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  • Abstract Number: 1202 • 2013 ACR/ARHP Annual Meeting

    Two Family Kindreds With Blau’s Syndrome Associated With Unusual NOD2 Mutations

    Qingping Yao, Rheumatic and Immunologic Dis, Cleveland Clinic, Cleveland, OH

    Background/Purpose: The aim of this study was to report families of Blau’s syndrome with unusual NOD2 gene variants. Methods: Two proband patients were seen, and their clinical…
  • Abstract Number: 1200 • 2013 ACR/ARHP Annual Meeting

    Proportion Of Patients Achieving Serum Urate Target In a Longitudinal Veterans Administration (VA) Gout Registry: Crystal Registry

    Puja Khanna1,2, Andreas M. Reimold3, Gail S. Kerr4, J. Steuart Richards5, Elizabeth Chang6, Jasvinder A. Singh7, H. Ralph Schumacher8, Tanima Bannerjee9 and Dinesh Khanna10, 1Rheumatology, Ann Arbor VA, Ann Arbor, MI, 2Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 3Rheumatology, Dallas VA and University of Texas Southwestern, Dallas, TX, 4Rheumatology, Washington DC VAMC, Georgetown and Howard University, Washington, DC, 5Rheumatology, Washington DC VAMC and Georgetown University, Washington, DC, 6Phoenix VAHCS, Phoenix, AZ, 7Department of Medicine, University of Alabama, Tuscaloosa, AL, 8Department of Medicine, University of Pennsylvania and VA Medical Center, Philadelphia, PA, 9Biostatistics, University of Michigan, Ann Arbor, MI, 10University of Michigan Health System, Ann Arbor, MI

    Background/Purpose: Gout is the most common inflammatory arthritis managed by healthcare providers at the VA Healthcare System. CRYSTAL registry is a longitudinal observational study at…
  • Abstract Number: 1201 • 2013 ACR/ARHP Annual Meeting

    A Progress Report On An Emerging Disease: NOD2-Associated Autoinflammatory Disease

    Qingping Yao, Rheumatic and Immunologic Dis, Cleveland Clinic, Cleveland, OH

    Background/Purpose: We recently reported a new disease designated as NOD2-associated autoinflammatory disease (NAID). The aim of this study was to update the progress on defining the disease. Methods: A…
  • Abstract Number: 1203 • 2013 ACR/ARHP Annual Meeting

    An Escalating Dose Of Anakinra In Patients With Autoinflammatory Disease Is a Safe and Reasonable Therapeutic Option

    Amanda K. Ombrello1, Karyl Barron2, Patrycja M. Hoffmann3, Anne Jones3, Deborah Stone4 and Daniel L. Kastner5, 1National Human Genome Research Institute,National Institute of Health, Bethesda, MD, 2Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, 3Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 4National Human Genome Research Institute, Bethesda, MD, 5Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, MD

    Background/Purpose:   The autoinflammatory diseases are diseases in which there is seemingly unprovoked stimulation of the innate immune system.  The enhanced release of cytokines in…
  • Abstract Number: 1204 • 2013 ACR/ARHP Annual Meeting

    Model-Based Pharmacokinetics Of Canakinumab and Pharmacodynamics Of IL-1Beta Binding In Cryopyrin Associated Periodic Syndromes, a Step Towards Personalized Medicine

    Aurélie Gautier1, Phil Lowe1, Andrej Skerjanec1, Phil McKernan1, Wenping Wang2 and Olivier Luttringer1, 1Novartis Pharma AG, Basel, Switzerland, 2Novartis Pharmaceuticals Corporation, East Hanover, NJ

    Background/Purpose: Cryopyrin-associated periodic syndrome (CAPS), comprises of extremely rare, inherited auto-inflammatory diseases, including the mildest form familial cold auto-inflammatory syndrome (FCAS), the more severe Muckle-Wells…
  • Abstract Number: 1205 • 2013 ACR/ARHP Annual Meeting

    Effectiveness Of Canakinumab In a Cryopyrin-Associated Periodic Syndrome Cohort.A Single Center Experience

    Virginia Moreira-Navarrete1, Francisco Javier Toyos Saenz de Miera2, Carmen Vargas Lebrón3 and F. Navarro Sarabia4, 1Rheumatology, University Hospital Virgen Macarena, Sevilla, Spain, 2Hospital Virgen de la Macarena, Sevilla, Spain, 3Hospital Virgen Macarena, SEVILLA, Spain, 4Rheumatologist Service, Hospital Universitario Virgen Macarena, Sevilla, Spain

