Evidence map›Paper›PMID 26000299›Full record

ArticleBioMed research international2015

Study of osteoarthritis treatment with anti-inflammatory drugs: cyclooxygenase-2 inhibitor and steroids.

Hongsik Cho, Andrew Walker, Jeb Williams, Karen A Hasty

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
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  11. Osteoarthritis and cartilage open · 2024
    Article
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  15. Review
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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

4 authors at 2 institutions in 1 country.

Hongsik ChoDepartment of Orthopaedic Surgery and Biomedical Engineering, University of Tennessee Health Science Center and Campbell Clinic, Memphis, TN, USA ; Veterans Affairs Medical Center, Memphis, TN, USA.
Andrew WalkerDepartment of Orthopaedic Surgery and Biomedical Engineering, University of Tennessee Health Science Center and Campbell Clinic, Memphis, TN, USA.
Jeb WilliamsDepartment of Orthopaedic Surgery and Biomedical Engineering, University of Tennessee Health Science Center and Campbell Clinic, Memphis, TN, USA.
Karen A HastyDepartment of Orthopaedic Surgery and Biomedical Engineering, University of Tennessee Health Science Center and Campbell Clinic, Memphis, TN, USA ; Veterans Affairs Medical Center, Memphis, TN, USA.
Campbell Clinic · USUniversity of Tennessee Health Science Center · US

Funding

Early Detection and Quantification of OAR21AR060408 · NIAMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI HASTY, KAREN A. · 2012 to 2013
$372k
NIAMS NIH HHS R21 AR060408
6 · The paper itself

Abstract

Patients with osteoarthritis (OA), a condition characterized by cartilage degradation, are often treated with steroids, nonsteroidal anti-inflammatory drugs (NSAIDs), and cyclooxygenase-2 (COX-2) selective NSAIDs. Due to their inhibition of the inflammatory cascade, the drugs affect the balance of matrix metalloproteinases (MMPs) and inflammatory cytokines, resulting in preservation of extracellular matrix (ECM). To compare the effects of these treatments on chondrocyte metabolism, TNF-α was incubated with cultured chondrocytes to mimic a proinflammatory environment with increasing production of MMP-1 and prostaglandin E2 (PGE2). The chondrocytes were then treated with either a steroid (prednisone), a nonspecific COX inhibitor NSAID (piroxicam), or a COX-2 selective NSAID (celecoxib). Both prednisone and celecoxib decreased MMP-1 and PGE-2 production while the nonspecific piroxicam decreased only the latter. Both prednisone and celecoxib decreased gene expression of MMP-1 and increased expression of aggrecan. Increased gene expression of type II collagen was also noted with celecoxib. The nonspecific piroxicam did not show these effects. The efficacy of celecoxib in vivo was investigated using a posttraumatic OA (PTOA) mouse model. In vivo, celecoxib increases aggrecan synthesis and suppresses MMP-1. In conclusion, this study demonstrates that celecoxib and steroids exert similar effects on MMP-1 and PGE2 production in vitro and that celecoxib may demonstrate beneficial effects on anabolic metabolism in vivo.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalCartilageCell SurvivalChondrocytesCyclooxygenase 2 InhibitorsDisease Models, AnimalFluorescent DyesGene Expression RegulationHumansKnee JointMaleMatrix Metalloproteinase 1Mice, Inbred C57BLOsteoarthritisSteroidsAnti-Inflammatory Agents, Non-SteroidalCyclooxygenase 2 InhibitorsFluorescent DyesMatrix Metalloproteinase 1SteroidsTumor Necrosis Factor-alpha

Identifiers

PMID26000299
PMCPMC4427003
OpenAlexW2086349374

What OpenQuestion holds

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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 OpenQuestion graph.