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Abstracts tagged "Myositis"

  • Abstract Number: 0451 • ACR Convergence 2020

    Prevalence, Therapy and Tumor Response in Patients with Rheumatic Immune-related Adverse Events Following Immune Checkpoint Inhibitor Therapy: A Single-Centre Analysis

    Sophia Verspohl1, Tobias Holderried1, Charlotte Behning2, Peter Brossart1 and Valentin Schaefer3, 1Clinic for Internal Medicine III, Department of Oncology, Hematology and Rheumatology, University Hospital Bonn, Germany, Bonn, Nordrhein-Westfalen, Germany, 2Institute for Medical Biometrics, Informatics and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany, Bonn, Nordrhein-Westfalen, Germany, 3Clinic of Internal Medicine III, Department of Oncology, Hematology and Rheumatology, University Hospital Bonn, Germany, Bonn, Nordrhein-Westfalen, Germany

    Background/Purpose: Immune checkpoint inhibitors (ICIs) have improved cancer therapy [1] by inducing a higher immune system activity and subsequent attack of tumor cells. However, this effect…
  • Abstract Number: 1073 • ACR Convergence 2020

    Anti Melanoma Differentiation-associated Protein Gene 5 Antibody Titer Monitoring Is a Useful Indicator for Early Detection of Recurrence in Rapidly Progressive Interstitial Lung Disease Associated with Dermatomyositis

    Yuji Hosono1, Azusa Kojima2, Keigo Shimura2, Akira Ishii2, Yuto Izumi2, Kazuki Hirano2, Sho Sasaki2, Takayoshi Kurabayashi2, Noriko Sasaki2, Chiho Yamada2 and Shinji Sato2, 1Tokai University School of Medicine, Kanagawa, Japan, 2Tokai University School of Medicine, Isehara, Kanagawa, Japan

    Background/Purpose: Anti melanoma differentiation-associated gene 5 (MDA5) antibody (Ab) positive dermatomyositis (DM) often complicates rapidly progressive interstitial lung disease (RP-ILD), which shows fatal prognosis at…
  • Abstract Number: 1093 • ACR Convergence 2020

    Impact of Blood Flow Restricted Strength Training on Myogenic Stem Cells and Myofiber Hypertrophy in Sporadic Inclusion Body Myositis Patients

    Kasper Yde Jensen1, Henrik Daa Schrøder2, Jakob Nielsen3, Mikkel Jacobsen3, Eleanor Boyle3, Anders Nørkær Jørgensen3, Rune Dueholm Bech4, Per Aagaard3 and Louise Pyndt Diederichsen1, 1Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark, 2Odense University Hospital, Odense, Denmark, 3University of Southern Denmark - Odense, Odense, Denmark, 4Zealand University Hospital, Copenhagen, Denmark

    Background/Purpose: Sporadic inclusion body myositis (sIBM) is clinically characterised by marked progressive muscle weakness and impaired physical function. Physical training has become an area of…
  • Abstract Number: 082 • 2020 Pediatric Rheumatology Symposium

    Anti-Mitochondrial Autoantibodies Are Associated with Dysphagia in Juvenile and Adult Myositis, and with Persistent Weakness and Cardiomyopathy in Adult Myositis

    Sara Sabbagh1, Iago Pinal-Fernandez 2, Maria Casal-Dominguez 3, Frederick W. Miller 4, Lisa G. Rider 5, Andrew Mammen 3 and Lisa Christopher-Stine 6, 1NIH/NIAMS, Bethesda, 2National Institutes of Health, Bethesda, 3NIH, Bethesda, 4Bethesda, 5NIEHS, NIH, Garrett Park, 6Johns Hopkins University, Baltimore

    Background/Purpose: We analyzed the prevalence of anti-mitochondrial autoantibodies (AMA) in both juvenile-(JM) and adult-onset myositis cohorts and investigated phenotype differences between juvenile and adult myositis…
  • Abstract Number: 389 • 2019 ACR/ARP Annual Meeting

