ACR Meeting Abstracts

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Abstracts tagged "cartilage"

  • Abstract Number: 1149 • 2015 ACR/ARHP Annual Meeting

    The Active Metabolite of Fostamatinib, R406, Only Decreases the Inflammation-Driven Extracellular Matrix Turnover of the Joint at High Concentrations Ex Vivo

    Cecilie F. Kjelgaard-Petersen1,2, Christian S. Thudium1, Anne Sofie Siebuhr1, Thorbjørn G. Christiansen3, Morten Asser Karsdal1, Per Hägglund2 and Anne C. Bay-Jensen4, 1Biomarkers and Research, Nordic Bioscience, Herlev, Denmark, 2Systems Biology, Technical University of Denmark, Kgs. Lyngby, Denmark, 3Gentofte University Hospital, Orthopaedicsurgery unit, Gentofte, Denmark, 4Biomarkers and Research, Rheumatology, Nordic Bioscience, Herlev, Denmark

    Background/Purpose: Osteoarthritis (OA) and rheumatoid arthritis are degenerative diseases of the whole joint.  The extracellular matrix (ECM) turnover is highly regulated in response to the…
  • Abstract Number: 1152 • 2015 ACR/ARHP Annual Meeting

    Comprehensive Novel Proteomic Analysis of RA Synovial Fluid Highlights the Distinct Protein Profiles of Bone and Cartilage Metabolism

    Yasushi Kondo1, Katsuya Suzuki1, Masaru Takeshita2, Yoshiaki Kassai3, Keiko Koga3, Yuumi Gotou4, Takahiro Miyazaki3, Rimpei Morita5, Yasuo Niki6, Atsuko Murota1, Ayumi Nishikawa1, Hironari Hanaoka1, Yuko Kaneko7, Hidekata Yasuoka7, Kunihiro Yamaoka1, Akihiko Yoshimura5 and Tsutomu Takeuchi8, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Division of Rheumatology and Clinical Immunology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 3Inflammation Drug Discovery Unit, Pharmaceutical Research Division, Takeda Pharmaceutical Company Ltd., Kanagawa, Japan, 4Inflammation Drug Discovery Unit, Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Tokyo, Tokyo, Japan, 5Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan, 6Department of Orthopaedic Surgery, Keio University, Tokyo, Japan, 7Division of Rheumatology, Keio University School of Medicine, Tokyo, Japan, 8Dept. of Internal Medicine, School of Medicine Keio University, Tokyo, Japan

    Background/Purpose: Growing interest has arisen in the search for specific pathophysiology and biomarker for rheumatoid arthritis (RA) utilizing synovial fluid (SF) proteomic analysis. However the…
  • Abstract Number: 1162 • 2015 ACR/ARHP Annual Meeting

    IL37 Reduces Pro-Inflammatory Cytokine and Catabolic Enzyme Production in Human Chondrocytes: A Protective Role in Osteoarthritis?

    Ellen van Geffen1, Arjan van Caam2, Elly Vitters2, Henk van Beuningen2, Esmeralda Blaney Davidson2 and Peter M. van der Kraan2, 1Experimential Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands

    Background/Purpose: Osteoarthritis (OA) is the most common joint disease, primarily characterized by progressive articular cartilage degradation. Cartilage destruction is assumed to be mediated by pro-inflammatory…
  • Abstract Number: 1312 • 2015 ACR/ARHP Annual Meeting

    Radiocarpal Cartilage Matrix Changes 3-Months after Anti-TNF Treatment for Rheumatoid Arthritis – Feasibility Study Using MR T1ρ� Imaging

