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Abstracts tagged "cartilage"

  • Abstract Number: 0700 • ACR Convergence 2020

    Lipoxin A4 Induces Lipid Class Switching and Inflammation Resolution at the Genomic Level in Human Osteoarthritis

    Mandar Dave1, Abul Islam2, Akshat Parekh3, Jay Patel4, Arushi Chawla5 and Ashok Amin6, 1Department of Rheumatology and Pathology, New York University Hospital for Joint Diseases, New York, 2Department of Genetic Engineering and Biotechnology, University of Dhaka, Dhaka, Bangladesh, 3Rutgers Robert Wood Johnson Medical School, Piscataway, NJ, 4Northeast Ohio Medical University, Rootstown, OH, 5Gujarat Forensic Science University, Gujarat, India, 6Department of Rheumatology and Pathology, New York University Hospital for Joint Diseases, New York, NY

    Background/Purpose: Human OA-affected cartilage does not show the cardinal signs of inflammation (redness and swelling with heat and pain—rubor et tumor cum calore et dolor) because…
  • Abstract Number: 0704 • ACR Convergence 2020

    The Murine Ear Wound Cartilage Superhealer Trait, Mediated by the Gut Microbiome, Is Transgenerationally Heritable Following Cecal Transplantation

    Christopher Dunn1, Cassandra Garman2, Cassandra Velasco2, Vladislav Izda2, Jake Martin2 and Matlock Jeffries2, 1University of Oklahoma Health Sciences Center, Oklahoma City, 2University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose: MRL/MpJ mice are substantially protected from developing post-traumatic osteoarthritis (OA), a trait with strong correlation to the ability to heal ear wounds. We have…
  • Abstract Number: 0706 • ACR Convergence 2020

    Adenosine A2A Receptor Activation Reduces Markers of Chondrocyte Senescence and Cartilage Inflammation Associated with Osteoarthritis

    Benjamin Friedman1 and Bruce Cronstein2, 1NYU Rheumatology, New York, NY, 2NYU Grossman School of Medicine, New York, NY

    Background/Purpose: Osteoarthritis is an aging-associated disorder linked to dysfunctional metabolism, chronic inflammation, oxidative stress, and cellular senescence. Cellular senescence is associated with stable cell cycle…
  • Abstract Number: 1846 • 2019 ACR/ARP Annual Meeting

    Does Cartilage Loss Cause Pain in Osteoarthritis?

    KATHRYN BACON1, Lavalley Michael 2 and David Felson 3, 1Boston University School of Medicine, Boston, MA, 2Boston University, Boston, 3Boston University School of Medicine, Department of Rheumatology, Boston

    Background/Purpose: Treatment development in osteoarthritis continues to focus on chondroprotection, but it is unclear if delaying cartilage loss would reduce joint pain. In published studies,…
  • Abstract Number: 1967 • 2019 ACR/ARP Annual Meeting

    Adenosine A2A Receptor Signals Through AMPK and SIRT1 to Increase Chondrocyte Homeostasis

    Benjamin Friedman1 and Bruce Cronstein 2, 1Department of Medicine, Division of Rheumatology NYUSoM, NYC, 2NYU Langone, New York

    Background/Purpose: OA is characterized by loss of cartilage and chondrocyte dysfunction. Our lab has shown CGS21680 (CGS, 1µM) activation of adenosine A2AR leads to chondrocyte…
  • Abstract Number: 1993 • 2019 ACR/ARP Annual Meeting

    Inhibition of Choline Kinase Alpha Improves Synovitis and Cartilage Damage in Animal Models of Osteoarthritis

    Roxana Coras1, Leening P Liu 2, Serena Z Shi 2, Anyan Cheng 3, Alexandra Stubelius 4, Elsa Sanchez-Lopez 5, Robert Sah 6, Ru Liu-Bryan 7 and Monica Guma 8, 1Department of Medicine, University of California San Diego, La Jolla, San Diego, CA, 2Department of Bioengineering, University of California San Diego, La Jolla, San Diego, 3Department of Medicine, University of California San Diego, La Jolla, San Diego, 4Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, San Diego, 5Department of Pharmacology, University of California San Diego, La Jolla, San Diego, 6Department of Bioengineering and Medicine, University of California San Diego, La Jolla, San Diego, 7San Diego VA/UCSD, La Jolla, CA, 8Department of Medicine, School of Medicine. University of California San Diego, La Jolla, United States

