Evidence map›Paper›PMID 31410880›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2019

Inhibition of COX-2 Pathway as a Potential Prophylaxis Against Arthrofibrogenesis in a Rabbit Model of Joint Contracture.

Christopher G Salib, Nicolas Reina, William H Trousdale, Afton K Limberg, Megan E Tibbo, Anthony G Jay, Joseph X Robin, Travis W Turner, Carter R Jones, Christopher R Paradise and 8 more

Open access · greenAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. New Clues to the Challenge of Knee Arthrofibrosis: From Molecules to Therapies.The Journal of the American Academy of Orthopaedic Surgeons · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. An Abbreviated Rabbit Knee Model of Joint Contracture.Tissue engineering. Part C, Methods · 2025
    Article
  11. Efficacy of ADIPOR1 and ADIPOR2 peptide-agonist AdipoRon in preventing contracture in a rabbit model of arthrofibrosis.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Biomechanical, histological, and molecular characterization of a new posttraumatic model of arthrofibrosis in rats.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2022
    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

18 authors at 2 institutions in 1 country.

Christopher G SalibDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Nicolas ReinaDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.ORCID 0000-0003-4059-9014
William H TrousdaleDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Afton K LimbergDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Megan E TibboDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Anthony G JayDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Joseph X RobinDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Travis W TurnerDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Carter R JonesDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Christopher R ParadiseDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Eric A LewallenDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Brad BolonGEMpath, Inc., 1610 Pace Street, Unit 900-343, Longmont, Colorado.
Jodi M CarterDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Daniel J BerryDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Mark E MorreyDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Joaquin Sanchez-SoteloDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Andre J van WijnenDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.
Matthew P AbdelDepartment of Orthopedic Surgery, Mayo Clinic, 200 First Street SW, Rochester, Minnesota.ORCID 0000-0002-2398-1724
Mayo Clinic · USNewPath Research · US

Funding

Pathologic Role of Inflammation and Mechanistic Analysis of Myofibroblastogenesis in ArthrofibrosisR01AR072597 · NIAMS · MAYO CLINIC ROCHESTER · PI ABDEL, MATTHEW P · 2018 to 2022
$1.7M
Anna- Maria and Stephen Kellen FoundationNIAMS NIH HHS AR072597-01A1NIAMS NIH HHS R01 AR072597
6 · The paper itself

Abstract

Arthrofibrosis is a common complication following total knee arthroplasty caused by pathologic fibroblast activation and excessive collagen deposition around a synovial joint leading to debilitating loss of motion. Treatment options are limited because the pathologic mechanisms remain to be characterized. Dysregulation of the inflammatory cascade may lead to communication between myofibroblasts and immune cells triggering tissue metaplasia, and excessive collagen deposition described clinically as arthrofibrosis. We explored the novel use of celecoxib (selective cyclooxygenase-2 [COX-2] inhibitor) to disrupt the downstream effects of the post-traumatic inflammatory cascade and inhibit scar tissue formation in a validated rabbit model of arthrofibrosis combined with new parameters for quantifying the stiffness of the posterior capsule. Biomechanical and molecular analyses, of contracted rabbit knee posterior capsule tissue after COX-2 inhibition revealed increased maximal passive extension and down-regulation of collagen messenger RNA compared with controls. Histopathologic examination suggested a trend of decreased quantities of dense fibrous connective tissue with COX-2 inhibition. These data may suggest that inhibiting the inflammatory cascade could potentially reduce pathologic myofibroblast activation, thereby reducing scar tissue formation and increasing the range of motion in arthrofibrotic joints. Implementing a multi-modal pharmacologic approach may simultaneously target numerous cellular components contributing to the complex process of arthrofibrogenesis. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:2609-2620, 2019.

Indexed as

AnimalsArthroplasty, Replacement, KneeBiomechanical PhenomenaCelecoxibCollagenContractureCyclooxygenase 2 InhibitorsDisease Models, AnimalFemaleFibrosisJointsMyofibroblastsRabbitsCelecoxibCollagenCyclooxygenase 2 InhibitorsarthrofibrosiscelecoxibCOX-2 inhibitionmyofibroblasttotal knee arthroplasty

Identifiers

PMID31410880
PMCPMC6848758
OpenAlexW2968101988

What OpenQuestion 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 OpenQuestion graph.