ACR Meeting Abstracts

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Abstracts tagged "pathogenesis"

  • Abstract Number: 2578 • 2016 ACR/ARHP Annual Meeting

    Plasma Levels of Bone Morphogenetic Protein (BMP) Subgroups and Their Inhibitors (noggin, sclerostin) in Rheumatoid Arthritis Patients and Correlation with Disease Activity, Clinical and Radiographic Progression

    Ozge Kockara1, Merve Sibel Gungoren2, Erdem Karabulut3, Sebnem Ataman4 and Filiz Akbiyik2, 1Physical Medicine and Rehabilitation, Ankara University Faculty of Medicine, Ankara, Turkey, 2Medical Biochemistry, Hacettepe University Faculty of Medicine, Ankara, Turkey, 3Biostatistics, Hacettepe University Faculty of Medicine, Ankara, Turkey, 4Rheumatology Department, Ankara University Faculty of Medicine, Ankara, Turkey

    Background/Purpose: Progressive bone destruction occurs in rheumatoid arthritis (RA) due to imbalance of osteoblast/osteoclast activity. Bone morphogenetic proteins (BMPs) regenerate bone damage by stimulating the…
  • Abstract Number: 570 • 2016 ACR/ARHP Annual Meeting

    A Molecular Timeline for Preclinical RA Pathogenesis Defined By Dysregulated PTPN22, Hypercitrullination, and Aberrant Cytokine/Metabolic Profiles in PBMC of at-Risk Individuals

    Hui-Hsin Chang1, Nishant Dwivedi2, Bo Sun2, Deepak A. Rao3, Jeffrey A. Sparks3, Jennifer Kinslow4, Yuko Okamoto4, Kevin D. Deane5, M. Kristen Demoruelle6, Jill M. Norris7, Elizabeth Karlson2, V. Michael Holers8 and I-Cheng Ho1, 1Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 3Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 4University of Colorado School of Medicine, Aurora, CO, 5Division of Rheumatology, University of Colorado School of Medicine, Aurora, CO, 6Rheumatology, University of Colorado School of Medicine, Aurora, CO, 7Epidemiology, Colorado School of Public Health, Aurora, CO, 8Rheumatology Division, University of Colorado School of Medicine, Aurora, CO

    Background/Purpose: One unique feature of RA is the presence of ACPA. PTPN22 is a phosphatase that also acts to suppress citrullination independently of its phosphatase…
  • Abstract Number: 2928 • 2016 ACR/ARHP Annual Meeting

    Hypomethylation of an Intragenic Alternative Promoter Contributes to Impaired Treg Function in Rheumatoid Arthritis By Transcriptional Interference with Expression of the Treg-Specific Protein, Glycoprotein a Repetitions Predominant (GARP)

    Alla Skapenko, Jan Leipe and Hendrik Schulze-Koops, Division of Rheumatology and Clinical Immunology, University of Munich, Munich, Germany

    Background/Purpose:  The expression of Treg specific genes, such as the master transcription factor of Tregs, FoxP3 or the Treg specific surface molecule, glycoprotein A repetitions…
  • Abstract Number: 581 • 2016 ACR/ARHP Annual Meeting

    Cell-Mediated Neutrophil Lysis-a Mechanism Promoting Hypercitrullination in Rheumatoid Arthritis?

    Tal Gazitt1, Christian Lood1, Xizhang Sun2, David Feith3, Jeffrey Ledbetter2, Gordon Starkebaum1, Thomas Loughran Jr.4 and Keith B. Elkon1, 1Department of Medicine, Division of Rheumatology, University of Washington, Seattle, WA, 2University of Washington, Seattle, WA, 3Hematology and Oncology, University of Virginia, Charlottesville, VA, 4Hematology Oncology, University of Virginia, Charlottesville, VA

    BACKGROUND/PURPOSE:Protein citrullination, the post-translational conversion of arginine to citrulline, mediated by peptidylarginine deiminase (PAD) enzymes, is considered a likely mechanism for the stimulation of anti-citrullinated…
  • Abstract Number: 3017 • 2016 ACR/ARHP Annual Meeting

    Elevated Neutrophil Extracellular Trap Levels Correlate with Anti-CCP3-IgG and Anti-CCP3-IgA Levels in the Sputum of Individuals at-Risk for Future Rheumatoid Arthritis

    M. Kristen Demoruelle1, Monica Purmalek2, Heather Rothfuss3, Michael Weisman4, Lindsay Kelmenson1, Michael Mahler5, Jill M. Norris6, Brian Cherrington3, Mariana Kaplan2, V. Michael Holers1 and Kevin D. Deane1, 1Rheumatology Division, University of Colorado Denver, Aurora, CO, 2Systemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 3Zoology and Physiology, University of Wyoming, Laramie, WY, 4Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 5Research and Development, Inova Diagnostics, San Diego, CA, 6Epidemiology, Colorado School of Public Health, Aurora, CO

    Background/Purpose: The initial site of anti-citrullinated protein antibody (ACPA) generation in RA has been proposed to be a mucosal site. We have previously demonstrated ACPA…
  • Abstract Number: 584 • 2016 ACR/ARHP Annual Meeting

    Glycoprotein VI: A Potential Target for ACPA-Mediated Platelet Activation?

