Evidence map›Paper›PMID 38689513›Full record

ArticleJournal of cachexia, sarcopenia and muscle2024

Metabolomic analysis of dietary-restriction-induced attenuation of sarcopenia in prematurely aging DNA repair-deficient mice.

Yupeng He, Wei Yang, Luojiao Huang, Marlien Admiraal-van Mever, Rawi Ramautar, Amy Harms, Yvonne Rijksen, Renata M C Brandt, Sander Barnhoorn, Kimberly Smit and 5 more

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2024. 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
–field-weighted citation impact
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.

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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

15 authors.

Yupeng HeMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.ORCID 0000-0002-3453-9499
Wei YangMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Luojiao HuangMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Marlien Admiraal-van MeverMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Rawi RamautarMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Amy HarmsMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Yvonne RijksenPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Renata M C BrandtDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
Sander BarnhoornDepartment of Molecular Genetics, Erasmus MC Cancer Institute, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
Kimberly SmitPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Dick JaarsmaDepartment of Neuroscience, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
Peter LindenburgMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
Jan H J HoeijmakersPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Wilbert P VermeijPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Thomas HankemeierMetabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.

Funding

THE IMPACT OF CELLULAR DEFENSE ON THE ROLE OF Ku80 IN GENOME MAINTENANCE AND LONGP01AG017242 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI VIJG, JAN · 1999 to 2023
$46.1M
China Scholarship Council (CSC) 201706320322Deutsche Forschungsgemeinschaft 73111208-SFB 829EJP-RD TC-NER RD20-113European Research Council Advanced Grant Dam2Age, NIH grant PO1 AG017242Medical Delta program METABODELTANetherlands Organisation for Scientific Research (NWO) in the Building Blocks of Life Program 737.016.015NIA NIH HHS P01 AG017242Oncode InstituteX-Omics 184.034.019ZonMW Memorabel 733050810
6 · The paper itself

Abstract

backgroundSarcopenia is characterized by loss of skeletal muscle mass and function, and is a major risk factor for disability and independence in the elderly. Effective medication is not available. Dietary restriction (DR) has been found to attenuate aging and aging-related diseases, including sarcopenia, but the mechanism of both DR and sarcopenia are incompletely understood.

methodsIn this study, mice body weight, fore and all limb grip strength, and motor learning and coordination performance were first analysed to evaluate the DR effects on muscle functioning. Liquid chromatography-mass spectrometry (LC-MS) was utilized for the metabolomics study of the DR effects on sarcopenia in progeroid DNA repair-deficient Ercc1

resultsMuscle mass was significantly (P < 0.05) decreased (13-20%) by DR; however, the muscle quality was improved with retained fore limbs and all limbs grip strength in Ercc1

conclusionsThis study provides fundamental supporting information on biomarkers and pathways related to the attenuation of sarcopenia, which might facilitate its diagnosis, prevention, and clinical therapy.

Indexed as

MetabolomicsSarcopeniaAging, PrematureAnimalsCaloric RestrictionDisease Models, AnimalDNA-Binding ProteinsDNA RepairEndonucleasesMaleMetabolomeMiceMice, KnockoutMuscle, SkeletalDNA-Binding ProteinsEndonucleasesErcc1 protein, mouseDietary restrictionEnergy generationInflammationMuscle agingOxidative stressProgeria

Identifiers

PMID38689513
PMCPMC11154776

What OpenQuestion holds

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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.