ACR Meeting Abstracts

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  • Abstract Number: 2247 • 2016 ACR/ARHP Annual Meeting

    REAL-Life Cost of UK Healthcare Resource for Patients with Rheumatoid Arthritis, Comparing High and Low/Remission Disease States

    Bruce Kirkham1, Estee Chan2, Alexandra Vincent2 and Alison Elliott3, 1Rheumatology, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom, 2Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom, 3Market Access Directorate, Roche Products LTD UK, Welwyn Garden City, United Kingdom

    Background/Purpose: Rheumatoid Arthritis (RA) has differing therapeutic outcomes, with resulting differences in function and quality of life. Little is known about the effects of disease…
  • Abstract Number: 2248 • 2016 ACR/ARHP Annual Meeting

    The “Financial Toxicity” of Therapy in Patients with Rheumatoid Arthritis

    Gary Craig1,2, Keith Knapp1,2, Karen Ferguson2 and Sergio Schwartzman3, 1Arthritis Northwest PLLC., Spokane, WA, 2Discus Analytics LLC., Spokane, WA, 3Rheumatology, Hospital for Special Surgery, New York, NY

    Background/Purpose: In the pre-biologic era, major costs faced by patients with RA included hospitalization and joint replacement. Biologic agent development has led to increasing outpatient…
  • Abstract Number: 2249 • 2016 ACR/ARHP Annual Meeting

    Comparison of Discontinuation Rates Among Patients with RA Initiating Biologics

    Sofia Pedro1 and Kaleb Michaud1,2, 1National Data Bank for Rheumatic Diseases, Wichita, KS, 2University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: While difficult to directly compare effectiveness of biologics in observational settings, drug discontinuation can be a useful substitute. We compared the discontinuation rates of…
  • Abstract Number: 2250 • 2016 ACR/ARHP Annual Meeting

    A Real World View of Rheumatoid Arthritis Patients Treated with Advanced Therapies: Comparing Patient Profiles and Outcomes

    Laurent Chanroux and Fara Mboge, Therapy Watch, Research Partnership, London, United Kingdom

    Background/Purpose: Advanced therapies including bDMARDs and tofacitinib have been shown to help control disease progression in rheumatoid arthritis (RA) and reduce joint damage. The aim…
  • Abstract Number: 2251 • 2016 ACR/ARHP Annual Meeting

    Secukinumab Vs Adalimumab for the Treatment of Ankylosing Spondylitis: A Cost per Responder Analysis at 52 Weeks from the US Perspective

    Jessica Walsh1, Efthalia Nikoglou2, Gunda Praveen3, Yujin Park4 and Steffen Jugl5, 1University of Utah School of Medicine, Salt Lake City, UT, 2Novartis Ireland, Ltd, Dublin, Ireland, 3Novartis Healthcare Pvt. Ltd., Hyderabad, India, Hyderabad, India, 4Novartis Pharmaceuticals Corporation, East Hanover, NJ, 5Novartis Pharma AG, Basel, Switzerland

    Secukinumab vs adalimumab for the treatment of ankylosing spondylitis: A cost per responder analysis at 52 weeks from the US perspectiveJessica Walsh1, Efthalia Nikoglou2, Praveen…
  • Abstract Number: 2252 • 2016 ACR/ARHP Annual Meeting

    Estimated Cost of SLE Hospitalizations

    Kayla Neville1, James Miceli1, Jianhua Li2, Samantha Nguyen3, Teja Kapoor3 and Anca Askanase3, 1Rheumatology, Columbia University Medical Center, New York, NY, 2Department of Biomedical Informatics, Columbia University Medical Center, New York, NY, 3Medicine, Division of Rheumatology, Columbia University Medical Center, New York, NY

    Background/Purpose:  Systemic lupus erythematosus (SLE) treatment comes at a high price, with both direct costs related to healthcare resource utilization and indirect ones related to…
  • Abstract Number: 2253 • 2016 ACR/ARHP Annual Meeting

