MRI overestimates articular cartilage thickness and volume compared to synchrotron radiation phase-contrast imaging.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 15 12 2022
accepted: 05 09 2023
medline: 5 10 2023
pubmed: 3 10 2023
entrez: 3 10 2023
Statut: epublish

Résumé

Accurate evaluation of morphological changes in articular cartilage are necessary for early detection of osteoarthritis (OA). 3T magnetic resonance imaging (MRI) has highly sensitive contrast resolution and is widely used clinically to detect OA. However, synchrotron radiation phase-contrast imaging computed tomography (SR-PCI) can also provide contrast to tissue interfaces that do not have sufficient absorption differences, with the added benefit of very high spatial resolution. Here, MRI was compared with SR-PCI for quantitative evaluation of human articular cartilage. Medial tibial condyles were harvested from non-OA donors and from OA patients receiving knee replacement surgery. Both imaging methods revealed that average cartilage thickness and cartilage volume were significantly reduced in the OA group, compared to the non-OA group. When comparing modalities, the superior resolution of SR-PCI enabled more precise mapping of the cartilage surface relative to MRI. As a result, MRI showed significantly higher average cartilage thickness and cartilage volume, compared to SR-PCI. These data highlight the potential for high-resolution imaging of articular cartilage using SR-PCI as a solution for early OA diagnosis. Recognizing current limitations of using a synchrotron for clinical imaging, we discuss its nascent utility for preclinical models, particularly longitudinal studies of live animal models of OA.

Identifiants

pubmed: 37788257
doi: 10.1371/journal.pone.0291757
pii: PONE-D-22-34378
pmc: PMC10547194
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0291757

Subventions

Organisme : CIHR
ID : 148683
Pays : Canada

Informations de copyright

Copyright: © 2023 Bairagi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Suranjan Bairagi (S)

Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

Mohammad-Amin Abdollahifar (MA)

Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

Oghenevwogaga J Atake (OJ)

Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

William Dust (W)

Department of Surgery, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

Sheldon Wiebe (S)

Department of Medical Imaging, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

George Belev (G)

Canadian Light Source Inc., Saskatoon, Saskatchewan, Canada.

L Dean Chapman (LD)

Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

M Adam Webb (MA)

Canadian Light Source Inc., Saskatoon, Saskatchewan, Canada.

Ning Zhu (N)

Canadian Light Source Inc., Saskatoon, Saskatchewan, Canada.

David M L Cooper (DML)

Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

B Frank Eames (BF)

Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

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