Evidence map›Paper›PMID 30932373›Full record

ArticleJournal of cachexia, sarcopenia and muscle2019

Insulin/IGF1 signalling mediates the effects of β

Dawit A Gonçalves, Wilian A Silveira, Leandro H Manfredi, Flávia A Graça, Andrea Armani, Enrico Bertaggia, Brian T O Neill, Natalia Lautherbach, Juliano Machado, Leonardo Nogara and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Respiratory Muscle Strength and Mortality in Patients with COPD: A Systematic Review and Meta-Analysis.International journal of chronic obstructive pulmonary disease · 2025
    Pooled it
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  15. Article
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  17. Unraveling the lost balance: Adrenergic dysfunction in cancer cachexia.Autonomic neuroscience : basic & clinical · 2024
    Review
  18. βFrontiers in physiology · 2024
    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

17 authors at 4 institutions in 3 countries.

Dawit A GonçalvesDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.ORCID 0000-0003-2621-3330
Wilian A SilveiraDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.ORCID 0000-0002-6171-7940
Leandro H ManfrediDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.
Flávia A GraçaDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.
Andrea ArmaniDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Enrico BertaggiaDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Brian T O NeillSection on Integrative Physiology and Metabolism, Joslin Diabetes Center, Harvard Medical School, Boston, MA, USA.
Natalia LautherbachDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.
Juliano MachadoDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.
Leonardo NogaraDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Marcelo G PereiraDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Diletta ArcidiaconoDigestive Endoscopy Unit, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Stefano RealdonDigestive Endoscopy Unit, Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
C Ronald KahnSection on Integrative Physiology and Metabolism, Joslin Diabetes Center, Harvard Medical School, Boston, MA, USA.
Marco SandriDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID 0000-0001-8509-7558
Isis C KettelhutDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.ORCID 0000-0002-9034-5357
Luiz Carlos C NavegantesDepartment of Physiology, Ribeirão Preto Medical School/University of São Paulo, Ribeirão Preto, SP, Brazil.ORCID 0000-0002-9870-9469
Universidade de São Paulo · BRUniversity of Padua · ITIstituto Oncologico Veneto · ITJoslin Diabetes Center · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI LAURIE J GOODYEAR · 1986 to 2026
$50.5M
Insulin Receptor Substrates and Insulin ActionR01DK033201 · NIDDK · JOSLIN DIABETES CENTER · PI KAHN, C RONALD · 1986 to 2016
$10.6M
Role of PI 3-Kinase Isoforms in Insulin ActionR01DK055545 · NIDDK · JOSLIN DIABETES CENTER · PI KAHN, C RONALD · 1999 to 2020
$8.3M
The Insulin Receptor and Its Signaling MechanismsR01DK031036 · NIDDK · JOSLIN DIABETES CENTER · PI C RONALD KAHN · 1986 to 2026
$4.2M
Regulation of Muscle Autophagy and Mitophagy by Insulin and IGF-1 SignalingK08DK100543 · NIDDK · UNIVERSITY OF IOWA · PI O'NEILL, BRIAN TIMOTHY · 2013 to 2017
$737k
NIDDK NIH HHS K08 DK100543NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R01 DK033201NIDDK NIH HHS R01 DK055545
6 · The paper itself

Abstract

backgroundStimulation of β

methodsFed wild type (WT), 2-day fasted WT, muscle-specific insulin (INS) receptor (IR) knockout (M-IR

resultsIn fed and fasted mice, one injection of FOR inhibited autophagosome formation (LC3-II content, 65%, P ≤ 0.05) that was paralleled by an increase in serum INS levels (4-fold to 25-fold, P ≤ 0.05) and the phosphorylation of Akt (4.4-fold to 6.5-fold, P ≤ 0.05) and ERK1/2 (50% to two-fold, P ≤ 0.05). This led to the suppression (40-70%, P ≤ 0.05) of the master regulators of atrophy, FoxOs, and the mRNA levels of their target genes. FOR enhanced (41%, P ≤ 0.05) protein synthesis only in fed condition and stimulated (4.4-fold to 35-fold, P ≤ 0.05) the prosynthetic Akt/mTOR/p70S6K pathway in both fed and fasted states. FOR effects on Akt signalling during fasting were blunted in both M-IR

conclusionsNS/IGF1 signalling is necessary for the anti-proteolytic and hypertrophic effects of in vivo β

Indexed as

Adrenergic beta-2 Receptor AgonistsAnimalsAutophagyInsulinInsulin-Like Growth Factor ILysosomesMaleMiceMice, KnockoutMuscle ProteinsMuscle, SkeletalMuscle StrengthPhosphatidylinositol 3-KinasesProteolysisProteostasisProto-Oncogene Proteins c-aktAdrenergic beta-2 Receptor AgonistsInsulinInsulin-Like Growth Factor IMuscle ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAutophagy-lysosomal systemInsulin/IGF1 signallingProtein metabolismSkeletal muscle functionSkeletal muscle plasticityβ2-adrenoceptor

Identifiers

PMID30932373
PMCPMC6463755
OpenAlexW2929263901

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.