Evidence map›Paper›PMID 25478225›Full record

ArticleArthritis2014

Progression of Gene Expression Changes following a Mechanical Injury to Articular Cartilage as a Model of Early Stage Osteoarthritis.

R S McCulloch, M S Ashwell, C Maltecca, A T O'Nan, P L Mente

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Arthritis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04222140 (Early Regenerative Intervention for Post-Traumatic Osteoarthritis), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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.

NCT04222140 naunknown statusnot on this mapstarted 2020, after this paper: background citation

Early Regenerative Intervention for Post-Traumatic Osteoarthritis

TypeinterventionalSponsorAffinity Health Research InstituteRan2020 to 2021Enrolled40ConditionsPost-Traumatic Osteoarthritis of KneeArmsERIPTO Protocol, BMAC Only
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Influence of the pericellular and extracellular matrix structural properties on chondrocyte mechanics.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
    Article
  7. Article
  8. 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

5 authors at 1 institution in 1 country.

R S McCullochJoint Department of Biomedical Engineering, North Carolina State University, Raleigh, NC 27695, USA ; University of North Carolina, Chapel Hill, NC 27599, USA ; Human Physiology Department, Gonzaga University, Spokane, WA 99258, USA.
M S AshwellDepartment of Animal Science, North Carolina State University, Campus Box 7621, Raleigh, NC 27695, USA.
C MalteccaDepartment of Animal Science, North Carolina State University, Campus Box 7621, Raleigh, NC 27695, USA.
A T O'NanDepartment of Animal Science, North Carolina State University, Campus Box 7621, Raleigh, NC 27695, USA.
P L MenteJoint Department of Biomedical Engineering, North Carolina State University, Raleigh, NC 27695, USA ; University of North Carolina, Chapel Hill, NC 27599, USA.
North Carolina State University · US

Funding

Cartilage Matrix Damage and Chondrocyte Response to Normal and Shear InjuryR03AR054557 · NIAMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MENTE, PETER LAWRENCE · 2007 to 2009
$210k
NIAMS NIH HHS R03 AR054557
6 · The paper itself

Abstract

An impact injury model of early stage osteoarthritis (OA) progression was developed using a mechanical insult to an articular cartilage surface to evaluate differential gene expression changes over time and treatment. Porcine patellae with intact cartilage surfaces were randomized to one of three treatments: nonimpacted control, axial impaction (2000 N), or a shear impaction (500 N axial, with tangential displacement to induce shear forces). After impact, the patellae were returned to culture for 0, 3, 7, or 14 days. At the appropriate time point, RNA was extracted from full-thickness cartilage slices at the impact site. Quantitative real-time PCR was used to evaluate differential gene expression for 18 OA related genes from four categories: cartilage matrix, degradative enzymes and inhibitors, inflammatory response and signaling, and cell apoptosis. The shear impacted specimens were compared to the axial impacted specimens and showed that shear specimens more highly expressed type I collagen (Col1a1) at the early time points. In addition, there was generally elevated expression of degradative enzymes, inflammatory response genes, and apoptosis markers at the early time points. These changes suggest that the more physiologically relevant shear loading may initially be more damaging to the cartilage and induces more repair efforts after loading.

Identifiers

PMID25478225
PMCPMC4248372
OpenAlexW2060428600

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.