al. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.106442 · Cited by 15 · see citing works
Hou, M., Song, P., Chen, Y., Yang, X., Chen, P., Cao, A., & Ni, Y. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117313 · Cited by 14 · see citing works
Chewing the Fat with Microbes: Lipid Crosstalk in the Gut
Lemons, J. M. S., & Liu, L. (2022) · Nutrients · doi:10.3390/nu14030573 · Cited by 14 · see citing works
Histamine Causes Pyroptosis of Liver by Regulating Gut-Liver Axis in Mice
Luo, Q., Shi, R., Liu, Y., Huang, L., Chen, W., & Wang, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073710 · Cited by 14 · see citing works
Tang, Q., & Evans, R. M. (2021) · Essays in Biochemistry · doi:10.1042/ebc20210038 · Cited by 14 · see citing works
Dietary Fiber Modulates the Window of Susceptibility to Clostridioides difficile Infection
Hewlett, K. K., PeBenito, A., Hecht, A. L., Tiffany, C. R., Tanes, C., Glover, R. C., Fawad, J. A., Friedman, E. S., Reynolds, J. C., Bittinger, K. L., et al. (2025) · Gastroenterology · doi:10.1053/j.gastro.2025.04.027 · Cited by 13 · see citing works
Self-citationNew insights into gut-liver axis in advanced liver diseases: A promising therapeutic target
Xing, Y., Ou, Y., Wang, Y., Hou, L., & Zhu, J. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117284 · Cited by 13 · see citing works
- Authors
- Friedman, E. S., Li, Y., Shen, T.-C. D., Jiang, J., Chau, L., Adorini, L., Babakhani, F., Edwards, J., Shapiro, D., Zhao, C., Carr, R. M., Bittinger, K., Li, H., & Wu, G. D.
- Affiliations
- University of Pennsylvania (US)
- Intercept Pharmaceuticals (United States) (US)
- Children's Hospital of Philadelphia (US)
- Corresponding author
- Wu, Gary D.
- ORCID
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2018-12
- Volume
- 155
- Issue
- 6
- Pages
- 1741-1752.e5
- ISSN
- 0016-5085 (ISSN-L)
- PMC
- PMC6279623
- OpenAlex
- W2888639734
- Semantic Scholar
- 112d9c4c64a59c5fa23a506e2249278055eca2ff
- Cited by
- 149
- References
- 44
- Citations by year
- 2026: 15 · 2025: 28 · 2024: 19 · 2023: 16 · 2022: 19 · 2021: 17 · 2020: 16 · 2019: 17
- FWCI
- 4.44
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Alcohol Abuse and Alcoholism (K08AA021424, R01AA026302)
- National Institute of General Medical Sciences (R01GM123056)
- National Institute of Diabetes and Digestive and Kidney Diseases (K08DK106457, P30DK019525, P30DK050306)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- obeticholic acid, farnesoid X receptor, bile acids, gut microbiota, bile acid synthesis inhibition, Gram-positive bacteria, Firmicutes, bacterial growth inhibition, microbiome biomarkers
- MeSH terms
- Gastrointestinal Microbiome, Receptor, Farnesoid X-Activated, Adult, Animals, Bile Acids and Salts, Chenodeoxycholic Acid, Female, Humans, Intestine, Small, Male, Mice, Inbred C57BL, Receptors, Cytoplasmic and Nuclear, Mice, Healthy Volunteers
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review