ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "systemic sclerosis and treatment"

  • Abstract Number: 800 • 2018 ACR/ARHP Annual Meeting

    Assessment of Recent Evidence to Support Treatment Recommendations in Patients with SSc-ILD

    Anna-Maria Hoffmann-Vold1, Toby Maher2, Edward Philpot3, Ali Ashrafzadeh4, Diwakar Jha5, Margarida Alves6 and Oliver Distler7, 1Oslo University Hospital, Oslo, Norway, 2Royal Brompton Hospital, London, United Kingdom, 3IQVIA, Durham, NC, 4IQVIA, Los Angeles, CA, 5IQVIA, Gurugram, India, 6Boehringer Ingelheim International GmbH, Ingelheim, Germany, 7Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland

    Background/Purpose: Systemic Sclerosis (SSc) is a chronic autoimmune disease characterized by fibrosis of skin and internal organs with an estimated worldwide prevalence of 110-430 cases/million.…
  • Abstract Number: 1724 • 2018 ACR/ARHP Annual Meeting

    Effectiveness and Safety of Rituximab for the Treatment of Refractory Systemic Sclerosis Associated Calcinosis: A Case Series

    Francisco Javier Narváez1, Juan Pablo Pirola2, Judit Lluch3, Pablo Juárez3, Isabel Morales3 and Joan Miquel Nolla3, 1Rheumatology Department, Hospital de Bellvitge. Barcelona. Spain, L’Hospitalet de Llobregat, Spain, 2Rheumatology, Hospital Privado Centro Médico de Córdoba, Cordoba, Argentina, 3Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain

    Background/Purpose: To analyze the effectiveness and safety of rituximab (RTX) for the treatment of refractory systemic sclerosis (SSc)–associated calcinosis. Methods: We undertook an observational study…
  • Abstract Number: 1877 • 2018 ACR/ARHP Annual Meeting

    Specific Pneumoproteins Predict Progression of Interstitial Lung Disease in Systemic Sclerosis Patients Undergoing Treatment with Immunosuppression

    Elizabeth R. Volkmann1, Donald P. Tashkin1, Masataka Kuwana2, Ning Li3, Julio Charles4, Faye N. Hant5, Galina S. Bogatkevich6, Tanjina Akter6, Michael Roth7, Hyun J. Grace Kim8, Jonathan Goldin9, Dinesh Khanna10, Philip J. Clements11, Daniel E. Furst7, Robert Elashoff12, Rick Silver13 and Shervin Assassi14, 1University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 2Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, 3Biomathematics, University of California, Los Angeles, Los Angeles, CA, 4University of Texas Health Science Center at Houston, Houston, TX, 5Rheumatology, Medical University of South Carolina, Charleston, SC, 6Division of Rheumatology and Immunology, Department of Medicine, Medical University of South Carolina, Charleston, SC, 7Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 8Department of Radiology, David Geffen School of Medicine at UCLA, Los Angeles, CA, 9Department of Radiological Sciences at UCLA, University of California, Los Angeles, David Geffen School of Medicine, Santa Monica, CA, 10Division of Rheumatology, Department of Internal Medicine, University of Michigan Scleroderma Program, University of Michigan, Ann Arbor, MI, 11Medicine, University of California, Los Angeles, Los Angeles, CA, 12University of California, Los Angeles, Los Angeles, CA, 13Rheumatology, Medical University of SC, Charleston, SC, 14University of Texas McGovern Medical School, Houston, TX

    Background/Purpose: Interstitial lung disease (ILD) is the leading cause of death in systemic sclerosis (SSc). While some SSc-ILD patients are stable or improve with immunosuppressive…
  • Abstract Number: 2708 • 2018 ACR/ARHP Annual Meeting

    Current Management of Early Diffuse Cutaneous Systemic Sclerosis in US Scleroderma Centers

