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

Abstracts tagged "Psoriatic arthritis"

  • Abstract Number: 0905 • ACR Convergence 2020

    Probability of Achieving Low Disease Activity or Remission with Apremilast Treatment Among DMARD-Naive Subjects with Active Psoriatic Arthritis

    Philip Mease1, Arthur Kavanaugh2, Alexis Ogdie3, Alvin Wells4, Martin Bergman5, Dafna Gladman6, Frank Behrens7, Sven Richter8, Michele Brunori9, Lichen Teng8, Benoit Guerette8 and Josef Smolen10, 1Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 2UC San Diego Health System, San Diego, CA, 3Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, 4Aurora Rheumatology and Immunotherapy Center, Franklin, 5Drexel University College of Medicine, Philadelphia, PA, 6Krembil Research Institute, Toronto Western Hospital, Toronto, ON, Canada, 7CIRI/Rheumatology & Fraunhofer IME, Research Division Translational Medicine and Pharmacology, Goethe University Hospital, Frankfurt, Hessen, Germany, 8Amgen Inc., Thousand Oaks, 9Amgen Europe GmbH, Rotkreuz, Switzerland, 10Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Apremilast (APR) is associated with comparable ACR response rates in DMARD-naive vs DMARD-experienced patients (pts) with PsA (Wells AF, et al. Rheumatology. 2018;57:1253-63; Kavanaugh…
  • Abstract Number: 1328 • ACR Convergence 2020

    Cardiac Biomarkers Are Associated with the Development of Cardiovascular Events in Patients with Psoriatic Arthritis and Psoriasis

    Keith Colaco1, Ker-Ai Lee2, Shadi Akhtari3, Raz Winer4, Paul Welsh5, Naveed Sattar5, Iain McInnes6, Vinod Chandran7, Paula Harvey8, Richard Cook2, Dafna Gladman7, Vincent Piguet8 and Lihi Eder9, 1Institute of Medical Science, University of Toronto; Women's College Research Institute, Women's College Hospital; and Toronto Western Hospital, University Health Network, Toronto, ON, Canada, 2University of Waterloo, Waterloo, ON, Canada, 3Women's College Hospital, University of Toronto, North York, ON, Canada, 4Rambam Health Care Campus, Haifa, Israel, 5University of Glasgow, Glasgow, Scotland, United Kingdom, 6Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow, United Kingdom, 7Krembil Research Institute, Toronto Western Hospital, Toronto, ON, Canada, 8Women's College Hospital, University of Toronto, Toronto, ON, Canada, 9Women’s College Research Institute, University of Toronto, Toronto, ON, Canada

    Background/Purpose: N-terminal pro-brain-type natriuretic peptide (NT-proBNP) and troponin I (TnI) are established cardiac biomarkers that predict cardiovascular events (CVEs) and mortality in apparently healthy individuals…
  • Abstract Number: 1355 • ACR Convergence 2020

    Characterization of Remission in Patients with Psoriatic Arthritis Treated with Upadacitinib: Post-hoc Analysis from Two Phase 3 Trials

    Philip Mease1, Arthur Kavanaugh2, Dafna Gladman3, Oliver FitzGerald4, Enrique Soriano5, Peter Nash6, Dai Feng7, Apinya Lertratanakul7, Kevin Douglas8, Ralph Lippe9 and Laure Gossec10, 1Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 2Division of Rheumatology, Allergy, & Immunology, University of California San Diego Medical School, San Diego, CA, 3Krembil Research Institute, Toronto Western Hospital, Toronto, ON, Canada, 4Conway Institute for Biomolecular Research, University College Dublin, Dublin, Ireland, 5Department of Public Health, Instituto Universitario, Escuela de Medicina Hospital Italiano de Buenos Aires, Buenos Aires, Argentina; Rheumatology Unit, Internal Medicine Services, Hospital Italiano de Buenos Aires, Capital Federal, Buenos Aires, Argentina, 6School of Medicine Griffith University, Brisbane, Queensland, Australia, 7AbbVie Inc., North Chicago, IL, 8AbbVie Inc., North Chicago, 9AbbVie Deutschland GmbH & Co. KG, Wiesbaden, Germany, 10Sorbonne Université and Hôpital Universitaire Pitié Salpêtrière, Paris, France

