ACR Meeting Abstracts

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Abstracts tagged "interstitial lung disease and myositis"

  • Abstract Number: 376 • 2018 ACR/ARHP Annual Meeting

    Antisynthetase Syndrome: Prevalence of Serositis in Autoantibody Subsets

    Alexis Katz1, James Bena2 and Soumya Chatterjee3, 1Internal Medicine, Cleveland Clinic, Cleveland, OH, 2Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, 3Rheumatic and Immunologic Diseases, Cleveland Clinic, Cleveland, OH

    Background/Purpose: Antisynthetase Syndrome (AS) is a relatively rare autoimmune disease characterized by interstitial lung disease (ILD), myositis, inflammatory arthritis, Raynaud phenomenon, and mechanic’s hands. Eight autoantibodies (Ab) to…
  • Abstract Number: 392 • 2018 ACR/ARHP Annual Meeting

    Autoantibody Profile and Clinical Characteristics in Patients with Idiopathic Inflammatory Myopathies

    Sung Hae Chang1, Sung Won Lee2, Mi-Il Kang3, Mihye Kwon4, Chung-Il Joung4, Seong-Wook Kang5, In-Seol Yoo5, Seung-Cheol Shim5, Su-Jin Yoo6, In Ah Choi7, Ji Hyoun Kim8, Seung-Jae Hong9, Yeon-Ah Lee9, Sang Wan Chung10 and Jinhyun Kim11, 1Department of Internal Medicine, Department of Internal Medicine, College of Medicine, Soonchunhyang University, Cheonan, Korea, Republic of (South), 2Division of Rheumatology, Department of Internal Medicine, Department of Rheumatology, Department of Internal Medicine, College of Medicine, Soonchunhyang University, Cheonan, Korea, Republic of (South), 3Department of Internal Medicine, Dankook University College of Medicine, Cheonan, Korea, Republic of (South), 4Department of Internal Medicine, Konyang University hospital, Daejeon, Korea, Republic of (South), 5Division of Rheumatology, Department of Internal Medicine, Daejeon Rheumatoid & Degenerative Arthritis Center, Chungnam National University Hospital, Daejeon, Korea, Republic of (South), 6Rheumatology, Daejeon Rheumatoid & Degenerative Arthritis Center, Chungnam National University Hospital, Daejeon, Korea, Republic of (South), 7Department of Internal Medicine, Chungbuk National University College of Medicine, Cheongju, Korea, Republic of (South), 8Department of Internal Medicine, Chungbuk National University College of Medicine, Cheong-ju, Korea, Republic of (South), 9Rheumatology, Kyung Hee University Hospital, Seoul, Korea, Republic of (South), 10Division of Rheumatology, Department of Internal Medicine, Kyung Hee University Hospital, Seoul, Korea, Republic of (South), 11Internal medicine, Daejeon Rheumatoid & Degenerative Arthritis Center, Chungnam National University Hospital, Deajeon, Korea, Republic of (South)

    Background/Purpose: Autoimmune myositis (AIM) is a constellation of rare chronic disease with progressive muscle weakness. Several autoantibodies are found to be highly correlated with IIM…
  • Abstract Number: 396 • 2018 ACR/ARHP Annual Meeting

    Clinical, Physiologic, and Radiologic Features Associated with Severe MDA5-Associated Interstitial Lung Disease

    Tracy Doyle1, Priya Borker2, Elaine Fletcher1, David Murphy3, Rachna Madan3 and Paul F. Dellaripa4, 1Brigham and Women's Hospital, Boston, MA, 2Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, Boston, MA, 3Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, Boston, MA, 4Brigham and Women's Hospital and Harvard Medical School, Boston, MA

    Background/Purpose: Autoantibodies against melanoma differentiation-associated protein 5 (MDA-5) have been described in patients with dermatomyositis (DM) and progressive interstitial lung disease (ILD). Previous cohorts have…
  • Abstract Number: 877 • 2018 ACR/ARHP Annual Meeting

    Serum Krebs Von Den Lungen-6 Is a Useful Biomarker for Assessing Activity of Myositis-Associated Interstitial Lung Disease

    Satoshi Takanashi1, Naoshi Nishina2, Maho Nakazawa2, Yuko Kaneko2 and Tsutomu Takeuchi2, 1Division of Rheumatoloy, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: Interstitial lung disease (ILD) is one of serious organ involvements in idiopathic inflammatory myositis. Krebs von den Lungen-6 (KL-6) is an antigen produced primarily…
  • Abstract Number: 1310 • 2018 ACR/ARHP Annual Meeting

    Diagnostic Utility of Myositis Antibodies in Patients with Interstitial Lung Disease and Suspected Underlying Connective Tissue Disease

    Verónica Wolff1, Juan Maya2, Carolina Cuéllar3, Matías Florenzano1, Alexis Peralta4 and Viviana Balboa4, 1Rheumatic Lung diseases Unit, Instituto Nacional del Tórax, Santiago, Chile, 2Rheumatology Unit, Hospital del Salvador. Facultad de Medicina. Universidad de Chile, Santiago, Chile, 3Rheumatology Section, Hospital del Salvador, Universidad de Chile, SANTIAGO, Chile, 4Laboratorio Inmunología, Hospital Del Salvador, SANTIAGO, Chile

     Background/Purpose: Interstitial Lung Disease (ILD) is a common manifestation of  Connective Tissue Diseases (CTD), mainly Systemic sclerosis (SSc), Rheumatoid Arthritis and Idiopathic Inflammatory Myositis (IIM)…
  • 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: 2144 • 2017 ACR/ARHP Annual Meeting