    ACR/EULAR Criteria for Myositis and Systemic Sclerosis Lack Sensitivity for Scleromyositis

    Alain Meyer1, Valérie Leclair 2, Océane Landon-Cardinal 3, Benjamin Ellezam 4, Julie D'Aoust 5, Margherita Giannini 6, Bernard Geny 6, Laurent Arnaud 7, Jacques-Eric Gottenberg 8, Jean Sibilia 9, Minoru Satoh 10, Marvin Fritzler 11, Yves Troyanov 12 and Marie Hudson 13, 1Centre de Reference des Maladies Autoimmunes Rares, Hôpitaux Universitaires de Strasbourg, Strasbourg, France, 2Division of Rheumatology, Department of Medicine, Jewish General Hospital; Clinical Epidemiology Unit, Department of Medicine, Karolinska Institutet, Montreal, QC, Canada, 3Centre Hospitalier de l'Université de Montréal, Montréal, Canada, 4Department of Pathology, Centre Hospitalier Universitaire Sainte-Justine, Montréal, Canada, 5McGill University, Montreal, QC, Canada, 6CHU de Strasbourg, Strasbourg, France, 7Service de Rhumatologie, Centre National de Référence des Maladies Autoimmunes Systemiques Rares (RESO), Hôpitaux Universitaires de Strasbourg, Strasbourg, France, Strasbourg, France, 8Department of Rheumatology, Strasbourg University Hospital, Strasbourg, France, 9CHU Strasbourg, Strasbourg, France, 10Department of Clinical Nursing, School of Health Sciences, University of Occupational and Environmental Health, Kitakyushu, Japan, 11Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, 12Division of Rheumatology, Department of Medicine, Hôpital du Sacre-Coeur de Montreal, Montreal, QC, Canada, 13Jewish General Hospital, Lady Davis Institute for Medical Research, and Department of Medicine, McGill University, Montreal, QC, Canada

    Background/Purpose: Autoimmune myositis consists of a group of diseases with heterogeneous muscular and systemic manifestations. Prognosis also varies widely across the spectrum. Thus, myositis subgroups…
  • Abstract Number: 399 • 2019 ACR/ARP Annual Meeting

    Seasonal and Temporal Analyses of Disease Onset and Diagnosis in Myositis Autoantibody Phenotypes in Juvenile Dermatomyositis (JDM)

    Gulnara Mamyrova1, Min Shi 2, Ira N. Targoff 3, Rodolfo V. Curiel 1, Frederick W. Miller 4 and Lisa G. Rider 5, 1George Washington University, School of Medicine and Health Sciences, Washington, DC, 2Biostatistics&Computational Biology Branch, NIEHS, NIH, Research Triangle Park, NC, 3Arthritis Immunology Section, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4NIEHS, NIH, Bethesda, MD, 5Environmental Autoimmunity Group, Clinical Research Branch, NIEHS, NIH, Bethesda, MD

    Background/Purpose: Published studies suggest seasonal occurrence of disease onset and disease activity in patients with adult idiopathic inflammatory myopathies (IIM).Our objective was to evaluate seasonal…
  • Abstract Number: 404 • 2019 ACR/ARP Annual Meeting