    Background/Purpose: Treat-to-target strategies in PsA recommend aiming for remission or low disease activity (LDA). Several disease activity measures are available including very low/minimal disease activity…
  • Abstract Number: 1549 • ACR Convergence 2020

    Joint Damage and Malalignment Determine Articular Tenderness More Than Inflammation in Rheumatoid Arthritis, Psoriatic Arthritis or Osteoarthritis in Established Disease

    Mihaela Popescu1, Victoria Schimpl2, Gabriela Supp3, Martina Durechova3, Paul Studenic3, Michael Zauner3, Josef Smolen3, Daniel Aletaha4, Peter Mandl3 and Irina Gessl3, 1Hôpital Maisonneuve-Rosemont, Montreal, Canada, 2Medical University of Vienna, Vienna, Austria, 3Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria, 4Division of Rheumatology, Department of Medicine III, Medical University of Vienna,, Vienna, Austria

    Background/Purpose: To determine whether clinical tenderness can be considered a sign of inflammatory joint activity in patients with rheumatoid arthritis (RA), osteoarthritis (OA) or psoriatic…
  • Abstract Number: 2021 • ACR Convergence 2020

    The Reliability of Scoring Sonographic Entheseal Abnormalities – the Diagnostic Ultrasound Enthesitis Tool (DUET) Study

    Lihi Eder1, Sibel Aydin2 and Gurjit Kaeley3, 1Women’s College Research Institute, University of Toronto, Toronto, ON, Canada, 2University of Ottawa Faculty of Medicine, Rheumatology, Ottawa, ON, CANADA; The Ottawa Hospital Research Institute, Ottawa, ON, CANADA, Ottawa, ON, Canada, 3University of Florida College of Medicine - Jacksonville, Jacksonville, FL

    Background/Purpose: DUET is a study supported by the Group for Assessment for Psoriasis and Psoriatic Arthritis (GRAPPA) that aims to develop a novel sonographic scoring…
  • Abstract Number: 0163 • ACR Convergence 2020

    Cost of Non-Persistence in the Treatment with Subcutaneous Tumor Necrosis Factor-Alpha Inhibitors of Inflammatory Arthritis: A Propensity Score Matching Approach

    Johan Dalén1, Karin Luttropp1, Tor Olofsson2, Christopher Black3 and Amy Puenpatom4, 1ICON plc, Stockholm, Sweden, Stockholm, Sweden, 2Department of Clinical Sciences, Lund, Rheumatology, Lund University, Sweden; Department of Rheumatology, Skåne University Hospital, Lund, Sweden, Lund, Sweden, 3Merck & Co., Inc., Kenilworth, NJ, USA, Rahway, NJ, 4Merck & Co., Inc., Kenilworth, NJ, USA, North Wales, PA

    Background/Purpose: Few studies have explored cost consequences of non-persistence in the treatment with Subcutaneous Tumor Necrosis Factor-Alpha Inhibitors (SC-TNFi) in Inflammatory Arthritis (IA; rheumatoid arthritis…
  • Abstract Number: 0316 • ACR Convergence 2020

    High-sensitivity 18F-FDG PET/CT: A Diagnostic Tool for Psoriatic Arthritis

    Siba Raychaudhuri1, Yasser Abdelhafez2, Soumajyoti Sarkar3, Smriti Raychaudhuri4 and Abhijit Chaudhari2, 1Division of Rheumatology, Allergy & Clinical Immunology, University of California School of Medicine, Davis, and VA Medical Center Sacramento, Sacramento, CA, 2University of California, Davis, Sacramento, CA, 3University of California, Davis, Davis, 4VA Sacramento Medical Center, Davis, CA

    Background/Purpose: To validate high-sensitivity PET/CT as a diagnostic test we have explored the association of total-body and extremity PET/CT measures with the standardized psoriatic arthritis…
  • Abstract Number: 0332 • ACR Convergence 2020

    Guselkumab Improved Work Productivity and Daily Activity in Patients with Psoriatic Arthritis: Results from a Phase 3 Trial

