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  • Abstract Number: 1330 • 2018 ACR/ARHP Annual Meeting

    Dyskeratotic Cells in Persistent Pruritic Skin Lesions Are Apoptotic and Associated with High Levels of Serum IL-18, and Possibly Predict the Outcomes in Adult-Onset Still’s Disease

    Hirofumi Nishikawa1, Yoshinori Taniguchi1, Natsuki Maeda1, Satoshi Inotani1, Kimiko Nakajima2, Kaoru Arii3 and Yoshio Terada1, 1Endocrinology, Metabolism, Nephrology and Rheumatology, Kochi Medical School Hospital, Nankoku, Japan, 2Dermatology, Kochi Medical School, Nankoku, Japan, 3Internal Medicine, Kochi Red Cross Hospital, Kochi, Japan

    Background/Purpose: To assess the clinical significance of dyskeratotic cells (DCs) in skin lesions of adult-onset Still’s disease (AOSD). Methods: We assessed clinical characteristics, serum markers,…
  • 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: 1332 • 2018 ACR/ARHP Annual Meeting

    Proteomic Discovery Analysis Identifies Unique Proteins and Pathways Correlating with Different Clinical Activity and Damage Measures in Juvenile Dermatomyositis (JDM)

    Hanna Kim1, Angelique Biancotto2, Foo Cheung2, Terrance P. O'Hanlon3, Yan Huang4, Frederick W. Miller3, Raphaela Goldbach-Mansky4 and Lisa G. Rider5, 1Pediatric Translational Research Branch, NIAMS, NIH, Bethesda, MD, 2Center for Human Immunology Autoimmunity and Inflammation (CHI), NIAID, NIH, Bethesda, MD, 3Environmental Autoimmunity Group, NIEHS, NIH, Bethesda, MD, 4Translational Autoinflammatory Disease Section (TADS), Laboratory of Clinical Investigation and Microbiology (LCIM), NIAID/NIH, Bethesda, MD, 5Environmental Autoimmunity Group, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD

    Background/Purpose: JDM is a complex heterogeneous autoimmune disease.  To define biomarkers and better understand JDM pathogenesis, aptamer-based proteomic technology was used to mine the serum…
  • Abstract Number: 1333 • 2018 ACR/ARHP Annual Meeting

    Abnormal Function of High Density Lipoproteins in Idiopathic Inflammatory Myopathies

    Sangmee Bae1, Jennifer Wang1, Ani Shahbazian1, Buzand Oganesian2, Ilana Golub1, Srinivasa T. Reddy1 and Christina Charles-Schoeman3, 1University of California, Los Angeles, Los Angeles, CA, 2University of California, Los Angeles, Los angeles, CA, 3Rheumatology, UCLA David Geffen School of Medicine, Los Angeles, CA

    Background/Purpose: Damage to the vascular endothelium is strongly implicated in the pathogenesis of dermatomyositis (DM) and to a lesser degree other idiopathic inflammatory myopathies (IIM).…
  • Abstract Number: 1334 • 2018 ACR/ARHP Annual Meeting

    Low Density Granulocytes As Biomarkers of Disease Activity and Damage in Patients with Idiopathic Inflammatory Myopathies

    Jiram Torres-Ruíz1, Araceli Leal-Alanis2, Ricardo Vazquez-Rodriguez3, Mario René Alvarado-Lara3, Edgar Rafael Carazo-Vargas3, José Luis Maravillas-Montero4, Jorge Alcocer-Varela5 and Diana Gómez-Martín5, 1Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico, 2Internal Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico, Mexico, 3Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico, Mexico, 4Red de Apoyo a la Investigación, UNAM, Mexico, Mexico, 5Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

    Background/Purpose: Low density granulocytes (LDGs) are a subset of neutrophils that spontaneously produce neutrophil extracellular traps (NETs) and type I IFN. The latter correlates with…
  • Abstract Number: 1335 • 2018 ACR/ARHP Annual Meeting

    Extracellular Vesicles Induce Pro-Inflammatory Cytokines in Dermatomyositis

    Krisha Desai1,2, Majid Zeidi3,4, Ming-Lin Liu1,2 and Victoria P. Werth1,2, 1Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, 2Department of Dermatology, Corporal Michael J. Crescenz VAMC, Philadelphia, PA, 3University of Pennsylvania, Philadelphia, PA, 4Philadelphia Veterans Affairs Medical Center, Philadelphia, PA

    Background/Purpose: Extracellular vesicles (EVs) are micron-scale bilayer membrane vesicles released from almost all cell types under activation or apoptosis. They have been detected in various…
  • Abstract Number: 1336 • 2018 ACR/ARHP Annual Meeting

    Functional, Radiographic and Serologic Correlates of Anti-SSA52 Kd – Associated Interstitial Lung Disease

