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  • Abstract Number: 400 • 2019 ACR/ARP Annual Meeting

    Performance of the European League Against Rheumatism/American College of Rheumatology Idiopathic Inflammatory Myopathies Classification Criteria in a Myositis Cohort from Argentina

    Belén Virasoro1, Ramiro Gomez 2, Dafne Capelusnik 3, Andrea Braillard Poccard 4, Emilce Schneeberger 5, Silvia Papasidero 6, Malena Viola 7, Maria de la Vega 8, Carolina Costi 9, Mercedes Garcia 10, Cecilia Asnal 11, Ana Cappuccio 12, Demelza Yucra 13, Natalia Tamborenea 14, Mariano Rivero 15, Amelia Granel 16, Linda Vergel Orduz 13, Marina Dalpiaz 14, Juan Bande 6, Carolina Segura Escobar 15 and Cecilia Pisoni 17, 1CEMIC, buenos aires, Buenos Aires, Argentina, 2Hospital de Clínicas José de San Martín, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina, 3Instituto de Rehabilitacion Psicofisica, CABA, Ciudad Autonoma de Buenos Aires, Argentina, 4Hospital de Clínicas José de San Martin, Buenos Aires, Buenos Aires, Argentina, 5Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina, 6Hospital General de Agudos Dr. E. Tornú, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina, 7Centro Reumatologia DOM, Buenos Aires, Buenos Aires, Argentina, 8CEIM Investigaciones Medicas, Buenos Aires, Argentina, 9Hospital General “San Martín” de la Plata, La Plata, Buenos Aires, Argentina, 10Hospital San Martín, La Plata, Argentina, 11Instituto Centenario, Buenos Aires, Buenos Aires, Argentina, 12Hospital Francés, Buenos Aires, Buenos Aires, Argentina, 13Sanatorio Güemes, Buenos Aires, Buenos Aires, Argentina, 14Hospital Rivadavia, Buenos Aires, Buenos Aires, Argentina, 15Hospital Británico, Buenos Aires, Buenos Aires, Argentina, 16Hospital San Roque,Gonnet,La Plata,Buenos Aires.Argentina, La Plata, Buenos Aires, Argentina, 17Centro de Educación Médica e Investigaciones Clínicas Norberto Quirno (CEMIC), Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina

    Background/Purpose: Patients with Idiopathic Inflammatory Myopathies (IIM) have been classified mainly according to Bohan and Peter (B&P) criteria, proposed in 1975. In 2017 the new…
  • Abstract Number: 401 • 2019 ACR/ARP Annual Meeting

    Performance of EULAR/ACR Classification Criteria for Idiopathic Inflammatory Myopathies in a Real-life Cohort of Adult Patients

    Ana Campar1 and Carlos Vasconcelos 2, 1Centro Hospitalar do Porto, Porto, Portugal, 2University of Porto, UMIB Abel Salazar Biomedical Sciences Institute, Porto, Portugal

    Background/Purpose: Idiopathic Inflammatory Myopathies (IIM) are rare and heterogenous diseases, remaining a clinical challenge and persisting with high morbidity and mortality. The lack of consensus…
  • Abstract Number: 402 • 2019 ACR/ARP Annual Meeting

    Chronic Disease Course and IVIg-dependance in Long-term Follow-up of Anti-HMGCR Immune-mediated Necrotizing Myopathy

    Océane Landon-Cardinal1, Kuberaka Mariampillai 2, Céline Anquetil 3, Aude Rigolet 2, Baptiste Hervier 4, Nicolas Champtiaux 2, Olivier Benveniste 3 and Yves Allenbach 3, 1Centre Hospitalier de l'Université de Montréal, Montréal, Canada, 2Pitié-Salpêtrière University Hospital, Paris, France, 3Sorbonne Université, Paris, France, 4Hopital Pitie-Salpetriere, Paris, France