    Jeffrey R Curtis1, Iain McInnes2, Proton Rahman3, William Tillett4, Philip Mease5, Alexa Kollmeier6, Elizabeth Hsia7, Bei Zhou8, Prasheen Agarwal8, Steven Peterson9 and Chenglong Han8, 1Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 2Institute of Infection, Immunity, and Inflammation, University of Glasgow, Glasgow, United Kingdom, 3Memorial University of Newfoundland, Department of Medicine, St John's, Canada, 4Royal National Hospital for Rheumatic Diseases, Bath, UK; Department of Pharmacy and Pharmacology, University of Bath, Bath, United Kingdom, 5Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 6Janssen Research & Development, LLC, La Jolla, CA, 7Janssen Research & Development, LLC and University of Pennsylvania Medical Center, Spring House, PA, 8Janssen Research & Development, LLC, Spring House, PA, 9Janssen Immunology Global Commercial Strategy Organization, Horsham, PA

    Background/Purpose: DISCOVER 2 (DISC 2) is a Phase 3 trial of anti-IL-23-specific MAb Guselkumab (GUS) in PsA patients, who experience impaired physical function, resulting in…
  • Abstract Number: 0352 • ACR Convergence 2020

    Efficacy and Safety of Ixekizumab versus Adalimumab with and Without Concomitant Conventional Synthetic Disease-Modifying Antirheumatic Drugs (DMARD) in Biologic DMARD-Naïve Patients with Psoriatic Arthritis: 52-Week Results

    Josef Smolen1, Anthony Sebba2, Eric Ruderman3, Amanda Gellett4, Christophe Sapin4, Aubrey Sprabery4, Soyi Liu-Leage4, Sreekumar Pillai4, Paulo Reis4 and Peter Nash5, 1Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria, 2Arthritis Associates, Palm Harbor, Tampa, FL, 3Feinberg School of Medicine, Northwestern University, Chicago, IL, 4Eli Lilly and Company, Indianapolis, IN, 5School of Medicine Griffith University, Brisbane, Queensland, Australia

    Background/Purpose: Ixekizumab (IXE), a high-affinity monoclonal antibody selectively targeting IL-17A, was superior to adalimumab (ADA) at Week (Wk) 24 for simultaneous achievement of ACR50 and…
  • Abstract Number: 0379 • ACR Convergence 2020

    Achievement of RAPID3 and cDAPSA Treatment Targets Is Associated with Control of Articular and Extra-Articular Manifestations of Active Psoriatic Arthritis in DMARD-Naive Patients Treated with Apremilast

    Philip Mease1, Arthur Kavanaugh2, Alexis Ogdie3, Alvin Wells4, Martin Bergman5, Dafna Gladman6, Sven Richter7, Michele Brunori8, Lichen Teng7, Benoit Guerette7 and Josef Smolen9, 1Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 2UC San Diego Health System, San Diego, CA, 3University of Pennsylvania, Philadelphia, PA, 4Aurora Rheumatology and Immunotherapy Center, Franklin, 5Drexel University College of Medicine, Philadelphia, PA, 6Krembil Research Institute, Toronto Western Hospital, Toronto, ON, Canada, 7Amgen Inc., Thousand Oaks, 8Amgen Europe GmbH, Rotkreuz, Switzerland, 9Division of Rheumatology, Department of Medicine III, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Phase III PALACE 4 (NCT01307423) assessed the efficacy of apremilast (APR) in DMARD-naive patients with PsA. The Routine Assessment of Patient Index Data 3…
  • Abstract Number: 0805 • ACR Convergence 2020

    The PROPER Study: Results of the First Interim Analysis of a Pan-EU Real-World Study of SB5 Biosimilar Following Transition from Reference Adalimumab in Patients with Rheumatoid Arthritis, Axial Spondyloarthritis or Psoriatic Arthritis

    Ulf Müller-Ladner1, Karl Gaffney2, Deepak Jadon3, Ulrich Freudensprung4 and Janet Addison5, 1Department of Rheumatology, Immunology, Osteology and Physical Medicine, Justus Liebig University Gießen, Campus Kerckhoff, Bad Nauheim, Germany, Bad Nauheim, Germany, 2Norfolk and Norwich University Hospital NHS Foundation Trust, Norfolk, United Kingdom, 3Cambridge University Hospitals NHSFT, Cambridge, United Kingdom, 4Biogen International GmbH, Baar, Switzerland, 5Biogen Idec, Maidenhead, United Kingdom