    Treatment Persistence with Subcutaneous TNF-Alpha Inhibitors in France

    Manon Belhassen1, Christophe Hudry2, Marie-Christine Woronoff3, Liliane Lamezec4, Najat Gouyette4, Marine Ginoux1, Eric Van Ganse1, Florence Tubach5 and Bruno Fautrel6, 1PELyon, Pharmacoepidemiologie Lyon, France, Lyon, France, 2AP-HP Hôpital Cochin, Paris, France, 3INSERM-U-1098, DRCI-CHRU Besançon, Franche-Comté University, UBFC, Besançon France, Besançon, France, 4MSD France, Courbevoie, France, 5Université Pierre et Marie Curie (UPMC)-Paris 6; APHP, Pitié Salpêtrière Hospital, Département Biostatistics and Public health, Pharmacoepidémiology center (Cephepi), 7501875013, Paris, France ;, Paris, France, 6Rheumatology, Pitié Salpêtrière Hospital, Paris, France

    Background/Purpose:  Immune-mediated rheumatic disease (IMRD) including rheumatoid arthritis (RA), psoriatic arthritis (PsA) and ankylosing spondylitis (AS), are severe and disabling chronic diseases in rheumatology. Biotherapies…
  • Abstract Number: 2254 • 2016 ACR/ARHP Annual Meeting

    Patient Adherence with Biologic Therapy in Rheumatoid Arthritis: A Real-World Review of Compliance

    Laurent Chanroux, Fara Mboge and Denise Baldock, Therapy Watch, Research Partnership, London, United Kingdom

    Background/Purpose: Biologic agents (bDMARDs) have been shown to help control disease progression in rheumatoid arthritis (RA) and reduce joint damage. The aim of our research…
  • Abstract Number: 2255 • 2016 ACR/ARHP Annual Meeting

    Characterization of Low-Density Granulocytes in Autoinflammatory Disorders

    Pragnesh Mistry1, Monica Purmalek1, Anne Jones2, Amanda K. Ombrello2, Daniel L. Kastner2, Ivona Aksentijevich2 and Mariana Kaplan1, 1NIAMS/NIH, Bethesda, MD, 2Inflammatory Disease Section, NHGRI/NIH, Bethesda, MD

    Background/Purpose: Autoinflammatory disorders (AD) are characterized by recurrent fevers associated with systemic symptoms involving joints, skin, muscles, and eyes in the absence of adaptive immune…
  • Abstract Number: 2256 • 2016 ACR/ARHP Annual Meeting

    Histopathologic Features and Tissue Interferon-Response Gene Scoring of Lesional Skin Samples for Diagnosis in Autoinflammatory Disorders

    Kyawt W. Shwin1,2, Chyi-Chia Richard Lee3, Adriana Almeida de Jesus4, Carmelo Carmona-Rivera5, Louise Malle4, Yanfeng Hou6, Gina A. Montealegre Sanchez4, Edward Cowen7 and Raphaela Goldbach-Mansky8, 1Translational Autoinflammatory Diseases Studies, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, 2National Institutes of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institutes of Health (NIH), Bethesda, MD, 3Dermatopathology Section, Laboratory of Pathology, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, 4National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD, 5Systemic Autoimmunity Branch/ NIAMS, National Institutes of Health, Bethesda, MD, 6Translational Autoinflammatory Disease Studies, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, 7Dermatology Branch, National Cancer Institute (NCI), National Institutes of Health, Bethesda, MD, 8Translational Autoinflammatory Disease Studies, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD

    Background/Purpose: Many genetically defined autoinflammatory diseases (AID) are caused by innate immune dysregulation and present with “neutrophilic dermatoses”. This study systematically assesses immune-cell infiltrates, and…
  • Abstract Number: 2257 • 2016 ACR/ARHP Annual Meeting

