Evidence map›Paper›PMID 37244285›Full record

ArticleAging2023

Changes in macrophage immunometabolism as a marker of skeletal muscle dysfunction across the lifespan.

Norika Liu, Joshua T Butcher, Atsushi Nakano, Andrea Del Campo

Abstract read
In one paragraph

Article in Aging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Lifelong Exercise as a Modulator of CD4European journal of clinical investigation · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Molecular Framework of the Onset and Progression of Skeletal Muscle Aging.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Probiotics and muscle health: the impact ofFrontiers in microbiology · 2025
    Review
  13. Article
  14. Article
  15. The immunology of sickness metabolism.Cellular & molecular immunology · 2024
    Review
  16. 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

4 authors.

Norika LiuDepartment of Cell Physiology, The Jikei University School of Medicine, Tokyo, Japan.
Joshua T ButcherDepartment of Physiological Sciences, College of Veterinary Medicine, Oklahoma State University, Stillwater, OK 74078, USA.
Atsushi NakanoDepartment of Cell Physiology, The Jikei University School of Medicine, Tokyo, Japan.
Andrea Del CampoLaboratorio de Fisiología y Bioenergetica Celular, Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Santiago 7810000, Chile.

Funding

ZFC3H1 Regulation of Host Defense and Influenza A Virus PathogenesisP20GM103648 · NIGMS · OKLAHOMA STATE UNIVERSITY STILLWATER · PI PATRAUCHAN, MARIANNA M. A. · 2013 to 2022
$22.3M
Metabolic regulation of heart formationR01HL142801 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NAKANO, ATSUSHI · 2019 to 2022
$1.6M
Hemogenic endocardium: contribution to the valvular tissue macrophagesR01HL127427 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NAKANO, ATSUSHI · 2016 to 2019
$1.5M
Skeletal Muscle as a Target for Cardio-Metabolic Disease in Sarcopenic ObesityK01AG064121 · NIA · OKLAHOMA STATE UNIVERSITY STILLWATER · PI BUTCHER, JOSHUA THOMAS · 2020 to 2024
$644k
NHLBI NIH HHS R01 HL127427NHLBI NIH HHS R01 HL142801NIA NIH HHS K01 AG064121NIGMS NIH HHS P20 GM103648
6 · The paper itself

Abstract

One of the most pronounced changes in the elderly is loss of strength and mobility due to the decline of skeletal muscle function, resulting in a multifactorial condition termed sarcopenia. Although significant clinical changes begin to manifest at advanced ages, recent studies have shown that changes at the cellular and molecular level precede the symptomatology of sarcopenia. By utilizing a single-cell transcriptomic atlas of mouse skeletal muscle across the lifespan, we identified a clear sign of immune senescence that presents during middle age. More importantly, the change in macrophage phenotype in middle age may explain the changes in extracellular matrix composition, especially collagen synthesis, that contributes to fibrosis and overall muscle weakness with advanced age. Our results show a novel paradigm whereby skeletal muscle dysfunction is driven by alterations in tissue-resident macrophages before the appearance of clinical symptoms in middle-aged mice, providing a new therapeutic approach via regulation of immunometabolism.

Indexed as

SarcopeniaAgingAnimalsLongevityMacrophagesMiceMuscle, SkeletalagingimmunometabolismmacrophagesarcopeniascRNA-seq

Identifiers

PMID37244285
PMCPMC10258037

What OpenQuestion holds

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LicenceCC BY
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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.