Evidence map›Paper›PMID 32165710›Full record

ArticleScientific reports2020

Exogenous GDF11, but not GDF8, reduces body weight and improves glucose homeostasis in mice.

Ryan G Walker, Ornella Barrandon, Tommaso Poggioli, Sezin Dagdeviren, Shannon H Carroll, Melanie J Mills, Kourtney R Mendello, Yanet Gomez, Francesco S Loffredo, James R Pancoast and 11 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. GDF11: An emerging therapeutic target for liver diseases and fibrosis.Journal of cellular and molecular medicine · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
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  15. 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

21 authors at 4 institutions in 1 country.

Ryan G Walker *Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Ornella Barrandon *Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Tommaso PoggioliDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Sezin DagdevirenDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Shannon H CarrollDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Melanie J MillsDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Kourtney R MendelloDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Yanet GomezDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Francesco S LoffredoDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
James R PancoastDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Claudio Macias-TrevinoDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Colin MartsDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Katherine B LeClairDivision of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 02139, USA.
Hye-Lim NohProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, 01605, USA.
Taekyoon KimProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, 01605, USA.
Alexander S BanksDivision of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Jason K KimProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, 01605, USA.
David E CohenDivision of Gastroenterology and Hepatology, Weill Cornell Medicine, New York, NY, USA.
Amy J WagersDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Douglas A MeltonDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA.
Richard T LeeDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, 02138, USA. Richard_Lee@harvard.edu.
Harvard University · USUniversity of Massachusetts Chan Medical School · USBrigham and Women's Hospital · USWeill Cornell Medicine · US

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI JONATHAN C KAGAN · 1986 to 2026
$32.4M
MULTIDISCIPLINARY RESEARCH TRAINING IN CARDIOLOGYT32HL007208 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Patrick Thomas Ellinor, David E Sosnovik · 1985 to 2026
$16.1M
UMass Mouse Metabolic Phenotyping Center - Metabolism CoreU2CDK093000 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2016 to 2021
$4.6M
Mechanism of Gdf3 action to limit insulin sensitivity in obesityR01DK107717 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BANKS, ALEXANDER · 2016 to 2023
$3.8M
Regulation and Function of Growth Differentiation Factor 11 During Development and AgingR01AG048917 · NIA · HARVARD UNIVERSITY · PI WAGERS, AMY JO · 2016 to 2020
$2.8M
Investigating GDF11 and MSTN as candidate circulating geronic factorsR01AG057428 · NIA · HARVARD UNIVERSITY · PI WAGERS, AMY JO · 2017 to 2020
$2.0M
Aging and Myocardial Progenitor RecruitmentR01AG032977 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LEE, RICHARD T · 2009 to 2013
$1.9M
A New Pathway for Reversing Cardiac AgingR01AG047131 · NIA · HARVARD UNIVERSITY · PI LEE, RICHARD T · 2015 to 2019
$1.7M
PREVENTING METABOLIC DECLINE IN ADOLESCENTS WITH IDDMR01DK046887 · NIDDK · JOSLIN DIABETES CENTER · PI LAFFEL, LORI M · 1993 to 2001
$515k
Circulating FSTL3 and Age-related Cardiac HypertrophyR03AG049657 · NIA · HARVARD UNIVERSITY · PI LEE, RICHARD T · 2015 to 2016
$339k
Regulation and function of Growth Differentiation Factor 11 during development and agingR56AG048917 · NIA · HARVARD UNIVERSITY · PI WAGERS, AMY JO · 2015 to 2015
$338k
NHLBI NIH HHS T32 HL007208NIA NIH HHS R01 AG032977NIA NIH HHS R01 AG047131NIA NIH HHS R01 AG048917NIA NIH HHS R01 AG057428NIA NIH HHS R03 AG049657NIA NIH HHS R56 AG048917NIDDK NIH HHS P30 DK034854NIDDK NIH HHS R01 DK046887NIDDK NIH HHS R01 DK107717NIDDK NIH HHS U2C DK093000
6 · The paper itself

Abstract

Insulin resistance is associated with aging in mice and humans. We have previously shown that administration of recombinant GDF11 (rGDF11) to aged mice alters aging phenotypes in the brain, skeletal muscle, and heart. While the closely related protein GDF8 has a role in metabolism, limited data are available on the potential metabolic effects of GDF11 or GDF8 in aging. To determine the metabolic effects of these two ligands, we administered rGDF11 or rGDF8 protein to young or aged mice fed a standard chow diet, short-term high-fat diet (HFD), or long-term HFD. Under nearly all of these diet conditions, administration of exogenous rGDF11 reduced body weight by 3-17% and significantly improved glucose tolerance in aged mice fed a chow (~30% vs. saline) or HF (~50% vs. saline) diet and young mice fed a HFD (~30%). On the other hand, exogenous rGDF8 showed signifcantly lesser effect or no effect at all on glucose tolerance compared to rGDF11, consistent with data demonstrating that GFD11 is a more potent signaling ligand than GDF8. Collectively, our results show that administration of exogenous rGDF11, but not rGDF8, can reduce diet-induced weight gain and improve metabolic homeostasis.

Indexed as

Insulin ResistanceAgingAnimalsBody WeightBone Morphogenetic ProteinsDiet, High-FatEnergy MetabolismGrowth Differentiation FactorsMaleMiceMice, Inbred C57BLMyostatinRecombinant ProteinsSignal TransductionBone Morphogenetic ProteinsGdf11 protein, mouseGrowth Differentiation FactorsMstn protein, mouseMyostatinRecombinant Proteins

Identifiers

PMID32165710
PMCPMC7067781
OpenAlexW3010802223

What OpenQuestion holds

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Registered trials

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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.