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  • Abstract Number: 216 • 2012 ACR/ARHP Annual Meeting

    Clinical and Serological Associations of Malignancy in Adult Patients with Polymyositis and Dermatomyositis

    Yuji Hosono1, Ran Nakashima1, Yoshitaka Imura2, Naoichiro Yukawa3, Hajime Yoshifuji1, Motomu Hashimoto4, Koichiro Ohmura5, Takao Fujii6 and Tsuneyo Mimori1, 1Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 2Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan, 3Department of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan, 4The Control for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 5Rheumatology & Clin Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 6Department of the Control for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan

    Background/Purpose: Polymyositis (PM) and dermatomyositis (DM) are systemic connective tissue disorders, which are often associated with internal malignancy. Several studies have reported the association between…
  • Abstract Number: 217 • 2012 ACR/ARHP Annual Meeting

    Myositis-Associated Usual Interstitial Pneumonia Has Better Survival Than Idiopathic Pulmonary Fibrosis

    Christine McBurney1, Rohit Aggarwal2, Kevin Gibson3, Kathleen Lindell4, Carl Fuhrman5, Diane Koontz6, Frank Schneider7, Naftali Kaminski4 and Chester V. Oddis8, 1Rheumatology, University of Pittsburgh, Pittsburgh, PA, 2Medicine, University of Pittsburgh, Pittsburgh, PA, 3Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, 4University of Pittsburgh Dorothy P. & Richard P. Simmons Center for Lung Disease, Pittsburgh, PA, 5Radiology, Division of Thoracic Imaging, University of Pittsburgh, Pittsburgh, PA, 6Department of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, 7Anatomic Pathology Department, Pittsburgh, PA, 8Rheum/Clinical Immunology, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: Usual interstitial pneumonia associated with idiopathic pulmonary fibrosis (IPF-UIP) has a poor prognosis with a median survival of 3 years. It is unknown whether…
  • Abstract Number: 218 • 2012 ACR/ARHP Annual Meeting

    Proteomics Study of a Phase 1b Trial with an Anti-IFN-α Monoclonal Antibody Indicates Association of Soluble Interleukin 2 Receptor with Type I Interferon Activity in Patients with Dermatomyositis or Polymyositis

    Xiang Guo1, Brandon W. Higgs1, Wei Zhu2, Yihong Yao1 and Wendy White3, 1Translational Sciences, MedImmune, LLC, Gaithersburg, MD, 2Translational Science, MedImmune, LLC, Gaithersburg, MD, 3Translational Sciences, MedImmune, Gaithersburg, MD

    Background/Purpose: To evaluate downstream effects of an anti-IFN-α monoclonal antibody (mAb) in adult dermatomyositis (DM) and polymyositis (PM) patients using serum proteomics and gene expression…
  • Abstract Number: 219 • 2012 ACR/ARHP Annual Meeting

    Significant Functional Improvement Using Aggressive Immunomodulatory Therapy in Patients with Inflammatory Myopathy and Interstitial Lung Disease

    Ramona Mihu1, Roger D. Rossen2, Jovan Popovich3 and Sandra L. Sessoms1, 1Immunology, Allergy and Rheumatology, Baylor College of Medicine, Houston, TX, 2Department of Pathology & Immunology, Baylor College of Medicine, Houston, TX, 3Medicine/Rheumatology, The Methodist Hospital, Houston, TX

    Background/Purpose: Pulmonary disease in patients with idiopathic inflammatory myopathies, polymyositis (PM), dermatomyositis (DM), and clinically amyopathic dermatomyositis (CADM) is a major cause of morbidity. Approximately…
  • Abstract Number: 220 • 2012 ACR/ARHP Annual Meeting

    Efficacy of Rituximab for the Treatment of Refractory Inflammatory Myopathies Associated with Anti-Histidyl-tRNA Synthetase Antibodies (the FORCE Jo1 Study)