    Multiple Serum Cytokine and Chemokine Profiling to Identify Combinational Biomarkers Toward Patients of Polymyositis/Dermatomyositis Complicated with Rapidly Progressive Interstitial Lung Disease

    Toshimasa Shimizu1, Tomohiro Koga1,2, Yoshiro Horai3, Keita Fujikawa4, Yushiro Endo1, Sousuke Tsuji1, Ayuko Takatani1, Masataka Umeda1, Shoichi Fukui1, Remi Sumiyoshi1, Ayako Nishino1, Shinya Kawashiri1, Naoki Iwamoto1, Takashi Igawa1, Kunihiro Ichinose1, Mami Tamai1, Noriho Sakamoto5, Hideki Nakamura1, Tomoki Origuchi6, Hiroshi Mukae5, Masataka Kuwana7 and Atsushi Kawakami1, 1Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 2Center for Bioinformatics and Molecular Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki City, Japan, 3Department of Rheumatology, National Hospital Nagasaki Medical Center, Nagasaki, Japan, 4Japan Community Health care Organization Isahaya General Hospital, Nagasaki, Japan, 5Department of RespiratoryMedicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 6Department of Rehabilitation Sciences, Nagasaki University, Nagasaki, Japan, 7Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan

    Background/Purpose: Polymyositis (PM)/dermatomyositis (DM) is a chronic inflammatory disorders involved in skeletal muscles. Interstitial lung disease (ILD) complicated with PM/DM patients is often developed as…
  • Abstract Number: 304 • 2015 ACR/ARHP Annual Meeting

    Abnormal Pulmonary Function Tests, Interstitial Lung Disease, and Lung Function Decline in Patients with Classic and Clinically Amyopathic Dermatomyositis

    Michael George1, Maryl Kreider2, Rupal Shah2, Wallace Miller Jr.3, Peter A. Merkel4 and Victoria Werth5,6, 1Department of Rheumatology, Hospital of the University of Pennsylvania, Philadelphia, PA, 2Pulmonary, Allergy & Critical Care, University of Pennsylvania, Philadelphia, PA, 3Radiology, University of Pennsylvania, Philadelphia, PA, 4Penn Vasculitis Center, Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, 5Dermatology, Veterans Affairs Medical Center, Philadelphia, PA, 6Dermatology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Interstitial lung disease (ILD) is common in classic dermatomyositis (DM) and clinically amyopathic dermatomyositis (CADM), in which rash is present without weakness. Previous studies…
  • Abstract Number: 2366 • 2015 ACR/ARHP Annual Meeting

    The Anti-MDA5 Autoantibody Phenotype: Defining Clinical, Biochemical and Radiological Features Suggestive of Anti-MDA5-Associated Rapidly Progressive Interstitial Lung Disease

    Sabrina Hoa1, Yves Troyanov1, Marvin J. Fritzler2, Ira N. Targoff3, Anne-Marie Mansour1, Eric Rich1, Hind Boudabbouz1, Josiane Bourré-Tessier1, Sandra Chartrand1, Marianne Landry1, Martin Albert1 and Jean-Luc Senécal1, 1Université de Montréal, Montreal, QC, Canada, 2Medicine, University of Calgary, Calgary, AB, Canada, 3Veterans Affairs Medical Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose: Anti-MDA5 autoantibody associated syndrome is a novel entity within the spectrum of autoimmune myositis. It has been described as a clinical mimic of the…
  • Abstract Number: 2371 • 2015 ACR/ARHP Annual Meeting

    The Clinical Features of Recurrent Interstitial Lung Disease in Dermatomyositis Patients with Anti- Melanoma Differentiation-Associated Gene 5 Antibody

    Yuji Hosono1, Ran Nakashima1, Kosaku Murakami2, Yoshitaka Imura2, Naoichiro Yukawa2, Hajime Yoshifuji2, Koichiro Ohmura2 and Tsuneyo Mimori2, 1Department of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan, 2Department of Rheumatology and Clinical Immunology, Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan

    Background/Purpose: Interstitial lung disease (ILD) is the most common cause of mortality in polymyosytis (PM) and dermatomyositis (DM). It is well known that the DM…
  • Abstract Number: 2376 • 2015 ACR/ARHP Annual Meeting

    Clinical Features in Dermatomyositis Patients with Novel Autoantibody to Small Ubiquitin-like Modifier Activating Enzymes (Anti-SAE Antibody) and Relationship to Interstitial Lung Disease: A Systematic Review of 29 Cases

    Sirada Panupattanapong1, Jessica Sun2 and Kevin Baszis1, 1Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, 2Pediatric, Division of Rheumatology, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO

    Background/Purpose: Anti-SAE antibody is a novel myositis-specific antibody first described in 2007. SAE is an enzyme that facilitates sumoylation, leading to the formation of stable…
  • Abstract Number: 1260 • 2014 ACR/ARHP Annual Meeting

    The Early Use of Cyclosporine Is Beneficial for Long-Term Prognosis in Patients of Polymyositis/Dermatomyositis-Associated Interstitial Lung Disease with Anti- Synthetase Antibodies

    Yuji Hosono1, Ran Nakashima2, Yoshitaka Imura3, Naoichiro Yukawa2, Hajime Yoshifuji2, Takaki Nojima4, Koichiro Ohmura2 and Tsuneyo Mimori2, 1Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 2Department of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan, 3Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan, 4Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Hiroshima, Japan

    Background/Purpose: Interstitial lung disesases (ILD) is the most common cause of mortality in polymyosotis (PM) and dermatomyositis (DM). Cyclosporine had been reported to improve clinical…
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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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