Evidence map›Paper›PMID 38131122›Full record

ArticleDisease models & mechanisms2024

Inescapable foot shock induces a PTSD-like phenotype and negatively impacts adult murine bone.

Sara J Sidles, Ryan R Kelly, Kirsten D Kelly, Jessica D Hathaway-Schrader, Stephanie K Khoo, Jeffrey A Jones, James J Cray, Amanda C LaRue

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Rat Models in Post-Traumatic Stress Disorder Research: Strengths, Limitations, and Implications for Translational Studies.Pathophysiology : the official journal of the International Society for Pathophysiology · 2024
    Review
  8. Article
  9. Connecting the dots: sex, depression, and musculoskeletal health.The Journal of clinical investigation · 2024
    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 3 institutions in 1 country.

Sara J SidlesResearch Service, Ralph H. Johnson Department of Veterans Affairs Health Care System, Charleston, SC 29401, USA.ORCID 0000-0001-7177-0270
Ryan R KellyResearch Service, Ralph H. Johnson Department of Veterans Affairs Health Care System, Charleston, SC 29401, USA.ORCID 0000-0002-3809-1302
Kirsten D KellyResearch Service, Ralph H. Johnson Department of Veterans Affairs Health Care System, Charleston, SC 29401, USA.
Jessica D Hathaway-SchraderResearch Service, Ralph H. Johnson Department of Veterans Affairs Health Care System, Charleston, SC 29401, USA.
Stephanie K KhooResearch Service, Ralph H. Johnson Department of Veterans Affairs Health Care System, Charleston, SC 29401, USA.
Jeffrey A JonesResearch Service, Ralph H. Johnson Department of Veterans Affairs Health Care System, Charleston, SC 29401, USA.
James J CrayDivision of Anatomy, The Ohio State University, Columbus, OH 43210, USA.
Amanda C LaRueResearch Service, Ralph H. Johnson Department of Veterans Affairs Health Care System, Charleston, SC 29401, USA.ORCID 0000-0003-4572-1496
Medical University of South Carolina · USRalph H. Johnson VA Medical Center · USThe Ohio State University · US

Funding

Potential of Hematopoietic Stem Cell-Based Therapies for Complicated FracturesI01BX000333 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI LARUE, AMANDA C. · 2009 to 2022
–
Transforming Growth Factor-beta Signaling Pathways in Thoracic Aortic AneurysmsI01BX000904 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI JONES, JEFFREY A. · 2011 to 2023
–
Exposing Invisible Wounds: Impacts of PTSD on Bone HealthI01BX005168 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI AMANDA C. LARUE · 2023 to 2026
–
BLRD VA I01 BX000333BLRD VA I01 BX000904BLRD VA I01 BX005168BLRD VA I01 BX005870
6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD) is associated with osteopenia, osteoporosis and increased fracture risk in the clinical population. Yet, the development of preclinical models to study PTSD-induced bone loss remains limited. In this study, we present a previously unreported model of PTSD in adult female C57BL/6 mice, by employing inescapable foot shock and social isolation, that demonstrates high face and construct validity. A subset of mice exposed to this paradigm (i.e. PTSD mice) display long-term alterations in behavioral and inflammatory indices. Using three-dimensional morphometric calculations, cyclic reference point indentation (cRPI) testing and histological analyses, we find that PTSD mice exhibit loss of trabecular bone, altered bone material quality, and aberrant changes in bone tissue architecture and cellular activity. This adult murine model of PTSD exhibits clinically relevant changes in bone physiology and provides a valuable tool for investigating the cellular and molecular mechanisms underlying PTSD-induced bone loss.

Indexed as

Stress Disorders, Post-TraumaticAnimalsBone and BonesDisease Models, AnimalFemaleMiceMice, Inbred C57BLPhenotypeAnimal modelBoneInescapable foot shockInflammationOsteoporosisPost-traumatic stress disorder

Identifiers

PMID38131122
PMCPMC10820809
OpenAlexW4390108382

What Socratic holds

Textmetadata
LicenceCC BY
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.