    Yves Allenbach1, Aude Rigolet2, Marguerite Guiguet3, Isabelle Marie4, Eric Hachulla5, Dominique Farge6, Kuberaka Mariampillai7, Serge Jacquot8, Fabienne Jouen9, Olivier Boyer10, Lucile Musset11, Serge Herson7 and Olivier Benveniste12, 1Internal Medicine Dpt 1, Pitié-Salpêtrière Hospital, APHP, Paris, France, 2Department: inflammation, immunopathology and biotherapy (DHU i2B), Assistance Publique - Hôpitaux de Paris, Pitié-Salpêtrière University Hospital, Paris, France, 3Biostatistique, Pitie-Salpetriere Hospital, Paris, France, 4Service de médecine interne, CHU de Rouen, Rouen, France., Rouen, France, 5Department of Internal Medicine, Claude Huriez University Hospital, Lille, France, 6Medicine, EBMT, Paris, France, 7Department: inflammation, immunopathology and biotherapy (DHU i2B), Assistance Publique - Hôpitaux de Paris, Pitié-Salpêtrière University, Paris, France, 8INSERM U905, University of Rouen, Rouen, France, 9Immunology, Rouen University Hospital, Rouen Cedex, France, 10Immunology, INSERM U905, University of Rouen, Rouen, France, 11Laboratoire d'Immunochimie, CHU Pitié-Salpêtrière, Paris, France, 12Internal Medecine Dpt 1, Pitié-Salpêtrière Hospital, APHP, Paris, France

    Background/Purpose: anti-histidyl-tRNA synthetase (anti-Jo1) antibodies are found in approximately 25–30% of patients with idiopathic inflammatory myopathies, frequently in the frame of an anti-synthetase syndrome characterized…
  • Abstract Number: 221 • 2012 ACR/ARHP Annual Meeting

    Expanding the Clinical and Serological Spectrum of MDA5-Associated Dermatomyositis

    John C. Hall1, Livia Casciola Rosen1, Sonye K. Danoff2, Lesly-Anne Samedy3 and Lisa Christopher-Stine4, 1Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 2Medicine/Pulmonary, Johns Hopkins University, Baltimore, MD, 3Division of Rheumatology, Johns Hopkins University, Baltimore, MD, 4Medicine and Neurology, Johns Hopkins University, Baltimore, MD

    Background/Purpose: Dermatomyositis (DM) is a heterogeneous systemic disease with specific autoantibodies (Abs) which correlate with unique clinical phenotypes.  Melanoma differentiation-associated gene 5 (MDA5) Abs have…
  • Abstract Number: 222 • 2012 ACR/ARHP Annual Meeting

    Lung Nodules in Patients with Idiopathic Inflammatory Myopathies

    Laura C. Cappelli1, Andrew L. Mammen2, Sonye K. Danoff3, Grant H. Louie4, Thomas E. Lloyd5 and Lisa Christopher-Stine6, 1Ste 4500, Johns Hopkins University, Baltimore, MD, 2NIAMS, NIH, Bethesda, MD, 3Medicine/Pulmonary, Johns Hopkins School of Medicine, Baltimore, MD, 4Rheumatology, Johns Hopkins University, Baltimore, MD, 5Neurology, Johns Hopkins, Baltimore, MD, 6Medicine and Neurology, Johns Hopkins University, Baltimore, MD

    Background/Purpose: The idiopathic inflammatory myopathies are associated with an increased incidence of malignancy, and interstitial lung disease (ILD) has been reported in as many as…
  • Abstract Number: 223 • 2012 ACR/ARHP Annual Meeting

    High Prevalence and Clustering Over Time of Anti-PL-7 Autoantibody-Positive Idiopathic Inflammatory Myopathies

    Yoshioki Yamasaki1, Minoru Satoh2, Hidehiro Yamada1, Machiko Mizushima1, Takahiro Okazaki1, Hiroko Nagafuchi1, Seido Ooka3, Tomohiko Shibata1, Hiromasa Nakano4, Hitoshi Ogawa1, Kohei Azuma1, Akihiko Maeda1, Hirofumi Mitomi1, Tomofumi Kiyokawa1, Kosei Tsuchida1, Hidenori Mikage1, Jason Y.F. Chan2 and Shoichi Ozaki1, 1Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan, 2Medicine, University of Florida, Gainesville, FL, 3St. Marianna University School of Medicine, Kawasaki, Japan, 4Division of Rheumatology and Allergy, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan

