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: 3155 • 2016 ACR/ARHP Annual Meeting

    Zygapophyseal Joint Fusion in Ankylosing Spondylitis Assessed Using Computed Tomography: Associations with Syndesmophytes and Spinal Motion

    Sovira Tan1, Jianhua Yao2, Lawrence Yao3, John Flynn4 and Michael Ward1, 1NIAMS/NIH, Bethesda, MD, 2Radiology and Imaging Sciences, NIH Clinical Center, Bethesda, MD, 3Radiology and Imaging Sciences, NIH, Bethesda, MD, 4Dept of Medicine, Johns Hopkins University, Baltimore, MD

    Background/Purpose: Both zygapophyseal joint (ZJ) fusion and syndesmophytes contribute to structural spine damage in Ankylosing Spondylitis (AS). However, because ZJs are difficult to visualize on…
  • Abstract Number: 3156 • 2016 ACR/ARHP Annual Meeting

    Adding MRI of the Spine to the ASAS Classification Criteria for Axial Spondyloarthritis, Redundant or Beneficial? Results from the Spondyloarthritis Caught Early (SPACE)-Cohort

    Zineb Ez-Zaitouni1, Pauline Bakker1, Miranda van Lunteren1, Rosaline van den Berg2, M. Reijnierse3, Karen M Fagerli4, Roberta Ramonda5, Robert Landewé6, Lennart T.H. Jacobsson7, Floris van Gaalen1 and Désirée van der Heijde1, 1Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 2Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 3Radiology, Leiden University Medical Center, Leiden, Netherlands, 4Dept. of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 5Rheumatology Unit, Department of Medicine DIMED, University of Padova, Padova, Italy, 6Clinical Immunology and Rheumatology, Amsterdam Rheumatology Center, Amsterdam, Netherlands, 7Department of Rheumatology and Inflammation Research, Sahlgrenska Academy at Gothenburg University, Gothenburg, Sweden

    Background/Purpose: The ASAS definition of a positive MRI is solely based on inflammation in the sacroiliac joints (SI), although spinal inflammatory lesions on MRI suggestive…
  • Abstract Number: 3157 • 2016 ACR/ARHP Annual Meeting

    The Association Between Sonographic Enthesitis and Radiographic Damage in Psoriatic Arthritis

    Ari Polachek1, Dafna D Gladman2, Richard J. Cook3, Vinod Chandran4 and Lihi Eder5, 1Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2University of Toronto, Toronto, ON, Canada, 3Statistics and Actuarial Science, University of Waterloo, Waterloo, ON, Canada, 4Rheumatology, University of Toronto, Toronto, ON, Canada, 5Medicine, University of Toronto, Women's College Hospital, Toronto, ON, Canada

    Background/Purpose: Enthesitis is a common clinical finding and a key pathogenic feature in psoriatic arthritis (PsA). Ultrasound is emerging as a preferred method to assess…
  • Abstract Number: 3158 • 2016 ACR/ARHP Annual Meeting

    What Predicts Absence of Spinal Damage in Patients with Spondyloarthritis after Prolonged Follow up?

    Walter Maksymowych1, Stephanie Wichuk1, Praveena Chiowchanwisawakit2, Robert G Lambert3 and Susanne J Pedersen4, 1Medicine, University of Alberta, Edmonton, AB, Canada, 2Medicine, Mahidol University, Bangkok, Thailand, 3Radiology, University of Alberta, Edmonton, AB, Canada, 4Rheumatology, Copenhagen University Hospitals, Copenhagen, Denmark

    Background/Purpose: After 20 years of follow up the majority of patients with aspondyloarthritis (SpA) have developed new bone in the spine although disease may remain…
  • Abstract Number: 3159 • 2016 ACR/ARHP Annual Meeting

    Validation of MRI Structural Lesions Using Computed Tomography in Patients with Axial Spondyloarthritis

    Robert G. Lambert1, Damien Loeuille2, Marie Raynal3, Jean Melchior2, Maria Antonietta D'Agostino4, Joel Paschke5 and Walter Maksymowych6, 1Radiology, University of Alberta, Edmonton, AB, Canada, 2Rheumatology, CHRU Vandoeuvre les Nancy, Nancy, France, 3Rheumatology, CHRU Nancy, Nancy, France, 4Rheumatology, Versailles-Saint Quentin en Yvelines University, Boulogne-Billancourt, France, 5CaRE Arthritis, Edmonton, AB, Canada, 6Medicine, University of Alberta, Edmonton, AB, Canada

