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      MMP-3 in the peripheral serum as a biomarker of knee osteoarthritis, 40 years after open total knee meniscectomy

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          Abstract

          Background

          To explore potential biomarkers in a meniscectomy-induced knee osteoarthritis model, at forty years after meniscectomy.

          Methods

          We carried out a forty-year study of 53 patients who, as adolescents, underwent open total meniscectomy and assessed two potential synovial and serum biomarkers, namely glycosaminoglycan (GAG) and matrix metalloproteinase-3 (MMP-3). Of the 30 patients available for review, 8 had contralateral knee operations and were excluded.

          Of the remaining 22 patients, 17 had successful operated knee synovial fluid aspirations and 8 also had successful contralateral control knee aspirations. GAG and MMP3 levels in the synovial fluid and peripheral serum was measured using Alcian blue precipitation and ELISA quantification, respectively. Patients also had their knee radiographs assessed and their radiographic osteoarthritis classified as per the Kellgren-Lawrence and Ahlbӓck systems.

          Results

          At forty years after meniscectomy, synovial MMP-3 levels remain increased ( p = 0.0132) while GAG levels were reduced ( p = 0.0487) when compared to controls and these two levels correlate inversely. Furthermore, levels of synovial MMP-3 significantly correlated ( p = 0.0032, r = 0.7734; p = 0.0256, r = 0.5552) and GAG levels significantly inversely correlated ( p = 0.0308, r = − 0.6220; p = 0.0135, r = − 0.6024), respectively, with both radiological scoring systems. Interestingly, we found that the levels of serum MMP-3 correlated only with the synovial fluid levels of MMP-3 in the operated knee and not with the non-operated joint ( p = 0.0252, r = 0.7706 vs. p = 0.0764, r = 0.6576). Multiple regression analysis for patient’s quality of life based on these biomarkers revealed an almost perfect result with an R2 of 0.9998 and a p value = 0.0087.

          Conclusion

          Our results suggest that serum levels of MMP3 could be used as a potential biomarker for knee osteoarthritis, using a simple blood test. Larger cohorts are desirable in order to prove or disprove this finding.

          Electronic supplementary material

          The online version of this article (10.1186/s40634-018-0132-x) contains supplementary material, which is available to authorized users.

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          Most cited references33

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          Tibiofemoral contact mechanics after serial medial meniscectomies in the human cadaveric knee.

          There is no consensus regarding the extent of meniscectomy leading to deleterious effects on tibiofemoral contact mechanics. The meniscus aids in optimizing tibiofemoral contact mechanics, increasing contact area, and decreasing contact stress. Controlled laboratory study. Twelve fresh-frozen human cadaveric knees each underwent 15 separate testing conditions-5 serial 20-mm posterior medial meniscectomy conditions (intact, 50% radial width, 75% radial width, segmental, and total meniscectomy) at 3 flexion angles (0 degrees , 30 degrees , and 60 degrees )-under an 1800-N axial load. Tekscan sensors were used to measure total force and medial force, contact area, mean contact stress, and peak contact stress. All posterior medial meniscectomy conditions resulted in significantly decreased contact areas and increased mean and peak contact stresses compared with the intact state (P .05). Incremental changes in contact area and mean contact stress increased as more peripheral portions of the medial meniscus were removed, whereas peak contact stresses exhibited similar incremental changes throughout all meniscectomy conditions. The meniscus is a crucial load-bearing structure, optimizing contact area and minimizing contact stress. Loss of hoop tension (ie, segmental meniscectomy) is equivalent to total meniscectomy in load-bearing terms. The peripheral portion of the medial meniscus provides a greater contribution to increasing contact areas and decreasing mean contact stresses than does the central portion, whereas peak contact stresses increase proportionally to the amount of meniscus removed. Because the degree of meniscectomy leading to clinically significant outcomes is unknown, a prudent strategy is to preserve the greatest amount of meniscus possible.
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            Aggrecan protects cartilage collagen from proteolytic cleavage.

            The matrix components responsible for cartilage mechanical properties, type II collagen and aggrecan, are degraded in osteoarthritis through proteolytic cleavage by matrix metalloproteinases (MMPs) and aggrecanases, respectively. We now show that aggrecan may serve to protect cartilage collagen from degradation. Although collagen in freeze-thawed cartilage depleted of aggrecan was completely degraded following incubation with MMP-1, collagen in cartilage with intact aggrecan was not. Using interleukin-1-stimulated bovine nasal cartilage explants where aggrecan depletion occurs during the first week of culture, followed by collagen loss during the second week, we evaluated the effect of selective MMP and aggrecanase inhibitors on degradation. A selective MMP inhibitor did not block aggrecan degradation but caused complete inhibition of collagen breakdown. Similar inhibition was seen with inhibitor addition following aggrecan depletion on day 6-8, suggesting that MMPs are not causing significant collagen degradation prior to the second week of culture. Inclusion of a selective aggrecanase inhibitor blocked aggrecan degradation, and, in addition, inhibited collagen degradation. When the inhibitor was introduced following aggrecan depletion, it had no effect on collagen breakdown, ruling out a direct effect through inhibition of collagenase. These data suggest that aggrecan plays a protective role in preventing degradation of collagen fibrils, and that an aggrecanase inhibitor may impart overall cartilage protection.
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              Osteo-Arthrosis: Prevalence in the Population and Relationship between Symptoms andX-ray Changes

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                Author and article information

                Contributors
                yiannispengas@yahoo.com
                Journal
                J Exp Orthop
                J Exp Orthop
                Journal of Experimental Orthopaedics
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2197-1153
                15 June 2018
                15 June 2018
                December 2018
                : 5
                : 21
                Affiliations
                [1 ]Consultant Trauma & Orthopaedic Knee Surgeon, Joint Preservation & Soft Tissue Knee Specialist, Royal Cornwall Teaching Hospitals NHS Trust Treliske, Truro, TR1 3LQ UK
                [2 ]ISNI 0000 0001 2171 1133, GRID grid.4868.2, Department of Experimental Medicine and Rheumatology, William Harvey Research Institute. Barts and The London, , Queen Mary’s School of Medicine and Dentistry, ; London, EC1M 6BQ UK
                [3 ]ISNI 0000 0004 0497 2835, GRID grid.428062.a, Specialist registrar in Trauma & Orthopaedics, , Chelsea & Westminster Hospital NHS Foundation Trust, ; 369 Fulham Rd, Chelsea, London, SW10 9NH UK
                [4 ]GRID grid.411255.6, Consultant Trauma & Orthopaedic Knee Surgeon, , Aintree University Hospital NHS Foundation Trust Longmoor Ln, ; Liverpool, L9 7AL UK
                [5 ]ISNI 0000 0001 2159 175X, GRID grid.10328.38, Orthopaedics Department of Minho University, R. da Universidade, , Minho University, ; 4710-057 Braga, Portugal
                [6 ]ISNI 0000 0004 0425 5852, GRID grid.416189.3, Department of Arthroscopy, , The Royal Orthopaedic Hospital, The Woodlands, ; Bristol Rd S, Birmingham, B31 2AP UK
                Author information
                http://orcid.org/0000-0001-9602-9104
                Article
                132
                10.1186/s40634-018-0132-x
                6003895
                29904905
                3ae918f5-5ff0-43e3-948b-ce81ca2fbcbe
                © The Author(s). 2018

                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
                : 1 March 2018
                : 17 May 2018
                Funding
                Funded by: The authors would like to thank the Warrington Hospital Charitable fund for covering the costs incurred in this study.
                Categories
                Research
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                © The Author(s) 2018

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