Evidence map›Paper›PMID 26069676›Full record

ArticleCartilage2013

Monounsaturated and Saturated, but Not n-6 Polyunsaturated Fatty Acids Decrease Cartilage Destruction under Inflammatory Conditions: A Preliminary Study.

Y M Bastiaansen-Jenniskens, M Siawash, C H A van de Lest, J A N Verhaar, M Kloppenburg, A-M Zuurmond, V Stojanovic-Susulic, G J V M Van Osch, S Clockaerts

Open access · greenAbstract read
In one paragraph

Article in Cartilage, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

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  14. Adiponectin, May Be a Potential Protective Factor for Obesity-Related Osteoarthritis.Diabetes, metabolic syndrome and obesity : targets and therapy · 2022
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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

9 authors at 5 institutions in 3 countries.

Y M Bastiaansen-JenniskensDepartment of Orthopaedics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
M SiawashDepartment of Orthopaedics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
C H A van de LestUniversity of Utrecht, Utrecht, The Netherlands.
J A N VerhaarDepartment of Orthopaedics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
M KloppenburgDepartment of Rheumatology, Leiden University Medical Center, Leiden, the Netherlands.
A-M ZuurmondTNO, Leiden, the Netherlands.
V Stojanovic-SusulicJanssen, The Pharmaceutical Companies of Johnson&Johnson, Fort Washington, PA, USA.
G J V M Van OschDepartment of Orthopaedics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands ; Department of Otorhinolaryngology, Ersamus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
S ClockaertsDepartment of Orthopaedics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands ; Department of Orthopaedic Surgery and Traumatology, University Hospital of Antwerp, Antwerp, Belgium.
Erasmus MC · NLJohnson & Johnson (United States) · USLeiden University Medical Center · NLNetherlands Organisation for Applied Scientific Research · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOsteoarthritis (OA) is associated with obesity in which altered fatty acid levels have been observed. We investigated whether the most common fatty acids in synovial fluid influence cartilage deterioration in OA.

designCartilage was obtained from OA patients undergoing total knee arthroplasty. Chondrocytes or cartilage explants were cultured with linoleic (n-6 polyunsaturated), oleic (monounsaturated), or palmitic (saturated) acid. After preculture, media were renewed and inflammation was simulated in half of the samples by addition of 10 ng/mL tumor necrosis factor-α (TNFα) with or without the fatty acids. Effects on lipid uptake (Oil-Red-O), cell toxicity (lactate dehydrogenase), prostaglandin-E2 (PGE2) release and gene expression for prostaglandin-endoperoxide synthase-2 (PTGS2), matrix metalloproteinase-1 (MMP1), and MMP13, and a disintegrin and metalloproteinase with thrombospondin motifs 4 were determined on chondrocytes in monolayer. Effects on glycosaminoglycan (GAG) release were evaluated on cartilage explants.

resultsNone of the fatty acids were cytotoxic and all were taken up by the cells, resulting in a higher amount of intracellular lipid in chondrocytes. Linoleic acid increased PGE2 production in the presence of TNFα. Oleic acid and palmitic acid inhibited MMP1 gene expression in chondrocytes stimulated with TNFα. In cartilage explants, GAG release was also inhibited by oleic acid and palmitic acid, and oleic acid decreased PTGS2 gene expression in stimulated chondrocytes.

conclusionsLinoleic acid has a pro-inflammatory effect on cartilage whereas oleic acid and palmitic acid seem to inhibit cartilage destruction. These results indicate that altered fatty acid levels may influence loss of cartilage structure in OA.

Indexed as

cartilagechondrocytefatty acids

Identifiers

PMID26069676
PMCPMC4297154
OpenAlexW2058931618

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.