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Abstracts tagged "dermatomyositis"

  • Abstract Number: 1098 • 2018 ACR/ARHP Annual Meeting

    Comparative Analysis of the Total Proteome of the Skin Lesions from Cutaneous Lupus Erythematosus (CLE) and Dermatomyositis (DM)

    Timothy B. Niewold1, Alexander Meves2, Julia S. Lehman3, Karin Popovic-Silwerfeldt4, Cristine Charlesworth5, Marie Wahren-Herlenius6, Elisabet Svenungsson7 and Vilija Oke8, 1Colton Center for Autoimmunity, New York University, New York, NY, 2Cancer Cenetr, Dermatology, Mayo Clinic, Rochester, MN, 3Pathology and Dermatology, Mayo Clinic College of Medicine and Science, Rochester, MN, MN, 4Department of Clinical Sciences, Dermatology Clinic, Danderyds Hospital,, Stockholm, Sweden, 5Mayo Clinic, Rochester, MN, 6Unit of Rheumatology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden, 7Division of Rheumatology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden, Stockholm, Sweden, 8Department of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden

    Background/Purpose: Cutaneous lupus erythematosus (CLE) and dermatomyositis (DM) are autoimmune diseases. The histopathological pattern of skin involvement can be similar, i.e. interface dermatitis, but the…
  • Abstract Number: 1331 • 2018 ACR/ARHP Annual Meeting

    Moving from Dermatomyositis Associated with Anti-Melanoma Differentiation-Associated Gene 5 Antibody to Anti-Melanoma Differentiation-Associated Gene 5 Syndrome

    Yves Allenbach1, Yurdagul Uzunhan2, Ségolène Toquet3, Gaëlle Leroux4, Laure Gallay5, Aude Rigolet6, Baptiste Hervier6, Nicolas Champtiaux6, Mathieu Vautier6, Perrine Guillaume6, Nicolas Limal7, Alain Meyer8, Christophe Deligny9, Bernard Bonnotte10, Hervé Devilliers11, Sylvain Audia12, Maxime Samson13, Amélie Servettaz14, Nathalie Costedoat15, David Saadoun16, elisabeth diot17, Alice Berezne18, Arsène Mékinian19, Kuberaka Mariampillai20, Hilario Nunes2 and Olivier Benveniste6, 1Internal Medicine and Clinical Immunology, Sorbonne University - Assistance Public - Hopitaux de Paris, Pitié-Salpêtrière University Hospital, Paris, France, 2Pulmonary diseases department, Avicenne Hospital (AP-HP), Bobigny, France, 3Sorbonne Universités, UPMC Univ Paris 06, INSERM UMRS_974, CNRS FRE 3617, Center of Research in Myology., Paris, France, 4Internal Medicine, Pitié-Salpêtrière University Hospital, Paris, France, 5Internal Medicine, Université de Lyon - CHU Lyon, Lyon, France, 6Department of Internal Medicine and Clinical Immunology and Inflammation-Immunopathology-Biotherapy Department (I2B), Pitié-Salpêtrière University Hospital, Assistance Publique-Hôpitaux de Paris, East Paris Neuromuscular Diseases Reference Center, Paris, France, 7Internal Medicine, APHP - Henri Mondor Hospital, Paris, France, 815Département de Rhumatologie, Centre de Référence des Maladies Auto-immunes Rares, Hôpitaux Universitaires de Strasbourg, Strasbourg, France, 9Zobda Quitman Hospital, Rheumatology and Internal Medicine, Fort de France, Martinique, 10Dijon, Dijon, France, 11Service de Médecine Interne et Maladies Systémiques, CHU de Dijon, Dijon, France, 12Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, CHU de Dijon; INSERM, UMR1098, University of Bourgogne Franche-Comté, FHU INCREASE, Dijon, France, 13Dijon University Hospital, Dijon, France, 14Internal Medicine, CHU - Reims University, Reims, France, 15Internal Medicine, Paris Descartes Université - APHP, paris, France, 16Sorbonne Universités, UPMC Univ Paris 06, UMR 7211, and Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75005, Paris, France; INSERM, UMR_S 959, F-75013, Paris, France; CNRS, FRE3632, F-75005, Paris, France; AP-HP, Groupe Hospitalier, Paris, France, 17Internal Medicine, Université Tours - CHU, Tours, France, 18Internal Medicine, CH Annecy, Annecy, France, 19Service de médecine interne. Hôpital Saint-Antoine., Paris, France, 20Département de Médecine Interne et Immunologie Clinique, Centre de Référence des Maladies Neuro-Musculaires Paris Est, Assistance Publique – Hôpitaux de Paris (AP-HP), Hôpital Universitaire Pitié-Salpêtrière, Paris, France

    Background/Purpose: Dermatomyositis (DM) is a heterogenous group of diseases ranging from skin limited disorders to non-specific auto-immune diseases with patients suffering from additional extra-cutaneous manifestations.…
  • Abstract Number: 1344 • 2018 ACR/ARHP Annual Meeting