    Eric Ku1, Valentina Pedoia2, Matthew Tanaka3, Ursula Heilmeier1, John Imboden4, Jonathan D. Graf5, Thomas M. Link6 and Xiaojuan Li7, 1Department of Radiology & Biomedical Imaging, Musculoskeletal Quantitative Imaging Research, UCSF, San Francisco, CA, 2Department of Radiology & Biomedical Imaging, Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, 3University of California Berkeley, Berkeley, CA, 4Rheumatology, Rheumatology, University of California San Francisco, San Francisco, CA, 5Rosalind Russell / Ephraim P. Engleman Rheumatology Research Center, University of California, San Francisco, San Francisco, CA, 6Department of Radiology and Biomedical Imaging, Musculoskeletal Quantitative Imaging Research, UCSF, San Francisco, CA, 7Radiology & Biomedical Imaging, Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA

    Background/Purpose: Standard assessment of Rheumatoid Arthritis (RA) on MRI relies on semi-quantitative joint space narrowing scores that are not sensitive to cartilage focal lesions or…
  • Abstract Number: 1341 • 2015 ACR/ARHP Annual Meeting

    Imaging Growing Joints By Diffraction Enhanced-Computed Tomography Using a Synchrotron Light Source

    Alan M. Rosenberg1, Glendon Rhoades2, Dean Chapman3, George Belev4, Sheldon Wiebe3, David Cooper3, Adelaine Wong3 and Brian Eames3, 1Department of Pediatrics, University of Saskatchewan, Saskatoon, SK, Canada, 2Biomedical Engineering, University of Saskatchewan, Saskatoon, SK, Canada, 3University of Saskatchewan, Saskatoon, SK, Canada, 4Canadian Light Source Inc, Ssasatoon, SK, Canada

    Background/Purpose: This project developed a new method for evaluating growing joints by employing diffraction enhanced imaging (DEI) with computed tomography (CT) using a synchrotron light…
  • Abstract Number: 2008 • 2015 ACR/ARHP Annual Meeting

    WISP1 Aggravates Osteoarthritis By Modulation of TGF-β Signaling and Positive Regulation of Canonical Wnt Signaling

    Martijn H. van den Bosch1, Arjen Blom1, Azusa Maeda2, Tina Kilts2, Wim van den Berg1, Floris Lafeber3, Peter van Lent1, Marian Young2 and Peter van der Kraan1, 1Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2NIDCR/NIH, Bethesda, MD, 3Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose: Many osteoarthritis (OA) patients show synovial activation, which is suggested to be involved in joint destruction. Previously, we found synovial overexpression of Wnt ligands in experimental…
  • Abstract Number: 2010 • 2015 ACR/ARHP Annual Meeting

    Adenosine A2A Receptor, but Not A2B Receptor, Deletion Leads to Development of Osteoarthritis (OA) in Mice and Administration of a Liposomal Suspension of Adenosine Prevents/Treats Osteoarthritis in Rats

    CARMEN CORCIULO1, MATIN Lendhey2, AUSTIN RAMME2, Tuere Wilder3, ORAN KENNEDY2 and Bruce Cronstein4, 1Medicine, NYU-School of Medicine, New York, NY, 2Department of Orthopaedic Surgery, NYU-School of Medicine, New York, NY, 3Dept of Med, Div of Rheum, NYU School of Medicine, New York, NY, 4Medicine, Division of Rheumatology, NYU School of Medicine, NEW YORK, NY

    Background/Purpose: Adenosine, acting at its receptors, regulates chondrocyte function and inflammation, two components of OA. Mice lacking adenosine A2A receptors (A2AR) have increasing difficulty walking…
  • Abstract Number: 170 • 2015 ACR/ARHP Annual Meeting

    Relationship Between Finger Joint Cartilage Evaluated By Ultrasound and Clinical Characteristics in Rheumatoid Arthritis (RA)

    Takehisa Ogura1, Ayako Hirata1, Hideki Ito2, Sayaka Takenaka2, Kennosuke Mizushina1, Yuki Fujisawa1, Naoko Yamashita1, Munetugu Imamura2, Norihide Hayashi2 and Hideto Kameda1, 1Department of Rheumatology, Toho University Ohashi Medical Center, Tokyo, Japan, 2Toho University Ohashi Medical Center, Tokyo, Japan

