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: 1742 • 2013 ACR/ARHP Annual Meeting

    Effects Of Blisibimod, An Inhibitor Of B Cell Activating Factor, On Serum Immunoglobulins and Infection Risk In Patients With Systemic Lupus Erythematosus: Observations From The Placebo-Controlled Pearl-SC and Open-Label Extension Studies

    Richard A. Furie1, Matthew Thomas2, Alvina Chu3, Renee S. Martin3, Colin Hislop3 and Morton A. Scheinberg4, 1The Feinstein Institute for Medical Research and North Shore-Long Island Jewish Health System, Lake Success, NY, 2Health and Research Centre, Trivandrum, Kerala, India, 3Anthera Pharmaceuticals Inc, Hayward, CA, 4Rheumatology Hospital Abreu Sodre Pesquisa Clínica, São Paulo, Brazil

    Background/Purpose: To evaluate the effects of subcutaneously-administered blisibimod (A-623, AMG 623), an inhibitor of B-cell activating factor (BAFF), on IgG, IgM and infection risk in patients…
  • Abstract Number: 1743 • 2013 ACR/ARHP Annual Meeting

    Administration Of AMG 557, a Human Anti-B7RP-1 (ICOSL) Antibody, Leads To The Selective Inhibition Of Anti-KLH IgG Responses In Subjects With SLE:  Results Of a Phase 1 Randomized, Double-Blind, Placebo-Controlled, Sequential, Rising, Multiple-Dose Study

    Barbara Sullivan1, Wayne H. Tsuji2, Vishala L. Chindalore3, Thomas D. Geppert4, Alla Rudinskaya5, Patricia Pardo6, Alan Kivitz7, C. Michael Neuwelt8, Meggan Mackay9, R. John Looney10, J. Carter Thorne11, Marilee Andrew12, Greg Arnold13, Michael Boedigheimer1, Kit Chiu1, Cherie Green1, Arunan Kaliyaperumal1, Christine Wang14, Andrew Welcher1 and James Chung1, 1Amgen, Thousand Oaks, CA, 2Clinical Research/Inflammation, Amgen, Seattle, WA, 3Anniston Medical Clinic PC, Anniston, AL, 4Metroplex Clinical Research Center, LLC, Dallas, TX, 5Danbury Hospital, Danbury, CT, 6MRA Clinical Research, Miami, FL, 7Altoona Center for Clinical Research, Duncansville, PA, 8East Bay Rheumatology Research Institute, San Leandro, CA, 9Autoimmune & Musculoskeletal Disease, Feinstein Institute for Medical Research, Manhasset, NY, 10Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY, 11Southlake Regional Health Centre, Newmarket, ON, Canada, 12Amgen, Seattle, WA, 13Medical Sciences, Amgen, Thousand Oaks, CA, 14Biostatistics, Amgen, Thousand Oaks, CA

    Background/Purpose: The interaction of inducible costimulator (ICOS) with its ligand, B7-related protein-1 (B7RP-1 or ICOSL), plays a role in T cell differentiation, cytokine production, and…
  • Abstract Number: 1744 • 2013 ACR/ARHP Annual Meeting

    Identifying Trajectories of Lung Function Change Over Time in Scleroderma

    Ada Man1, Todd Davidyock2, Laura Western3, Michael Ieong2, Yuqing Zhang4 and Robert W. Simms1, 1Rheumatology, Boston University School of Medicine, Boston, MA, 2Boston University School of Medicine, Boston, MA, 3University of Maryland, Baltimore, MD, 4Clinical Epidemiology Unit, Boston University School of Medicine, Boston, MA

    Background/Purpose: Interstitial lung disease (ILD) is a leading cause of scleroderma (SSc) mortality, yet little is known about how changes in lung function over time…
  • Abstract Number: 1745 • 2013 ACR/ARHP Annual Meeting

    Prediction Of Pulmonary Complications In Systemic Sclerosis – Model Development and Validation

    Svetlana I. Nihtyanova1, Benjamin E. Schreiber2, Voon H. Ong3, John G. Coghlan4, Athol U. Wells5 and Christopher P. Denton6, 1Department of Rheumatology, Royal Free and University College Medical School, London, United Kingdom, 2Royal Free Hospital NHS Foundation Trust, National Pulmonary Hypertension Service, London, United Kingdom, 3Department of Rheumatology, The Royal Free and University College Medical School, London, United Kingdom, 4National Pulmonary Hypertension Service, The Royal Free Hospital NHS Foundation Trust, London, United Kingdom, 5Royal Brompton and Harefield NHS Foundation Trust, Department of Radiology, London, United Kingdom, 6Centre for Rheumatology, Royal Free and University College Medical School, London, United Kingdom

    Background/Purpose:  Pulmonary complications contribute substantially to systemic sclerosis (SSc) associated morbidity and are the most frequent disease-related cause of death. We explore predictors of clinically…
  • Abstract Number: 1746 • 2013 ACR/ARHP Annual Meeting

    Pericardial Effusions Are Not a Poor Prognostic Factor In Systemic Sclerosis Patients With Pulmonary Hypertension

