Evidence map›Paper›PMID 24185113›Full record

ArticleOsteoarthritis and cartilage2014

Identification of cartilage injury using quantitative multiphoton microscopy.

K D Novakofski, R M Williams, L A Fortier, H O Mohammed, W R Zipfel, L J Bonassar

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Osteoarthritis and cartilage, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.1field-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

11 citing papers in PubMed, 27 citations in OpenAlex.

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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 1 institution in 1 country.

K D NovakofskiDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
R M WilliamsDepartment of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
L A FortierDepartment of Clinical Sciences, Cornell University, Ithaca, NY, USA.
H O MohammedPopulation Medicine and Diagnostic Sciences, Cornell University, Ithaca, NY 14853, USA.
W R ZipfelDepartment of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
L J BonassarDepartment of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA. Electronic address: lb244@cornell.edu.
Cornell University · US

Funding

Clinical and Translational Science CenterUL1TR000457 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2012 to 2016
$46.0M
Biotechnology Resource Digital Electro-Optical ImagingP41EB001976 · NIBIB · CORNELL UNIVERSITY ITHACA · PI ZIPFEL, WARREN R · 2003 to 2010
$6.9M
Clinical and Translational Science CenterTL1TR000459 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2012 to 2016
$451k
NCATS NIH HHS TL1 TR000459NCATS NIH HHS UL1 TR000457NCRR NIH HHS TL1RR000459NIBIB NIH HHS P41 EB001976NIBIB NIH HHS P41-EB01976
6 · The paper itself

Abstract

objectiveCartilage injury can lead to post-traumatic osteoarthritis (PTOA). Immediate post-trauma cellular and structural changes are not widely understood. Furthermore, current cellular-resolution cartilage imaging techniques require sectioning of cartilage and/or use of dyes not suitable for patient imaging. In this study, we used multiphoton microscopy (MPM) data with FDA-approved sodium fluorescein to identify and evaluate the pattern of chondrocyte death after traumatic injury.

methodMature equine distal metacarpal or metatarsal osteochondral blocks (OCBs) were injured by 30 MPa compressive loading delivered over 1 s. Injured and control sites were imaged unfixed and in situ 1 h post-injury with sodium fluorescein using rasterized z-scanning. MPM data was quantified in MATLAB, reconstructed in 3-D, and projected in 2-D to determine the damage pattern.

resultsMPM images (600 per sample) were reconstructed and analyzed for cell death. The overall distribution of cell death appeared to cluster into circular (n = 7) or elliptical (n = 4) patterns (p = 0.006). Dead cells were prevalent near cracks in the matrix, with only 26.3% (SE = 5.0%, p < 0.0001) of chondrocytes near cracks being viable.

conclusionThis study demonstrates the first application of MPM for evaluating cellular-scale cartilage injury in situ in live tissue, with clinical potential for detecting early cartilage damage. With this technique, we were able to uniquely observe two death patterns resulting from the same compressive loading, which may be related to local variability in matrix structure. These results also demonstrate proof-of-concept MPM diagnostic use in detecting subtle and early cartilage damage not detectable in any other way.

Indexed as

AnimalsCartilage, ArticularCell DeathChondrocytesDisease Models, AnimalEarly DiagnosisFeasibility StudiesHorsesImage Processing, Computer-AssistedMetacarpusMetatarsal BonesMicroscopy, Fluorescence, MultiphotonStress, MechanicalWeight-BearingCartilageImagingInjuryMultiphoton microscopyPost-traumatic osteoarthritis

Identifiers

PMID24185113
PMCPMC4117377
OpenAlexW2113712596

What OpenQuestion holds

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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.