    Background/Purpose: Osteoarthritis (OA) is a disease of the whole joint, affecting cartilage, ligaments, menisci, bone and synovial tissue. We previously found that choline kinase alpha…
  • Abstract Number: 2761 • 2019 ACR/ARP Annual Meeting

    Cartilage Thickness Modification with Sprifermin in Knee Osteoarthritis Patients Translates into Symptomatic Improvement over Placebo in Patients at Risk of Further Structural and Symptomatic Progression: Post-Hoc Analysis of a Phase II Trial

    Hans Guehring1, Jeffrey Kraines 2, Flavie Moreau 2, Benjamin Daelken 1, Christoph Ladel 1, Wolfgang Wirth 3, Philip G Conaghan 4, Felix Eckstein 5 and Marc C. Hochberg 6, 1Merck KGaA, Darmstadt, Germany, 2EMD Serono Research and Development Institute, Inc. (a business of Merck KGaA, Darmstadt, Germany), Billerica, MA, 3Paracelsus Medical University, Salzbury, Austria, 4Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds & NIHR Leeds Biomedical Research Centre, Leeds, United Kingdom, 5Paracelsus Medical University, Salzburg, Austria, 6University of Maryland School of Medicine, Baltimore, MD

    Background/Purpose: Results from the 5-year Phase II FORWARD study showed significant dose-dependent modification of total femorotibial joint (TFTJ) cartilage thickness change with sprifermin at 2…
  • Abstract Number: 28 • 2019 ACR/ARP Annual Meeting

    Novel Ex Vivo Model of Septic Arthritis Identifies Role of Neutrophils in Joint Destruction

    Kathryn McCall1, Caroline Atherton 2, Neal Millar 2, Carl Goodyear 3, Tom Evans 4 and Iain McInnes 2, 1Institute of Infection, Immunity & Inflammation, University of Glasgow, Galsgow, United Kingdom, 2Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, United Kingdom, 3University of Glasgow, Glasgow, United Kingdom, 4Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow

    Background/Purpose: Septic arthritis (SA) caused by bacterial species, such as Staphylococcus aureus, has high morbidity and mortality1. Currently diagnosis is often prolonged and unreliable, with…
  • Abstract Number: 1001 • 2019 ACR/ARP Annual Meeting

    Oral Collagen Type V Supplementation Inhibits Cartilage Degeneration in Experimental Arthritis

    Lizandre Keren Silveira 1, José Eduardo Rodrigues 1, Silvana Atayde 1, Sergio Catanozi 1, Antonio dos Santos Filho 2, Vera Luiza Capelozzi 1, Ricardo Fuller 2, Ana Paula Velosa 2 and Walcy Teodoro1, 1Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR, Sao Paulo, Sao Paulo, Brazil, 2Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, BR, Sao Paulo, Sao Paulo, Brazil

    Background/Purpose: It is known that collagen V (col V) can generate autoimmunity when exposed. In contrast, induction of tolerance with col V supplementation is able…
  • Abstract Number: 1180 • 2019 ACR/ARP Annual Meeting

    Confirmation of Manual Cartilage Segmentation Findings by Automated Segmentation: Retrospective Analysis of MRI Images from a Sprifermin Phase II Study

    Alan Brett1, Michael A Bowes 1, Philip G Conaghan 2, Christoph Ladel 3, Jeffrey Kraines 4, Hans Guehring 3, Flavie Moreau 4 and Felix Eckstein 5, 1Imorphics, Manchester, United Kingdom, 2Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds & NIHR Leeds Biomedical Research Centre, Leeds, United Kingdom, 3Merck KGaA, Darmstadt, Germany, 4EMD Serono Research and Development Institute, Inc. (a business of Merck KGaA, Darmstadt, Germany), Billerica, MA, 5Paracelsus Medical University, Salzburg, Austria

    Background/Purpose: Sprifermin is under investigation as a potential disease-modifying osteoarthritis drug (DMOAD). 2-yr results from the FORWARD study showed significant dose-dependent modification of cartilage thickness…
  • Abstract Number: 850 • 2018 ACR/ARHP Annual Meeting

    Long Term Efficacy of Cartilage Repair Induced By scSOX9 in Situ with Bone Marrow-Derived Mesenchymal Stem Cells

    Xiaowei Zhang1,2, Shili Wu3, Yong Zhu3 and Cong-Qiu Chu4,5, 1Oregon Health & Science University, Portland, OR, 2VA Portland Health Care System, Portland, OR, 3VivoScript, Inc, Costa Mesa, CA, 4Rheumatology, Oregon Health & Science University, Portland, OR, 5Rheumatology, VA Portland Health Care System, Portland, OR