    Estefania Calle Botero1, Benjamin Wang2, Juan J Maya2, Isabel Mira-Avendano3 and Andy Abril2, 1Rheumatology, Universidad de Antioquia, Medellin, Colombia, 2Rheumatology, Mayo Clinic Florida, Jacksonville, FL, 3Pulmonary and Critical Care, Mayo Clinic Florida, Jacksonville, FL

    Background/Purpose: Autoantibodies against the SSA52 Kd protein (anti-SSA52) have been cataloged as myositis-associated antibodies, occurring in up to 30% of cases idiopathic inflammatory myopathies (IIM),…
  • Abstract Number: 1337 • 2018 ACR/ARHP Annual Meeting

    Myocardial Fatty Acid Metabolism and Perfusion Mismatch in Scintigraphy Predicts Worse Prognosis in Clinically Amyopathic Dermatomyositis

    Harunobu Iida1, Hironari Hanaoka1, Kana Ishimori2, Tomofumi Kiyokawa1, Yukiko Takakuwa1 and Kimito Kawahata1, 1Division of Rheumatology and Allergology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan, 2Division of Rheumatology and Allergy, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan

    Background/Purpose: Clinically amyopathic dermatomyositis (CADM) patients are frequently manifested by rapidly progressive interstitial lung disease (ILD) and associated with a poor prognosis. Recently cardiac involvement…
  • Abstract Number: 1338 • 2018 ACR/ARHP Annual Meeting

    Validation of the Diagnostic Accuracy of Myositis-Related Antibodies in a Large Patient-Cohort

    Angelika Lackner1, Viktoria Tiefenthaler2, Jalia Mirzayeva2, Winfried Graninger3 and Martin Stradner4, 1Rheumatology and Immunology, Medical University of Graz, Graz, Austria, 2Department of Rheumatology & Immunology, Medical University of Graz, Graz, Austria, 3Division of Rheumatology and Immunology, Medical University of Graz, Graz, Austria, 4Department of Rheumatology and Immunology, Medical University of Graz, Graz, Austria

    Validation of the diagnostic accuracy of myositis-related antibodies in a large patient-cohortLackner, A; Tiefenthaler, V; Mirzayeva, J; Graninger, W; Stradner, MH Background/Purpose: Myositis-specific antibodies (MSA) and…
  • Abstract Number: 1339 • 2018 ACR/ARHP Annual Meeting

    Myositis Specific Anti-Histidyl tRNA Synthetase (HisRS) Autoantibodies Display High Reactivity Against Hisrs Conformational Epitopes and Associate with Lung and Joint Involvement

    Catia Fernandes-Cerqueira1,2, Nuria Renard1,2, Antonella Notarnicola1,2, Edvard Wigren1,2,3, Per-Johan Jakobsson2,4, Susanne Graslund1,2,3 and Ingrid E. Lundberg1,2, 1Department of Medicine, Division of Rheumatology, Karolinska Institutet, Stockholm, Sweden, 2Center for Molecular Medicine, Stockholm, Sweden, 3Structural Genomics Consortium, Stockholm, Sweden, 4Rheumatology Unit, Dept. of Medicine, Karolinska Institutet, Stockholm, Sweden

    Background/Purpose: Autoimmune myositis (rheumatic muscle inflammation) associated with interstitial lung disease (ILD) and arthritis is strongly correlated with the presence of anti-histidyl tRNA synthetase (HisRS)…
  • Abstract Number: 1340 • 2018 ACR/ARHP Annual Meeting

    Anti-Aminoacyl-tRNA-Synthetase Antibodies Which Are Positive By ELISA but Negative By RNA-Immunoprecipitation Suggest Different Antigen Recognition and Clinical Relevance Different from Typical Anti-Synthetase Syndrome

    Tsuneo Sasai1, Ran Nakashima2, Yuki Ishikawa3, Takuya Isayama4 and Tsuneyo Mimori2, 1Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Japan, Kyoto, Japan, 2Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 3One Joslin Place, Joslin Diabetes Center, Harvard Medical School, Boston, MA, 4Medical & Biological Laboratories CO.,LTD., Nagoya, Japan

    Background/Purpose: Anti-aminoacyl-tRNA-synthetase (ARS) antibodies are myositis specific autoantibodies and associated with common clinical characteristics called anti-synthetase syndrome (ASS). Recently anti-ARS detecting enzyme-linked immunosorbent assay (ELISA)…
  • Abstract Number: 1341 • 2018 ACR/ARHP Annual Meeting

