Evidence map›Paper›PMID 35288246›Full record

ArticleThe Journal of arthroplasty2022

Otto Aufranc Award: Identification of Key Molecular Players in the Progression of Hip Osteoarthritis Through Transcriptomes and Epigenetics.

Cecilia Pascual-Garrido, Tomoyuki Kamenaga, Robert H Brophy, Jie Shen, Regis J O'Keefe, John C Clohisy

Open access · greenAbstract read
In one paragraph

Article in The Journal of arthroplasty, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Revealing a Natural Model of Pre-Osteoarthritis of the Hip Through Study of Femoroacetabular Impingement.HSS journal : the musculoskeletal journal of Hospital for Special Surgery · 2023
    Article
  8. Review
  9. Epigenetic dysregulation of articular cartilage during progression of hip femoroacetabular impingement disease.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    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

6 authors at 1 institution in 1 country.

Cecilia Pascual-GarridoDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri.
Tomoyuki KamenagaDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri.
Robert H BrophyDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri.
Jie ShenDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri.
Regis J O'KeefeDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri.
John C ClohisyDepartment of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri.
Washington University in St. Louis · US

Funding

Resource Based Center for Musculoskeletal Biology and Medicine (Overall Application)P30AR074992 · NIAMS · WASHINGTON UNIVERSITY · PI MATTHEW J SILVA · 2019 to 2026
$6.8M
Mediators of the OA Cascade in the Pre-Arthritic HipK08AR077740 · NIAMS · WASHINGTON UNIVERSITY · PI PASCUAL-GARRIDO, CECILIA · 2020 to 2024
$779k
NIAMS NIH HHS K08 AR077740NIAMS NIH HHS P30 AR074992
6 · The paper itself

Abstract

backgroundThis study aimed: (1) to compare the transcriptome profile of articular cartilage in cam-FAI (early stage) to advanced OA secondary to cam-FAI (late stage) and (2) to investigate epigenetic changes through the expression of DNA methylation enzymes DNMT3B, DNMT1, and DNMT3A and peroxisome proliferator-activated receptor gamma (PPARγ) in human cartilage samples during the progression of hip OA.

methodsFull-thickness cartilage samples were collected from the anterolateral head-neck junction (impingement zone) of 22 patients (9 early-FAI and 13 late-FAI). RNA sequencing and in vitro cartilage cultures with histological analysis and immunohistochemistry staining for PPARγ and DNMT3B were performed. Target gene validation was confirmed with RT-PCR.

resultsFifty genes and 42 pathways were identified differentially between early and late-FAI (fold change <-1.5 or >1.5, P < .01). PPARγ and DNMT3B were gradually suppressed with disease progression. Contrarily, disease progression induced expression of DNMT1/3A.

conclusionBy comparing comprehensive gene expression in early and late stage hip degeneration at the whole-genome level, distinct transcriptome profiles for early and late stage disease were identified along with key molecular contributors to the progression of hip OA. Preservation of endogenous PPARγ may have therapeutic potential to delay or prevent hip OA.

Indexed as

Cartilage, ArticularEpigenesis, GeneticFemoracetabular ImpingementOsteoarthritis, HipTranscriptomeDisease ProgressionHip JointHumansPPAR gammaPPAR gammaepigeneticshiposteoarthritispreosteoarthritistranscriptomes

Identifiers

PMID35288246
PMCPMC9208365
OpenAlexW4220972795

What OpenQuestion holds

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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.