Evidence map›Paper›PMID 38466454›Full record

ArticleGeroScience2024

The common marmoset as a translational model of age-related osteoarthritis.

Dennis M Minton, Aditya R Ailiani, Michael D K Focht, Mariana E Kersh, Angela J Marolf, Kelly S Santangelo, Adam B Salmon, Adam R Konopka

Open access · greenAbstract read
In one paragraph

Article in GeroScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Inhibition of mTORC1 by rapamycin results in feedback activation of AktbioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
  5. Review
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

8 authors at 5 institutions in 1 country.

Dennis M MintonDivision of Geriatrics and Gerontology, Department of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Aditya R AilianiDivision of Geriatrics and Gerontology, Department of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Michael D K FochtDepartment of Mechanical Science and Engineering, University of Illinois Urbana-Champaign, Champaign, IL, USA.
Mariana E KershDepartment of Mechanical Science and Engineering, University of Illinois Urbana-Champaign, Champaign, IL, USA.
Angela J MarolfDepartment of Veterinary Clinical Sciences, Ohio State University, Columbus, OH, USA.
Kelly S SantangeloDepartment of Microbiology, Immunology, and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.
Adam B SalmonBarshop Institute for Longevity and Aging Studies, San Antonio, TX, USA.
Adam R KonopkaDivision of Geriatrics and Gerontology, Department of Medicine, University of Wisconsin-Madison, Madison, WI, USA. akonopka@medicine.wisc.edu.ORCID 0000-0001-6655-6747
University of Wisconsin–Madison · USUniversity of Illinois Urbana-Champaign · USColorado State University · USThe Ohio State University · USThe University of Texas Health Science Center at San Antonio · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JAMES FLOYD NELSON · 1995 to 2026
$30.6M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon · 2015 to 2026
$14.1M
Biology of Aging and Age-Related Diseases Training GrantT32AG000213 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Rozalyn M. Anderson, Sanjay Asthana · 1991 to 2026
$9.9M
Clinical evaluation of mTORC1 inhibition for geroprotection.U01AG076941 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI KONOPKA, ADAM R · 2022 to 2024
$4.3M
The role of mTOR inhibition on longevity and healthy aging in a non-human primateR01AG050797 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SALMON, ADAM · 2015 to 2019
$2.7M
Safer mTOR inhibition for human geroprotectionU01AG081482 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Adam R Konopka, Dudley William Lamming · 2023 to 2026
$1.8M
Characterization of Marmosets as a Geroscience Model by the San Antonio MAPU34AG068482 · NIA · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI ROSS, CORINNA NICOLE, SALMON, ADAM · 2020 to 2022
$1.4M
Developing the common marmoset as a translational model of age-related osteoarthritisR21AG067464 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI KONOPKA, ADAM R · 2020 to 2021
$399k
NCI NIH HHS P30 CA014520NIA NIH HHS AG000213NIA NIH HHS AG013319NIA NIH HHS AG044271NIA NIH HHS AG050797NIA NIH HHS AG067464NIA NIH HHS P30 AG013319NIA NIH HHS P30 AG044271NIA NIH HHS R01 AG050797NIA NIH HHS R21 AG067464NIA NIH HHS T32 AG000213NIA NIH HHS U01 AG076941NIA NIH HHS U01 AG081482NIA NIH HHS U34 AG068482NIH HHS P51 OD011133
6 · The paper itself

Abstract

Age-related osteoarthritis (OA) is a degenerative joint disease characterized by pathological changes in nearly every intra- and peri-articular tissue that contributes to disability in older adults. Studying the etiology of age-related OA in humans is difficult due to an unpredictable onset and insidious nature. A barrier in developing OA modifying therapies is the lack of translational models that replicate human joint anatomy and age-related OA progression. The purpose of this study was to determine whether the common marmoset is a faithful model of human age-related knee OA. Semi-quantitative microCT scoring revealed greater radiographic OA in geriatric versus adult marmosets, and the age-related increase in OA prevalence was similar between marmosets and humans. Quantitative assessments indicate greater medial tibial cortical and trabecular bone thickness and heterogeneity in geriatric versus adult marmosets which is consistent with an age-related increase in focal subchondral bone sclerosis. Additionally, marmosets displayed an age-associated increase in synovitis and calcification of the meniscus and patella. Histological OA pathology in the medial tibial plateau was greater in geriatric versus adult marmosets driven by articular cartilage damage, proteoglycan loss, and altered chondrocyte cellularity. The age-associated increase in medial tibial cartilage OA pathology and meniscal calcification was greater in female versus male geriatric marmosets. Overall, marmosets largely replicate human OA as evident by similar 1) cartilage and skeletal morphology, 2) age-related progression in OA pathology, and 3) sex differences in OA pathology with increasing age. Collectively, these data suggest that the common marmoset is a highly translatable model of the naturally occurring, age-related OA seen in humans.

Indexed as

Cartilage, ArticularOsteoarthritis, KneeAgedAnimalsCallithrixFemaleHumansKnee JointMaleTibiaBoneCartilageKneeMeniscusNaturally occurring osteoarthritisNon-human primatePatella

Identifiers

PMID38466454
PMCPMC11009185
OpenAlexW4392649849

What OpenQuestion holds

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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.