Evidence map›Paper›PMID 31167139›Full record

ArticleCell reports2019

FGF21 Signals Protein Status to the Brain and Adaptively Regulates Food Choice and Metabolism.

Cristal M Hill, Thomas Laeger, Madeleine Dehner, Diana C Albarado, Blaise Clarke, Desiree Wanders, Susan J Burke, J Jason Collier, Emily Qualls-Creekmore, Samantha M Solon-Biet and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 1 pooled it
9.2field-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

131 citing papers in PubMed, 1 synthesis or guideline pooled it, 223 citations in OpenAlex.

  1. Liver Brain Interactions: Focus on FGF21 a Systematic Review.International journal of molecular sciences · 2022
    Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Protein Decoys, Alcohol, and Energy Intake: Testing a Mechanistic-Ecological Model.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. FGF21 analogue PF-05231023 on alcohol consumption and neuronal activity in the nucleus accumbens.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  17. Review
  18. Article
  19. Article
  20. Article

71 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

14 authors at 3 institutions in 2 countries.

Cristal M HillPennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Thomas LaegerPennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Madeleine DehnerPennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Diana C AlbaradoPennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Blaise ClarkePennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Desiree WandersGeorgia State University, Atlanta, GA 30302, USA.
Susan J BurkePennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
J Jason CollierPennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Emily Qualls-CreekmorePennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Samantha M Solon-BietCharles Perkins Centre, School of Life and Environmental Sciences, The University of Sydney, NSW 2006, Australia.
Stephen J SimpsonCharles Perkins Centre, School of Life and Environmental Sciences, The University of Sydney, NSW 2006, Australia.
Hans-Rudolf BerthoudPennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Heike MünzbergPennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Christopher D MorrisonPennington Biomedical Research Center, Baton Rouge, LA 70808, USA. Electronic address: morriscd@pbrc.edu.
Pennington Biomedical Research Center · USUniversity of Sydney · AUGeorgia State University · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
Transgenics CoreP30GM118430 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2016 to 2020
$5.8M
Neural mechanisms controlling food intake and body weight after bariatric surgeryR01DK047348 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI BERTHOUD, HANS-RUDOLF · 1994 to 2018
$5.0M
Leptin and Central Control of ThermoregulationR01DK092587 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MUENZBERG-GRUENING, HEIKE · 2012 to 2024
$3.5M
FGF21 is an endocrine signal of protein restrictionR01DK105032 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2016 to 2019
$1.4M
Sable Systems Promethion for Mouse Metabolic AnalysisS10OD023703 · OD · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2017 to 2017
$626k
A Unique Receptor Agonist Approach for Type 1 Diabetes PreventionR21AI138136 · NIAID · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI COLLIER, JAMES JASON · 2018 to 2019
$436k
Neuronal FGF21 Signaling in the Detection of Dietary Protein RestrictionF32DK115137 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI HILL, CRISTAL MONIQUE · 2017 to 2019
$185k
NIAID NIH HHS R21 AI138136NIDDK NIH HHS F32 DK115137NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R01 DK047348NIDDK NIH HHS R01 DK092587NIDDK NIH HHS R01 DK105032NIGMS NIH HHS P30 GM118430NIH HHS S10 OD023703
6 · The paper itself

Abstract

Reduced dietary protein intake induces adaptive physiological changes in macronutrient preference, energy expenditure, growth, and glucose homeostasis. We demonstrate that deletion of the FGF21 co-receptor βKlotho (Klb) from the brain produces mice that are unable to mount a physiological response to protein restriction, an effect that is replicated by whole-body deletion of FGF21. Mice forced to consume a low-protein diet exhibit reduced growth, increased energy expenditure, and a resistance to diet-induced obesity, but the loss of FGF21 signaling in the brain completely abrogates that response. When given access to a higher protein alternative, protein-restricted mice exhibit a shift toward protein-containing foods, and central FGF21 signaling is essential for that response. FGF21 is an endocrine signal linking the liver and brain, which regulates adaptive, homeostatic changes in metabolism and feeding behavior during protein restriction.

Indexed as

Diet, Protein-RestrictedFeeding BehaviorAdipose TissueAnimalsBrainDiet, High-FatFibroblast Growth FactorsFood PreferencesGlucose IntoleranceInsulin ResistanceKlotho ProteinsLiverMaleMembrane ProteinsMiceMice, Inbred C57BLFGF21 protein, humanfibroblast growth factor 21Fibroblast Growth FactorsKlb protein, mouseKlotho ProteinsMembrane Proteinscentral nervous systemdietary protein restrictionFGF21Klbmacronutrientnutrition

Identifiers

PMID31167139
PMCPMC6579533
OpenAlexW2948182761

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.