Evidence map›Paper›PMID 40881276›Full record

ArticleEuropean cells & materials

BURN-SYNOVECTOMY MOUSE MODEL FOR TEMPOROMANDIBULAR JOINT OSTEOARTHRITIS.

Ginny Ching-Yun Hsu

Abstract read
In one paragraph

Article in European cells & materials. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Ginny Ching-Yun HsuDepartment of Orthodontics, Oregon Health & Science University, Portland, OR 97201, USA.

Funding

TIAM1 dictates lineage commitment in skeletal and soft tissue pericytesK08DE031347 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI Ginny Ching-Yun Hsu · 2022 to 2026
$830k
NIDCR NIH HHS K08 DE031347
6 · The paper itself

Abstract

Temporomandibular joint osteoarthritis (TMJ OA) occurs in 8 to 16 % of the population. Currently available animal models do not faithfully simulate the native disease progression of TMJ OA. The initiation of TMJ OA requires both local trauma and extended inflammation. In this study, we present a novel mouse model that reproduces these two conditions. This is achieved by a procedure involving both synovectomy (local trauma) and a distant burn injury (systemic inflammation). Its efficacy at inducing TMJ OA was assessed by histomorphologic and radiographic evaluation at 1, 3, and 9 weeks after the procedure. Burn-synovectomy mice exhibited significantly more degenerative hard and soft tissue changes in the TMJ than uninjured control or synovotomy mice. The observed histology in burn-synovectomy mice faithfully mimicked synovitis-induced TMJ OA progression. This animal model is invaluable in future research of the mechanism and risk factors of TMJ OA.

Indexed as

mouse modeltemporomandibular disordersTemporomandibular joint osteoarthritis

Identifiers

PMID40881276
PMCPMC12382779

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.