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      Triple Contrast CT Method Enables Simultaneous Evaluation of Articular Cartilage Composition and Segmentation

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          Abstract

          Early degenerative changes of articular cartilage are detected using contrast-enhanced computed tomography (CT) with a cationic contrast agent (CA). However, cationic CA diffusion into degenerated cartilage decreases with proteoglycan depletion and increases with elevated water content, thus hampering tissue evaluation at early diffusion time points. Furthermore, the contrast at synovial fluid-cartilage interface diminishes as a function of diffusion time hindering accurate cartilage segmentation. For the first time, we employ quantitative dual-energy CT (QDECT) imaging utilizing a mixture of three CAs (cationic CA4+ and non-ionic gadoteridol which are sensitive to proteoglycan and water contents, respectively, and bismuth nanoparticles which highlight the cartilage surface) to simultaneously segment the articulating surfaces and determine of the cartilage condition. Intact healthy, proteoglycan-depleted, and mechanically injured bovine cartilage samples ( n = 27) were halved and imaged with synchrotron microCT 2-h post immersion in triple CA or in dual CA (CA4+ and gadoteridol). CA4+ and gadoteridol partitions were determined using QDECT, and pairwise evaluation of these partitions was conducted for samples immersed in dual and triple CAs. In conclusion, the triple CA method is sensitive to proteoglycan depletion while maintaining sufficient contrast at the articular surface to enable detection of cartilage lesions caused by mechanical impact.

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          X-ray-computed tomography contrast agents.

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            Tests for comparing elements of a correlation matrix.

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              Post-traumatic osteoarthritis: improved understanding and opportunities for early intervention.

              Even with current treatments of acute joint injuries, more than 40% of people who suffer significant ligament or meniscus tears, or articular surface injuries, will develop osteoarthritis (OA). Correspondingly, 12% or more of all patients with lower extremity OA have a history of joint injury. Recent research suggests that acute joint damage that occurs at the time of an injury initiates a sequence of events that can lead to progressive articular surface damage. New molecular interventions, combined with evolving surgical methods, aim to minimize or prevent progressive tissue damage triggered by joint injury. Seizing the potential for progress in the treatment of joint injuries to forestall OA will depend on advances in (1) quantitative methods of assessing the injury severity, including both structural damage and biologic responses, (2) understanding of the pathogenesis of post-traumatic OA, taking into account potential interactions among the different tissues and the role of post-traumatic incongruity and instability, and (3) application of engineering and molecular research to develop new methods of treating injured joints. This paper highlights recent advances in understanding of the structural damage and the acute biological response following joint injury, and it identifies important directions for future research. Copyright © 2011 Orthopaedic Research Society.
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                Author and article information

                Contributors
                miitu.honkanen@uef.fi
                annina.saukko@uef.fi
                mikael.turunen@uef.fi
                wujun.xu@uef.fi
                goran.lovric@psi.ch
                juuso.honkanen@uef.fi
                mgrin@bu.edu
                vesa-pekka.lehto@uef.fi
                juha.toyras@uef.fi
                Journal
                Ann Biomed Eng
                Ann Biomed Eng
                Annals of Biomedical Engineering
                Springer US (New York )
                0090-6964
                1573-9686
                1 October 2019
                1 October 2019
                2020
                : 48
                : 2
                : 556-567
                Affiliations
                [1 ]GRID grid.9668.1, ISNI 0000 0001 0726 2490, Department of Applied Physics, , University of Eastern Finland, ; P.O. Box 1627, 70211 Kuopio, Finland
                [2 ]GRID grid.410705.7, ISNI 0000 0004 0628 207X, Diagnostic Imaging Center, , Kuopio University Hospital, ; Kuopio, Finland
                [3 ]GRID grid.410552.7, ISNI 0000 0004 0628 215X, Department of Medical Physics, , Turku University Hospital, ; Turku, Finland
                [4 ]GRID grid.9668.1, ISNI 0000 0001 0726 2490, SIB-labs, , University of Eastern Finland, ; Kuopio, Finland
                [5 ]GRID grid.5333.6, ISNI 0000000121839049, Centre d’Imagerie BioMédicale, , École Polytechnique Fédérale de Lausanne, ; Lausanne, Switzerland
                [6 ]GRID grid.5991.4, ISNI 0000 0001 1090 7501, Swiss Light Source, Paul Scherrer Institute, ; Villigen, Switzerland
                [7 ]GRID grid.410705.7, ISNI 0000 0004 0628 207X, Center of Oncology, , Kuopio University Hospital, ; Kuopio, Finland
                [8 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Departments of Biomedical Engineering, Chemistry, and Medicine, , Boston University, ; Boston, MA USA
                [9 ]GRID grid.1003.2, ISNI 0000 0000 9320 7537, School of Information Technology and Electrical Engineering, , The University of Queensland, ; Brisbane, Australia
                Author notes

                Associate Editor Sean S. Kohles oversaw the review of this article.

                Author information
                http://orcid.org/0000-0002-2548-4457
                http://orcid.org/0000-0001-8678-4675
                http://orcid.org/0000-0003-1093-1178
                http://orcid.org/0000-0002-3177-4709
                http://orcid.org/0000-0002-0833-4043
                http://orcid.org/0000-0002-9150-9253
                http://orcid.org/0000-0002-5453-3668
                http://orcid.org/0000-0001-8153-1070
                http://orcid.org/0000-0002-8035-1606
                Article
                2362
                10.1007/s10439-019-02362-6
                6949199
                31576504
                185987e3-a534-4317-b647-3f0124d8310c
                © The Author(s) 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 7 April 2019
                : 11 September 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004212, Päivikki ja Sakari Sohlbergin Säätiö;
                Funded by: The Vilho, Yrjö and Kalle Väisälä Foundation of the Finnish Academy of Science and Letters
                Funded by: The Research Committee of the Kuopio University Hospital Catchment Area for the State Research Funding
                Award ID: 5041769
                Award ID: 5654199
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002341, Academy of Finland;
                Award ID: 307932
                Award Recipient :
                Funded by: Doctoral Program in Science, Technology and Computing, University of Eastern Finland
                Funded by: FundRef http://dx.doi.org/10.13039/501100004022, Jenny ja Antti Wihurin Rahasto;
                Categories
                Original Article
                Custom metadata
                © Biomedical Engineering Society 2020

                Biomedical engineering
                triple contrast agent,dual contrast agent,computed tomography,contrast-enhanced computed tomography,post-traumatic osteoarthritis,synchrotron microct

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