    Background/Purpose: Anti-HMGCR antibodies have been associated with a severe form of immune-mediated necrotizing myopathy (IMNM) with a poor muscle strength recovery and early muscle damage.…
  • Abstract Number: 403 • 2019 ACR/ARP Annual Meeting

    Single-specificity Anti-SMN Autoantibodies Are Associated with a Novel Scleromyositis Overlap Syndrome

    Alexandra Baril-Dionne 1, Océane Landon-Cardinal2, Alain Meyer 3, Josiane Bourre-Tessier 1, Yves Troyanov 4, Anne-Marie Mansour 5, Farah Zarka 5, Jean-Paul Makhzoum 6, Jessica Nehme 5, Eric Rich 1, Jean-Richard Goulet 1, Tamara Grodzicky 1, Isabelle Richard 7, Marie Hudson 8, Valérie Leclair 9, Ira Targoff 10, Minoru Satoh 11, Marvin Fritzler 12 and Jean-Luc Senecal 1, 1Centre hospitalier de l'Universite de Montreal, Montreal, QC, Canada, 2Division of Rheumatology, Centre hospitalier de l'Université de Montréal; Department of Medicine, Université de Montréal, Montreal, QC, Canada, 3Centre de Reference des Maladies Autoimmunes Rares, Hôpitaux Universitaires de Strasbourg, Strasbourg, France, 4Division of Rheumatology, Department of Medicine, Hôpital du Sacre-Coeur de Montreal, Montreal, QC, Canada, 5Hôpital du Sacre-Coeur de Montreal, Montreal, QC, Canada, 6Vasculitis Clinic, Hopital du Sacre-Coeur de Montreal, Montreal, QC, Canada, 7CISSS AT Rouyn-Noranda, Rouyn-Noranda, QC, Canada, 8Jewish General Hospital, Lady Davis Institute for Medical Research, and Department of Medicine, McGill University, Montreal, QC, Canada, 9Division of Rheumatology, Department of Medicine, Jewish General Hospital; Clinical Epidemiology Unit, Department of Medicine, Karolinska Institutet, Montreal, QC, Canada, 10University of Oklahoma Health Sciences Center, Oklahoma City, OK, 11Department of Clinical Nursing, School of Health Sciences, University of Occupational and Environmental Health, Kitakyushu, Japan, 12Cumming School of Medicine, University of Calgary, Calgary, AB, Canada

    Background/Purpose: Autoantibodies (aAbs) to proteins comprising the survival of motor neuron (SMN) macromolecular complex have not been thoroughly studied. Only two publications described clinical associations…
  • 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: 405 • 2019 ACR/ARP Annual Meeting

    Anti-MDA5 Dermatomyositis: A Case Series, Systematic Review and Meta-analysis of the Literature

    Mohammad Ryadh Pokeerbux1, Luc Dauchet 2, Benjamin Lopez 3, Hélène Maillard 1, Sandrine Morell-Dubois 1, Eric Auxenfants 4 and Eric Hachulla 5, 1Department of Internal Medicine and Clinical Immunology, CHU Lille, University of Lille, Lille, France, 2Department of Epidemiology, CHU Lille, University of Lille, Lille, France, 3Institute of Immunology, CHU Lille, University of Lille, Lille, France, 4Department of Internal Medicine, Roubaix Hospital, Roubaix, France, 5Dept. of Internal Medicine and Clinical Immunology, Hôpital Claude Huriez, University of Lille, Lille, France, Lille, France

    Background/Purpose: Anti-MDA5 dermatomyositis is characterized by little or no muscle involvement, distinct cutaneous features and an increased risk of severe interstitial lung disease (ILD) with…
  • Abstract Number: 406 • 2019 ACR/ARP Annual Meeting

    Myositis Related Antibodies and Interstitial Lung Disease: Variables Associated with Baseline Lung Function and Functional Improvement: Results from a Multicentric Latin-american Cohort

