Evidence map›Paper›PMID 33761350›Full record

ArticleCell reports2021

FoxO1 suppresses Fgf21 during hepatic insulin resistance to impair peripheral glucose utilization and acute cold tolerance.

Oliver Stöhr, Rongya Tao, Ji Miao, Kyle D Copps, Morris F White

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  9. Review
  10. Article
  11. The role of hepatokines in NAFLD.Cell metabolism · 2023
    Review
  12. Article
  13. 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

5 authors at 2 institutions in 1 country.

Oliver StöhrDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02215, USA.
Rongya TaoDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02215, USA.
Ji MiaoDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02215, USA.
Kyle D CoppsDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02215, USA.
Morris F WhiteDivision of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02215, USA. Electronic address: morris.white@childrens.harvard.edu.
Boston Children's Hospital · USHarvard University · US

Funding

CAREER DEVELOPMENT IN DIABETES RESEARCH FOR PEDIATRIC ENDOCRINOLOGISTSK12DK094721 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI LAFFEL, LORI M, WHITE, MORRIS F. · 2011 to 2021
$6.3M
Metabolic Crosstalk During Hepatic Insulin ResistanceR01DK098655 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI WHITE, MORRIS F. · 2013 to 2020
$4.0M
Regulation of hippocampal function by central and peripheral IRS signalingR01AG067913 · NIA · BOSTON CHILDREN'S HOSPITAL · PI WHITE, MORRIS F. · 2020 to 2024
$3.1M
Role of TAZ in metabolic regulation in both normal and insulin resistant statesR01DK124328 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI MIAO, JI · 2021 to 2025
$2.2M
Insulin Regulation of Liver X Receptor in Normal and Insulin Resistant StatesR00DK100539 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI MIAO, JI · 2016 to 2018
$747k
Hepatic insulin resistance integrates T2D and NAFLDR56DK098655 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI WHITE, MORRIS F. · 2023 to 2023
$150k
NIA NIH HHS R01 AG067913NIDDK NIH HHS K12 DK094721NIDDK NIH HHS R00 DK100539NIDDK NIH HHS R01 DK098655NIDDK NIH HHS R01 DK124328NIDDK NIH HHS R56 DK098655
6 · The paper itself

Abstract

Fgf21 (fibroblast growth factor 21) is a regulatory hepatokine that, in pharmacologic form, powerfully promotes weight loss and glucose homeostasis. Although "Fgf21 resistance" is inferred from higher plasma Fgf21 levels in insulin-resistant mice and humans, diminished Fgf21 function is understood primarily via Fgf21 knockout mice. By contrast, we show that modestly reduced Fgf21-owing to cell-autonomous suppression by hepatic FoxO1-contributes to dysregulated metabolism in LDKO mice (Irs1

Indexed as

Adaptation, PhysiologicalCold TemperatureInsulin ResistanceAdipocytes, BrownAdipose Tissue, BrownAnimalsBlood GlucoseBody WeightDiet, High-FatFibroblast Growth FactorsForkhead Box Protein O1Gene Expression RegulationGlucoseHomeostasisInsulinInsulin Receptor Substrate ProteinsBlood Glucosefibroblast growth factor 21Fibroblast Growth FactorsForkhead Box Protein O1GlucoseInsulinInsulin Receptor Substrate ProteinsIrs2 protein, mousebrown adipose tissuecold intoleranceFGF21FoxO1glucose disposalhepatic insulin resistancehepatokineinsulin receptor substrateperipheral insulin resistance

Identifiers

PMID33761350
PMCPMC8529953
OpenAlexW3136943178

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.