    Background/Purpose:  Unusually high prevalence of autoantibodies to threonyl tRNA (PL-7) [17% in polymyositis/dermatomyositis (PM/DM) associated with lower levels of serum creatine kinase (CK) and milder…
  • Abstract Number: 224 • 2012 ACR/ARHP Annual Meeting

    Standardized Incidence Ratios and Predictors of Malignancies in 215 Southern Chinese Patients with Inflammatory Myopathies

    Chi Chiu Mok1, Chi Hung To1, ML Yip2 and King Yee Ying3, 1Medicine, Tuen Mun Hospital, Hong Kong, Hong Kong, 2Division of Rheumatology, Department of Medicine, Kwong Wah Hospital, Kowloon, Hong Kong, 3Department of Medicine, Princess Margaret Hospital, Hong Kong, Hong Kong

    Background/Purpose: To examine the standardized incidence ratios (SIRs) and predictive factors for malignancy in a cohort of southern Chinese patients with inflammatory myopathies (IM). Methods:…
  • Abstract Number: 225 • 2012 ACR/ARHP Annual Meeting

    Polymyositis in HIV+ Patients Is Associated to Uncontrolled Viral Load

    Yves Allenbach1, Odile Dubourg2, Thierry Maisonobe2, Anthony Behin3, Charles Duyckaerts2, Guillaume Breton4, Olivier Fain5, Marie-Caroline Meyhoas6, Catherine Leport7, Marc-Antoine Valentin8, Daniel Vittecoq9, Jean-François Bergmann10, Thomas Anslik11, Marie-Paule Chauveheid12, Zahir Amoura13, Thomas de Broucker14, Pierre Bourgeois15, Bruno Eymard3, Serge Herson16 and Olivier Benveniste17, 1Internal Medicine Dpt 1, Pitié-Salpêtrière Hospital, APHP, Paris, France, 2Neuropathology, Pitie-Salpetriere Hospital, Paris, France, 3Institute of Myology, Pitie-Salpetriere Hospital, Paris, France, 4Internal Medecine, Pitie-Salpetriere Hospital, Paris, France, 5Internal Medicine, Jean Verdier Hospital, Bondy, France, 6Department of Infectious Diseases, Saint Antoine Hospital, Paris, France, 7Epidemic and biological risk coordination unit, AP-HP, Paris, France, 8Department of Infectious Diseases, Pitié-Salpetriere Hospital, Paris, France, 9Department of Infectious Diseases, K Bicetre Hospital, Kremlin-Bicetre, France, 10Internal Medicine, Lariboisiere Hospital, Paris, France, 11Internal Medicine, Ambroise Pare Hospital, Boulogne Billancourt, France, 12Internal Medicine,, University Paris-7, APHP, Bichat Hospital, Paris, France, 13Department of Internal Medicine 2. Referal center for SLE/APS, CHU Pitié-Salpêtrière, Paris, France, 14Department of Neurology, Delafontaine Hospital, Saint Denis, France, 15Rheumatology, APHP,Pitie-Salpetriere Hospital, Paris 6, Paris, France, 16Department: inflammation, immunopathology and biotherapy (DHU i2B), Assistance Publique - Hôpitaux de Paris, Pitié-Salpêtrière University, Paris, France, 17Internal Medecine Dpt 1, Pitié-Salpêtrière Hospital, APHP, Paris, France

    Background/Purpose: Different myopathies can be observed in HIV-infected patients, such as idiopathic inflammatory myopathies (inclusion-body myositis or polymyositis) or toxic mitochondrial myopathies secondary to antiretroviral…
  • Abstract Number: 226 • 2012 ACR/ARHP Annual Meeting

    Autoantibodies to Small Ubiquitin-Like Modifier Activating Enzymes in Japanese Patients with Dermatomyositis

