Evidence map›Paper›PMID 23933983›Full record

ArticleNature medicine2013

FGF21 contributes to neuroendocrine control of female reproduction.

Bryn M Owen, Angie L Bookout, Xunshan Ding, Vicky Y Lin, Stan D Atkin, Laurent Gautron, Steven A Kliewer, David J Mangelsdorf

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
11.1field-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

128 citing papers in PubMed, 224 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Hypothalamus-liver talks: whispers in the language of metabolism.Reviews in endocrine & metabolic disorders · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Hepatic FGF21 Deletion Improves Glucose Metabolism, Alters Lipogenic andInternational journal of molecular sciences · 2025
    Article
  12. Review
  13. Review
  14. Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
  15. Observational
  16. Review
  17. Review
  18. Article
  19. Metabolic Crosstalk between Liver and Brain: From Diseases to Mechanisms.International journal of molecular sciences · 2024
    Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Bryn M OwenDepartment of Pharmacology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Angie L Bookout
Xunshan Ding
Vicky Y Lin
Stan D Atkin
Laurent Gautron
Steven A Kliewer
David J Mangelsdorf
The University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

ProteomicsU19DK062434 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MANGELSDORF, DAVID J · 2002 to 2011
$37.4M
PROJECT 3 - Steroid-Metabolic Interactions In the Control of GnRH NeuronsU54HD028934 · NICHD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI MARSHALL, JOHN C · 1998 to 2013
$16.5M
MECHANISMS OF DRUG ACTION AND DISPOSITIONT32GM007062 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI MANGELSDORF, DAVID J · 1985 to 2020
$7.4M
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
Role of FGF21 as a Hormonal Mediator of PPARalpha Actions, Project 4 of 10RL1GM084436 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI MANGELSDORF, DAVID J · 2007 to 2011
$1.9M
The PPARgamma-FGF21 Signaling Pathway: Its Role in Thiazolidinedione Drug ActionR56DK089600 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI KLIEWER, STEVEN A. · 2010 to 2010
$238k
Howard Hughes Medical InstituteNICHD NIH HHS U54 HD028934NICHD NIH HHS U54-HD28934NIDDK NIH HHS R01 DK067158NIDDK NIH HHS R01DK067158NIDDK NIH HHS R56 DK089600NIDDK NIH HHS R56DK089600NIDDK NIH HHS U19 DK062434NIDDK NIH HHS U19DK62434NIGMS NIH HHS GM007062NIGMS NIH HHS RL1 GM084436NIGMS NIH HHS RL1GM084436NIGMS NIH HHS T32 GM007062
6 · The paper itself

Abstract

Preventing reproduction during nutritional deprivation is an adaptive process that is conserved and essential for the survival of species. In mammals, the mechanisms that inhibit fertility during starvation are complex and incompletely understood. Here we show that exposure of female mice to fibroblast growth factor 21 (FGF21), a fasting-induced hepatokine, mimics infertility secondary to starvation. Mechanistically, FGF21 acts on the suprachiasmatic nucleus (SCN) in the hypothalamus to suppress the vasopressin-kisspeptin signaling cascade, thereby inhibiting the proestrus surge in luteinizing hormone. Mice lacking the FGF21 co-receptor, β-Klotho, in the SCN are refractory to the inhibitory effect of FGF21 on female fertility. Thus, FGF21 defines an important liver-neuroendocrine axis that modulates female reproduction in response to nutritional challenge.

Indexed as

ReproductionAnimalsEnergy MetabolismFemaleFibroblast Growth FactorsHypothalamusInfertility, FemaleKisspeptinsKlotho ProteinsLuteinizing HormoneMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutProestrusSignal Transductionfibroblast growth factor 21Fibroblast Growth FactorsKisspeptinsKlb protein, mouseKlotho ProteinsLuteinizing HormoneMembrane ProteinsVasopressins

Identifiers

PMID23933983
PMCPMC3769455
OpenAlexW1963690531

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.