Evidence map›Paper›PMID 35751529›Full record

ArticleAnatomical record (Hoboken, N.J. : 2007)2023

Contrast-enhanced micro-computed tomography of compartment and time-dependent changes in femoral cartilage and subchondral plate in a murine model of osteoarthritis.

Deva D Chan, Maleeha Mashiatulla, Jun Li, Ryan D Ross, Meghana Pendyala, Amit Patwa, Mark W Grinstaff, Anna Plaas, D Rick Sumner

Open access · bronzeAbstract read
In one paragraph

Article in Anatomical record (Hoboken, N.J. : 2007), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors at 3 institutions in 2 countries.

Deva D ChanDepartment of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.ORCID 0000-0003-1508-1045
Maleeha MashiatullaDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, USA.ORCID 0000-0003-2847-2766
Jun LiDepartment of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.ORCID 0000-0002-3257-9315
Ryan D RossDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, USA.ORCID 0000-0003-3760-234X
Meghana PendyalaDepartment of Biomedical Engineering, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, New York, USA.ORCID 0000-0003-2968-1746
Amit PatwaDepartment of Biomedical Engineering Department of Chemistry, Boston University, Boston, Massachusetts, USA.ORCID 0000-0002-9323-3262
Mark W GrinstaffDepartment of Biomedical Engineering Department of Chemistry, Boston University, Boston, Massachusetts, USA.ORCID 0000-0002-5453-3668
Anna PlaasDepartment of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.ORCID 0000-0001-5205-0892
D Rick SumnerDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, USA.
Rush University Medical Center · USBoston University · USRensselaer Polytechnic Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A lack of understanding of the mechanisms underlying osteoarthritis (OA) progression limits the development of effective long-term treatments. Quantitatively tracking spatiotemporal patterns of cartilage and bone degeneration is critical for assessment of more appropriately targeted OA therapies. In this study, we use contrast-enhanced micro-computed tomography (μCT) to establish a timeline of subchondral plate (SCP) and cartilage changes in the murine femur after destabilization of the medial meniscus (DMM). We performed DMM or sham surgery in 10-12-week-old male C57Bl/6J mice. Femora were imaged using μCT after 0, 2, 4, or 8 weeks. Cartilage-optimized scans were performed after immersion in contrast agent CA4+. Bone mineral density distribution (BMDD), cartilage attenuation, SCP, and cartilage thickness and volume were measured, including lateral and medial femoral condyle and patellar groove compartments. As early as 2 weeks post-DMM, cartilage thickness significantly increased and cartilage attenuation, SCP volume, and BMDD mean significantly decreased. Trends in cartilage and SCP metrics within each joint compartment reflected those seen in global measurements, and both BMDD and SCP thickness were consistently greater in the lateral and medial condyles than the patellar groove. Sham surgery also resulted in significant changes to SCP and cartilage metrics, highlighting a potential limitation of using surgical models to study tissue morphology or composition changes during OA progression. Contrast-enhanced μCT analysis is an effective tool to monitor changes in morphology and composition of cartilage, and when combined with bone-optimized μCT, can be used to assess the progression of degenerative changes after joint injury.

Indexed as

CartilageAnimalsDisease Models, AnimalMaleMiceX-Ray Microtomographycartilagecontrast-enhanced micro-computed tomographymurine modelpost-traumatic osteoarthritissubchondral plate

Identifiers

PMID35751529
PMCPMC10084428
OpenAlexW4283511014

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.