Evidence map›Paper›PMID 33089625›Full record

ArticleThe FEBS journal2021

Short-term protein restriction at advanced age stimulates FGF21 signalling, energy expenditure and browning of white adipose tissue.

Marleen B Dommerholt, Maaike Blankestijn, Marcel A Vieira-Lara, Theo H van Dijk, Henk Wolters, Mirjam H Koster, Albert Gerding, Ronald P van Os, Vincent W Bloks, Barbara M Bakker and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The FEBS journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  15. Thermogenic adipose tissue aging: Mechanisms and implications.Frontiers in cell and developmental biology · 2022
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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.

Marleen B DommerholtSections of Molecular Metabolism and Nutrition, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0002-1930-5336
Maaike BlankestijnSections of Molecular Metabolism and Nutrition, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0002-6805-3470
Marcel A Vieira-LaraSections of Systems Medicine of Metabolism and Signaling, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0003-3115-3520
Theo H van DijkDepartment of Laboratory Medicine, University Medical Center Groningen, University of Groningen, the Netherlands.ORCID 0000-0003-2713-049X
Henk WoltersSections of Molecular Metabolism and Nutrition, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Mirjam H KosterSections of Molecular Metabolism and Nutrition, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Albert GerdingSections of Systems Medicine of Metabolism and Signaling, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Ronald P van OsMouse Clinic for Cancer and Aging, Central Animal Facility, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0001-6188-1540
Vincent W BloksSections of Molecular Metabolism and Nutrition, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0001-6493-7482
Barbara M BakkerSections of Systems Medicine of Metabolism and Signaling, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0001-6274-3633
Janine K KruitSections of Molecular Metabolism and Nutrition, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0002-5414-0485
Johan W JonkerSections of Molecular Metabolism and Nutrition, Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0002-3919-5437
University Medical Center Groningen · NL

Funding

Coordinating and Bioinformatics Unit for the MMPC/DiaCompU24DK076169 · NIDDK · AUGUSTA UNIVERSITY · PI MCINDOE, RICHARD A. · 2006 to 2018
$42.4M
Coordinating Unit for DiaCompU24DK115255 · NIDDK · AUGUSTA UNIVERSITY · PI MCINDOE, RICHARD A. · 2017 to 2020
$11.6M
NIDDK NIH HHS U24 DK076169NIDDK NIH HHS U24 DK115255
6 · The paper itself

Abstract

Dietary protein restriction has been demonstrated to improve metabolic health under various conditions. However, the relevance of ageing and age-related decline in metabolic flexibility on the effects of dietary protein restriction has not been addressed. Therefore, we investigated the effect of short-term dietary protein restriction on metabolic health in young and aged mice. Young adult (3 months old) and aged (18 months old) C57Bl/6J mice were subjected to a 3-month dietary protein restriction. Outcome parameters included fibroblast growth factor 21 (FGF21) levels, muscle strength, glucose tolerance, energy expenditure (EE) and transcriptomics of brown and white adipose tissue (WAT). Here, we report that a low-protein diet had beneficial effects in aged mice by reducing some aspects of age-related metabolic decline. These effects were characterized by increased plasma levels of FGF21, browning of subcutaneous WAT, increased body temperature and EE, while no changes were observed in glucose homeostasis and insulin sensitivity. Moreover, the low-protein diet used in this study was well-tolerated in aged mice indicated by the absence of adverse effects on body weight, locomotor activity and muscle performance. In conclusion, our study demonstrates that a short-term reduction in dietary protein intake can impact age-related metabolic health alongside increased FGF21 signalling, without negatively affecting muscle function. These findings highlight the potential of protein restriction as a strategy to induce EE and browning of WAT in aged individuals.

Indexed as

Adipose Tissue, BrownAdipose Tissue, WhiteAge FactorsAgingAnimalsCaloric RestrictionDietary ProteinsEnergy MetabolismFibroblast Growth FactorsHumansMiceSignal TransductionDietary ProteinsFGF21 protein, humanfibroblast growth factor 21Fibroblast Growth Factorsbrowning of white adipose tissuedietary protein restrictionenergy metabolismFGF21 signallingthermogenesis

Identifiers

PMID33089625
PMCPMC8048886
OpenAlexW3093652796

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.