Evidence map›Paper›PMID 38797244›Full record

ReviewNeuropharmacology2024

FGF21 as a mediator of adaptive changes in food intake and macronutrient preference in response to protein restriction.

Sora Q Kim, Redin A Spann, Md Shahjalal H Khan, Hans-Rudolf Berthoud, Heike Münzberg, Vance L Albaugh, Yanlin He, David H McDougal, Paul Soto, Sangho Yu and 1 more

Abstract readReview
In one paragraph

Review in Neuropharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
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

11 authors.

Sora Q KimPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Redin A SpannPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Md Shahjalal H KhanPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Hans-Rudolf BerthoudPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Heike MünzbergPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Vance L AlbaughPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA; Department of Surgery, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Yanlin HePennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
David H McDougalPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Paul SotoDepartment of Psychology, Louisiana State University, Baton Rouge, LA, 70810, USA.
Sangho YuPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Christopher D MorrisonPennington Biomedical Research Center, Baton Rouge, LA, 70808, USA. Electronic address: Christopher.Morrison@pbrc.edu.

Funding

Training in Obesity ResearchT32DK064584 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI CORBY K MARTIN, Christopher D Morrison · 2003 to 2026
$5.3M
Neural circuits coordinating protein intake: Role of FGF21R01DK123083 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2020 to 2024
$1.6M
FGF21-dependent mechanisms driving changes in energy expenditure during dietary protein restrictionR01DK121370 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MORRISON, CHRISTOPHER D · 2020 to 2023
$1.5M
Central FGF21-mediated control of energy expenditure.F32DK130544 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI SPANN, REDIN A · 2021 to 2022
$134k
NIDDK NIH HHS F32 DK130544NIDDK NIH HHS R01 DK121370NIDDK NIH HHS R01 DK123083NIDDK NIH HHS T32 DK064584
6 · The paper itself

Abstract

Free-feeding animals navigate complex nutritional landscapes in which food availability, cost, and nutritional value can vary markedly. Animals have thus developed neural mechanisms that enable the detection of nutrient restriction, and these mechanisms engage adaptive physiological and behavioral responses that limit or reverse this nutrient restriction. This review focuses specifically on dietary protein as an essential and independently defended nutrient. Adequate protein intake is required for life, and ample evidence exists to support an active defense of protein that involves behavioral changes in food intake, food preference, and food motivation, likely mediated by neural changes that increase the reward value of protein foods. Available evidence also suggests that the circulating hormone fibroblast growth factor 21 (FGF21) acts in the brain to coordinate these adaptive changes in food intake, making it a unique endocrine signal that drives changes in macronutrient preference in the context of protein restriction. This article is part of the Special Issue on "Food intake and feeding states".

Indexed as

EatingFibroblast Growth FactorsFood PreferencesAdaptation, PhysiologicalAnimalsBrainDietary ProteinsDiet, Protein-RestrictedHumansNutrientsDietary Proteinsfibroblast growth factor 21Fibroblast Growth FactorsNutrientsDopamineFeeding behaviorFibroblast growth factor 21 (FGF21)PreferenceProtein restrictionReward

Identifiers

PMID38797244
PMCPMC11156534

What Socratic 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 Socratic graph.