ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 2985 • 2016 ACR/ARHP Annual Meeting

    Practice-Level Variation in Quality of Care in the Acr’s Rheumatology Informatics System for Effectiveness (RISE) Registry

    Jinoos Yazdany1, Nick Bansback2, Megan E. B. Clowse3, Deborah Collier4, Karen Law5, Katherine Liao6, Kaleb Michaud7, Esi Morgan8, Jim Oates9, Catalina Orozco10, Andreas Reimold11, Julia F Simard12, Rachel Myslinski13, Tracy Johansson14 and Salahuddin Kazi15, 1Medicine/Rheumatology, University of California, San Francisco, San Francisco, CA, 2School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada, 3Rheumatology, Duke University School of Medicine, Durham, NC, 4Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 5Internal Medicine, Emory University School of Medicine, Atlanta, GA, 6Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, MA, 7University of Nebraska Medical Center, Omaha, NE, 8Pediatric rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 9Medicine/Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 10Rheumatology Associates, Dallas, TX, 11Hospital of Southern Norway, Kristiansand, Norway, 12Division of Epidemiology, Health Research and Policy Department, and Division of Immunology & Rheumatology, Department of Medicine, Stanford School of Medicine, Stanford, CA, 13Governance & Ethics Specialist, Amer College of Rheumatology, Atlanta, GA, 14Practice, Advocacy & Quality, American College of Rheumatology, Atlanta, GA, 15Rheumatology, UT Southwestern Medical Center, Dallas, TX

    Background/Purpose:  The Medicare Access and CHIP Reauthorization Act (MACRA) of 2015 has put into place an aggressive timeline for a Merit-Based Incentive Payment System (MIPS)…
  • Abstract Number: 2986 • 2016 ACR/ARHP Annual Meeting

    Trends and Determinants of Osteoporosis Prevention and Management in Patients with Rheumatoid Arthritis Compared to Osteoarthritis

    Gulsen Ozen1,2, Diane L. Kamen3, Ted R Mikuls2, Frederick Wolfe4 and Kaleb Michaud2,4, 1Rheumatology, Marmara University Faculty of Medicine, Istanbul, Turkey, 2Rheumatology, University of Nebraska Medical Center, Omaha, NE, 3Medicine/Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 4National Data Bank for Rheumatic Diseases, Wichita, KS

    Background/Purpose: Despite more aggressive treatment strategies and new biologic DMARDs, the prevalence of osteoporosis (OP) leading to fracture in RA remains high. It is unknown…
  • Abstract Number: 2987 • 2016 ACR/ARHP Annual Meeting

    Comparison of Certolizumab Pegol Versus Adalimumab: 2 Year Efficacy and Safety Results from a Superiority, Investigator-Blind, Head-to-Head Study

    Roy Fleischmann1, Gerd-Rüdiger Burmester2, Bernard Combe3, Jeffrey R. Curtis4, Stephen Hall5, Boulos Haraoui6, Ronald van Vollenhoven7, Christopher Cioffi8, Cécile Ecoffet9, Lucian Ionescu9, Leon Gervitz10, Luke Peterson8 and Josef Smolen11, 1University of Texas Southwestern Medical Center at Dallas Metroplex Clinical Research Center, Dallas, TX, 2Charité – University Medicine Berlin, Berlin, Germany, 3Montpellier University Hospital, Montpellier, France, 4Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 5Cabrini Medical Centre, Monash University, Melbourne, Australia, 6Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada, 7Amsterdam Rheumatology and Immunology Center (ARC), Amsterdam, Netherlands, 8UCB Pharma, Raleigh, NC, 9UCB Pharma, Brussels, Belgium, 10RA Patient Value Mission, UCB Pharma, Brussels, Belgium, 11Medical University of Vienna and Hietzing Hospital, Vienna, Austria

    Background/Purpose: Head-to-head comparisons of biological (b)DMARDs in the treatment of RA should provide rigorous evidence on the comparative efficacy of different treatments. Although there are…
  • Abstract Number: 2988 • 2016 ACR/ARHP Annual Meeting

    Cigarette Smoking Increases the Risk of Anti-Double-Stranded DNA Positive SLE Among Women in the Nurses’ Health Studies

    Medha Barbhaiya1, Sara Tedeschi2, Bing Lu1, Susan Malspeis3, Jeffrey A. Sparks3, Elizabeth W. Karlson1 and Karen H. Costenbader1, 1Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 2Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 3Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA

