Evidence map›Paper›PMID 38708778›Full record

ArticleAging cell2024

Clinical validation of C

William S Hambright, Victoria R Duke, Adam D Goff, Alex W Goff, Lucas T Minas, Heidi Kloser, Xueqin Gao, Charles Huard, Ping Guo, Aiping Lu and 11 more

Abstract read
In one paragraph

Article in Aging cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Murine Progeria Model Exhibits Delayed Fracture Healing With Senescent Phenotype and Dysregulated Immune Response.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. What's New in Musculoskeletal Basic Science.The Journal of bone and joint surgery. American volume · 2025
    Article
  10. Review
  11. Review
  12. Observational
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Clinical validation of CAging cell · 2024
    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

21 authors.

William S HambrightCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Victoria R DukeCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.ORCID 0000-0001-6949-1862
Adam D GoffCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Alex W GoffCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Lucas T MinasCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Heidi KloserCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.ORCID 0000-0003-3087-9661
Xueqin GaoCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Charles HuardCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Ping GuoCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Aiping LuCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.ORCID 0000-0001-5529-6599
John MitchellCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Michael MullenCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Charles SuCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.
Tamara TchkoniaDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, USA.
Jair M Espindola NettoDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-0387-5059
Paul D RobbinsDepartment of Biochemistry and Molecular Biology and Biophysics, Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0003-1068-7099
Laura J NiedernhoferDepartment of Biochemistry and Molecular Biology and Biophysics, Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0002-1074-1385
James L KirklandDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, USA.
Chelsea S BahneyCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.ORCID 0000-0001-9808-8888
Marc PhilipponCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.ORCID 0000-0002-0358-3331
Johnny HuardCenter for Regenerative Sports Medicine, Steadman Philippon Research Institute, Vail, Colorado, USA.ORCID 0000-0002-2926-569X

Funding

Targeting Cellular Senescence to Extend HealthspanP01AG062413 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, Nathan K LeBrasseur · 2019 to 2026
$28.7M
The Use of Senolytic and Anti-Fibrotic Agents to Improve the Beneficial Effect of Bone Marrow Stem Cells for OsteoarthritisUH3AR077748 · NIAMS · STEADMAN PHILIPPON RESEARCH INSTITUTE · PI HUARD, JOHNNY, PHILIPPON, MARC · 2021 to 2024
$2.6M
PORT (Portland Oral health Research Training)T90DE030859 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI WU, HUI · 2021 to 2025
$2.1M
Department of Defense Office of Naval Research N00014-19-C-2052NIAMS NIH HHS 3 UH3 AR077748-02S1NIAMS NIH HHS UH3 AR077748NIAMS NIH HHS UH3AR077748NIA NIH HHS P01 AG062413NIDCR NIH HHS T90 DE030859Orthopaedic Research and Education Foundation TAF-21-059
6 · The paper itself

Abstract

Chronic conditions associated with aging have proven difficult to prevent or treat. Senescence is a cell fate defined by loss of proliferative capacity and the development of a pro-inflammatory senescence-associated secretory phenotype comprised of cytokines/chemokines, proteases, and other factors that promotes age-related diseases. Specifically, an increase in senescent peripheral blood mononuclear cells (PBMCs), including T cells, is associated with conditions like frailty, rheumatoid arthritis, and bone loss. However, it is unknown if the percentage of senescent PBMCs associated with age-associated orthopedic decline could be used for potential diagnostic or prognostic use in orthopedics. Here, we report senescent cell detection using the fluorescent compound C

Indexed as

BiomarkersCellular SenescenceOsteoarthritisPhenotypeAgedAged, 80 and overAgingFemaleHumansLeukocytes, MononuclearMaleMiddle AgedBiomarkersagingcell senescenceosteoarthritissenolytics

Identifiers

PMID38708778
PMCPMC11113632

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.