ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 1384 • ACR Convergence 2022

    Echocardiographic Screening in Childhood Onset Systemic Lupus Erythematosus

    Amanda Marsden1, Georgina Tiller2, Angelyne Rivera3, Maitri Deep Rai3, Lori Tucker3, Jaime Guzman4, Kimberly Morishita2, Kristin Houghton2, Shreya Moodley3 and David Cabral5, 1BC Children's Hospital, Castle Hill, Australia, 2University of British Columbia - Vancouver, Vancouver, BC, Canada, 3British Columbia Children's Hospital, Vancouver, BC, Canada, 4University of British Columbia and BC Children's Hospital, Vancouver, BC, Canada, 5BC Children's Hospital and University of British Columbia, Vancouver, BC, Canada

    Background/Purpose: Childhood onset SLE is an autoantibody mediated, multisystem disease which can include cardiac manifestations. Because cardiac involvement can develop insidiously, an earlier review from…
  • Abstract Number: 1414 • ACR Convergence 2022

    2022 Revision of the ACR/EULAR Remission Criteria for Rheumatoid Arthritis

    Paul Studenic1, Daniel Aletaha2, Maarten de Wit3, Tanja Stamm4, Farideh Alasti5, Diane Lacaille6, Josef Smolen1 and David Felson7, 1Medical University of Vienna, Vienna, Austria, 2Medical University Vienna, Wien, Austria, 3Patient research partner, Amsterdam, Netherlands, 4Medical University of Vienna, CeMSIIS - Center for Medical Statistics, Informatics, and Intelligent Systems, Section for Outcomes Research, Wien, Austria, 5Medical University of Vienna, Department of Internal Medicine 3, Division of Rheumatology, Vienna, Austria, 6Arthritis Research Canada, University of British Columbia, Vancouver, BC, Canada, 7Boston University, Boston, MA

    Background/Purpose: More than 10 years ago ACR and EULAR endorsed provisional criteria to define remission in RA, both Boolean and index-based. However, the agreement between…
  • Abstract Number: 1415 • ACR Convergence 2022

    Different Bioactive Lipid Profile Predicts Response to TNF or IL6 Inhibitors in Rheumatoid Arthritis: Result of the CorEvitas CERTAIN Comparative Effectiveness Study

    Mona Alotaibi1, Roxana Coras2, Dimitrios Pappas3, Ted Mikuls4, Joel Kremer5, Geoffrey Thiele6, mohit jain1 and Monica Guma7, 1Department of Medicine, School of Medicine, University of California San Diego, San Diego, CA, 2University of California San Diego, San Diego, CA, 3CorEvitas, LLC, Waltham, MA, 4Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE, 5The Corrona Research Foundation, Delray Beach, FL, 6University of Nebraska Medical Center, Omaha, NE, 7UCSD, La Jolla, CA

    Background/Purpose: Circulating bioactive lipids can provide information about the pathogenesis of specific diseases and potentially help predict therapeutic response. Choosing the right biological therapy earlier…
  • Abstract Number: 1412 • ACR Convergence 2022

    Coronary Microvascular Dysfunction in Patients with Rheumatoid Arthritis and Diabetes Mellitus: A Cross-sectional Study with 13NH3 Myocardial PET/CT

    Bas Dijkshoorn1, Remco Knol2, Friso Van Der Zant2, Michael Nurmohamed3 and Suat Simsek2, 1Reade Rheumatology Center, Amsterdam, Netherlands, 2Noord-west Ziekenhuis groep, Alkmaar, Netherlands, 3Amsterdam University Medical Center, Kortenhoef, Netherlands

    Background/Purpose: Patients with rheumatoid arthritis (RA) are at increased risk of cardiovascular disease. This risk is similar to that of diabetes mellitus (DM). There have…
  • Abstract Number: 1418 • ACR Convergence 2022

    Change in Disease Activity and Occurrence of Adverse Events After Initiation of Etanercept in Pediatric Patients with Juvenile Psoriatic Arthritis in the CARRA Registry

    Colleen Correll1, Scott Stryker2, David Collier3, Anne Dennos4, Stephen Balevic5, Thomas Phillips5 and Tim Beukelman6, 1University of Minnesota, Minneapolis, MN, 2Amgen Inc., San Francisco, CA, 3Amgen Inc., Simi Valley, CA, 4Duke University, Durham, NC, 5Duke Clinical Research Institute, Durham, NC, 6Childhood Arthritis and Rheumatology Research Alliance (CARRA), Birmingham, AL

    Background/Purpose: Juvenile psoriatic arthritis (JPsA) constitutes ~5% of juvenile idiopathic arthritis (JIA). Several therapeutics are available for JPsA; however, given the low JPsA incidence, important…
  • Abstract Number: 1420 • ACR Convergence 2022

    Outcomes in Patients with Rheumatoid Arthritis Initiating Monotherapy with Etanercept, Adalimumab, or Janus Kinase Inhibitors