    Background/Purpose: SB5, an adalimumab biosimilar received EU marketing authorisation in August 2017, based on the totality of evidence from pre-clinical and clinical Phase I and…
  • Abstract Number: 0906 • ACR Convergence 2020

    Bimekizumab Treatment Is Associated with Improvements in Back Pain and Fatigue in Patients with Active Psoriatic Arthritis: 48-Week Results from a Phase 2b Study

    Atul Deodhar1, Laure Gossec2, Philip Mease3, Jason Coarse4, Heather Edens5, Natasha de Peyrecave6, Deepak Assudani6, Barbara Ink7 and Christopher Ritchlin8, 1Oregon Health & Science University, Portland, OR, 2Sorbonne Université and Hôpital Universitaire Pitié Salpêtrière, Paris, France, 3Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 4UCB Pharma, Raleigh, NC, 5UCB Pharma, Smyrna, GA, 6UCB Pharma, Slough, United Kingdom, 7UCB Pharma, Slough, 8Department of Medicine, University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Patients (pts) with psoriatic arthritis (PsA) require effective treatment across all symptoms. Bimekizumab (BKZ) is a humanized IgG1 monoclonal antibody which selectively neutralizes interleukin…
  • Abstract Number: 1329 • ACR Convergence 2020

    Subclinical Atherosclerosis Risk in Psoriatic Arthritis: Could It Be Prevented?

    Mai Farouk1, Salwa Moussa1 and Rowaida Abdou1, 1Rhuematology Ain Shams University Hospitals, Cairo, Egypt

    Background/Purpose: Psoriatic arthritis (PsA) is an immune-mediated inflammatory arthritis associated with psoriasis that can cause remarkable joint damage (1). Subclinical cardiovascular disease (CVD) due to…
  • Abstract Number: 1356 • ACR Convergence 2020

    Efficacy of Upadacitinib in Patients with Psoriatic Arthritis Stratified by Number of Prior Biologic Disease-modifying Anti-rheumatic Drugs

    Philip Mease1, Apinya Lertratanakul2, Bruce Strober3, Shigeyoshi Tsuji4, Pascal Richette5, Charlie Lovan6, Dai Feng2, Jaclyn K Anderson2 and Filip Van den Bosch7, 1Seattle Rheumatology Associates, P.L.L.C., Seattle, WA, 2AbbVie Inc., North Chicago, IL, 3Yale University School of Medicine and Central Connecticut Dermatology, New Haven, 4Department of Orthopaedics/Rheumatology, National Hospital Organization, Osaka Minami Medical Center, Osaka, Japan, 5Department of Rheumatology, Lariboisière Hospital, Paris, France, 6AbbVie Inc., North Chicago, 7Ghent University Hospital, Ghent, Belgium

    Background/Purpose: Upadacitinib (UPA) has shown efficacy and safety in patients (pts) with active PsA in the Phase 3 SELECT-PsA 1 and SELECT-PsA 2 clinical trials.1,2…
  • Abstract Number: 1552 • ACR Convergence 2020

    Ultrasound Doppler Enthesitis Shows Sensitivity to Change After Biological Therapy in Spondyloarthritis and Psoriatic Arthritis Patients

    Juan Molina Collada1, Cristina Macía-Villa2, Chamaida Plasencia3, Jose Maria Alvaro-Gracia4 and Eugenio De Miguel5, 1Hospital General Universitario Gregorio Marañón, Madrid, Spain, 2Hospital Universitario Severo Ochoa, Madrid, Spain, 3Rheumatology, La Paz University Hospital-IdiPAZ, madrid, Spain, 4CEIMI, Hospital General Universitario Gregorio Marañón, Madrid, Spain, 5Rheumatology Department, Hospital Universitario La Paz, Madrid, Spain

    Background/Purpose: The assessment of activity in spondyloarthritis (SpA) and psoriatic arthritis (PsA) involves several domains, including enthesitis. Clinical enthesitis has shown low sensitivity, specificity and…
  • « Previous Page
  • 1
  • …
  • 65
  • 66
  • 67
  • 68
  • 69
  • …
  • 93
  • 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