    Autoantibodies to Mi-2 Alpha and Mi-2 Beta in Patients with Myositis

    Michaelin Richards1, Ignacio Garcia-De La Torre2, Yelitza Gonzalez-Bello3, Monica Vazquez-Del Mercado4, Lilia Andrade-Ortega5, Gabriel Medrano-Rameriz6, Jose Eduardo Navarro-Zarza7, Marco Maradiaga8, Esthela Loyo9, Armando Rojo-Mejía10, Graciela N Gómez11, Andrea Seaman1, Marvin J. Fritzler12, Martial Koenig13 and Michael Mahler1, 1Research and Development, Inova Diagnostics, San Diego, CA, 2Immunology & Rheumatology, Centro de Est. de Invest. Bas. y Clin., S.C., Guadalajara, JAL, Mexico, 3Immunology and Rheumatology, Hospital General de Occidente, Secretaria de Salud Jalisco, Guadalajara, Jalisco, Mexico, 4Centro Universitario de Ciencias de la Salud, Instituto de Investigación en Reumatología y del Sistema Músculo Esquelético, Universidad de Guadalajara, Guadalajara, Mexico, 5Rheumatology Department, CMN 20 de Noviembre ISSSTE,, CDMX, Mexico, 6Hospital General de México, "Dr. Eduardo Liceaga, Mexico City, Mexico, 7Hospital General “Dr. Raymundo Abarca Alarcón”, Chilpancingo, Mexico, 8Centro de Investigación de Tratamientos Innovadores de Sinaloa, Culiacán, Mexico, 9Departamento de Reumatologia, Hospital Regional Universitario José Ma Cabral Baez, Santiago, Dominican Republic, 10Clínica San Pablo, Lima, Peru, 11Diaz Colodrero 2537 8° A, Instituto de Investigaciones Medicas Alfredo Lanari, Capital Federal, Argentina, 12Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, 13Internal Medicine, Hôpital Notre-Dame du CHUM, Montréal, QC, Canada

     Background/Purpose: Myositis specific antibodies (MSA) represent not only important diagnostic tools, but also help stratify myositis patients with particular clinical features, treatment responses and disease…
  • Abstract Number: 1342 • 2018 ACR/ARHP Annual Meeting

    Myositis Specific Antibodies Measured Using a Novel Particle Based Multi-Analyte Assay Resemble Myositis Subsets By Principle Component Analysis

    Michaelin Richards1, Ignacio Garcia de la Torre2, Yelitza Gonzalez-Bello3, Monica Vazquez-Del Mercado4, Lilia Andrade-Ortega5, Gabriel Medrano-Rameriz6, Jose Eduardo Navarro-Zarza7, Marco Maradiaga8, Esthela Loyo9, Armando Rojo-Mejía10, Graciela N Gómez11, Andrea Seaman1, Marvin J. Fritzler12 and Michael Mahler1,13, 1Research and Development, Inova Diagnostics, San Diego, CA, 2Hospital General de Occidente, Guadalajara, Mexico, 3Immunology and Rheumatology, Hospital General de Occidente, Secretaria de Salud Jalisco, Guadalajara, Jalisco, Mexico, 4Centro Universitario de Ciencias de la Salud, Instituto de Investigación en Reumatología y del Sistema Músculo Esquelético, Universidad de Guadalajara, Guadalajara, Mexico, 5Rheumatology Department, CMN 20 de Noviembre ISSSTE,, CDMX, Mexico, 6Hospital General de México, "Dr. Eduardo Liceaga, Mexico City, Mexico, 7Hospital General “Dr. Raymundo Abarca Alarcón”, Chilpancingo, Mexico, 8Centro de Investigación de Tratamientos Innovadores de Sinaloa, Culiacán, Mexico, 9Departamento de Reumatologia, Hospital Regional Universitario José Ma Cabral Baez, Santiago, Dominican Republic, 10Clínica San Pablo, Lima, Peru, 11Diaz Colodrero 2537 8° A, Instituto de Investigaciones Medicas Alfredo Lanari, Capital Federal, Argentina, 12Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, 139900 Old Grove road, INOVA Diagnostics, San Diego, CA

     Background/Purpose: Myositis specific antibodies (MSA) represent important diagnostic tools and also help stratify idiopathic inflammatory myositis (IIM) patients with particular clinical features, treatment responses, and…
  • Abstract Number: 1343 • 2018 ACR/ARHP Annual Meeting

    A Novel Autoantibody Against DNA Damage Binding Protein-1 in Idiopathic Inflammatory Myopathy

    Yuji Hosono1,2, Ran Nakashima1, Koji Kitagori1, Kosaku Murakami1, Hajime Yoshifuji1, Koichiro Ohmura3 and Tsuneyo Mimori1, 1Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan, 2National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 3Department of Rheumatology and Clinical Immunology, Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan

    Background/Purpose: Many kinds of autoantibodies are detected in idiopathic inflammatory myopathy (IIM) patients. Some of them are useful to diagnose, predict the clinical course, and…
  • 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…
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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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