Evidence map›Paper›PMID 30797944›Full record

ArticleOsteoarthritis and cartilage2019

Distinct degenerative phenotype of articular cartilage from knees with meniscus tear compared to knees with osteoarthritis.

M F Rai, E D Tycksen, L Cai, J Yu, R W Wright, R H Brophy

Open access · bronzeAbstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Loss of periostin function impairs ligament fibroblast activity and facilitates ROS-mediated cellular senescence.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Non-Coding RNAs in Cartilage Development: An Updated Review.International journal of molecular sciences · 2019
    Review
  17. Review
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

6 authors at 1 institution in 1 country.

M F RaiDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: rai.m@wustl.edu.
E D TycksenGenome Technology Access Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: etycksen@wustl.edu.
L CaiDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: lei.cai@wustl.edu.
J YuGenome Technology Access Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: jinsheng.yu@wustl.edu.
R W WrightDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: rwright@wustl.edu.
R H BrophyDepartment of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: brophyrh@wustl.edu.
Washington University in St. Louis · US

Funding

Genetic and Molecular Insights into Cartilage Regeneration, Primary and Posttraumatic OsteoarthritisR00AR064837 · NIAMS · WASHINGTON UNIVERSITY · PI RAI, MUHAMMAD FAROOQ · 2017 to 2019
$747k
NIAMS NIH HHS R00 AR064837
6 · The paper itself

Abstract

objectiveTo compare the transcriptome of articular cartilage from knees with meniscus tears to knees with end-stage osteoarthritis (OA).

designArticular cartilage was collected from the non-weight bearing medial intercondylar notch of knees undergoing arthroscopic partial meniscectomy (APM; N = 10, 49.7 ± 10.8 years, 50% females) for isolated medial meniscus tears and knees undergoing total knee arthroplasty (TKA; N = 10, 66.0 ± 7.6 years, 70% females) due to end-stage OA. Ribonucleic acid (RNA) preparation was subjected to SurePrint G3 human 8 × 60K RNA microarrays to probe differentially expressed transcripts followed by computational exploration of underlying biological processes. Real-time polymerase chain reaction amplification was performed on selected transcripts to validate microarray data.

resultsWe observed that 81 transcripts were significantly differentially expressed (45 elevated, 36 repressed) between APM and TKA samples (≥ 2 fold) at a false discovery rate of ≤ 0.05. Among these, CFD, CSN1S1, TSPAN11, CSF1R and CD14 were elevated in the TKA group, while CHI3L2, HILPDA, COL3A1, COL27A1 and FGF2 were highly expressed in APM group. A few long intergenic non-coding RNAs (lincRNAs), small nuclear RNAs (snoRNAs) and antisense RNAs were also differentially expressed between the two groups. Transcripts up-regulated in TKA cartilage were enriched for protein localization and activation, chemical stimulus, immune response, and toll-like receptor signaling pathway. Transcripts up-regulated in APM cartilage were enriched for mesenchymal cell apoptosis, epithelial morphogenesis, canonical glycolysis, extracellular matrix organization, cartilage development, and glucose catabolic process.

conclusionsThis study suggests that APM and TKA cartilage express distinct sets of OA transcripts. The gene profile in cartilage from TKA knees represents an end-stage OA whereas in APM knees it is clearly earlier in the degenerative process.

Indexed as

AdultAgedArthroplasty, Replacement, KneeCartilage, ArticularCase-Control StudiesCaseinsChitinasesCollagen Type IIIComplement Factor DFemaleFibrillar CollagensFibroblast Growth Factor 2Gene Expression ProfilingHumansLipopolysaccharide ReceptorsMaleCaseinsCFD protein, humanCHI3L2 protein, humanChitinasesCOL27A1 protein, humanCOL3A1 protein, humanCollagen Type IIIComplement Factor DCSF1R protein, humanFibrillar CollagensFibroblast Growth Factor 2HILPDA protein, humanLipopolysaccharide ReceptorsNeoplasm ProteinsReceptor, Macrophage Colony-Stimulating FactorReceptors, Granulocyte-Macrophage Colony-Stimulating FactorRNARNA, AntisenseRNA, Long NoncodingRNA, MessengerRNA, Small NuclearTetraspaninsTSPAN11 protein, humanExtracellular matrix organizationImmune responseKnee arthroplastylincRNAsMicroarraysPartial meniscectomy

Identifiers

PMID30797944
PMCPMC6536326
OpenAlexW2916763796

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.