    Background/Purpose: Microfracture induces fibrocartilage or fibro-hyaline cartilage both are biomechanically inferior to hyaline cartilage. We reported previously that a super positively charged SOX9 (scSOX9) improved…
  • Abstract Number: 912 • 2018 ACR/ARHP Annual Meeting

    Association of Adiposity Measures in Childhood and Adulthood with Knee Cartilage Thickness, Volume and Bone Area in Young Adults

    Tao Meng1, Alison Venn1, Felix Eckstein2,3, Wolfgang Wirth2,3, Flavia Cicuttini4, Lyn March5, Terence Dwyer1,6, Marita Cross5, Laura Laslett1, Graeme Jones1, Changhai Ding1,7 and Benny Samuel Eathakkattu Antony1, 1Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia, 2Chondrometrics GmbH, Ainring, Germany, 3Institute of Anatomy, Paracelsus Medical University, Salzburg, Austria, 4Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia, 5Institute of Bone and Joint Research, University of Sydney, Sydney, Australia, 6The George Institute for Global Health, Nuffield Department of Obstetrics & Gynaecology, University of Oxford, Oxford, United Kingdom, 7Clinical Research Centre, Zhujiang Hospital, Southern Medical University, Guangzhou, China

    Background/Purpose: Adiposity is associated with increased risk of knee osteoarthritis; cartilage thickness, cartilage volume and subchondral bone area are established biomarkers in knee osteoarthritis. We…
  • Abstract Number: 954 • 2018 ACR/ARHP Annual Meeting

    A New Way to Think about Composite Magnetic Resonance Imaging Scores to Measure Osteoarthritis Severity and Progression

    Lori Lyn Price1,2, Jeffrey B. Driban3, Grace H. Lo4, Ming Zhang5, Michael P. LaValley6 and Timothy E. McAlindon7, 1Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, 2Tufts Clinical and Translational Science Institute, Tufts University, Boston, MA, 3Medicine, Division of Rheumatology, Tufts Medical Center, Boston, MA, 4Michael E. DeBakey Veterans Affairs Medical Center / Baylor College of Medicine, Houston, TX, 5Tufts Medical Center, Boston, MA, 6Biostatistics, Boston University School of Public Health, Boston, MA, 7Division of Rheumatology, Tufts Medical Center, Boston, MA

    Background/Purpose: For some rheumatologic diseases (e.g. lupus), separate scores evaluate cumulative damage and disease activity.  No such strategy exists for osteoarthritis (OA).  The prevailing approach…
  • Abstract Number: 1035 • 2018 ACR/ARHP Annual Meeting

    Different Cartilage-Bone Unit in Patients with Primary Osteoarthritis and Secondary Osteoarthritis Caused By Rheumatoid Arthritis

    Rasmus Klose-Jensen1, Anne Friesgaard Christensen2, Kresten Krarup Keller3 and Ellen-Margrethe Hauge3,4, 1Department of Rheumatology, Aarhus University Hospital, Aarhus, Aarhus C, Denmark, 2Department of Internal Medicine, Lillebaelt Hospital, Vejle, Vejle, Denmark, 3Department of Rheumatology, Aarhus University Hospital, Aarhus, Aarhus, Denmark, 4Clinical medicine, Department of Clinical Medicine, Aarhus University Hospital, Århus N, Denmark

    Background/Purpose: Despite distinct aetiologies of joint diseases, the osteoarthritic end-stage of primary osteoarthritis (OA) and rheumatoid arthritis (RA) are described using similar radiological features. However,…
  • Abstract Number: 1041 • 2018 ACR/ARHP Annual Meeting

    The Anti-Adamts-5 Nanobody®, M6495, Protects Against Cartilage Breakdown in Cartilage and Synovial Joint Tissue Explant Models

    Anne Sofie Siebuhr1, Anne C. Bay-Jensen2, Christian S. Thudium2, Morten A. Karsdal2, Benedikte Serruys3, Daniela Werkmann4, Martin Michaelis4, Christoph Ladel4 and Sven Lindemann4, 1Biomarkers and Research, Nordic Bioscience, Herlev, Denmark, 2Nordic Bioscience, Herlev, Denmark, 3Ablynx NV, Zwijnaarde, Belgium, 4Merck KGaA, Darmstadt, Germany

    Background/Purpose: Osteoarthritis (OA) is associated with cartilage breakdown, where degradation of aggrecan by ADAMTS-5 (a disintegrin and metalloproteinase with thrombospondin motifs 5) is thought to…
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

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