    Manabu Fujimoto1, Takashi Matsushita2, Yasuhito Hamaguchi3, Kenzo Kaji3, Minoru Hasegawa1 and Kazuhiko Takehara4, 1Dermatology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan, 2Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan, 3Department of Dermatology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan, 4Dermatology, Kanazawa University, Kanazawa, Japan

    Background/Purpose: Myositis-specific autoantibodies (MSAs) are closely associated with distinct clinical subsets within idiopathic inflammatory myopaties, and thus serve as useful diagnostic tools. Recently, anti-small ubiquitin-like modifier…
  • Abstract Number: 187 • 2012 ACR/ARHP Annual Meeting

    Effect of Colchicine On Cholesterol Levels in Patients with Familial Mediterranean Fever and Behçet’s Syndrome

    SerdaL Ugurlu1, Emire Seyahi2, Idil Hanci3, Huri Ozdogan4, Seval Masatlioglu-Pehlivan5 and Hasan Yazici6, 1Division of Rheumatology,Department of Medicine, Cerrahpasa Medical Faculty, University of Istanbul, Istanbul, Turkey, 2Rheumatology, Cerrahpasa Faculty of Medicine, Istanbul University, Istanbul, Turkey, 3Department of Neurology, Krankrenhaus Nordwest, Frankfurt am Main, Frankfurt, Germany, 4Division of Rheumatology, Department of Internal Medicine, Cerrahpasa Medical Faculty, University of Istanbul, Istanbul, Turkey, 5Haydarpasa Numune Research and Education Hospital, MD,Rheumatology, Istanbul, Turkey, 6Istanbul University, Cerrahpasa Medical School, Istanbul University, Cerrahpasa Medical School, Rheumatology, Istanbul, Turkey

    Background/Purpose: We and others have previously shown that patients with Familial Mediterranean Fever (FMF) had low cholesterol levels when compared to healthy controls (1-2). The…
  • Abstract Number: 188 • 2012 ACR/ARHP Annual Meeting

    Etiology of Uveitis: A Hospital-Based Study in a Referral Centre

    Claudia Ferrari1, Rosaria Talarico1, Michele Figus2, Chiara Stagnaro3, Anna d'Ascanio4 and Stefano Bombardieri5, 1University of Pisa, Rheumatology Unit, Pisa, Italy, 2Neurosciences Department, Ophthalmology Unit, University of Pisa, Pisa, Italy, 3Rheumatology Unit, University of Pisa, Pisa, Italy, 4Department of Internal Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy, 5Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy

    Background/Purpose: Defined as an intraocular inflammation, uveitis may be associated to a systemic disease or represent an isolated entity. It affects people from all parts…
  • Abstract Number: 189 • 2012 ACR/ARHP Annual Meeting

    Pedal Swelling As a Characteristic Phenotype of the New Category of Autoinflammatory Disease Associated with NOD2 Gene Mutations

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

    Background/Purpose: Autoinflammatory diseases are characterized by seemingly unprovoked episodes of inflammation, without high titer autoantibodies or antigen specific T cells, and derive from genetic variants…
  • Abstract Number: 190 • 2012 ACR/ARHP Annual Meeting

    NLRP3 Gene Analysis for Patients with Schnitzler’s Syndrome

    Cong-Qiu Chu1, Carrie R. Austin2, Trudy M. Doyle2, Kelley A. Goodwin2, Noha El Torgomen2, Regina Treudler3 and Tammy M. Martin4, 1Rheumatology, Oregon Health & Science Univ and Portland VA Medical Center, Portland, OR, 2Casey Eye Institute, Oregon Health & Science University, Portland, OR, 3Department of Dermatology, Venereology and Allergology, Universitätsklinikum Leipzig AöR, Leipzig, Germany, 4Ophthalmology/L467AD, Oregon Health & Science Univ, Portland, OR

    Background/Purpose: Schnitzler's syndrome is characterized by chronic urticaria, intermittent fever, arthralgia, bone pain, gammopathy and marked systemic inflammation. The striking response to IL-1 blockade suggests…
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