    Background/Purpose: Joint destruction is the primary lesion by bone and cartilage damage in RA. By X-ray examination, cartilage destruction is evaluated as a joint space…
  • Abstract Number: 2722 • 2015 ACR/ARHP Annual Meeting

    Cyclic Phosphatidic Acid (CPA) Suppresses Expression of Cartilage Degrading Enzymes Such As MMP-3, MMP-13 and Adamts-4 in Inflammatory Synovial Fibroblasts and Articular Chondrocytes Induced By IL-1 Beta and/or TNF ALFA

    Ikuko Masuda1,2, Kodo Okada3, Hisashi Yamanaka1 and Shigeki Momohara1, 1Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 2Rheumatology, Jyujyo Takeda Rehabilitation Hospital, Kyoto, Japan, 3SANSHO, Co. Ltd., Tokyo, Japan

    Background/Purpose: Cyclic phosphatidic acid (cPA) is one of bioactive lipid, has been implicated as an mediator of various biological effects including inhibitory effects of proliferation,…
  • Abstract Number: 312 • 2015 ACR/ARHP Annual Meeting

    Safety, Efficacy and Biomarker Outcomes of a Novel, Intra-Articular, Injectable, Wnt Inhibitor (SM04690) in the Treatment of Osteoarthritis of the Knee: Interim, Exploratory Analysis of Results from a Randomized, Double-Blind, Placebo-Controlled Phase 1 Study

    Yusuf Yazici1, Timothy E. McAlindon2, Roy Fleischmann3, Allan Gibofsky4, Nancy E. Lane5, Alan J. Kivitz6, Nebojsa Skrepnik7, Eddie Armas8, Christopher J. Swearingen1, Anita DiFrancesco1, Jeyanesh R. S. Tambiah1, John Hood1 and Marc C. Hochberg9, 1Samumed, San Diego, CA, 2Tufts Medical Center, Boston, MA, 3University of Texas Southwestern Medical Center, Dallas, TX, 4Weill Cornell Medical College and Hospital for Special Surgery, New York, NY, 5UC Davis Medical Center, Sacramento, CA, 6Altoona Center for Clinical Research, Duncansville, PA, 7Tucson Orthopaedic Institute, Tucson, AZ, 8Well Pharma Medical Research, Miami, FL, 9University of Maryland School of Medicine, Baltimore, MD, USA, Baltimore, MD

    Background/Purpose: Knee osteoarthritis (OA) is characterized by the destruction of articular cartilage, subchrondral bone alterations and varying degrees of synovitis. Current OA treatments are limited…
  • Abstract Number: 313 • 2015 ACR/ARHP Annual Meeting

    Magnetic Resonance Imaging Outcomes Using an Intra-Articular Injection (SM04690) in the Treatment of Osteoarthritis of the Knee: Interim, Exploratory Analysis of Results from a Randomized, Double-Blind, Placebo-Controlled, Phase 1 Study

    Yusuf Yazici1, Sharmila Majumdar2, Timothy E. McAlindon3, Roy Fleischmann4, Allan Gibofsky5, Marc C. Hochberg6, Christopher J. Swearingen1, Anita DiFrancesco1, Jeyanesh R. S. Tambiah1, John Hood1 and Nancy E. Lane7, 1Samumed, San Diego, CA, 2Radiology, UCSF School of Medicine, San Francisco, CA, 3Rheumatology, Tufts Medical Center, Boston, MA, 4University of Texas Southwestern Medical Center, Dallas, TX, 5Weill Cornell Medical College and Hospital for Special Surgery, New York, NY, 6Department of Medicine, University of Maryland, Baltimore, MD, 7Center for Musculoskeletal Health, Univ of California at Davis, Sacramento, CA