    John Stack1, Anne Madigan2, Laura Helbert1, Niamh Redmond1, Eimear Dunne3, Dermot Kenny3 and Geraldine M. McCarthy2, 1Rheumatology, Mater Misericordiae University Hospital, Dublin, Ireland, 2Rheumatology, Mater Misericordiae University Hospital, Dublin 7, Ireland, 3Molecular and Cellular Therapeutics, RCSI, Dublin 2, Ireland

    Background/Purpose: Arterial thrombosis is a major cause of mortality in  rheumatoid arthritis (RA),especially in anti-citrullinated protein antibody (ACPA)-positive patients Recent studies suggest that platelet activation…
  • Abstract Number: 3019 • 2016 ACR/ARHP Annual Meeting

    Sputum Antibodies to Individual Citrullinated Protein/Peptide Antigens Are Elevated in Subjects at-Risk of Future RA and Subjects with Established Disease

    Emily Bowers1, M. Kristen Demoruelle2, Michael Weisman3, Jill M. Norris4, William H. Robinson5, V. Michael Holers2 and Kevin D. Deane2, 1Medicine, University of Colorado Denver, Aurora, CO, 2Rheumatology Division, University of Colorado Denver, Aurora, CO, 3Cedars-Sinai Medical Center, Los Angeles, CA, 4Epidemiology, Colorado School of Public Health, Aurora, CO, 5Stanford University School of Medicine, Stanford, CA

    Background/Purpose: Multiple studies demonstrate that ACPAs are elevated in the serum years prior to the onset of seropositive RA during a preclinical period of autoimmunity.…
  • Abstract Number: 988 • 2016 ACR/ARHP Annual Meeting

    Risk of Rheumatoid Arthritis after Transfusion of Blood from Donors Later Diagnosed with  Rheumatoid Arthritis: A Retrospective Cohort Study

    Søren Andreas Just1, Kjell Titlestad2, Gustaf Edgren3, Klaus Rostgaard4, Johan Askling5, Hanne Lindegaard1 and Henrik Hjalgrim4, 1Department of Rheumatology, Department of Rheumatology, Odense University Hospital, Odense, Denmark, Odense, Denmark, 2Department of Clinical Immunology, Department of Clinical Immunology, Odense Unversity Hospital, Odense, Denmark, Odense, Denmark, 3Department of Medical Epidemiology and Biostatistics, Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden, Stockholm, Sweden, 4Epidemiology Research, Department of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark, Copenhagen, Denmark, 5Clinical Epidemiology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden, Stockholm, Sweden

    Background/Purpose: Rheumatoid Arthritis (RA) is a disease that can have a long sub-clinical phase. During this phase the person with pre-RA could have factors in…
  • Abstract Number: 3022 • 2016 ACR/ARHP Annual Meeting

    Autoantibodies to Peptidylarginine Deiminase 2 Protect Against Radiographic Progression in Patients with Rheumatoid Arthritis

    Erika Darrah1, Jon T. Giles2, Ryan Davis1, Pooja Naik1, Maximilian Konig1 and Felipe Andrade1, 1Department of Medicine, Division of Rheumatology, The Johns Hopkins University, Division of Rheumatology, Baltimore, MD, 2Columbia University, College of Physicians and Surgeons, Division of Rheumatology, New York, NY

    Background/Purpose:  The mechanisms that drive clinical heterogeneity and outcomes in patients with rheumatoid arthritis (RA) are poorly understood, but precise biomarkers may identify clinically unique…
  • Abstract Number: 1040 • 2016 ACR/ARHP Annual Meeting

    Stressful Life Events : A Trigger for Rheumatoid Arthritis Onset within a Year. a Case-Control Study

    Jimmy Gross1, Nadia Oubaya2,3, Florent Eymard1, Alexia Hourdille1, Xavier Chevalier1 and Sandra Guignard1, 1Department of Rheumatology, APHP Henri Mondor hospital, Créteil, France, 2Public Health Department, F-94000, APHP Henri Mondor hospital, Créteil, France, 3DHU A-TVB, IMRB- EA 7376 CEpiA (Clinical Epidemiology And Ageing Unit), F-94000, Université Paris-Est, UPEC,, Créteil, France