    Background/Purpose: SLE is heterogeneous with subtypes characterized by different systemic manifestations and autoantibodies. Past studies suggest that smoking may be a risk factor for SLE,…
  • Abstract Number: 2989 • 2016 ACR/ARHP Annual Meeting

    Risk of Cardiovascular Disease Events Among Patients with Systemic Lupus Erythematosus Compared to Those with Diabetes Mellitus in a Nationwide Medicaid Cohort

    Medha Barbhaiya1, Candace H. Feldman1, Sarah K. Chen2, Hongshu Guan3, Tzu-Chieh Lin1, Michael A. Fischer4, Daniel H. Solomon5, Brendan M. Everett6 and Karen H. Costenbader1, 1Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 2Beth Israel Deaconess Medical Center, Boston, MA, 3Rheumatology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 4Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 5Division of Rheumatology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 6Division of Cardiovascular Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA

    Background/Purpose: Cardiovascular disease (CVD) risk is elevated in SLE patients compared to non-SLE patients.  However, how CVD rates differ in SLE patients compared with other…
  • Abstract Number: 2990 • 2016 ACR/ARHP Annual Meeting

    Cancer in Systemic Lupus Erythematosus: Results from the Systemic Lupus International Collaborating Clinics Inception Cohort

    Sasha Bernatsky1, Murray Urowitz2, John Hanly3, Ann E. Clarke4, Caroline Gordon5, Juanita Romero-Diaz6, Graciela S. Alarcon7, Sang-Cheol Bae8, Michelle Petri9, Joan T. Merrill10, Daniel J Wallace11, Paul R. Fortin12, Dafna D. Gladman13, David A. Isenberg14, Anisur Rahman15, Susan Manzi16, Ola Nived17, Gunnar K. Sturfelt18, Christine Peschken19, Jorge Sánchez-Guerrero20, Guillermo Ruiz-Irastorza21, Cynthia Aranow22, Ronald F. van Vollenhoven23, Asad Zoma24, Kristján Steinsson25, M Khamashta26, Ellen M. Ginzler27, Anca Askanase28, Kenneth C. Kalunian29, Mary Anne Dooley30, S. Sam Lim31, Diane L. Kamen32, Søren Jacobsen33, Manuel Ramos-Casals34, Murat Inanc35, Jeremy Labrecque36, Jennifer LF Lee37 and Rosalind Ramsey-Goldman38, 1Divisions of Rheumatology and Clinical Epidemiology, McGill University Health Centre, Montreal, QC, Canada, 2Medicine, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 3Division of Rheumatology, Department of Medicine and Department of Pathology, Queen Elizabeth II Health Sciences Centre and Dalhousie University, Halifax, NS, Canada, 4Division of Rheumatology, University of Calgary, Calgary, AB, Canada, 5NIHR/Wellcome Trust Clinical Research Facility, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom, 6Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico city, Mexico, 7Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 8Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of, 9Rheumatology Division, Johns Hopkins University School of Medicine, Baltimore, MD, 10Oklahoma Medical Research Foundation, Oklahoma City, OK, 11Division of Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 12Université Laval, CHU de Québec, Québec, QC, Canada, 13Rheumatology, Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 14Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom, 15Rayne Institute, Centre for Rheumatology Research, UCL Division of Medicine, London, United Kingdom, 16Lupus Center of Excellence, West Penn Allegheny Health System, Pittsburgh, PA, 17Department of Rheumatology, University Hospital, Lund, Sweden, 18Department of Rheumatology, Univ Hospital Lund, Lund, Sweden, 19Medicine & Community Health Sciences, University of Manitoba, Winnipeg, MB, Canada, 20Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, Mexico, 21Universidad del Pais Vasco, Servicio de Medicina Interna, Hospital de Cruces, Bizkaia, Spain, 22Feinstein Institute for Medical Research, Manhasset, NY, 23Amsterdam Rheumatology and Immunology Center (ARC), Amsterdam, Netherlands, 24Hairmyres Hospital, Scotland, United Kingdom, 25Rheumatology, Univ. Hospital, Reykjavik, Iceland, 26Lupus Research Unit, Lupus Research Unit, The Rayne Institute, King's College London School of Medicine, St Thomas' Hospital, London, United Kingdom, 27Rheumatology, SUNY Downstate Medical Center, Brooklyn, NY, 28NYU, Seligman Centre for Advanced Therapeutics, New York, NY, 29Division of Rheumatology, Allergy & Immunology, UCSD School of Medicine Center for Innovative Therapy, La Jolla, CA, 30Dooley Rheumatology, Chapel Hill Doctors, Chapel Hill, NC, 31Medicine, Emory University School of Medicine, Atlanta, GA, 32Medicine/Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 33Rheumatology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark, 34Department of Autoimmune Diseases, ICMiD, Hospital Clínic, Sjögren Syndrome Research Group (AGAUR), Laboratory of Autoimmune Diseases Josep Font, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain, 35Internal Medicine, Istanbul University, Istanbul, Turkey, 36Clinical Epidemiology, McGill UHC/RVH, Montreal, QC, Canada, 37Clinical Epidemiology Rheum, McGill UHC/RVH, Montreal, QC, Canada, 38FSM, Northwestern University, Chicago, IL