    Background/Purpose: Knee osteoarthritis (OA) is characterized by the destruction of articular cartilage, subchrondral bone alterations and varying degrees of synovitis. Current OA treatments are limited…
  • Abstract Number: 315 • 2015 ACR/ARHP Annual Meeting

    Structural Effects of Sprifermin in Knee Osteoarthritis: A Post-Hoc Analysis on Cartilage and Non-Cartilaginous Tissue Alterations

    Frank Roemer1, Aida Aydemir2, Stefan Lohmander3, Michel Crema4, Monica D. Marra5, Norma Muurahainen2, Felix Eckstein6 and Ali Guermazi7, 1Radiology, Boston University School of Medicine, Boston, MA, 2EMD Serono, Billerica, MA, 3Lund University, Lund, Sweden, 4Department of Radiology, Boston University School of Medicine, Boston, MA, 5Department of Radiology, BUSM, Boston, MA, 6Paracelsus Med Univ, Chondrometrics GmbH, Salzburg, Austria, 7Boston University School of Medicine, Boston, MA

    Background/Purpose: A randomized, double-blind, placebo-controlled phase 1b clinical trial of sprifermin (rhFGF18) in knee OA assessed central medial tibio-femoral compartment cartilage thickness on quantitative MRI…
  • Abstract Number: 1018 • 2015 ACR/ARHP Annual Meeting

    A 32-Mer Aggrecan Fragment Generated through Adamts-4/5 and MMP-Mediated Cleavage Can Directly Excite Nociceptive Neurons

    Rachel E. Miller1, Richard J. Miller2, Abdelhak Belmadani3, Suzanne Golub4, Amanda J. Fosang4 and Anne-Marie Malfait5, 1Biochemistry, Rush University Medical Center, Chicago, IL, 2Molecular Biochemistry and Pharmacology, Northwestern University, Chicago, IL, 3Northwestern University, Chicago, IL, 4University of Melbourne, Melbourne, Australia, 5Rush University Medeical Center, Chicago, IL

    Background/Purpose: Cleavage of aggrecan in the interglobular domain (E373-374A) by ADAMTS-4/5 is an early event in osteoarthritis pathogenesis. Further cleavage by MMPs (N341-342F) releases a…
  • Abstract Number: 1133 • 2015 ACR/ARHP Annual Meeting

    Microrna-128 Interference Mitigates the Progression of Keen Osteoarthritis By Regulating Sirtuin-1

    Feng-Sheng Wang1, Yi-Chih Sun1, Yu-Shan Chen1 and Jih-Yang Ko2, 1Core Facility for Phenomics & Diagnostics, Department of Medical Research, Core Facility for Phenomics & Diagnostics, Department of Medical Research, Kaohsiung Chang Gung Memorial Hospital, Taiwan, Kaohsiung, Taiwan, 2Department of Orthopedic Surgery, Department of Orthopedic Surgery, Kaohsiung Chang Gung Memorial Hospital, Taiwan, Kaohsiung, Taiwan

    Background/Purpose:  MicroRNAs, non-coding small RNAs, reportedly regulate development, remodeling and pathogenesis activities in various tissues through silencing mRNA targets and protein translation. This study is…
  • Abstract Number: 1145 • 2015 ACR/ARHP Annual Meeting

    Expression of Xylosyltransferase-1 Is Modulated By Fibronectin Fragment in Human Articular Chondrocytes

    Mi Hyun Lee1, Min Ha Choi1, Hyun Sook Hwang1 and Hyun Ah Kim2, 1Division of rheumatology, Hallym University Sacred Heart Hospital, Kyunggi, South Korea, 2Internal Medicine, Hallym Univ Sacred Heart Hosp, Anyang, South Korea

    Background/Purpose: Xylosyltransferase-1 (XT-1), encoded by xylt1 gene, is an essential anabolic enzyme to catalyze the initial and rate-determining step in glycosaminoglycan chain synthesis. The effect…
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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 ET on November 14, 2024. 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.).

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Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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