    VERONICA WOLFF1, MARIA LAURA ALBERTI 2, FELIPE REYES 3, ERNESTO JUAREZ 4, JORGE ROJAS-SERRANO 4, FABIAN CARO 2, IVETTE BUENDIA 4, MAYRA MEJIA 4, MATIAS FLORENZANO 5 and FRANCISCO PAULIN 2, 1INSTITUTO NACIONAL DEL TORAX - UNIVERSIDAD DE CHILE, SANTIAGO, Chile, 2HOSPITAL MARIA FERRER, BUENOS AIRES, Argentina, 3HOSPITAL CLINICO UNIVERSIDAD DE CHILE, SANTIAGO, Chile, 4INSTITUTO NACIONAL DE ENFERMEDADES RESPIRATORIAS DE MEXICO DF, CIUDAD DE MEXICO, Mexico, 5INSTITUTO NACIONAL DEL TORAX, SANTIAGO, Chile

    Background/Purpose: Idiopathic inflammatory myopathies (IIM) comprise a group of autoimmune diseases associated to different myositis related antibodies (MRA), that determine distinct phenotypes but share some…
  • Abstract Number: 407 • 2019 ACR/ARP Annual Meeting

    Utility of Anti-SSA/SSB Assay and Anti-Ro 52 Antibody Assay in Routine Clinical Practice for Risk Assessment of Patients with Idiopathic Inflammatory Myositis

    Galina Marder 1, Sonali Narain2, Maria-Louise Barilla-Labarca 1 and Ana Valle 1, 1Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, 2Northwell Health, Great Neck, Long Island, NY

    Background/Purpose: Idiopathic inflammatory myopathies (IIM) are chronic autoimmune diseases affecting multiple organ systems and associated with a diverse autoantibody profile. Anti-SSA/SSB are the most frequent…
  • Abstract Number: 408 • 2019 ACR/ARP Annual Meeting

    Frequency of Concomitant Non-aminoacyl-transfer-RNA Synthetase Autoantibodies in Patients with Antisynthetase Syndrome

    Alexis Katz1, Soumya Chatterjee 2 and Yuxuan Jin 3, 1Cleveland Clinic, Cleveland, OH, 2Cleveland Clinic, Cleveland, 3Quantitative Health Science, Cleveland Clinic, Cleveland, OH

    Background/Purpose: Antisynthetase syndrome (ASSD) is an autoimmune disease with features including interstitial lung disease (ILD), myositis, inflammatory arthritis, Raynaud phenomenon, and mechanic’s hands.¹ Eight aminoacyl-transfer-RNA…
  • Abstract Number: 409 • 2019 ACR/ARP Annual Meeting

    Antisynthetase Syndromes: Correlation of Indirect Immunofluorescence Patterns with Diagnosis Criteria Fulfillment

    Martín Greco1, María Jesús García De Yébenes 2, Inmaculada Alarcón 3, Iñigo Rua Figueroa 4, Estíbaliz Loza 2, Carlos Rodriguez-Lozano 5, Anahy Brandy-Garcia 6 and Loreto Carmona 2, 1Rheumatology Department. Hospital Universitario de Gran Canaria Dr. Negrín., Las Palmas, Spain, 2Instituto de Salud Musculoesquelética - Inmusc., Madrid, Spain, 3Biochemical Department, Autoimmunity Laboratory. Hospital Universitario de Gran Canaria Dr. Negrín., Las Palmas, Canarias, Spain, 4Hospital Doctor Negrin, Las Palmas, 5Rheumatology Department. Hospital Universitario de Gran Canaria Dr. Negrín., Madrid, Spain, 6Hospital Universitari Germans Trias i Pujol, Badalona, Spain

    Background/Purpose: The antisynthetase syndromes (ASSD) are characterized by the presence of anti-aminoacyl transfer RNA synthetase (ARS) autoantibodies and a clinical classic triad of myositis, arthritis,…
  • Abstract Number: 410 • 2019 ACR/ARP Annual Meeting

    Prevalence of Malignancy in Myositis Patients with Anti-aminoacyl-tRNA Synthetase Antibodies: A Single Center Retrospective Study and Literature Review

