Evidence map›Paper›PMID 16476713›Full record

Trial reportAnnals of the rheumatic diseases2006

Long term NSAID treatment inhibits COX-2 synthesis in the knee synovial membrane of patients with osteoarthritis: differential proinflammatory cytokine profile between celecoxib and aceclofenac.

M A Alvarez-Soria, R Largo, J Santillana, O Sánchez-Pernaute, E Calvo, M Hernández, J Egido, G Herrero-Beaumont

Open access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Annals of the rheumatic diseases, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.2field-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

32 citing papers in PubMed, 98 citations in OpenAlex.

  1. Effect of Celecoxib on Surgical Site Inflammation after Total Knee Arthroplasty: A Randomized Controlled Study.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2018
    Trial
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Imaging of Synovial Inflammation in Osteoarthritis, From theAJR. American journal of roentgenology · 2022
    Review
  8. Observational
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Macrophages in osteoarthritis: pathophysiology and therapeutics.American journal of translational research · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

M A Alvarez-SoriaServicio de Reumatología, Fundación Jiménez Díaz, Avenida Reyes Católicos 2, 28040 Madrid, Spain.
R Largo
J Santillana
O Sánchez-Pernaute
E Calvo
M Hernández
J Egido
G Herrero-Beaumont
Hospital Universitario Fundación Jiménez Díaz · ESHospital de Tortosa Virgen de la Cinta · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo compare the effect of celecoxib with that of a classic non-steroidal anti-inflammatory drug (NSAID) on synovial inflammation and on the synovial expression of proinflammatory genes in patients with knee osteoarthritis (OA).

methods30 patients with severe knee OA scheduled for total knee replacement surgery were included in a 3 month clinical trial. They were randomised to two groups: patients treated with celecoxib (CBX) (200 mg/24 h) and patients treated with aceclofenac (ACF) (100 mg/12 h). Those patients with OA who did not want to be treated with NSAIDs served as a control group. During knee surgery, synovial fluid (SF) and synovial membrane (SM) were collected. A SM specimen was fixed and embedded in paraffin and another part was frozen for molecular biology studies.

resultsAt the end of study both CBX and ACF treated patients showed a significant improvement in pain and knee function compared with controls. Both drugs significantly reduced prostaglandin E(2) (PGE(2)) SF concentration and down regulated COX-2 mRNA and protein expression at the SM. However, synovial macrophage infiltration (CD68 antigen staining) and expression of proinflammatory mediators, such as interleukin 1beta and tumour necrosis factor alpha, were decreased only by CBX treatment.

conclusionBoth drugs improved joint pain and function, inhibited SF PGE(2) concentration, and induced a decrease in synovial COX-2 expression and synthesis not related to the tissue inflammatory status. These data suggest that PGE(2) blocking agents may decrease PGE(2) production not only by direct COX-2 inhibition but also by down regulating COX-2 expression and synthesis. However, CBX and ACF appear to have different anti-inflammatory profiles in controlling OA synovial macrophage infiltration and proinflammatory expression.

Indexed as

Osteoarthritis, KneeAgedAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory Agents, Non-SteroidalBlotting, WesternCD68 MoleculeCelecoxibCyclooxygenase 1Cyclooxygenase 2Depression, ChemicalDiclofenacDinoprostoneFemaleGene ExpressionHumansaceclofenacAntigens, CDAntigens, Differentiation, MyelomonocyticAnti-Inflammatory Agents, Non-SteroidalCD68 antigen, humanCD68 MoleculeCelecoxibCyclooxygenase 1Cyclooxygenase 2DiclofenacDinoprostoneInterleukin-1Membrane ProteinsPTGS1 protein, humanPTGS2 protein, humanPyrazolesRNA, MessengerSulfonamidesTumor Necrosis Factor-alpha

Identifiers

PMID16476713
PMCPMC1798252
OpenAlexW2096938558

What OpenQuestion holds

Textmetadata
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.