    Elana J. Bernstein1, Jessica K. Gordon2, Wei-Ti Huang3 and Virginia D. Steen4, 1Rheumatology, Columbia University College of Physicians & Surgeons, New York, NY, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Biostatistics, Hospital for Special Surgery, New York, NY, 4Department of Rheumatology, Georgetown University Medical Center, Washington, DC

    Background/Purpose: Pulmonary hypertension (PH) (defined as a mean pulmonary arterial pressure ≥ 25 mmHg on right heart catheterization) is a leading cause of death in…
  • Abstract Number: 1747 • 2013 ACR/ARHP Annual Meeting

    Plasma MCP-1 and IL-10 Levels Predict Long-Term Progression Of Interstitial Lung Disease In Patients With Early Systemic Sclerosis

    Minghua Wu1, Claudia Pedroza2, Gloria Salazar1, Xiaodong Zhou1, John D. Reveille1, Maureen D. Mayes1 and Shervin Assassi1, 1Rheumatology, University of Texas Health Science Center at Houston, Houston, TX, 2Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX

    Background/Purpose: The currently available clinical markers are not reliable predictors of long-term progression of systemic sclerosis (SSc) related interstitial lung disease (ILD). SSc patients have…
  • Abstract Number: 1714 • 2013 ACR/ARHP Annual Meeting

    Grey-Scale and Power Doppler Findings Of Lower Extremity Entheses In Healthy Children

    Clara Lin1 and Diana Milojevic2, 1Pediatric Rheumatology, University of California-San Francisco, San Francisco, CA, 2Dept of Pediatric Rheumatology, University of California, San Francisco, San Francisco, CA

    Background/Purpose: The aim of our study is to describe the grey-scale and Power Doppler findings in lower extremity entheses in healthy children ages 5-18 years.…
  • Abstract Number: 1723 • 2013 ACR/ARHP Annual Meeting

    Lesinurad, An Inhibitor Of The Uric Acid Transporter URAT1 and a Potential Therapy For Gout, Requires URAT1 Phenylalanine 365 For High Affinity Inhibition

    Philip K. Tan, David Hyndman and Jeffrey N. Miner, Ardea Biosciences, Inc., San Diego, CA

    Background/Purpose:  Gout is caused by a lack of efficient excretion of uric acid, resulting in hyperuricemia and the formation of crystal deposits of uric acid. …
  • Abstract Number: 1706 • 2013 ACR/ARHP Annual Meeting

    Fine-Mapping Major Histocompatibility Complex Variation Associated With Ankylosing Spondylitis Susceptibility

    Adrian Cortes1, International Genetics of Ankylosing Spondylitis Consortium (IGAS)2, Paul de Bakker3 and Matthew A. Brown4, 1Human Genetics Group, The University of Queensland Diamantina Insititute, Brisbane, Australia, 2University of Queensland Diamantina Institute, brisbane, Australia, 3Medical Genetics, University Medical Center Utrecht, Utrecht, Netherlands, 4University of Queensland Diamantina Institute, Brisbane, Australia

    Background/Purpose: Ankylosing spondylitis (AS) is a common, highly heritable, inflammatory arthritis. Thus far, 27 susceptibility loci have been identified in and outside the MHC in…
  • Abstract Number: 1707 • 2013 ACR/ARHP Annual Meeting

    Biological Insights From Genetics Of Rheumatoid Arthritis Contribute To Drug Discovery

    Yukinori Okada1,2,3, Di Wu2,4,5,6, Chikashi Terao7,8, Katsunori Ikari9, Yuta Kochi10, Koichiro Ohmura11, Akari Suzuki10, Hisashi Yamanaka9, Joshua C. Denny12, Jeffrey D. Greenberg13, Robert R. Graham14, Matthew A. Brown15, Sang-Cheol Bae16, Jane Worthington17, Leonid Padyukov18, Lars Klareskog19, Peter K. Gregersen20, Peter M. Visscher21,22, Katherine A. Siminovitch23,24 and Robert M. Plenge25, 1Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 2Division of Genetics, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 3Broad Institute, Cambridge, MA, 4Division of Rheumatology, Immunology, and Allergy, Brigham and Women’s Hospital, Boston, MA, 5Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, 6Department of Statistics, Harvard University, Cambridge, MA, 7Center for Genomic Medicine, Kyoto University, Kyoto, Japan, 8Department of Rheumatology and Clinical immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 9Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 10Laboratory for Autoimmune Diseases, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan, 11Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 12Department of Biomedical Informatics, Vanderbilt University School of Medicine, Nashville, TN, 13Rheumatology, NYU Hospital for Joint Diseases, New York, NY, 14ITGR Human Genetics, Genentech, Inc., South San Francisco, CA, 15Human Genetics Group, The University of Queensland Diamantina Insititute, Brisbane, Australia, 16Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, South Korea, 17Arthritis Research UK Epidemiology Unit, Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester, United Kingdom, 18Rheumatology Unit, Department of Medicine, Karolinska University Hospital, Solna, Karolinska Institutet, Stockholm, Sweden, 19Rheumatology Unit, Department of Medicine, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden, 20Genomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, NY, 21The University of Queensland Diamantina Institute, Princess Alexandra Hospital, University of Queensland, Brisbane, Australia, 22Queensland Brain Institute, The University of Queensland, St Lucia, Brisbane, Australia, 23Mount Sinai Hospital, Toronto, ON, Canada, 24University of Toronto, Toronto, ON, Canada, 25Division of Rheumatology, Immunology and Allergy and Division of Genetics, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA

