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  • Abstract Number: 2730 • 2019 ACR/ARP Annual Meeting

    Efficacy and Safety of Romosozumab vs Placebo Among Patients with Mild-to-Moderate Chronic Kidney Disease

    Paul Miller1, Arkadi Chines 2, Ben-Hur Albergaria 3, Evelien Gielen 4, Bente Langdahl 5, Akimitsu Miyauchi 6, Mark Vanderkelen 7, Cassandra Milmont 2, Judy Maddox 2 and Jonathan Adachi 8, 1Colorado Center for Bone Research at Panorama Orthopedics and Spine Center, Golden, CO, 2Amgen Inc., Thousand Oaks, CA, 3Federal University of Espirito Santo, Vitória, Brazil, 4Gerontology and Geriatrics, Department of Chronic Diseases, Metabolism and Aging, KU Leuven & Center for Metabolic Bone Diseases, UZ Leuven, Leuven, Belgium, 5Aarhus University Hospital, Aarhus, Denmark, 6Miyauchi Medical Center, Osaka, Japan, 7UCB Pharma, Brussels, Belgium, 8McMaster University and St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada

    Background/Purpose: Osteoporosis and renal insufficiency are coexisting disease states in a substantial proportion of postmenopausal women. Since bisphosphonates are generally contraindicated in patients with estimated…
  • Abstract Number: 2731 • 2019 ACR/ARP Annual Meeting

    Decomposition Analysis of Spending and Price Trends for Biologic Anti-Rheumatic Drugs in Medicare and Medicaid

    Natalie McCormick1, Zachary Wallace 2, Chana Sacks 3, John Hsu 4 and Hyon K. Choi 5, 1Massachusetts General Hospital and Harvard Medical School, Boston, MA, 2Massachusetts General Hospital, Boston, 3Department of General Internal Medicine, Massachusetts General Hospital; Department of Medicine, Harvard Medical School, Boston, MA, 4Mongan Institute, Massachusetts General Hospital; Department of Health Care Policy, Harvard Medical School, Boston, MA, 5Massachusetts General Hospital, Boston, MA

    Background/Purpose: Billions of public dollars are spent each year on biologic disease-modifying anti-rheumatic drugs (bDMARDs), but the drivers of bDMARD spending and per-patient cost increases…
  • Abstract Number: 2732 • 2019 ACR/ARP Annual Meeting

    The Relationship Between Gout and Cardiovascular Disease Outcomes: A Health Data Linkage Study of 1 Million New Zealanders Using Population-level Cardiovascular Risk Prediction Equations

    Ken Cai1, Billy Wu 2, Suneela Mehta 2, Nicola Dalbeth 2, Rod Jackson 2 and Poppe Katrina 2, 1University of Auckland, Auckland, Auckland, New Zealand, 2University of Auckland, Auckland, New Zealand

    Background/Purpose: Some studies have reported that gout is an independent risk factor for cardiovascular events. Furthermore, urate-lowering therapy such as allopurinol may be associated with…
  • Abstract Number: 2733 • 2019 ACR/ARP Annual Meeting

    Inhibition of Neutrophil Elastase Reduces Autoantibody Levels and Renal Inflammation in Murine Lupus

    Gautam Sule1, Kristen Gilley 1, Andrew Fernandes 1, Srilakshmi Yalavarthi 1 and Jason Knight 2, 1University of Michigan, Ann Arbor, MI, 2Division of Rheumatology, Department of Internal Medicine, Michigan Medicine, Ann Arbor, MI

    Background/Purpose: Dysregulated neutrophil extracellular trap (NET) release has been proposed as a source of autoantigens in lupus.  Furthermore, it has recently been shown that the…
  • Abstract Number: 2734 • 2019 ACR/ARP Annual Meeting

    Signaling Lymphocytic Activation Molecule Family (SLAMF) Receptors Deregulation Is Implicated in the Altered Function of NK Cells in Systemic Lupus Erythematosus

    Morgane Humbel 1, Florence Bellanger 1, Craig Fenwick 2, Alice Horisberger 3, Camillo Ribi 3 and Denis Comte1, 1Service of Immunology and Allergy, Lausanne University Hospital and University of Lausanne, Epalinges, Vaud, Switzerland, 2Service of Immunology and Allergy, Lausanne University Hospital and University of Lausanne, Epalinhes, Vaud, Switzerland, 3Service of Immunology and Allergy, Lausanne University Hospital and University of Lausanne, Lausanne, Vaud, Switzerland

    Background/Purpose: Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease characterized by quantitative and qualitative deficiencies of immune cells. Natural killer (NK) cells are innate…
  • Abstract Number: 2735 • 2019 ACR/ARP Annual Meeting

