Evidence map›Paper›PMID 26045265›Full record

ReviewDigestive diseases (Basel, Switzerland)2015

Bile Acids as Hormones: The FXR-FGF15/19 Pathway.

Steven A Kliewer, David J Mangelsdorf

Open access · bronzeAbstract readReview
In one paragraph

Review in Digestive diseases (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 221 papers.

0numbers the graph read from it
0cells of the map it votes in
221citing papers in PubMed
10.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

221 citing papers in PubMed, 400 citations in OpenAlex.

  1. Trial
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  7. Review
  8. Article
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  10. The Role of Gut Microbiota in Liver Regeneration After Partial Hepatectomy: New Evidence From Animal and Human Studies.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  11. Article
  12. Article
  13. TheJHEP reports : innovation in hepatology · 2026
    Article
  14. Review
  15. Review
  16. Bile acid signaling, metabolism, and aging.Liver research (Beijing, China) · 2026
    Review
  17. Article
  18. Review
  19. Article
  20. Review

161 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Steven A KliewerDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Tex., USA.
David J Mangelsdorf
The University of Texas Southwestern Medical Center · US

Funding

Tissue-specific Mechanism of Action of the Metabolic Hormones FGF19 and FGF21R01DK067158 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI KLIEWER, STEVEN A. · 2004 to 2017
$4.1M
Howard Hughes Medical InstituteNIDDK NIH HHS DK067158NIDDK NIH HHS R01 DK067158
6 · The paper itself

Abstract

While it has long been recognized that bile acids are essential for solubilizing lipophilic nutrients in the small intestine, the discovery in 1999 that bile acids serve as ligands for the nuclear receptor farnesoid X receptor (FXR) opened the floodgates in terms of characterizing their actions as selective signaling molecules. Bile acids act on FXR in ileal enterocytes to induce the expression of fibroblast growth factor (FGF)15/19, an atypical FGF that functions as a hormone. FGF15/19 subsequently acts on a cell surface receptor complex in hepatocytes to repress bile acid synthesis and gluconeogenesis, and to stimulate glycogen and protein synthesis. FGF15/19 also stimulates gallbladder filling. Thus, the bile acid-FXR-FGF15/19 signaling pathway regulates diverse aspects of the postprandial enterohepatic response. Pharmacologically, this endocrine pathway provides exciting new opportunities for treating metabolic disease and bile acid-related disorders such as primary biliary cirrhosis and bile acid diarrhea. Both FXR agonists and FGF19 analogs are currently in clinical trials.

Indexed as

Signal TransductionAnimalsBile Acids and SaltsCholesterol 7-alpha-HydroxylaseEnterocytesFibroblast Growth FactorsGene Expression RegulationGluconeogenesisGlycogenHomeostasisHumansInsulin ResistanceLipid MetabolismMiceReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearBile Acids and SaltsCholesterol 7-alpha-HydroxylaseCyp7a1 protein, mouseFGF19 protein, humanfibroblast growth factor 15, mouseFibroblast Growth FactorsGlycogennuclear receptor subfamily 0, group B, member 2Receptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and Nuclear

Identifiers

PMID26045265
PMCPMC4465534
OpenAlexW1555526329

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.