    Autoantibody Profiles Delineate Three Distinct Subsets of Scleromyositis

    Julie D'Aoust1, Valérie Leclair 2, Geneviève Gyger 3, Alain Meyer 4, Marvin Fritzler 5, Océane Landon-Cardinal 6, Erin O'Ferrall 7, Jason Karamchandani 7, Benjamin Ellezam 8, Rami Massie 7, Minoru Satoh 9, Yves Troyanov 10 and Marie Hudson 11, 1McGill University, Montreal, QC, Canada, 2Division of Rheumatology, Department of Medicine, Jewish General Hospital; Clinical Epidemiology Unit, Department of Medicine, Karolinska Institutet, Montreal, QC, Canada, 3Division of Rheumatology, Department of Medicine, Jewish General Hospital, Montreal, QC, Canada, 4Centre de Reference des Maladies Autoimmunes Rares, Hôpitaux Universitaires de Strasbourg, Strasbourg, France, 5Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, 6Division of Rheumatology, Centre hospitalier de l'Université de Montréal; Department of Medicine, Université de Montréal, Montreal, QC, Canada, 7Montreal Neurological Institute, Montreal, QC, Canada, 8Centre hospitalier universitaire Sainte-Justine, Montreal, QC, Canada, 9Department of Clinical Nursing, School of Health Sciences, University of Occupational and Environmental Health, Kitakyushu, Japan, 10Division of Rheumatology, Department of Medicine, Hôpital du Sacre-Coeur de Montreal, Montreal, QC, Canada, 11Jewish General Hospital, Lady Davis Institute for Medical Research, and Department of Medicine, McGill University, Montreal, QC, Canada

    Background/Purpose: Myopathy is an important cause of morbidity in systemic sclerosis (SSc).  Nevertheless, scleromyositis remains incompletely characterized owing at least in part to its clinical…
  • Abstract Number: 881 • 2019 ACR/ARP Annual Meeting

    Auto-antibodies Targeting Components of Sarcolemma Repair: A Pathogenic Mechanism in Human Inflammatory Myopathies

    Kevin McElhanon1, Ana Capati 2, Nicholas Young 3, Brian Paleo 2, Eric Beck 2, Zarife Sahenk 4, Rohit Aggarwal 5, Chester Oddis 5, Noah Weisleder 1 and Wael Jarjour 6, 1Dorothy M. Davis Heart and Lung Research Institute & Dept. of Physiology & Cell Biology, The Ohio State University Wexner Medical Center, Columbus, OH, 2The Ohio State University Wexner Medical Center, Columbus, OH, 3The Ohio State University Wexner Medical Center, Division of Immunology and Rheumatology, Columbus, OH, 4Nationwide Children's Hospital, Columbus, OH, 5University of Pittsburgh Medical Center, Pittsburgh, PA, 6Ohio State College of Medicine, Columbus, OH

    Background/Purpose: Idiopathic inflammatory myopathies (IIM) represent a group of disorders causing chronic inflammation and significant damage to skeletal muscle due to an unchecked autoimmune response. …
  • Abstract Number: 1286 • 2019 ACR/ARP Annual Meeting

    Patients with Anti-tRNA Synthetase Syndrome Are More Likely to Present to Pulmonary Clinic and Have a Higher Prevalence and Severity of Lung Disease Than Patients with Other Types of Myositis or Systemic Sclerosis

    Bret Sohn1, Erin Wilfong 1 and Leslie Crofford 1, 1Vanderbilt University, Nashville

    Background/Purpose: Interstitial lung disease (ILD) is a significant cause of morbidity and mortality in idiopathic inflammatory myopathies (IIM) as well as systemic sclerosis (SSc). The…
  • Abstract Number: 1288 • 2019 ACR/ARP Annual Meeting

    Line Blot Immunoassay in Inflammatory Myopathies: Diagnostic Accuracy and Factors Predicting Positive Results in Routine Clinical Practice

    Fergus To1, Clara Ventín Rodríguez 2, Shuayb Elkhalifa 3, James Lilleker 4 and Hector Chinoy 4, 1University of British Columbia, Vancouver, Canada, 2Complejo Hospitalario Universitario de A Coruña, A Coruña, Spain, 3(3) Department of Immunology, Salford Royal NHS Foundation, Salford, United Kingdom, 4University of Manchester, Manchester, United Kingdom

    Background/Purpose: To evaluate the real-world accuracy of a line blot immunoassay (LIA) for myositis-specific (MSA) and myositis-associated (MSA) autoantibody testing in patients at a tertiary…
  • Abstract Number: 1291 • 2019 ACR/ARP Annual Meeting

    Semi-Quantitative and Quantitative Evaluation of Magnetic Resonance Imaging in Patients with Idiopathic Inflammatory Myopathies – a Subanalysis of the Prometheus Study