    Background/Purpose:  Published studies of cancer risk in SLE to date have never focussed solely on clinically confirmed, incident patients. Prior studies thus may not reflect the cancer…
  • Abstract Number: 2991 • 2016 ACR/ARHP Annual Meeting

    A Molecular Signature Based on IFN Gene Signature and Serology Defines Two Populations of Patients with Different Baseline Disease Activity in a Large Multinational Phase 3 SLE Trial Population

    Michelle Petri1, Kenneth C. Kalunian2, Murray Urowitz3, David A. Isenberg4, Richard Furie5, MaryAnn Morgan-Cox6, Maria Silk7, Ernst R. Dow8, Richard Higgs7, Steven Watts7 and Matthew D Linnik9, 1Rheumatology Division, Johns Hopkins University School of Medicine, Baltimore, MD, 2Division of Rheumatology, Allergy & Immunology, UCSD School of Medicine Center for Innovative Therapy, La Jolla, CA, 3Medicine, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 4Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom, 5North Shore University Hospital, Great Neck, NY, 6Eli Lilly and Company, Indianapolis, IN, 7Eli Lilly, Indianapolis, IN, 8Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, 9Immunology, Lilly Biotechnology Center, San Diego, CA

    Background/Purpose: Registration trials for SLE therapeutics require large numbers of patients with active disease, which in turn necessitates the trials be multinational with many participating…
  • Abstract Number: 2992 • 2016 ACR/ARHP Annual Meeting

    In Systemic Lupus Erythematosus with Antiphospholipid Antibodies, Hypocomplementemia Associates with Thrombosis

    Laura Durcan1, Wei Fu2 and Michelle Petri3, 1University of Washington, Seattle, WA, 2Division of Rheumatology, School of Medicine, Johns Hopkins University, Baltimore, MD, 3Rheumatology Division, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Hypocomplementemia is a common phenomenon in systemic lupus erythematosus (SLE) and antiphospholipid antibody syndrome (APS). Robust mechanistic data implicate complement activation in antiphospholipid antibody…
  • Abstract Number: 2993 • 2016 ACR/ARHP Annual Meeting

    Membrane-Type 1 Matrix Metalloproteinase Controls Osteo- and Chondrogenesis By a Proteolysis-Independent Mechanism Mediated By Its Cytoplasmic Tail

    Yang Qing1, Mukundan Attur2, Thorsten Kirsch3, You Jin Lee3, Shoshana Yakar4, Zhomgbo Liu5, Steven B. Abramson6 and Paolo Mignatti7, 1Medicine, New York University School of Medicine, New York, NY, 2Rheumatology Research, NYU - Hospital for Joint Diseases, New York, NY, 3Orthopaedic Surgery, New York University, New York, NY, 4Basic Science and Craniofacial Biology, College of Dentistry, New York University, New York, NY, 5New York University, New York, NY, 6Dept of Rheumatology/Medicine, Hosp for Joint Diseases/NYU, New York, NY, 7Medicine, New York University, New York, NY

    Background/Purpose:  We aimed to understand the mechanism by which membrane-type 1 matrix metalloproteinase (MT1-MMP, MMP-14) controls bone and cartilage homeostasis. MT1-MMP, a cell-membrane-bound proteinase with…
  • Abstract Number: 2994 • 2016 ACR/ARHP Annual Meeting

    Binding of Periostin to Discoidin Domain Receptor-1 (DDR1) Promotes Cartilage Degeneration By Inducing MMP-13 Expression

