Evidence map›Paper›PMID 25854584›Full record

ArticleAnnals of the rheumatic diseases2015

Differential DNA methylation and expression of inflammatory and zinc transporter genes defines subgroups of osteoarthritic hip patients.

Michael D Rushton, David A Young, John Loughlin, Louise N Reynard

Open access · hybridAbstract read
In one paragraph

Article in Annals of the rheumatic diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.7field-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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  9. Review
  10. Role of low-grade inflammation in osteoarthritis.Current opinion in rheumatology · 2017
    Review
  11. Review
  12. Article
  13. Article
  14. DNA Methylation in Osteoarthritis.Current genomics · 2015
    Article
  15. 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

4 authors at 1 institution in 1 country.

Michael D RushtonMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
David A YoungMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
John LoughlinMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Louise N ReynardMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Newcastle University · GB

Funding

Medical Research Council MR/K006312/1Versus Arthritis 18746Versus Arthritis 20028
6 · The paper itself

Abstract

objectivesWe have previously shown that the cartilage DNA methylome delineates two clusters of osteoarthritic (OA) hip patients, characterised by differential methylation of inflammatory genes, while others have demonstrated a link between zinc homeostasis and inflammation in OA. We aimed to investigate these effects at the methylation and gene expression level.

methodsWe used our previously generated methylation data while quantitative PCR was used to measure gene expression using RNA from the hip cartilage of members of both clusters and from control individuals without hip OA.

resultsOne of the OA clusters is characterised by the promoter hypomethylation and increased expression of inflammation-associated genes including IL1A and TNF. Furthermore, we show that the increase in expression of these genes is accompanied by increased expression of several zinc transporter genes. In addition, the zinc responsive transcription factor MTF1 is also upregulated, which is accompanied by an increase in the expression of its targets the metalloproteinases MMP13 and ADAMTS5.

conclusionsWe have identified a subgroup of OA hip patients that are epigenetically and transcriptiomically characterised by a cartilage inflammatory phenotype with concurrent differential regulation of zinc regulators. The identification of subgroups enhances stratified phenotyping of OA patients and has important implications for future therapeutic applications.

Indexed as

DNA MethylationADAM ProteinsADAMTS5 ProteinAgedAged, 80 and overCartilage, ArticularCase-Control StudiesDNA-Binding ProteinsEpigenesis, GeneticFemaleGene Expression RegulationHumansInterleukin-1alphaMaleMatrix Metalloproteinase 13Middle AgedADAM ProteinsADAMTS5 ProteinADAMTS5 protein, humanDNA-Binding ProteinsIL1A protein, humanInterleukin-1alphaMatrix Metalloproteinase 13MMP13 protein, humanRNA, MessengerTranscription Factor MTF-1Transcription FactorsTumor Necrosis Factor-alphaChondrocytesInflammationOsteoarthritis

Identifiers

PMID25854584
PMCPMC4552898
OpenAlexW2166323245

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LicenceCC BY
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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.