    Katerina Kubinova1 and Jiří Vencovský 2, 1Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Prague, Czech Republic, Prague 2, 2Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Prague, Czech Republic, Prague 2, Czech Republic

    Background/Purpose: Prometheus study was a prospective, randomized, assessor-blind multicenter trial, comparing the efficacy and safety of the glucocorticoid (GC) monotherapy versus combination therapy with methotrexate…
  • Abstract Number: 1292 • 2019 ACR/ARP Annual Meeting

    Abnormal High Density Lipoprotein Particle Size and Number in Idiopathic Inflammatory Myopathies

    Sangmee Bae1, Ilana Golub 2, Ani Shahbazian 3, Jennifer Wang 3 and Christina Charles-Schoeman 4, 1UCLA, Los Angeles, CA, 2UCLA, Los Angeles, 3UCLA Medical Center, Los Angeles, 4University of California, Los Angeles, CA

    Background/Purpose: Vascular inflammation and damage are implicated in the pathogenesis of idiopathic inflammatory myopathies (IIM), particularly dermatomyositis (DM). High and low density lipoprotein (HDL, LDL)…
  • Abstract Number: 1294 • 2019 ACR/ARP Annual Meeting

    Alterations in Activin A-Myostatin-Follistatin System Associate with Disease Activity in Inflammatory Myopathies

    Lucia Vernerová1, Veronika Horvathová 2, Tereza Kropáčková 3, Martina Vokurková 2, Martin Klein 1, Sabina Oreska 4, Katerina Kubinova 5, Herman Mann 4, Maja Spiritovic 6, Hana Storkanova 1, Olga Kryštůfková 1, Michal Tomcik 4, Jozef Ukropec 7, Barbara Ukropcová 7 and Jiří Vencovský 4, 1Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Prague, Czech Republic, Prague, Czech Republic, 2Institute of Rheumatology, Prague, Czech Republic, 3Institute of Rheumatology, Prague, 4Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Prague, Czech Republic, Prague 2, Czech Republic, 5Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Prague, Czech Republic, Prague 2, 6Faculty of Physical Education and Sport, Department of Physiotherapy, Charles University, Prague, Czech Republic, Prague 2, Hlavni mesto Praha, Czech Republic, 7Institute of Experimental Endocrinology, Biomedical center, Slovak Academy of Sciences, Bratislava, Slovakia

    Background/Purpose: The aim of this study was to investigate myokines involved in muscle atrophy such as myostatin, follistatin and activin A, in idiopathic inflammatory myopathies…
  • Abstract Number: 2245 • 2019 ACR/ARP Annual Meeting

    Polymyositis (PM) and Dermatomyositis (DM) Symptom Flares and Associated Impact from the Patient Perspective

    Lisa Christopher-Stine1, William Kelly 2, George Wan 3, Linda Kobert 4 and Michael Reed 5, 1Johns Hopkins University School of Medicine, Baltimore, MD, 2Johns Hopkins Myositis Center, Baltimore, MD, 3Mallinckrodt Pharmaceuticals, Bedminster, NJ, 4The Myositis Association, Alexandria, VA, 5Vedanta Research, Chapel Hill, NC

    Background/Purpose: Flare activity or worsening symptoms are not well defined for myositis. This analysis characterizes PM and DM flares from the patient perspective and reports…
  • Abstract Number: 2840 • 2019 ACR/ARP Annual Meeting

    Reliability, Validity and Responsiveness of PROMIS PF-20 in Patients with Inflammatory Myopathy

    Didem Saygin1, Chester Oddis 1, Nicole Neiman 1, Diane Koontz 1, Siamak Moghadam-Kia 1 and Rohit Aggarwal 1, 1University of Pittsburgh Medical Center, Pittsburgh, PA

    Background/Purpose: Idiopathic inflammatory myopathies (IIM) are a group of rare, debilitating systemic diseases characterized by proximal muscle weakness, which limit activities of daily living and…
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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.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

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