    Background/Purpose: To assess the association between recent stressful life events and rheumatoid arthritis (RA) onset. Methods: We conducted a monocentric case-control study of in and…
  • Abstract Number: 3217 • 2016 ACR/ARHP Annual Meeting

    Broad-Based Interrogation of the Serum Proteome Suggests That RA Onset Is Associated with Activation of the Intrinsic Coagulation Cascade

    Liam O'Neil1, Xiaobo Meng2, Irene Smolik3, Carol Hitchon2 and Hani El-Gabalawy4, 1Rheumatology, University of Manitoba, Winnipeg, MB, Canada, 2University of Manitoba, Winnipeg, MB, Canada, 3Arthritis Center, University of Manitoba, Winnipeg, MB, Canada, 4University of Manitoba Arthritis Center, Winnipeg, MB, Canada

    Background/Purpose: The establishment of longitudinal pre-clinical RA cohorts is beginning to provide important insights into the mechanisms that precede the onset of clinically detectable disease.…
  • Abstract Number: 1111 • 2016 ACR/ARHP Annual Meeting

    Huntingtin Interactin Protein 1 (HIP1) Regulates Receptor Tyrosine Kinases Mediated Activity and Cell Invasiness in Fibroblast-like Synoviocytes

    Teresina Laragione, Nasim Azizgolshani, Carolyn Harris, Erjing Gao and Percio Gulko, Medicine/Rheumatology, Icahn School of Medicine at Mount Sinai, New York, NY

    Background/Purpose: Huntingtin-interacting protein 1 (Hip1) is a new arthritis severity gene recently identified in the Pristane and Collagen-induced arthritis (PIA, CIA) quantitative trait locus Cia25/Pia42…
  • Abstract Number: 1207 • 2016 ACR/ARHP Annual Meeting

    Design of a Multiplex Serum Proteome Assay to Monitor Biologic Drug Response in Rheumatoid Arthritis Patients

    Niamh Callan1, Aisha Butt1, Stephen R. Pennington2, Cathy McGeough3, Philip Gardiner4, Gary Wright5, Tony Bjourson3 and David S. Gibson6, 1Proteome Research Centre, Conway Institute, University College Dublin, Dublin, Ireland, 2Proteome Research Centre, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland, 3Northern Ireland Centre for Stratified Medicine, Ulster University, Londonderry, United Kingdom, 4Rheumatology, Altnagelvin Hospital, Londonderry, United Kingdom, 5Rheumatology, Musgrave Park Hospital, BELFAST, United Kingdom, 6Inflammatory Disease Research Group, Northern ireland Centre for Stratified Medicine, Ulster University, Londonderry, United Kingdom

    Background/Purpose: Biologic drugs have revolutionised the treatment of Rheumatoid Arthritis (RA), however these therapies are expensive and exhibit a high non–response rate (30%). Currently there…
  • Abstract Number: 1213 • 2016 ACR/ARHP Annual Meeting

    Targeted Next-Generation Sequencing of 128 Genes Associated with Rheumatoid Arthritis

    Khai Pang Leong1, Liuh Ling Goh2, Edward Yu Wing Chee2, Petrina Pei Qin Lim2, Grace Li-Xian Toh2, Ee Tzun Koh3 and Tan Tock Seng Hospital Rheumatoid Arthritis Study Group, 1Rheumatology/Allerg/Immunology, Tan Tock Seng Hospital, Singapore, Singapore, 2Clinical Research & Innovation Office, Tan Tock Seng Hospital, Singapore, Singapore, 3Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Singapore, Singapore

    Background/Purpose: Through genome-wide association scans (GWAS), more than 120 genes have been found to be associated with rheumatoid arthritis (RA). This study aims to search…
  • Abstract Number: 1247 • 2016 ACR/ARHP Annual Meeting

    Diagnostic Modeling of Rheumatoid Arthritis in Oklahoma Tribal Members Using Soluble Mediators

    Lucas Adams1, Carla J. Guthridge1, Tim Gross1, Hua Chen1, Krista M. Bean1, Virginia C. Roberts1, Julie M. Robertson2, Melissa E. Munroe1, Joel M. Guthridge3, Roger Montgomery4, M. Sohail Khan4, Fabio Mota5, Michael Peercy6, Bobby Saunkeah7 and Judith A. James8,9, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Acelity, San Antonio, TX, 3Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Cherokee Nation Health Services, Tahlequah, OK, 5Chickasaw Nation Medical Center, Ada, OK, 6Epidemiology, Chickasaw Nation Department of Health, Ada, OK, 7Chickasaw Nation Department of Health, Ada, OK, 8Department of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 9Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Diagnosis of RA is difficult in American Indian (AI) patients who often have atypical autoantibodies (e.g. ANA) with erosive arthritis. Soluble mediators may serve…
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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].

ACR Abstract Embargo Policy

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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