    Background/Purpose: MRI can detect both inflammatory and structural lesions in the sacroiliac joints (SIJ) of patients with axial SpA. However, standard MRI sequences do not…
  • Abstract Number: 3160 • 2016 ACR/ARHP Annual Meeting

    Scoring Syndesmophytes on CT Spine Images of Patients with Radiographic Axial Spondyloarthritis from the Sensitive Imaging of Axial Spondyloarthritis (SIAS) Cohort

    F. de Bruin1, R van den Berg2, Xenofon Baraliakos3, Monique Reijnierse4 and Désirée van der Heijde1, 1Leiden University Medical Center, Leiden, Netherlands, 2Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 3Rheumazentrum Ruhrgebiet Herne, Ruhr-University Bochum, Herne, Germany, 4Department of Radiology, Leiden University Medical Center, Leiden, Netherlands

    Background/Purpose: Low dose Computed Tomography (CT) could potentially be more sensitive than radiographs in the follow up of patients with axial spondyloarthritis (axSpA). First goal…
  • Abstract Number: 3161 • 2016 ACR/ARHP Annual Meeting

    The Association Between HLA Genetic Susceptibility Markers and Sonographic Enthesitis in Psoriatic Arthritis

    Ari Polachek1, Richard J. Cook2, Vinod Chandran1, Fatima Abji1, Dafna D Gladman3 and Lihi Eder4, 1Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Statistics and Actuarial Science, University of Waterloo, Waterloo, ON, Canada, 3University of Toronto, Toronto, ON, Canada, 4Rheumatology, University of Toronto, Women's College Hospital, Toronto, ON, Canada

    Background/Purpose: Enthesitis is an important pathophysiologic component in psoriatic arthritis (PsA). Ultrasound is emerging as an optimal method to evaluate enthesitis. HLA genes are implicated…
  • Abstract Number: 3162 • 2016 ACR/ARHP Annual Meeting

    Symmetric and Asymmetric Sacroiliitis Are Associated with Different Major Histocompatibility Class I Alleles in Psoriatic Arthritis

    Jon T. Giles1, Muhammad Haroon2, Deepak R. Jadon3, Raj Sengupta4, Alison L Nightingale5, Eleanor Korendowych3, Jing Bi6, Neil J. McHugh3, Oliver FitzGerald7 and Robert Winchester6, 1Division of Rheumatology, Columbia University, College of Physicians & Surgeons, New York, NY, 2Rheumatology, Kerry General Hospital, Co Kerry, Ireland, 3Rheumatology, Royal National Hospital for Rheumatic Diseases, Bath, United Kingdom, 4Rheumatology, Royal National Hospital for Rheumatic Diseases,, Bath, United Kingdom, 5Pharmacy and Pharmacology, University of Bath, Bath, United Kingdom, 6Rheumatology, Columbia University, College of Physicians & Surgeons, New York, NY, 7St. Vincent's University Hospital, Department of Rheumatology, Dublin, Ireland

    Background/Purpose: HLA-B27 has been linked to sacroiliitis (SII) in psoriatic arthritis (PsA); however, the contribution to SII of other human leukocyte antigen (HLA) Class I…
  • Abstract Number: 3163 • 2016 ACR/ARHP Annual Meeting

    SEC16A and Intracellular Trafficking Abnormalities in Axial Spondyloarthritis

    Fanxing Zeng1, Zhenbo Zhang1, Vidya Ranganathan2, Darren Orielly3, Proton Rahman4 and Nigil Haroon5, 1Krembil research institute, Toronto, ON, Canada, 2University Health Network, Toronto, ON, Canada, 3Faculty of Medicine, Memorial University of Newfoundland, St. John’s, NF, Canada, 4Rheumatology, St Claires Mercy Hospital, St Johns, NF, Canada, 5Rheumatology, Toronto Western Hospital, University of Toronto, Spondylitis Clinic, Toronto, ON, Canada