    Background/Purpose: A major challenge in human genetics is to devise a systematic strategy to integrate disease-associated variants with diverse genomic and biological datasets to provide…
  • Abstract Number: 1708 • 2013 ACR/ARHP Annual Meeting

    Can People With Rheumatoid Arthritis Self Monitor Their Disease Activity?

    Noura AL Osaimi1, Erin Carruthers2, Charles H Goldsmith3,4, Paul M Adam5 and Diane Lacaille1,6, 1Medicine, University of British Columbia, Vancouver, BC, Canada, 2Arthritis Research Centre of Canada, Richmond, BC, Canada, 3Biostatistics, Arthritis Research Centre of Canada, Richmond, BC, Canada, 4Health Sciences, Simon Fraser University, Burnaby, BC, Canada, 5Rheumatology Liaison, Mary Pack Arthritis Centre, Vancouver, BC, Canada, 6Rheumatology, Arthritis Research Centre of Canada, University of British Columbia, Richmond, BC, Canada

    Background/Purpose: In rheumatoid arthritis (RA) the target for treatment is clinical remission or minimal disease activity. Active involvement of patients in monitoring their own disease…
  • Abstract Number: 1709 • 2013 ACR/ARHP Annual Meeting

    Rheumatoid Arthritis Patient Cardiovascular Disease Prevention Experiences: Qualitative Analysis and Implications

    Christie M. Bartels1, Sarah Tweddell2, Barbara Bowers3, Elizabeth Jacobs4 and Tonya Roberts3, 1Rheumatology/Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, 2UW School of Medicine and Public Health, Madison, WI, 3UW School of Nursing, Madison, WI, 4Internal Medicine, UW School of Medicine and Public Health, Madison, WI

    Background/Purpose:  Although rheumatoid arthritis (RA) increases cardiovascular disease (CVD) risk, RA patients receive less CVD preventive care than peers. We previously showed gaps in lipid…
  • Abstract Number: 1711 • 2013 ACR/ARHP Annual Meeting

    Folic Acid Prescription Among Older Adult Methotrexate Initiators Is Poor

    Gabriela Schmajuk1, Jinoos Yazdany2, Yinghui Miao3, David I. Daikh4 and Michael Steinman3, 1Rheumatology, UCSF / San Francisco VA Medical Center, San Francisco, CA, 2Medicine, University of California, San Francisco, San Francisco, CA, 3Division of Geriatrics, UCSF, San Francisco Veterans Affairs Medical Center, San Francisco, CA, 4Rheumatology, University of California, San Francisco, San Francisco, CA

    Background/Purpose: Methotrexate (MTX) is the most commonly used disease modifying agent for rheumatoid arthritis (RA), although liver enzyme (LFT) elevations limit its use in some…
  • Abstract Number: 1712 • 2013 ACR/ARHP Annual Meeting

    Identification Of Factors Associated With Agreement Between Rheumatoid Arthritis Electronic Medication Lists and Prescribed Disease Modifying Treatment Plans

    Ilinca D. Metes1, Heather Eng2, June Feng2, G.K. Balasubramani3, Stephen R. Wisniewski3 and Marc C. Levesque4, 1Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Pittsburgh, Pittsburgh, PA, 2Epidemiology Data Center, University of Pittsburgh, Graduate School of Public Health, Pittsburgh, PA, 3Epidemiology, University of Pittsburgh, Graduate School of Public Health, Pittsburgh, PA, 4Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: Federal government programs incentivize the use of Electronic Health Records (EHR) including accurate medication lists.  The accuracy of a patient’s EHR medication list is…
  • Abstract Number: 1713 • 2013 ACR/ARHP Annual Meeting

    Disparity In Biologic Therapy In Ethnic Minorities With Rheumatoid Arthritis: Can It All Be Due To Lack Of Access To Drug?

    Gail S. Kerr1, Ted R. Mikuls2, Christopher J. Swearingen3, Chunqiao Luo4 and Yusuf Yazici5, 1Rheumatology, Washington DC VAMC, Georgetown and Howard University, Washington, DC, 2Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE, 3Pediatric Biostatistics, University of Arkansas for Medical Sciences, Little Rock, AR, 4Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, 5Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY

    Background/Purpose: Ethnic disparities in the administration of DMARDs exist, but the impact of differing health care systems on access in ethnic minorities treated by rheumatologists,…
  • « Previous Page
  • 1
  • …
  • 2134
  • 2135
  • 2136
  • 2137
  • 2138
  • …
  • 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