    Taiga Kuga1, Yoshiyuki Abe 2, Kurisu Tada 3, Masakazu Matsushita 1, Ken Yamaji 1 and Naoto Tamura 1, 1Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 2Department of Rheumatology, Juntendo University, Tokyo, Japan, Tokyo, Japan, 3Juntendo University School of Medicine, Tokyo, Japan

    Background/Purpose: Anti-aminoacyl-tRNA synthetase antibodies (anti-ARS antibodies) are related to Idiopathic Inflammatory Myopathy (IIM) and Anti-Synthetase Syndrome (ASS). While anti-TIF1-γ antibody and anti-NXP-2 antibody are highly…
  • Abstract Number: 411 • 2019 ACR/ARP Annual Meeting

    Frequency and Staining Patterns of Antinuclear Antibodies in Myositis Patients Without Known Myositis-specific Autoantibodies

    Maria casal-Dominguez1, Iago Pinal-Fernandez 1, Ana Marin 2, Maria Teresa Sanz-Martinez 2, Andres Baucells-de la Pena 3, Katherine Pak 4, Yuji Hosono 1, Lisa Christopher-Stine 5 and Andrew L Mammen 4, 1NIH, Bethesda, 2Vall d'Hebron Hospital, Barcelona, Spain, 3Hospital de la Santa Creu i Sant Pau, Barcelona, Spain, 4National Institutes of Health, Bethesda, 5Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Objective:To determine the frequency and staining patterns of antinuclear antibodies (ANA) in myositis patients who do not have known myositis-specific autoantibodies.Methods: Material and methods:Sera…
  • Abstract Number: 412 • 2019 ACR/ARP Annual Meeting

    Elevated Serum BAFF Levels in Patients with Dermatomyositis: Association with Interstitial Lung Disease

    Takashi Matsushita1, Tadahiro Kobayashi 1, Miyu Kano 1, Yasuhito Hamaguchi 1 and Kazuhiko Takehara 2, 1Kanazawa University, Kanazawa, Japan, 2Department of Dermatology, Kanazawa University, Kanazawa, Japan

    Background/Purpose: Patients with dermatomyositis (DM) frequently have myositis-specific autoantibodies (MSAs), which are closely associated with different clinical features. Patients with anti-aminoacyl-tRNA synthetase (ARS) antibody (Ab)…
  • Abstract Number: 413 • 2019 ACR/ARP Annual Meeting

    Performance of the Patient Reported Outcomes Measurement Information System 29-item Profile in Comparison to the Clinical Disease Activity Index (CDAI) and Routine Assessment of Patient Index Data 3 (RAPID3) in an Australian Rheumatoid Arthritis Cohort

    Kathryn Gibson1, Dana Gerogevsky 2, Frank Huang 3, Ray Fang 3 and Joseph Descallar 4, 1Liverpool Hospital, Sydney, New South Wales, Australia, 2Royal Prince Alfred Hospital, Sydney, Australia, 3University of New South Wales, Sydney, New South Wales, Australia, 4Ingham Research Institute, Sydney, New South Wales, Australia

    Background/Purpose: The Patient-Reported Outcomes Measurement Information System (PROMIS) was developed to improve measurement of patient-reported outcomes. A large study from the US reported guarded support…
  • Abstract Number: 414 • 2019 ACR/ARP Annual Meeting

    Treat-to-Target Approach in the Management of Elderly Rheumatoid Arthritis Patients

    Vivek Joseph 1, Swetha Vontela 2, Surjeet Dheer3, Molly Weinberg 4, Zuhayr Haq 2 and Arundathi Jayatilleke 5, 1Drexel University, PHILADELPHIA, PA, 2Drexel University, Philadelphia, 3Mercy Catholic Medical Center, Philadelphia, 4Drexel University, Philadlephia, 5Drexel, Philadelphia, PA

    Background/Purpose: With the advent of biologic therapy for RA, the American College of Rheumatology advocates a treat to target (TTT) approach in the treatment of…
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