    Background/Purpose: Cryopyrin-associated periodic syndrome (CAPS) comprises a group of rare, but severe, autoinflammatory diseases, characterized by urticaria, periodic fever, central nervous system inflammation, arthropathy, and…
  • Abstract Number: 1206 • 2013 ACR/ARHP Annual Meeting

    Canakinumab Treatment Regimens In CAPS Patients

    Ferdinand Hofer1, Theresa Endres1, Birgit Kortus-Goetze2, Norbert Blank3, Elisabeth Weissbarth-Riedel4, Catharina Schuetz5, Tilmann Kallinich6, Karoline Krause7, Christoph Rietschel8, Gerd Horneff9 and Jasmin B. Kuemmerle-Deschner10, 1Department of Pediatrics, Division of Pediatric Rheumatology, University Hospital Tuebingen, Tuebingen, Germany, 2Klinik für Innere Medizin, Klinikum der Philipps-Universität Marburg, Marburg, Germany, 3University of Heidelberg, Heidelberg, Germany, 4Kinderrheumatologische Ambulanz, Universitätsklinikum Eppendorf, Hamburg, Germany, 5Klinik für Kinder und Jugendmedizin, Universitätsklinikum Ulm, Ulm, Germany, 6Charite, University Medicine Berlin, Berlin, Germany, 7Dept. of Dermatology and Allergy, Allergie-Centrum-Charité, Charité – Universitätsmedizin Berlin, Germany, Berlin, Germany, 8Kinder- und Jugendrheumatologie, Clementine-Kinderhospital, Frankfurt, Germany, 9Department of Pediatrics, Asklepios Klinik Sankt Augustin, Sankt Augustin, Germany, 10University Hospital Tuebingen, Tuebingen, Germany

    Background/Purpose: Canakinumab is a recombinant monoclonal fully human antibody against Interleukin-1β and approved for the treatment of CAPS in many countries including Europe and the…
  • Abstract Number: 1207 • 2013 ACR/ARHP Annual Meeting

    Efficacy Of Tocilizumab In Patients With AA Amyloidosis Secondary To Familial Mediterranean Fever: A Single Centre Experience

    Sedat Yilmaz1, Muhammet Cinar2, Ismail Simsek1, Hakan Erdem3 and Salih Pay3, 1Gulhane School of Medicine, Ankara, Turkey, 2Rheumatology, Gulhane School of Medicine, Ankara, Turkey, 3Division of Rheumatology, Gulhane School of Medicine, Ankara, Turkey

    Background/Purpose: The most frequent underlying diseases responsible for AA amyloidosis worldwide are rheumatoid arthritis, juvenile idiopathic arthritis and ankylosing spondylitis, while familial Mediterranean fever (FMF)…
  • Abstract Number: 1208 • 2013 ACR/ARHP Annual Meeting

    Canakinumab In Patients With FMF

    Serdal Ugurlu1, Emire Seyahi1, Gulen Hatemi2, Ayse Hacioglu2 and Huri Ozdogan2, 1Division of Rheumatology,Department of Medicine, Cerrahpasa Medical Faculty, University of Istanbul, Istanbul, Turkey, 2Division of Rheumatology, Department of Internal Medicine, Cerrahpasa Medical Faculty, University of Istanbul, Istanbul, Turkey

    Background/Purpose: In a recent pilot study, it was reported that Canakinumab reduced the frequency of attacks in 9 patients with Familial Mediterranean Fever (FMF) resistant…
  • Abstract Number: 1209 • 2013 ACR/ARHP Annual Meeting

    Starting Time Of Inflammatory Attacks In Patients With Familial Mediterranean Fever

    Feyza Berktas1, Nilufer Alpay Kanitez1, Bahtiyar Toz1, Oguz Kaan Bakkaloglu1, Burak Erer2 and Ahmet Gul1, 1Department of Internal Medicine, Rheumatology Division, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey, 2Department of Internal Medicine, Rheumatology Division, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey

    Background/Purpose: Familial Mediterranean fever (FMF), the most common form of the hereditary autoinflammatory diseases, is characterized by recurrent self-limiting attacks of fever and/or serositis accompanied…
  • Abstract Number: 1210 • 2013 ACR/ARHP Annual Meeting

    Epicardial Adipose Tissue and Atherosclerosis In Patients With Familial Mediterranean Fever