    Response Gene to Complement -32 Exerts Proinflammatory and Profibrotic Effects in Immune Complex Gediated Glomerulonephritis

    Vinh Nguyen 1, Alexandru Tatomir 2, Horea Rus 3, Cinthia Drachenberg 1, John Papdimitriou 1, Tudor Badea 4, Irina Luzina 5 and Violeta Rus1, 1Univ of Maryland Sch of Medicine, Baltimore, MD, 2Univ of Maryland Sch of Medicine, Baltimore, 3Univ of Maryland Sch of Med and VAMHCS, Baltimore, MD, 4NIH, NEI, Bethesda, MD, 5Univ of Maryland Sch of Med AND VAMHCS, Baltimore

    Background/Purpose: Response Gene to Complement (RGC)-32 is a cell cycle regulator widely expressed in normal tissues, multiple tumors and  a variety of cell lines. RGC-32…
  • Abstract Number: 2736 • 2019 ACR/ARP Annual Meeting

    Mucosal-associated Invariant T Cells Can Be Therapeutically Targeted in Lupus

    Goh Murayama1, Asako Chiba 2, Tomohiro Mizuno 3, Atsushi Nomura 2, Taiga Kuga 4, HIrofumi Amano 4, Ken Yamaji 4, Naoto Tamura 4 and Sachiko Miyake 2, 1Department of Internal Medicine and Rhumatology, Juntendo University School of Medicine, Tokyo, Japan, 2Department of Immunology, Juntendo University School of Medicine, Tokyo, Japan, 3Department of Immunlogy, Juntendo University School of Medicine, Tokyo, Japan, 4Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan

    Background/Purpose: Mucosal-associated invariant T (MAIT) cells are innate T cells that are restricted by the nonpolymorphic MHC-related molecule-1 (MR1) and express a semi-invariant TCRα chain:…
  • Abstract Number: 2737 • 2019 ACR/ARP Annual Meeting

    HIF-1α and miR-210 Differential and Lineage-specific Expression in Systemic Lupus Erythematosus

    Barry Garchow1 and Marianthi Kiriakidou 1, 1Thomas Jefferson University, Philadelphia, PA

    Background/Purpose: Hypoxia inducible factor 1 is a key transcription factor that regulates the cellular response to oxygen stress. In the adaptive immune system, HIF-1α is…
  • Abstract Number: 2738 • 2019 ACR/ARP Annual Meeting

    Differential Methylation of Peripheral Blood Adaptive Immune Cells in Individuals at High Risk for RA and with Early RA Compared with Controls Identifies Pathways Important in Transition to Arthritis

    Rizi Ai1, David Boyle 2, Deepa Hammaker 3, Kevin Deane 4, V. Michael Holers 5, Andre Matti 6, William Robinson 7, Jane Buckner 8, Navin Rao 9, Frédéric Baribaud 10, George Vratsanos 11, Sunil Nagpal 9, Wei Wang 2 and Gary Firestein 3, 1University of California San Diego, San Diego, 2University of California, San Diego, San Diego, CA, 3University of California, San Diego, San Diego, 4University of Colorado Denver, Division of Rheumatology, Aurora, CO, USA, Aurora, CO, 5University of Colorado Denver, Division of Rheumatology, Aurora, CO, USA, Denver, 6UCSD, La Jolla, CA, 7Stanford University, Stanford, CA, 8Benaroya Research Institute, Seattle, WA, 9Janssen R&D, Spring House, PA, 10Janssen Research & Development, LLC, Spring House, PA, 11JNJ, Raritan, NJ

    Background/Purpose: The “Targeting Immune Responses for Prevention of RA” (TIP-RA) collaboration studies individuals at high risk for developing RA because of serum anti-citrullinated protein antibody…
  • Abstract Number: 2739 • 2019 ACR/ARP Annual Meeting

    Skin Disease Activity and Autoantibody Phenotype Are Major Determinants of Blood Interferon Signatures in Dermatomyositis

    Mika Tabata1, Kavita Sarin 2, Karen Page 3, Christine Huard 3, Shanrong Zhao 3, Donald Bennett 3, Jillian Johnson 3, Kristen Johnson 3 and David Fiorentino 2, 1Stanford University School of Medicine, Stanford, CA, 2Department of Dermatology, Stanford University School of Medicine, Redwood City, CA, 3Pfizer, Boston

    Background/Purpose: Interferon (IFN) signaling is upregulated in dermatomyositis (DM) and thought to play a role in pathogenesis. An IFN gene signature in peripheral blood of…
  • Abstract Number: 2740 • 2019 ACR/ARP Annual Meeting

    Takayasu Arteritis Associated Risk Locus in IL6 Represses the Anti-inflammatory Gene GPNMB Through Chromatin Looping and Recruiting MEF2-HDAC Complex

