Evidence map›Paper›PMID 23124630›Full record

ArticleArthritis and rheumatism2013

Quantitative imaging of murine osteoarthritic cartilage by phase-contrast micro-computed tomography.

Merry Z C Ruan, Brian Dawson, Ming-Ming Jiang, Francis Gannon, Michael Heggeness, Brendan H L Lee

Abstract read
In one paragraph

Article in Arthritis and rheumatism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 58 citations in OpenAlex.

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  12. Targeted Near-Infrared Fluorescence Imaging for Regenerative Medicine.Tissue engineering and regenerative medicine · 2019
    Review
  13. Article
  14. Animal Models for the Study of Bone-Derived Pain.Methods in molecular biology (Clifton, N.J.) · 2019
    Article
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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

6 authors at 2 institutions in 1 country.

Merry Z C RuanBaylor College of Medicine, Houston, Texas 77030, USA.
Brian Dawson
Ming-Ming Jiang
Francis Gannon
Michael Heggeness
Brendan H L Lee
Baylor College of Medicine · USHoward Hughes Medical Institute · US

Funding

UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI TOLIAS, KIMBERLY R · 1988 to 2013
$29.4M
THE SKELETAL DYSPLASIASP01HD022657 · NICHD · CEDARS-SINAI MEDICAL CENTER · PI LEE, BRENDAN · 1987 to 2011
$17.0M
PROGRAM IN HUMAN MOLECULAR GENETICST32GM008307 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI SHAULSKY, GAD · 1990 to 2020
$6.6M
Mouse mutations that model human craniofacial/limb abnormalitiesP01ES011253 · NIEHS · BAYLOR COLLEGE OF MEDICINE · PI LEE, BRENDAN HL · 2001 to 2005
$5.4M
Transcriptional Regulation of Craniofacial SkeletogenesisR01DE016990 · NIDCR · BAYLOR COLLEGE OF MEDICINE · PI LEE, BRENDAN · 2005 to 2009
$1.6M
TRANSCRIPTIONAL REGULATORS IN CHONDROGENESISR29AR044738 · NIAMS · BAYLOR COLLEGE OF MEDICINE · PI LEE, BRENDAN HL · 1998 to 1999
–
Howard Hughes Medical InstituteNIAMS NIH HHS R29 AR044738NICHD NIH HHS P01 HD022657NICHD NIH HHS P30 HD024064NIDCR NIH HHS R01 DE016990NIEHS NIH HHS P01 ES011253NIGMS NIH HHS T32 GM008307
6 · The paper itself

Abstract

objectiveThe mouse is an optimal model organism in which gene-environment interactions can be used to study the pathogenesis of osteoarthritis (OA). The gold standard for arthritis research in mice is based on histopathology and immunohistochemistry, which are labor-intensive, prone to sampling bias and technical variability, and limited in throughput. The aim of this study was to develop a new technique that assesses mouse cartilage by integrating quantitative volumetric imaging techniques.

methodsA novel mouse model of OA was generated by cruciate ligament transection (CLT) and evaluated by histopathology and immunohistochemistry. Knee joint specimens were then imaged using a new technique that combines high-resolution micro-computed tomography (micro-CT) and phase-contrast optics followed by quantitative analyses. A comparative analysis was also performed in a previously established mouse model of OA generated by destabilization of the medial meniscus (DMM).

resultsPhase-contrast micro-CT achieved cellular resolution of chondrocytes and quantitative assessment of parameters such as articular cartilage volume and surface area. In mouse models of OA generated by either CLT or DMM, we showed that phase-contrast micro-CT distinguished control and OA cartilage by providing quantitative measures with high reproducibility and minimal variability. Features of OA at the cellular or tissue level could also be observed in images generated by phase-contrast micro-CT.

conclusionWe established an imaging technology that comprehensively assessed and quantified the 2-dimensional and 3-dimensional changes of articular cartilage. Application of this technology will facilitate the rapid and high-throughput assessment of genetic and therapeutic models of OA in mice.

Indexed as

Microscopy, Phase-ContrastAnimalsAnterior Cruciate LigamentArthritis, ExperimentalCartilage, ArticularChondrocytesKnee JointMaleMiceOsteoarthritis, KneeX-Ray Microtomography

Identifiers

PMID23124630
PMCPMC3779602
OpenAlexW2138236384

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.