    Background/Purpose: The pathogenesis of Axial Spondyloarthritis (AxSpA) is not well understood. A rare 9 base-pair deletion of SEC16A was recently identified to be strongly associated with AxSpA in a multiplex…
  • Abstract Number: 3164 • 2016 ACR/ARHP Annual Meeting

    Spondyloarthritis Pathogenesis Involves Interplay Between Gut Microbiota and Genetic Background

    Tejpal Gill1, Mark Asquith2, Stephen Brooks3, James T. Rosenbaum2 and Robert A. Colbert1, 1National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Oregon Health & Science University, Portland, OR, 3NIAMS/NIH, Bethesda, MD

    Background/Purpose: HLA-B27 and human b2m expression in rats induces a spontaneous inflammatory disease resembling human spondyloarthritis (SpA). While aspects of rat SpA have been studied…
  • Abstract Number: 3165 • 2016 ACR/ARHP Annual Meeting

    HLA-B27 Expression Is Accompanied By a Profoundly Altered IgA Response to the Intestinal Microbiota and Microbial Translocation to the Joint

    Mark Asquith1, Sean Davin1, Patrick Stauffer1, Claire Mitchell2 and James T. Rosenbaum1, 1Oregon Health & Science University, Portland, OR, 2Division of Arthritis and Rheumatology, Oregon Health & Science University, Portland, OR

    Background/Purpose:  HLA-B27 is the strongest known genetic risk factor for ankylosing spondylitis and other spondyloarthropathies (SpAs). We have shown previously that Fisher 344 rats that…
  • Abstract Number: 3166 • 2016 ACR/ARHP Annual Meeting

    HLA-B27 and Ankylosing Spondylitis Have Shared Effects on the Gut Microbiome

    Mary-Ellen Costello1, Mark Asquith2, Kim-Anh Lê Cao3, Tammy Martin4, Sarah Diamond2, Michelle Beaumont5, Timothy D. Spector5, James T. Rosenbaum2 and Matthew A. Brown1, 1Translational Research Institute, Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia, 2Oregon Health & Science University, Portland, OR, 3Translational Research Instiute, The University of Queensland Diamantina Institute, Brisbane, Australia, 4Ophthalmology, Oregon Health & Science Univ, Portland, OR, 5Dept of Twin Research and Genetic Epidemiology, King's College London, London, United Kingdom

    Background/Purpose: Evidence for a discrete intestinal microbiome signature in the terminal ileum (TI) of ankylosing spondylitis (AS) patients, compared to healthy controls, has recently been…
  • Abstract Number: 3167 • 2016 ACR/ARHP Annual Meeting

    Total and Glucocorticoid-Related Damage Accrual in the Systemic Lupus International Collaborating Clinics Inception Cohort

    Jayne Little1,2, Mark Lunt3, Benjamin Parker1,2, Ian N. Bruce2,4 and The Systemic Lupus International Collaborating Clinics (SLICC) Group, 1Centre for Musculoskeletal Research, Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 2NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom, 3Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 4Central Manchester University Hospital NHS Foundation Trust and Manchester Academic Health Science Centre, Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom

    Total and Glucocorticoid-Related Damage Accrual in The Systemic Lupus International Collaborating Clinics Inception Cohort.   Jayne Little1, Mark Lunt1, Ben Parker1, Ian N. Bruce1 and The…
  • Abstract Number: 3168 • 2016 ACR/ARHP Annual Meeting

