Evidence map›Paper›PMID 35773785›Full record

ReviewJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2022

Similarities Between Disuse and Age-Induced Bone Loss.

Evan G Buettmann, Galen M Goldscheitter, Gabriel A Hoppock, Michael A Friedman, Larry J Suva, Henry J Donahue

Open access · greenAbstract readReview
In one paragraph

Review in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Botulinum toxin (A)-induced bone loss is associated with increased blood velocity and reduced vascular bone porosity.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Connecting the dots: sex, depression, and musculoskeletal health.The Journal of clinical investigation · 2024
    Review
  14. Review
  15. Article
  16. The heart-bone connection: relationships between myocardial infarction and osteoporotic fracture.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  17. Article
  18. Article
  19. Genetic variation influences the skeletal response to hindlimb unloading in the eight founder strains of the diversity outbred mouse population.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2024
    Article
  20. 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

6 authors at 2 institutions in 1 country.

Evan G BuettmannDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-8439-477X
Galen M GoldscheitterDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0002-6721-3161
Gabriel A HoppockDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-5673-6234
Michael A FriedmanDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-8279-0306
Larry J SuvaDepartment of Veterinary Physiology and Pharmacology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.ORCID 0000-0002-2892-9757
Henry J DonahueDepartment of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0002-9238-4157
Virginia Commonwealth University · USTexas College · US

Funding

The role of oxidative stress in alcohol-induced osteopeniaR37AA018282 · NIAAA · LSU HEALTH SCIENCES CENTER · PI RONIS, MARTIN J J · 2016 to 2025
$4.7M
Understanding the skeleton in Down SyndromeR01HD102909 · NICHD · TEXAS A&M AGRILIFE RESEARCH · PI SUVA, LARRY J. · 2021 to 2025
$2.8M
Gap Junction and Bone Cell Response to Physical SignalsR01AR068132 · NIAMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DONAHUE, HENRY J · 2014 to 2019
$1.5M
NASA 80NSSC18K1473National Space Biomedical Research Institute Grant MA02802NIAAA NIH HHS R37 AA018282NIAMS NIH HHS R01 AR068132NICHD NIH HHS R01 HD102909Translational Research Institute for Space Health NNX16AO69A
6 · The paper itself

Abstract

Disuse and aging are known risk factors associated with low bone mass and quality deterioration, resulting in increased fracture risk. Indeed, current and emerging evidence implicate a large number of shared skeletal manifestations between disuse and aging scenarios. This review provides a detailed overview of current preclinical models of musculoskeletal disuse and the clinical scenarios they seek to recapitulate. We also explore and summarize the major similarities between bone loss after extreme disuse and advanced aging at multiple length scales, including at the organ/tissue, cellular, and molecular level. Specifically, shared structural and material alterations of bone loss are presented between disuse and aging, including preferential loss of bone at cancellous sites, cortical thinning, and loss of bone strength due to enhanced fragility. At the cellular level bone loss is accompanied, during disuse and aging, by increased bone resorption, decreased formation, and enhanced adipogenesis due to altered gap junction intercellular communication, WNT/β-catenin and RANKL/OPG signaling. Major differences between extreme short-term disuse and aging are discussed, including anatomical specificity, differences in bone turnover rates, periosteal modeling, and the influence of subject sex and genetic variability. The examination also identifies potential shared mechanisms underlying bone loss in aging and disuse that warrant further study such as collagen cross-linking, advanced glycation end products/receptor for advanced glycation end products (AGE-RAGE) signaling, reactive oxygen species (ROS) and nuclear factor κB (NF-κB) signaling, cellular senescence, and altered lacunar-canalicular connectivity (mechanosensation). Understanding the shared structural alterations, changes in bone cell function, and molecular mechanisms common to both extreme disuse and aging are paramount to discovering therapies to combat both age-related and disuse-induced osteoporosis. © 2022 American Society for Bone and Mineral Research (ASBMR).

Indexed as

Bone Diseases, MetabolicOsteoporosisAdipogenesisAgingBone and BonesHumansOsteocytesAGINGBONE DISORDERS AND DISEASES-OSTEOPOROSISCELLS OF BONE-OSTEOCYTESMOLECULAR PATHWAYS-REMODELINGPRECLINICAL STUDIESSENESCENCE

Identifiers

PMID35773785
PMCPMC9378610
OpenAlexW4283763313

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

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 Socratic graph.