    Xiufang Kong 1 and Amr Sawalha2, 1University of Michigan & Fudan University, Ann Arbor, MI, 2University of Pittsburgh & University of Michigan, Pittsburgh, PA

    Background/Purpose: Previous work has revealed a genetic association between Takayasu arteritis and a non-coding genetic variant in an enhancer region within IL6 (rs2069837 A/G). The…
  • Abstract Number: 2741 • 2019 ACR/ARP Annual Meeting

    Integration of Single Cells from Inflammatory Disease Tissues Reveals Common and Unique Pathogenic Cell States

    Fan Zhang1, Joseph Mears 1, ilya Korsunsky 1, Kevin Wei 2, Anna Helena Jonsson 2, Deepak Rao 1, Edy Kim 3, Laura Donlin 4, Jill Buyon 5, Michelle Petri 6, Chaim Putterman 7, Thomas Tuschl 8, Nir Hacohen 9, Betty Diamond 10, Michael Brenner 11 and Soumya Raychaudhuri 1, 1Brigham and Women's Hospital, Boston, MA, 2Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 3Brigham and Women's Hospital, Boton, MA, 4Hospital For Special Surgery, New York, NY, 5New York University School of Medicine, New York, NY, 6Johns Hopkins University School of Medicine, Baltimore, MD, 7Albert Einstein College of Medicine, New York, NY, 8Rockefeller Research Laboratories, New York, 9Broad Institute, Cambridge, 10Feinstein Institutes for Medical Research, Manhasset, 11Brigham and Women’s Hospital:, Boston

    Background/Purpose: Different autoimmune diseases can co-exist in an individual and share similar genetic associations, autoimmune signaling pathways, and clinical manifestations. However, autoimmune diseases present varied…
  • Abstract Number: 2742 • 2019 ACR/ARP Annual Meeting

    Toward a Liquid Biopsy for Lupus Nephritis: Urine Proteomic Analysis of SLE Identifies Inflammatory and Macrophage Signatures

    Andrea Fava1, Yuji Zhang 2, Jill Buyon 3, H. Michael Belmont 4, Peter Izmirly 5, Chandra Mohan 6, Ting Zhang 7, The Accelerating Medicines Partnership 8 and Michelle Petri 9, 1Johns Hopkins University, Baltimore, 2University of Maryland, Baltimore, 3NYU School of Medicine, New York, 4New York University School of Medicine, Ney York, 5New York University School of Medicine, New York, 6University of Houston, Houston, 7Biomedical Engineering, University of Houston, Houston, TX, 8Multiple Organizations, USA, 9Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Lupus nephritis (LN) complicates up to 60% of patients with systemic lupus erythematosus (SLE) and carries a high morbidity and mortality. The definitive diagnosis…
  • Abstract Number: 2743 • 2019 ACR/ARP Annual Meeting

    Characterizing the Epigenomic Landscape of Psoriasis Patients Destined to Develop Psoriatic Arthritis

    Remy Pollock1, Rohan Machhar 1, Vinod Chandran 2 and Dafna Gladman 3, 1Krembil Research Institute, University Health Network, Toronto, Canada, 2University Health Network, University of Toronto, Toronto, Canada, 3Toronto Western Hospital, Toronto, Canada, Toronto, ON, Canada

    Background/Purpose: Approximately 30% of psoriasis patients develop psoriatic arthritis (PsA), an inflammatory musculoskeletal disease, usually after psoriasis onset. A large proportion of individuals with PsA…
  • Abstract Number: 2744 • 2019 ACR/ARP Annual Meeting

    Altered Expression of CD52 Facilitates Adhesion of Circulating CD14+ Monocytes in Systemic Sclerosis

    Michal Rudnik1, Mara Stellato 1, Filip Rolski 2, Przemyslaw Blyszczuk 3, Karin Klingel 4, Joerg Henes 5, Carol Feghali-Bostwick 6, Oliver Distler 7 and Gabriela Kania 3, 1Center of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Department of Clinical Immunology, Jagiellonian University Medical College, Krakow, Poland, 3Centre of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 4Institute for Pathology and Neuropathology, University Hospital Tuebingen, Tuebingen, Germany, 5University Hospital Tuebingen, Department of Internal Medicine II (Oncology, Haematology, Immunology and Rheumatology), Tuebingen, Germany, 6Division of Rheumatology & Immunology, Medical University of South Carolina, Charlston, SC, 7Dept. of Rheumatology, University Hospital Zürich, Zürich, Switzerland, Zürich, Switzerland

    Background/Purpose: Infiltration of inflammatory cells, including monocytes, into the organs is a major process leading to fibrosis, remodelling and organ dysfunction in systemic sclerosis (SSc).…
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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 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].

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