Evidence map›Paper›PMID 35998055›Full record

ArticleJCI insight2022

FGF21 controls hepatic lipid metabolism via sex-dependent interorgan crosstalk.

Aki T Chaffin, Karlton R Larson, Kuei-Pin Huang, Chih-Ting Wu, Nadejda Godoroja, Yanbin Fang, Devi Jayakrishnan, Karla A Soto Sauza, Landon C Sims, Niloufar Mohajerani and 2 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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
  5. Article
  6. 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
  7. Hepatic FGF21 Deletion Improves Glucose Metabolism, Alters Lipogenic andInternational journal of molecular sciences · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. FGF21 mediating the Sex-dependent Response to Dietary Macronutrients.The Journal of clinical endocrinology and metabolism · 2024
    Review
  18. Article
  19. Article
  20. Article
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

12 authors at 1 institution in 1 country.

Aki T ChaffinDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Karlton R LarsonDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Kuei-Pin HuangDepartment of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California, Davis, Davis, California, USA.
Chih-Ting WuDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Nadejda GodorojaDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Yanbin FangDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Devi JayakrishnanDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Karla A Soto SauzaDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Landon C SimsDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Niloufar MohajeraniDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Michael L GoodsonDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
Karen K RyanDepartment of Neurobiology, Physiology and Behavior, College of Biological Sciences, and.
University of California, Davis · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
UC Davis CTSC TL1 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility MentorshipTL1TR001861 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MEDICI, VALENTINA · 2016 to 2025
$4.7M
Predoctoral Training in Pharmacological SciencesT32GM099608 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2021
$2.2M
Training Program in PharmacologyT32GM144303 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Donald M Bers, JOHANNES W HELL · 2022 to 2026
$2.1M
The novel role of FGF21 in mediating sex-dependent responses to dietary macronutrientsR01DK121035 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RYAN, KAREN · 2019 to 2023
$1.9M
Acquisition of Covaris E220 and Sciclone G3 systems for high throughput sequencinS10OD010786 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI COMAI, LUCA · 2012 to 2012
$311k
Central mechanisms of fibroblast growth factor-21 to decrease hepatic triglyceridesF31DK124080 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHAFFIN, AKI TERATA-BOWERS · 2020 to 2021
$76k
NCATS NIH HHS TL1 TR001861NCATS NIH HHS UL1 TR001860NIDDK NIH HHS F31 DK124080NIDDK NIH HHS R01 DK121035NIGMS NIH HHS T32 GM007377NIGMS NIH HHS T32 GM099608NIGMS NIH HHS T32 GM144303NIH HHS S10 OD010786
6 · The paper itself

Abstract

The liver regulates energy partitioning and use in a sex-dependent manner, coupling hepatic substrate availability to female reproductive status. Fibroblast growth factor 21 (FGF21) is a hepatokine produced in response to metabolic stress that adaptively directs systemic metabolism and substrate use to reduce hepatic lipid storage. Here we report that FGF21 altered hepatic transcriptional and metabolic responses, and reduced liver triglycerides, in a sex-dependent manner. FGF21 decreased hepatic triglycerides in obese male mice in a weight loss-independent manner; this was abrogated among female littermates. The effect of FGF21 on hepatosteatosis is thought to derive, in part, from increased adiponectin secretion. Accordingly, plasma adiponectin and its upstream adrenergic receptor → cAMP → exchange protein directly activated by cAMP signaling pathway was stimulated by FGF21 in males and inhibited in females. Both ovariectomized and reproductively senescent old females responded to FGF21 treatment by decreasing body weight, but liver triglycerides and adiponectin remained unchanged. Thus, the benefit of FGF21 treatment for improving hepatosteatosis depends on sex but not on a functional female reproductive system. Because FGF21 provides a downstream mechanism contributing to several metabolic interventions, and given its direct clinical importance, these findings may have broad implications for the targeted application of nutritional and pharmacological treatments for metabolic disease.

Indexed as

AdiponectinFibroblast Growth FactorsLipid MetabolismAnimalsFemaleLipidsLiverMaleMiceMice, ObeseReceptors, AdrenergicTriglyceridesAdiponectinfibroblast growth factor 21Fibroblast Growth FactorsLipidsReceptors, AdrenergicTriglyceridesEndocrinologyGrowth factorsHepatologyObesitySex hormones

Identifiers

PMID35998055
PMCPMC9675565
OpenAlexW4292774827

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.