    Yang Qing1, Paolo Mignatti2, Austin Ramme3, Thorsten Kirsch3, Jyoti Patel4 and Mukundan Attur4, 1Medicine, New York University School of Medicine, New York, NY, 2Medicine, New York University, New York, NY, 3Orthopaedic Surgery, New York University, New York, NY, 4Rheumatology Research, NYU - Hospital for Joint Diseases, New York, NY

    Background/Purpose:  We and others have previously shown that periostin (Postn) expression is dramatically elevated in cartilage and sub-chondral bone in OA patients and surgical models…
  • Abstract Number: 2995 • 2016 ACR/ARHP Annual Meeting

    WISP1/CCN4 Aggravates Experimental Osteoarthritis and Is Associated with Disease Progression in Early Osteoarthritis Patients

    Martijn H. van den Bosch1, Arjen B. Blom1, Azusa Maeda2, Tina Kilts2, Wim B. van den Berg3, Peter L. van Lent3, Marian F. Young2 and Peter M. van der Kraan1, 1Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2NIDCR/NIH, Bethesda, MD, 3Radboud university medical center, Nijmegen, Netherlands

    Background/Purpose:  Many osteoarthritis (OA) patients show synovial activation, which is thought to be involved in joint destruction. Previously, we described strongly increased expression of Wnt2b…
  • Abstract Number: 2996 • 2016 ACR/ARHP Annual Meeting

    High Fat Diet-Induced Osteoarthritis Progression Is Dependent on Toll-like Receptor 4

    Mary Beth Humphrey1, Evangelia Kalaitzoglou2, Camille Herron2, Yanqing HU2, Yao Fu3, Erika Barboza Prado Lopes3, Elise Donovan3, Joanna Hudson3 and Timothy Griffin3, 1Medicine/Rheumatology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 2Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 3Aging and Metabolism, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose:   Obesity is considered the primary preventable risk factor for OA, increasing the risk of developing OA in weight-bearing joints, especially the knee, as…
  • Abstract Number: 2997 • 2016 ACR/ARHP Annual Meeting

    Microrna-29a Curtails Synovitis in the Development of Knee Osteoarthritis By Disrupting VEGF

    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:  Intensive synovitis is a prominent feature that progressively aggravated excessive fibrosis reactions relative to joint stiffness in the pathogenesis of osteoarthritis (OA). MicroRNA-29a (miR-29a)…
  • Abstract Number: 2998 • 2016 ACR/ARHP Annual Meeting

    Gut Microbiota Induce IGF-1 and Promote Bone Formation and Growth

    Jing Yan1, Jeremy Herzog2, Kelly Tsang1, R. Balfour Sartor2, Antonios Aliprantis3 and Julia F. Charles1, 1Medicine/Rheumatology, Brigham and Women's Hospital, Boston, MA, 2National Gnotobiotic Rodent Resource Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 3Rheumatology, Allergy and Immunology, Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Appreciation of the role of the gut microbiome in regulating vertebrate metabolism has exploded recently. However, the effects of gut microbiota on skeletal growth…
  • Abstract Number: 2999 • 2016 ACR/ARHP Annual Meeting

    Autologous Osteoblastic Cells Versus Concentrated Bone Marrow Implantation in Osteonecrosis of the Femoral Head: A Randomized Controlled Single Blind Study

    Valérie Gangji1, Michel Toungouz2, Chantal Lechanteur3, Yves Beguin3, Etienne Baudoux3, Michel Malaise4, Viviane De maertelaer5, Sanjiva Pather6, Julia Ino7 and Jean-Philippe Hauzeur4, 1Rheumatology, Hôpital Erasme, brussels, Belgium, 2Hemobiology and Transfusion Dept, Hôpital Erasme, brussels, Belgium, 3Hematology & Laboratory of Cell Therapy,, Sart Tilman, Liège, Belgium, 4Rheumatology, Sart Tilman, Liège, Belgium, 5Faculty of Medicine, Université Libre de Bruxelles, brussels, Belgium, 6Radiology, Hopital Erasme, Brussels, Belgium, 7Bone Therapeutics, Gosselies, Belgium

    Background/Purpose: Non traumatic osteonecrosis (ON) of the femoral head is characterized by epiphyseal necrosis leading to femoral head collapse and eventually hip replacement. The physiopathology…
  • « Previous Page
  • 1
  • …
  • 1614
  • 1615
  • 1616
  • 1617
  • 1618
  • …
  • 2425
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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.).

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology