ACR Meeting Abstracts

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Abstracts tagged "dermatomyositis"

  • Abstract Number: 1347 • 2018 ACR/ARHP Annual Meeting

    A Semi-Quantitative Whole Body Magnetic Resonance Imaging Assessment Tool to Define Musculoskeletal Abnormalities in Patients with Idiopathic Inflammatory Myopathies

    Sara Faghihi-Kashani1, Lisa G. Rider2, David Bluemke3, Ashkan Malayeri4, Evrim Turkbey4, Joseph Shrader5, John McGrath6, Elizabeth Jones7, Jamie Marco8, Frederick W. Miller9 and Adam Schiffenbauer10, 1Environmental Autoimmunity Group, National Institute of Environmental Health, Bethesda, MD, 2Environmental Autoimmunity Group, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, 3Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison, WI, 4Radiology and Imaging Sciences, National Institutes of Health, Bethesda, MD, 5Rehabilitation Medicine, National Institutes of Health, Bethesda, MD, 6Social and Scientific Systems, Inc., Durham, NC, 7Radiology and Imaging Sciences, National Institutes of Health Clinical Center, Bethesda, MD, 8Radiology and Imaging Sciences National Institutes of Health, Bethesda, MD, 9Environmental Autoimmunity Group, NIEHS, NIH, Bethesda, MD, 10NIEHS, NIH, Bethesda, MD

    Background/Purpose: There is a lack of standardized methodology for assessing whole body MRI (WBMRI) in idiopathic inflammatory myopathy (IIM) patients. This leads to difficulty in…
  • Abstract Number: 1382 • 2018 ACR/ARHP Annual Meeting

    Evaluating Results of an Interferon-γ Release Assay in Patients with Autoimmune Skin Disease on Hydroxychloroquine

    Rebecca Gaffney1 and Victoria P. Werth2, 1Dermatology, University of Pennsylvania, Philadelphia, PA, 2Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA

    Background/Purpose: QuantiFERON-TB Gold is commercial interferon-γ release assay used to screen patients for tuberculosis before starting or while on immunosuppressive therapies. Clinical studies on efficacy…
  • Abstract Number: 1851 • 2018 ACR/ARHP Annual Meeting

    Physical Function Trajectories in Children with Juvenile Myositis

    Kaveh Ardalan1, Elizabeth L. Gray2, Julia (Jungwha) Lee2, Madison L. Wolfe3, Gabrielle A. Morgan4 and Lauren M. Pachman5, 1Departments of Pediatrics and Medical Social Sciences, Division of Rheumatology, Northwestern University Feinberg School of Medicine/Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, 2Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 3Creighton University School of Medicine, Omaha, NE, 4Cure JM Program of Excellence in Myositis Research, Stanley Manne Children’s Research Institute, affiliated with Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL, 5Cure JM Program of Excellence in Juvenile Myositis Research, Stanley Manne Children’s Research Institute, affiliated with Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL

    Background/Purpose: Juvenile myositis (JM) is an inflammatory disease that causes muscle weakness, skin rashes, and significant deconditioning. Little is known about long-term resolution of physical…
  • Abstract Number: 2163 • 2018 ACR/ARHP Annual Meeting

    Prevalence and Incidence of Idiopathic Inflammatory Myopathies in Korea:a Nationwide Population-Based Study over 10 Years

    Yoon-Kyoung Sung1, Hyoungyoung Kim2, Jisun Myung3, Eunwoo Nam3, Sun-Young Jung4, Eun Jin Jang5, Dae-Hyun Yoo6 and Soo-Kyung Cho2, 1Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South), 2Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South), 3Biostatistical Consulting and Research Lab, Medical Research Collaborating Center, Hanyang University, Seoul, Korea, Republic of (South), 4College of Pharmacy, Chung-Ang University, Seoul, Korea, Republic of (South), 5Information Statistics, Andong National University, Andong-si, Korea, Republic of (South), 6Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South)

    Prevalence and Incidence of idiopathic Inflammatory Myopathies in Korea: a Nationwide Population-based Study over 10 yearsYoon-Kyoung Sung1, Hyoungyoung Kim1, Jisun Myung2, Eunwoo Nam2, Sun-young Jung3,…
  • Abstract Number: 2169 • 2017 ACR/ARHP Annual Meeting

    A Two-Center Experience with Rituximab in Patients with Primary Idiopathic Myositis and Overlap Myositis: A Retrospective Observational Study

    Kimberly A. Rehberg1, Morgan M. Brown2, Anna K. Shmagel1, Elie Gertner3 and Jerry A. Molitor1, 1Rheumatic & Autoimmune Diseases, University of Minnesota, Minneapolis, MN, 2HealthPartners Institute, St. Paul, MN, 3Section of Rheumatology, Regions Hospital, St. Paul, MN

    Background/Purpose: Recent studies have suggested the possible benefit of the anti-CD20 agent Rituximab (RTX) in autoimmune myositis (AIM). As AIM is a rare and heterogeneous…
  • Abstract Number: 2170 • 2017 ACR/ARHP Annual Meeting

    Near Patient Detection of Anti-MDA5 Antibodies Using Photonic Ring Immunoassays

    Makoto Miyara1, Rémi Chieze2, Yurdagul Uzunhan3, Jean- Luc Charuel4, Pascale Ghillani-Dalbin4, Sasi Mudumba5, Alice Wu5, Hilario Nunes3, Zahir Amoura6, Rufus Burlingame5 and Lucile Musset1, 1Department of immunology, Pitié-Salpêtrière Hospital (AP-HP), Paris, France, 2department of Immunology, Pitié-Salpêtrière Hospital (AP-HP), Paris, France, 3Pulmonary diseases department, Avicenne Hospital (AP-HP), Bobigny, France, 4Department of Immunology, Pitié-Salpêtrière Hospital (AP-HP), Paris, France, 5Genalyte Inc., San Diego, CA, 6Hôpital Pitié-Salpêtrière, AP-HP, UPMC Univ Paris 06 & French National Reference Center For Systemic Lupus and Antiphospholipid Syndrome, Paris, France

    Background/Purpose: The presence of anti-MDA5 antibody is associated with amyopathic dermatomyositis and/or rapidly progressive interstitial lung disease that can be fatal.In the latter case, it…
  • Abstract Number: 851 • 2017 ACR/ARHP Annual Meeting

    Autoantibodies Predict Long Term Survival in Myositis Associated Interstitial Lung Disease

    Silvia Martinez1, Rohit Aggarwal2,3 and Chester V. Oddis4, 1Internal Medicine, UPMC, pittsburgh, PA, 2Department of Medicine / Rheumtology, University of Pittsburgh Medical Center, Pittsburgh, PA, 3Rheumatology, University of Pittsburgh, Pittsburgh, PA, 4Rheumatology/Clinical Immunology, Unviersity of Pittsburgh/University of Pittsburgh Medical Center, Pittsburgh, PA

    Background/Purpose: Interstitial lung disease (ILD) significantly contributes to morbidity and mortality in adult polymyositis (PM) and dermatomyositis (DM). Myositis associated autoantibodies (MAA) are associated with…
  • Abstract Number: 2172 • 2017 ACR/ARHP Annual Meeting

    Clinical Significance of Serum Levels of Anti-Transcriptional Intermediary Factor 1-γ Antibody in Patients with Dermatomyositis

    Nobuaki Ikeda, Yukie Yamaguchi, Miwa Kanaoka, Yasushi Ototake, Eriko Takebayashi and Michiko Aihara, Department of Environmental Immuno-Dermatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan

    Background/Purpose: Dermatomyositis (DM) is an autoimmune inflammatory disease characterized by skin eruptions and myositis, which is occasionally complicated by interstitial lung disease (ILD) or concomitant…
  • Abstract Number: 854 • 2017 ACR/ARHP Annual Meeting

    Predictive Modeling of Mortality in Polymyositis/Dermatomyositis Patients with Interstitial Lung Disease Based on Combination of Serum Myositis-Specific Autoantibodies and Conventional Biomarkers

    Takahisa Gono1, Kenichi Masui2, Yasushi Kawaguchi3, Kei Ikeda4, Atsushi Kawakami5, Maasa Tamura6, Yoshinori Tanino7, Takahiro Nunokawa8, Yuko Kaneko9, Shinji Sato10, Katsuaki Asakawa11, Naoshi Nishina9 and Masataka Kuwana1, 1Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, 2Department of Anesthesiology, National Defense Medical College School of Medicine, Tokorozawa, Japan, 3Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 4Department of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan, 5Department of Immunology and Rheumatology, Division of Advanced Preventive Medical Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki City, Japan, 6Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan, 7Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan, 8Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan, 9Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 10Division of Rheumatology, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan, 11Division of Respiratory Medicine, Niigata University Medical and Dental Hospital, Niigata, Japan

    Background/Purpose: Interstitial lung disease (ILD) is one of the leading causes of mortality in patients with polymyositis or dermatomyositis (PM/DM). Since clinical courses and outcomes…
  • Abstract Number: 2173 • 2017 ACR/ARHP Annual Meeting

    Characteristics Unique to MDA5 and Anti-Ro/SSA-52 Kda Dual Antibody Positive Patients with Inflammatory Myopathies

    Juan J Maya, Olga Pinkston, Florentina Berianu, Benjamin Wang and Andy Abril, Rheumatology, Mayo Clinic Florida, Jacksonville, FL

    Background/Purpose: The anti-melanoma differentiation-associated gene 5 antibody (MDA5) was recently classified as a myositis-specific antibody (MSA), and has been associated with rapidly progressive interstitial lung…
  • Abstract Number: 1732 • 2017 ACR/ARHP Annual Meeting

    The Characteristic T-Cell Receptor-Mediated Signaling of Peripheral Blood T Cells in Dermatomyositis and Polymyositis

    Yasuhiro Shimojima1, Dai Kishida2 and Yoshiki Sekijima2, 1Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, Japan, 2Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, Japan

    Background/Purpose: In dermatomyositis (DM) and polymyositis (PM), the characteristics of T cell expression in peripheral blood have been previously described; especially, decreased expression of interferon-γ…
  • Abstract Number: 2613 • 2017 ACR/ARHP Annual Meeting

    Antimalarial Drug Toxicities in Rheumatic Skin Disease Patients

    Lavanya Mittal1, Lingqiao Zhang2, Rui Feng2 and Victoria Werth1, 1Department of Dermatology, Corporal Michael J. Crescenz VAMC, Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, 2Department of Biostatistics and Epidemiology at the Hospital of the University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Although existing evidence demonstrates the efficacy of antimalarials for rheumatic skin disease, the safety of these medications, and particularly quinacrine, remain debated. Quinacrine may…
  • Abstract Number: 1801 • 2017 ACR/ARHP Annual Meeting

    Quantifying Clinical and Economic Outcomes Associated with Chronic Corticosteroid Exposure in a US Population

    J. Bradford Rice1, Alan White1, Andrea Lopez1, Aneesha Wagh1, Yimin Qin2, Ghaith Mitri2, Laura Bartels-Peculis2, Gosia Ciepielewska2 and Winnie Nelson3, 1Analysis Group, Inc., Boston, MA, 2Mallinckrodt Pharmaceuticals, Hampton, NJ, 3Health Economics and Outcomes Research, Mallinckrodt Pharmaceuticals, Hampton, NJ

    Background/Purpose:  Corticosteroids (CS) are commonly used for rheumatologic conditions, and known to cause systemic adverse events (AEs), particularly when used at high doses for prolonged…
  • Abstract Number: 2130 • 2017 ACR/ARHP Annual Meeting

    Joint Manifestations in Patients Diagnosed with Idiopathic Inflammatory Myopathy: Multicenter Registry on Inflammatory Myositis from the Rheumatology Society in Madrid, Spain

    Larissa Valor1, Diana Hernández-Flórez2, Julia Martínez-Barrio3, Beatriz E. Joven4, Laura Nuño5, Carmen Larena6, Irene Llorente7, Carmen Barbadillo8, Paloma Garcia De La Peña9, Lucía Ruíz Gutiérrez10, Henry Moruno Cruz11, Tatiana Cobo-Ibáñez12, Raquel Almodóvar González13, Leticia Lojo14, MARIA JESUS GARCIA DE YEBENES Y PROUS15 and Francisco Javier López Longo16, 1Rheumatology, Hospital General Universitario Gregorio Marañón, Madrid, Spain, 2Rheumatology, Gregorio Marañón University General Hospital, Madrid, Spain, 3Servicio de Reumatologia, Hospital General Universitario Gregorio Marañón, Madrid, Spain, 4Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Spain, 5Servicio de Reumatologia, Hospital Universitario La Paz, Madrid, Spain, 6Hospital Gregorio Marañón, Madrid, Spain, 7Rheumatology, H.U. La Princesa, Madrid, Spain, 8Hospital Universitario Puerta de Hierro, Madrid, Spain, 9Rheumatology, Hospital Madrid Norte Sanchinarro, Madrid, Spain, 10Pediatric Rheumathology Unit, University Children's Hospital Niño Jesús, Madrid, Spain, 11University Hospital Príncipe de Asturias, Immune System Diseases, Rheumatology department, Alcalá de Henares, Madrid, Spain, 12Hospital Universitario Reina Sofía, Universidad Europea de Madrid, Madrid, Spain, 13Rheumatology Unit, Hospital Universitario Fundación Alcorcón, Madrid, Spain, 14Rheumatology, Hospital Universitario La Paz, Spain, Spain, 15Institute for Musculoskeletal Health, Madrid, Spain, 16Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain

    Background/Purpose: Idiopathic inflammatory myopathies (IIM) comprise a heterogeneous group of autoimmune conditions characterized by muscle non-suppurative inflammation, progressive muscle weakness and a variety of extra-muscular…
  • Abstract Number: 2132 • 2017 ACR/ARHP Annual Meeting

    Angiogenesis and VEGF-Expressing Cells Are Identified Predominantly in the Fascia Rather Than the Muscle in the Early Phase of Dermatomyositis

    Ken Yoshida1,2, Haruyasu Ito1, Kazuhiro Furuya1, Taro Ukichi1, Kentaro Noda1 and Daitaro Kurosaka1, 1Division of Rheumatology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan, 2Internal Medicine, Jikei University School of Medicine, Tokyo, Japan

    Background/Purpose: We previously showed that fasciitis is a frequent manifestation of the disease in dermatomyositis (DM) but not in polymyositis (PM) and that DM-associated fasciitis…
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