    Dimitrios Pappas1, Jacqueline O'Brien2, Mike Kelleman2, Lin Guo2, Ying Shan2, Joshua Baker3, Greg Kricorian4, Scott Stryker5 and David Collier6, 1Corrona Research Foundation; CorEvitas, LLC, Albany, NY, 2CorEvitas, LLC, Waltham, MA, 3University of Pennsylvania and Corporal Michael J. Crescenz VA Medical Center, Philadelphia, 4Amgen, Inc., Thousand Oaks, CA, 5Amgen Inc., San Francisco, CA, 6Amgen Inc., Simi Valley, CA

    Background/Purpose: Biologic/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) often are used as monotherapy in rheumatoid arthritis (RA). However, little is known about the comparative effectiveness of…
  • Abstract Number: 1419 • ACR Convergence 2022

    Time to Discontinuation and Effectiveness with Baricitinib in Rheumatoid Arthritis: 12-Month European Data from a Multinational, Prospective, Observational Study

    Rieke Alten1, Gerd Burmester2, Marco Matucci-Cerinic3, Andrew Ostor4, Liliana Zaremba-Pechmann5, Tamas Treuer6, Khai Jing Ng6, Jens Gerwien6, Kathryn Gibson7 and Bruno Fautrel8, 1SCHLOSSPARK KLINIK, University Medicine Berlin, Berlin, Germany, 2Charité University Medicine Berlin, Berlin, Germany, 3University of Florence, Florence, Italy, 4Cabrini Hospital, Monash University & Emeritus Research, Melbourne, Australia, 5HaaPACS GmbH, Schriesheim, Germany, 6Eli Lilly and Company, Indianapolis, IN, 7Eli Lilly and Company, Indianapolis, United States of America, Sydney, Australia, 8Sorbonne University Paris, France and Pierre Louis Institute of Epidemiology and Public Health, Paris, France, Paris, France

    Background/Purpose: RA-BE-REAL is a 3-year, multinational, prospective, observational study of adult patients with rheumatoid arthritis (RA) evaluating time to discontinuation of initial RA treatment. Baricitinib…
  • Abstract Number: 1421 • ACR Convergence 2022

    Pharmacokinetics, Safety, Tolerability, and Immunogenicity of a Proposed Tocilizumab Biosimilar (MSB11456) versus US‑licensed Tocilizumab: Results of a Randomized, Double-blind, Parallel‑group, Single‑intravenous Dose Study in Healthy Adults (APTURA II)

    Monika Tomaszewska-Kiecana1, Martin Ullmann2, Emmanuelle Vincent2, Corinne Petit-frere2, Joëlle Monnet3 and Andras Illes2, 1Biokinetica S.A., Jozefow, Poland, 2Fresenius Kabi SwissBioSim, Eysins, Switzerland, 3Fresenius Kabi Swiss BioSim, Eysins, Switzerland

    Background/Purpose: Tocilizumab is a biologic anti-interleukin-6 receptor monoclonal immunoglobin G1 antibody indicated for treating inflammatory diseases, including RA, and cytokine release syndrome. MSB11456 is a…
  • Abstract Number: 1423 • ACR Convergence 2022

    Long-Term Treatment with Golimumab Is a Safe Treatment Option Regardless of Risk Factors in Patients with Rheumatoid Arthritis, Psoriatic Arthritis, and Axial Spondyloarthritis: Results from a Real-World Canadian Setting

    Regan Arendse1, Proton Rahman2, Philip Baer3, Derek Haaland4, Dalton Sholter5, Odalis Asin-Milan6, Meagan Rachich7, Emmanouil Rampakakis8, A. Marilise Marrache9 and Allen J. Lehman10, 1Community Rheumatology Care, Saskatoon, Canada, 2Memorial University, St. John's, NL, Canada, 3Baer Weinberg MPC, Scarborough, ON, Canada, 4The Waterside Clinic, Oro Medonte, ON, Canada, 5University of Alberta, Edmonton, AB, Canada, 6Janssen Canada, Laval, QC, Canada, 7Janssen Inc., Guelph, ON, Canada, 8McGill University, Department of Pediatrics and JSS Medical Research, Montréal, QC, Canada, 9Janssen Inc., Dollard-des-Ormeaux, QC, Canada, 10Janssen Inc., Toronto, ON, Canada

    Background/Purpose: Golimumab (GLM), a tumor necrosis factor inhibitor (TNFi), has demonstrated efficacy and a favorable safety profile in inflammatory rheumatic diseases. Recent safety studies with…
  • Abstract Number: 1409 • ACR Convergence 2022

    Impact of a Hybrid Medical Care Model in the Rheumatoid Arthritis Patient-Reported Outcomes: A Non-inferiority Crossover Randomized Study