    Adem Kucuk1, Yalcin Solak2, Hakan Akilli3, Oguzhan Yildirim3, Ibrahim Guler4, Ramazan Ucar5, Alpay Aribas3, Orhan Ozbek6, Mehmet Kayrak3 and Recep Tunc1, 1Necmettin Erbakan University, Meram Medical Faculty,Division of Rheumatology, Konya, Turkey, 2Karaman State Hospital, Division of Nephrology, Karaman, Turkey, 3Necmettin Erbakan University, Division of Cardiology, Konya, Turkey, 4Konya Research and Education Hospital, Division of Radiology, Konya, Turkey, 5Konya Education and Research Hospital, Department ofInternal Medicine, Konya, Turkey, 6Necmettin Erbakan University, Division of Radiology, Konya, Turkey

    Background/Purpose : Familial Mediterranean Fever (FMF) is a chronic autosomal recessive hereditary disease characterized by episodic attacks of fever and inflammation of serosal and synovial…
  • Abstract Number: 1211 • 2013 ACR/ARHP Annual Meeting

    Adult Autoinflammatory Phenotypes Associated With Heterozygous MEFV Mutations: A Continuum of Familial Mediterranean Fever?

    Qingping Yao, Rheumatic and Immunologic Dis, Cleveland Clinic, Cleveland, OH

    Background/Purpose: Familial Mediterranean fever (FMF) is traditionally regarded as an autosomal recessive disease characterized by periodic fever, serositis, erysipelas-like erythema and good response to colchicine. The…
  • Abstract Number: 1212 • 2013 ACR/ARHP Annual Meeting

    Are Different Disease Subtypes With Distinct Clinical Expression Present In Familial Mediterranean Fever: Results Of a Cluster Analysis

    Servet Akar1, Timucin Kasifoglu2, Dilek Solmaz1, Sule Yasar Bilge2, Ismail Sari1 and Mehmet Tunca3, 1Rheumatology, Dokuz Eylul University School of Medicine, Izmir, Turkey, 2Rheumatology, Eskisehir Osmangazi University School of Medicine, Eskisehir, Turkey, 3Internal Medicine, Dokuz Eylul University School of Medicine, Izmir, Turkey

    Background/Purpose: Familial Mediterranean fever (FMF) is an auto-inflammatory disorder characterized by self limited attacks of fever and serositis. The disease expression may be different in…
  • Abstract Number: 1213 • 2013 ACR/ARHP Annual Meeting

    Low-Penetrance NLRP3-Variants

    Theresa Endres1, Ferdinand Hofer1, Raphaela T. Goldbach-Mansky2, Hal M. Hoffman3, Norbert Blank4, Karoline Krause5, Christoph Rietschel6, Gerd Horneff7, Peter Lohse8 and Jasmin B. Kuemmerle-Deschner9, 1Department of Pediatrics, Division of Pediatric Rheumatology, University Hospital Tuebingen, Tuebingen, Germany, 2Translational Autoinflammatory Diseases Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD, 3Division of Allergy, Immunology and Rheumatology, University of California at San Diego, La Jolla, CA, 4University of Heidelberg, Heidelberg, Germany, 5Dept. of Dermatology and Allergy, Allergie-Centrum-Charité, Charité – Universitätsmedizin Berlin, Germany, Berlin, Germany, 6Kinder- und Jugendrheumatologie, Clementine-Kinderhospital, Frankfurt, Germany, 7Department of Pediatrics, Asklepios Klinik Sankt Augustin, Sankt Augustin, Germany, 8Institut für Laboratoriumsmedizin und Humangenetik, Singen, Germany, 9University Hospital Tuebingen, Tuebingen, Germany

    Background/Purpose: Cryopyrin-associated periodic syndrome (CAPS) presents as rare, autosomal dominant disease spectrum, due to mutations in the NLRP3-gene which lead to excessive interleukin-1 (IL-1) release.…
  • Abstract Number: 1174 • 2013 ACR/ARHP Annual Meeting

    Impact Of Bariatric Surgery On Serum Urate Targets in People With Morbid Obesity and Diabetes: A Prospective Longitudinal Study

    Nicola Dalbeth1, Peggy Chen2, Marie White3, Gregory Gamble4, Caran Barratt-Boyes2, Peter J. Gow5 and Brandon Orr-Walker2, 1Medicine, University of Auckland, Auckland, New Zealand, 2Counties Manukau District Health Board, Auckland, New Zealand, 3CCRep, Auckland, New Zealand, 4Department of Medicine, University of Auckland, Auckland, New Zealand, 5Rheumatology Dept, Middlemore Hospital, Auckland, New Zealand

    Background/Purpose: Weight loss leads to reduced serum urate (SU) in people with obesity. However, the clinical relevance of such reductions in SU are unknown. This…
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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.

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