    Regulation of Mitochondrial Proton Gradient Is Critical for NLRP3 Inflammasome Activation

    Jehad H. Edwan, Raphaela Goldbach-Mansky and Robert A. Colbert, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD

    Background/Purpose:  Self-activating mutations in NLRP3 cause a spectrum of autoinflammatory diseases known as cryopyrin-associated periodic syndromes (CAPS). NLRP3 is a key component of a multiprotein…
  • Abstract Number: 2258 • 2016 ACR/ARHP Annual Meeting

    Role of NLRP12 on Disease Severity in Autoimmune Arthritis

    Ryan Lupo and Peng Liu, Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC

    Background/Purpose:  Nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) are cytoplasmic sensors that response to danger signals released by invading pathogen or self-damaged tissues. NLRP12 is a member…
  • Abstract Number: 2259 • 2016 ACR/ARHP Annual Meeting

    Suppression of Monosodium Urate Crystal-Induced Cytokine Production Via Inhibition of Histone Deacetylases 1/2

    Maartje Cleophas1, Tania Crisan2, Charles Dinarello3, M.G. Netea2 and Leo .A.B. Joosten2, 1Department of Medicine, Radboud University Medical Center, Nijmegen, Netherlands, 2Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands, 3Department of Medicine, Division of Infectious Diseases, University of Colorado, Denver, CO

    Background/Purpose: Acute gout is a highly common and painful form of inflammatory arthritis, occurring mainly in men above the age of 50. The recurring flares…
  • Abstract Number: 2260 • 2016 ACR/ARHP Annual Meeting

    Anti-Inflammatory Role of Lubricin/Proteoglycan 4 (PRG4) in Monosodium Urate (MSU)-Crystal Induced Arthritis.

    Anthony M. Reginato1, Marwa Qadri2, Changqi Sun3, Tannin Schmidt4, Nicole Yang5, Khaled Elsaid6 and Gregory Jay7, 1Rhode Island Hospital, The Warren Alpert School of Medicine at Brown University, Providence, RI, 2Department of Pharmaceutical Science, School of Pharmacy, MCHS University, Boston, MA, 3Division of Rheumatology, Rhode Island Hospital, The Warren Alpert School of Medicine at Brown University, Providence, RI, 4Kinesiology and Schulich School of Engineering, University of Calgary, Calgary, AB, Canada, 5Division of Rheumatology, Immunology and Allergy, Brigham and Women’s Hospital, Boston, MA, USA., Boston, MA, 6Biomedical and Pharmaceutical Sciences, Chapman University, Irvine, CA, 7Emergency Medicine, Brown University, Providence, RI

    Background/Purpose: Lubricin/proteoglycan-4 (PRG4) is a mucinous glycoprotein secreted by synovial fibroblast and superficial zone chondrocyte. PRG4 has a homeostatic multifaceted role in the joint including…
  • Abstract Number: 2261 • 2016 ACR/ARHP Annual Meeting

    Methotrexate Inhibits Intracellular Redox Signaling Induced By the Reactive Oxygen Species; Malondialdehyde and Acetaldehyde

    Andrew Chiou1, Michael J. Duryee1,2, Cleofes Sarmiento3, Matthew Zimmerman4, Carlos D. Hunter1, Lynell W. Klassen5, James R. O'Dell5, Daniel R. Anderson3, Geoffrey M. Thiele3 and Ted R Mikuls6, 1Internal Medicine Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE, 2Research Services, Omaha VA Medical Center, Omaha, NE, 3University of Nebraska Medical Center, Omaha, NE, 4Cell Biology and Physiology, University of Nebraska Medical Center, Omaha, NE, 5Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 6Internal Medicine, Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: Inflammatory diseases such as rheumatoid arthritis (RA) are associated with oxidative stress as a result of elevated levels of reactive oxygen species (ROS). Oxidative…
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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.).

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