    Guillermo Guaracha Basañez1, Irazu Contreras-Yáñez2, Vivian Estrada-González2, Lexli Pacheco-Santiago2, Salvador Valverde-Hernández2 and Virginia Pascual Ramos3, 1Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirn", Ciudad de México, Mexico, 2Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México, Mexico, 3Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ciudad de México, Mexico

    Background/Purpose: Patients and physicians can naturally adopt hybrid healthcare models (HC), that combine face-to-face consultations (FFC) with telemedicine. The study's objective was to compare the…
  • Abstract Number: 1387 • ACR Convergence 2022

    Real-World Utilization of Adalimumab Biosimilar (ABP 501) in Patients with Rheumatoid Arthritis, Ankylosing Spondylitis and Psoriatic Arthritis in Europe

    Ran Jin1, Megan Hughes2, Emily Goddard2, James Piercy2, Delphine Courmier2, Rachael Meadows2 and Waldemar Radziszewski1, 1Amgen, Inc., Thousand Oaks, CA, 2Adelphi Group, Bollington, United Kingdom

    Background/Purpose: ABP 501 is the first adalimumab biosimilar approved by the European Medicines Agency. A clinical trial demonstrated biosimilarity between ABP 501 and the reference…
  • Abstract Number: 1427 • ACR Convergence 2022

    Impact of Upadacitinib versus Abatacept on Individual Disease Outcomes in Patients with Rheumatoid Arthritis and Inadequate Responses to Biologic DMARDs

    Ronald van Vollenhoven1, Andrea Rubbert-Roth2, Stephen Hall3, Ricardo Xavier4, Anna K Shmagel5, Yanna Song5, Samuel Anyanwu5 and Vibeke Strand6, 1Amsterdam University Medical Centers, Amsterdam, Netherlands, 2Division of Rheumatology, Cantonal Clinic St Gallen, St.Gallen, Switzerland, 3Emeritus Research and Monash University, Melbourne, Australia, 4Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil, 5AbbVie, Inc., North Chicago, IL, 6Stanford University School of Medicine, Stanford, CA

    Background/Purpose: The phase 3 SELECT-CHOICE trial of patients with rheumatoid arthritis (RA) and prior inadequate response to biologic DMARD(s) (bDMARD-IR) demonstrated superiority of the JAK…
  • Abstract Number: 1425 • ACR Convergence 2022

    Treatment Persistence and Switching Patterns of ABP 501 (AMGEVITA®) in German Patients with Rheumatic Diseases

    Ran Jin1, Silvia Kruppert2, Florian Scholz2, Marc Hammer2, Greg Kricorian1, David Collier3 and Jonathan Kay4, 1Amgen, Inc., Thousand Oaks, CA, 2IQVIA, Frankfurt, Germany, 3Amgen Inc., Simi Valley, CA, 4Division of Rheumatology, Department of Medicine, UMass Chan Medical School and UMass Memorial Medical Center, Worcester, MA

    Background/Purpose: ABP 501 is the first adalimumab (ADA) biosimilar approved by the European Medical Association and the Food and Drug Administration for the treatment of…
  • Abstract Number: 1429 • ACR Convergence 2022

    Acute Cardiovascular Events Risk in Rheumatoid Arthritis Patients Treated with Tofacitinib or TNF Inhibitors, a Nationwide Cohort Study: RELATION Study

    jacques-eric gottenberg1, Nadir Mammar2, Meriem Kessouri2, Jeremie RUDANT2, nada Assi3, Benjamin grenier3 and julien kirchgesner4, 1Strasbourg University Hospital, Strasbourg, France, 2Pfizer, Paris, France, 3HEVA, Lyon, France, 4AP-HP, Paris, France

    Background/Purpose: Patients with IMID, and notably patients with rheumatoid arthritis (RA), are at increased risk of major adverse cardiovascular event (MACE) compared with the general…
  • Abstract Number: 1431 • ACR Convergence 2022

    Impact of Tofacitinib on Fracture Risk in Rheumatoid Arthritis

    Karen E Hansen1, Mahta Mortezavi2, Edward Nagy3, Cunshan Wang4, Carol A Connell4, Zaher Radi5, Heather J Litman6, Giovanni Adami7 and Maurizio Rossini7, 1Rheumatology Division, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, 2Pfizer Inc, New York, NY, 3Pfizer Ltd, Tadworth, United Kingdom, 4Pfizer Inc, Groton, CT, 5Pfizer Inc., Cambridge, MA, 6CorEvitas, LLC, Waltham, MA, 7Rheumatology Unit, Department of Medicine, University of Verona, Verona, Italy

    Background/Purpose: Preclinical data suggest that tofacitinib stimulates osteoblast function and would have a protective effect on bone health and fracture risk in RA.1 We report…
  • « Previous Page
  • 1
  • …
  • 648
  • 649
  • 650
  • 651
  • 652
  • …
  • 2607
  • 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 »

Embargo Policy

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].

Wiley

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

© Copyright 2026 American College of Rheumatology