    Anti-Splicing Factor Proline/Glutamine-Richautoantibodies Rarely Co-Exist with Anti-Melanoma Differentiation-Associated Gene 5 Autoantibodies in a Cohort of Dermatomyositis Patients from the United States

    Yuji Hosono1, Iago Pinal-Fernandez1, Katherine Pak1, Jemima Albayda2, Eleni Tiniakou3, Julie J. Paik4, Christopher A. Mecoli5, Sonye K. Danoff6, Lisa Christopher-Stine6 and Andrew Mammen1,7, 1National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Johns Hopkins University School of Medicine, Baltimore, MD, 3Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 4Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 5Internal Medicine/Rheumatology, Johns Hopkins University, Baltimore, MD, 6Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 7Neurology, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Anti-melanoma differentiation-associated gene 5 (MDA5) autoantibodies are common among Japanese dermatomyositis (DM) and clinically amyopathic DM (CADM) patients who develop rapidly progressive interstitial lung…
  • Abstract Number: 2158 • 2017 ACR/ARHP Annual Meeting

    HLA-DRB1*04:03/*04:06 As the Genetic Susceptibility to Dermatomyositis Positive for Anti-Transcriptional Intermediary Factor 1-γ Antibody in Japanese Population

    Yukie Yamaguchi1, Masataka Kuwana2, Miwa Kanaoka1, Tomoya Watanabe1, Naoko Okiyama3, Takahisa Gono2, Masanari Kodera4, Takeshi Kambara5, Yasuhito Hamaguchi6, Mariko Seishima7, Kazuhiko Takehara6, Manabu Fujimoto3 and Michiko Aihara1, 1Department of Environmental Immuno-Dermatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan, 2Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, 3Department of Dermatology, University of Tsukuba, Tsukuba, Japan, 4Department of Dermatology, Japan Community Health care Organization Chukyo Hospital, Nagoya, Japan, 5Department of Dermatology, Yokohama City University Medical Center, Yokohama, Japan, 6Department of Dermatology, Kanazawa University, Kanazawa, Japan, 7Department of Dermatology, Gifu University Graduate School of Medicine, Gifu, Japan

    Background/Purpose: Dermatomyositis (DM) is characterized by inflammation of the skin and skeletal muscle, and is occasionally complicated by interstitial lung disease or concomitant malignancy. It…
  • Abstract Number: 2159 • 2017 ACR/ARHP Annual Meeting

    Dermatomyositis Acute Onset/Flares Following Ingestion of Isalean® Herbal Supplement: Clinical and Immunostimulatory Findings

    Majid Zeidi1,2, Peter B Chansky1,2 and Victoria P Werth3,4, 1Department of Dermatology, Corporal Michael J. Crescenz VAMC, PHILADELPHIA, PA, 2Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, 3University of Pennsylvania and the VA Medical Center, Philadelphia, PA, 4Department of Dermatology, Corporal Michael J. Crescenz VAMC, Philadelphia, PA

    Background/Purpose : The use of complementary and alternative medicine (CAM) has gained popularity in the United States over the last few decades. Herbal supplements have…
  • Abstract Number: 2164 • 2017 ACR/ARHP Annual Meeting

    Prognostic Factors in Polymyositis/ Dermatomyositis Patients with Anti-Synthetase Antibodies

    Masashi Taniguchi1, Ran Nakashima1, Nobuo Kuramoto1, Kosaku Murakami1, Motomu Hashimoto2, Hajime Yoshifuji1, Masao Tanaka2, Koichiro Ohmura1 and Tsuneyo Mimori1, 1Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 2Department of Advanced Medicine for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan

    Background/Purpose: Anti-aminoacyl-tRNA synthetase antibodies (Abs), which mainly consists of anti-Jo1, PL-7, PL-12, EJ, OJ and KS, are the most common myositis-specific autoantibodies (MSAs). It has…
  • Abstract Number: 2165 • 2017 ACR/ARHP Annual Meeting

    Easily Obtainable Myositis Autoantibody Panel Predictive Factors

    Jason Weiner1, Ryan Jessee2, Amanda M. Eudy3, Robert T. Keenan4, Michael Datto5 and Lisa Criscione-Schreiber6, 1Department of Medicine, Division of Rheumatology and Immunology, Duke University Medical Center, Durham, NC, 2Department of Medicine, Division of Rheumatology and Immunology, Duke University, Durham, NC, 3Duke University Medical Center, Chapel Hill, NC, 4Rheumatology, NYU-HJD, New York, NY, 5Department of Pathology, Duke University, Durham, NC, 6Internal Medicine, Duke University Medical Center, Durham, NC

    Background/Purpose: Myositis autoantibodies have diagnostic, therapeutic and prognostic implications, but their utility in clinical practice is unclear.  We aimed to describe our institutionÕs ordering practices…
  • 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…
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