Evidence map›Paper›PMID 32259714›Full record

ArticleEBioMedicine2020

Fibroblast Growth Factor 19 modulates intestinal microbiota and inflammation in presence of Farnesoid X Receptor.

Raffaella Maria Gadaleta, Oihane Garcia-Irigoyen, Marica Cariello, Natasha Scialpi, Claudia Peres, Stefania Vetrano, Gionatha Fiorino, Silvio Danese, Brian Ko, Jian Luo and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

  1. Pooled it
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  7. Role of Bile Acid Receptors in Non-Infectious Diarrhea: A Narrative Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
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  10. Regulation of Tph cell differentiation via farnesoid X receptor of dendritic cells in inflammatory bowel disease.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 2 countries.

Raffaella Maria GadaletaDepartment of Interdisciplinary Medicine, "Aldo Moro" University, Piazza Giulio Cesare 11, 70124 Bari, Italy; National Institute for Biostructures and Biosystems, Via delle Medaglie d'Oro 135, 00136 Rome, Italy.
Oihane Garcia-IrigoyenDepartment of Interdisciplinary Medicine, "Aldo Moro" University, Piazza Giulio Cesare 11, 70124 Bari, Italy.
Marica CarielloDepartment of Interdisciplinary Medicine, "Aldo Moro" University, Piazza Giulio Cesare 11, 70124 Bari, Italy.
Natasha ScialpiNational Institute for Biostructures and Biosystems, Via delle Medaglie d'Oro 135, 00136 Rome, Italy.
Claudia PeresNational Institute for Biostructures and Biosystems, Via delle Medaglie d'Oro 135, 00136 Rome, Italy.
Stefania VetranoDepartment of Biomedical Sciences, Humanitas University, Via Alessandro Manzoni, 56, 20089 Rozzano, Milan, Italy; Inflammatory Bowel Disease Center, Humanitas Cancer Center, via Rita Levi Montalcini 4, 20090 Milan, Italy.
Gionatha FiorinoInflammatory Bowel Disease Center, Humanitas Cancer Center, via Rita Levi Montalcini 4, 20090 Milan, Italy.
Silvio DaneseDepartment of Biomedical Sciences, Humanitas University, Via Alessandro Manzoni, 56, 20089 Rozzano, Milan, Italy; Inflammatory Bowel Disease Center, Humanitas Cancer Center, via Rita Levi Montalcini 4, 20090 Milan, Italy.
Brian KoNGM Biopharmaceuticals Inc., 333 Oyster Point Blvd, South San Francisco, CA 94080, USA.
Jian LuoNGM Biopharmaceuticals Inc., 333 Oyster Point Blvd, South San Francisco, CA 94080, USA.
Emanuele PorruDepartment of Chemistry "Giacomo Ciamician", Alma Mater Studiorum, University of Bologna, Via Selmi, 2, 40126 Bologna, Italy.
Aldo RodaDepartment of Chemistry "Giacomo Ciamician", Alma Mater Studiorum, University of Bologna, Via Selmi, 2, 40126 Bologna, Italy.
Carlo SabbàDepartment of Interdisciplinary Medicine, "Aldo Moro" University, Piazza Giulio Cesare 11, 70124 Bari, Italy.
Antonio MoschettaDepartment of Interdisciplinary Medicine, "Aldo Moro" University, Piazza Giulio Cesare 11, 70124 Bari, Italy; National Cancer Center, IRCCS Istituto Tumori "Giovanni Paolo II", Viale Orazio Flacco, 65, 70124 Bari, Italy. Electronic address: antonio.moschetta@uniba.it.
Humanitas University · ITUniversity of Bari Aldo Moro · ITNGM Biopharmaceuticals (United States) · USUniversity of Bologna · ITIstituto Nazionale Biostrutture e Biosistemi · ITIstituto Tumori Bari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDisruption of bile acid (BA) homeostasis plays a key role in intestinal inflammation. The gut-liver axis is the main site for the regulation of BA synthesis and BA pool size via the combined action of the nuclear Farnesoid X Receptor (FXR) and the enterokine Fibroblast Growth Factor 19 (FGF19). Increasing evidence have linked derangement of BA metabolism with dysbiosis and mucosal inflammation. Thus, here we aimed to investigate the potential action of an FGF19 analogue on intestinal microbiota and inflammation.

methodsA novel engineered non-tumorigenic variant of the FGF19 protein, M52-WO 2016/0168219 was generated. WT and FXR

findingsFGF19-M52 reduced BA synthesis and pool size, modulated its composition and protected mice from intestinal inflammation. These events were coupled with preservation of the intestinal epithelial barrier integrity, inhibition of inflammatory immune response and modulation of microbiota composition. Interestingly, FGF19-M52-driven systemic and local anti-inflammatory activity was completely abolished in Farnesoid X Receptor (FXR)

interpretationReactivation of the FXR-FGF19 axis in a murine model of intestinal inflammation could bona fide provide positive changes in BA metabolism with consequent reduction of intestinal inflammation and modulation of microbiota. These results point to the therapeutic potential of FGF19 in the treatment of intestinal inflammation with concomitant derangement of BA homeostasis.

fundingA. Moschetta is funded by MIUR-PRIN 2017 <- 2017J3E2W2; Italian Association for Cancer Research (AIRC, IG 23239); Interreg V-A Greece-Italy 2014-2020-SILVER WELLBEING, MIS5003627; HDHL-INTIMIC EuJPI-FATMAL; MIUR PON "R&I" 2014-2020-ARS01_01220. No money has been paid by NGM Biopharmaceuticals or any other agency to write this article.

Indexed as

Gastrointestinal MicrobiomeAnimalsAnti-Inflammatory AgentsBile Acids and SaltsColitis, UlcerativeCrohn DiseaseFemaleFibroblast Growth FactorsHumansMaleMiceMice, Inbred C57BLPeptidesReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearRecombinant ProteinsAnti-Inflammatory AgentsBile Acids and Saltsfibroblast growth factor 15, mouseFibroblast Growth FactorsPeptidesReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearRecombinant ProteinsBile acidsDSS-colitisEnterokineIntestinal inflammationNuclear receptors

Identifiers

PMID32259714
PMCPMC7136604
OpenAlexW3014272029

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.