    Economic Evaluation of Damage Accrual in an International SLE Inception Cohort

    Megan Barber1, Ian N. Bruce2, Murray Urowitz3, John G. Hanly4, Li Su5, Juanita Romero-Diaz6, Caroline Gordon7, Sang-Cheol Bae8, Sasha Bernatsky9, Daniel J Wallace10, Joan T. Merrill11, David A. Isenberg12, Anisur Rahman13, Ellen M. Ginzler14, Michelle Petri15, Mary Anne Dooley16, Paul R. Fortin17, Dafna D. Gladman18, Jorge Sanchez-Guerrero19, Kristján Steinsson20, Rosalind Ramsey-Goldman21, M Khamashta22, Cynthia Aranow23, Graciela S. Alarcon24, Barri J. Fessler25, Susan Manzi26, Ola Nived27, Andreas Jönsen28, Asad Zoma29, Ronald F. van Vollenhoven30, Manuel Ramos-Casals31, Guillermo Ruiz-Irastorza32, S. Sam Lim33, Kenneth C. Kalunian34, Murat Inanc35, Diane L. Kamen36, Christine A. Peschken37, Søren Jacobsen38, Anca Askanase39, Jill P. Buyon40, Chris Theriault41, Vernon Farewell42 and Ann E. Clarke43, 1Division of Rheumatology, University of Calgary, Caglary, AB, Canada, 2Central Manchester University Hospital NHS Foundation Trust and Manchester Academic Health Science Centre, Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 3Medicine, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 4Rheumatology, Division of Rheumatology, Capital Health and Dalhousie University, Halifax, NS, Canada, 5Nova Scotia Rehab Site, Division of Rheumatology, Capital Health and Dalhousie University, Halifax, NS, Canada, 6Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico city, Mexico, 7NIHR/Wellcome Trust Clinical Research Facility, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom, 8Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of, 9Divisions of Rheumatology and Clinical Epidemiology, McGill University Health Centre, Montreal, QC, Canada, 10Cedars-Sinai Medical Center, West Hollywood, CA, 11Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 12Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom, 13Rayne Institute, Centre for Rheumatology Research, UCL Division of Medicine, London, United Kingdom, 14Rheumatology, SUNY Downstate Medical Center, Brooklyn, NY, 15Rheumatology Division, Johns Hopkins University School of Medicine, Baltimore, MD, 16Dooley Rheumatology, Chapel Hill Doctors, Chapel Hill, NC, 17Rheumatology, University of Laval, Quebec, QC, Canada, 18Rheumatology, Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 19Rheumatology, Toronto Western Hospital, Toronto, ON, Canada, 20Rheumatology, Univ. Hospital, Reykjavik, Iceland, 21FSM, Northwestern University, Chicago, IL, 22Lupus Research Unit, Lupus Research Unit, The Rayne Institute, King's College London School of Medicine, St Thomas' Hospital, London, United Kingdom, 23Molecular Medicine and Medicine, Hofstra Northwell School of Medicine, Hempstead, NY, 24Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 25Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 26Lupus Center of Excellence, West Penn Allegheny Health System, Pittsburgh, PA, 27Department of Rheumatology, University Hospital, Lund, Sweden, 28Lund University, Department of Clinical Sciences, Rheumatology, Lund, Sweden, 29Rheumatology, Hairmyres Hospital, East Kilbride, Great Britain, 30Amsterdam Rheumatology and Immunology Center (ARC), Amsterdam, Netherlands, 31Department 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, 32Universidad del Pais Vasco, Servicio de Medicina Interna, Hospital de Cruces, Bizkaia, Spain, 33Medicine, Emory University School of Medicine, Atlanta, GA, 34Division of Rheumatology, Allergy & Immunology, UCSD School of Medicine Center for Innovative Therapy, La Jolla, CA, 35Department of Internal Medicine, Division of Rheumatology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey, 36Medicine/Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 37RR 149G, Univ of Manitoba, Winnipeg, MB, Canada, 38Rheumatology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark, 39Rheumatology, Columbia University Medical Center, New York, NY, 40Medicine, New York University School of Medicine, New York, NY, 41Medicine, Queen Elizabeth II Health Sciences Centre and Dalhousie University, Halifax, NS, Canada, 42Medicine, Division of Rheumatology, Capital Health and Dalhousie University, Halifax, NS, Canada, 43Division of Rheumatology, University of Calgary, Calgary, AB, Canada

    Background/Purpose: Little is known about the association of healthcare costs with damage accrual in SLE. We describe the costs associated with damage states across the disease…
  • Abstract Number: 3169 • 2016 ACR/ARHP Annual Meeting

    Mortality Trends in Systemic Lupus Erythematosus: A General Population-Based Cohort Study

    April Jorge1, Na Lu1,2, Sharan K. Rai3 and Hyon Choi1, 1Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 2Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 3Arthritis Research Canada, Vancouver, BC, Canada

    Background/Purpose: Systemic lupus erythematosus (SLE) is associated with an increased risk of mortality. Despite improvements in the recognition and treatment of SLE, it remains a challenging…
  • « Previous Page
  • 1
  • …
  • 1807
  • 1808
  • 1809
  • 1810
  • 1811
  • …
  • 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 2025 American College of Rheumatology