    Rebecca B. Blank1, Jessica K. Gordon2, Jackie Szymonifka3, Shervin Assassi4, Elana J. Bernstein5, Flavia V. Castelino6, Robyn T. Domsic7, Faye N. Hant8, Monique Hinchcliff9, Kate Homer10, Ami A. Shah11, Victoria Shanmugam12, Virginia D. Steen13, Tracy M. Frech14 and Dinesh Khanna15, 1Internal Medicine, New York Presbyterian-Weill Cornell Hospital, New York, NY, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Hospital for Special Surgery, New York, NY, 4University of Texas McGovern Medical School, Houston, TX, 5Rheumatology, Columbia University, New York, NY, 6Rheumatology, Harvard Medical School, Boston, MA, 7Medicine - Rheumatology, University of Pittsburgh, Pittsburgh, PA, 8Rheumatology, Medical University of South Carolina, Charleston, SC, 9Division of Rheumatology, Northwestern University Medical School, Chicago, IL, 10Department of Internal Medicine, Rheumatology Division, Scleroderma Program, University of Michigan, Ann Arbor, MI, 11Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 12Rheumatology, The George Washington University, Washington, DC, 13Rheumatology, MedStar Georgetown University Hospital, Washington, DC, 14Division of Rheumatology, University of Utah, Salt Lake City, UT, 15Division of Rheumatology, Department of Internal Medicine, University of Michigan Scleroderma Program, University of Michigan, Ann Arbor, MI

    Background/Purpose: Standard treatment for the diverse aspects of diffuse cutaneous systemic sclerosis (dcSSc) is not yet well defined although experts have described therapeutic algorithms.  The…
  • Abstract Number: 749 • 2017 ACR/ARHP Annual Meeting

    Treatment with Cyclophosphamide for Systemic Sclerosis-Interstitial Lung Disease Does Not Lead to a Sustained Improvement in Lung Function in Two Independent Cohorts

    Elizabeth R. Volkmann1, Donald P. Tashkin1, Myung Sim1, Ning Li2, Dinesh Khanna3, Michael Roth4, Philip J. Clements4, Anna-Maria Hoffmann-Vold5, Daniel E. Furst1, Grace Kim6, Jonathan Goldin1 and Robert Elashoff7, 1University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 2Biomathematics, University of California, Los Angeles, Los Angeles, CA, 3University of Michigan, Ann Arbor, MI, 4Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 5Oslo University Hospital, Oslo, Norway, 6Radiology, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 7University of California, Los Angeles, Los Angeles, CA

    Background/Purpose: Compared with placebo, treatment with cyclophosphamide (CYC) improved lung function in patients with systemic sclerosis-related interstitial lung disease (SSc-ILD) after 1 year in Scleroderma…
  • Abstract Number: 943 • 2017 ACR/ARHP Annual Meeting

    The Course of the Forced Vital Capacity during Treatment for Systemic Sclerosis-Related Interstitial Lung Disease Predicts Long-Term Survival in 2 Independent Cohorts

    Elizabeth R. Volkmann1, Donald P. Tashkin1, Myung Sim1, Dinesh Khanna2, Michael Roth3, Philip J. Clements3, Daniel E. Furst1, Lynette Keyes-Elstein4, Ashley Pinckney4, Ellen Goldmuntz5, Robert Elashoff6 and Keith Sullivan7, 1University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 2University of Michigan, Ann Arbor, MI, 3Medicine, University of California, Los Angeles, David Geffen School of Medicine, Los Angeles, CA, 4Rho Federal Systems, Inc., Chapel Hill, NC, 5NIAID, NIH, Bethesda, MD, 6University of California, Los Angeles, Los Angeles, CA, 7Duke University, Durham, NC

    Background/Purpose: While prior observational studies have identified predictors of mortality in systemic sclerosis-interstitial lung disease (SSc-ILD), no studies have evaluated predictors of long-term mortality in…
  • Abstract Number: 2692 • 2017 ACR/ARHP Annual Meeting

    Vitamin D Deficiency in Systemic Sclerosis Patients: Relations with Multiple Clinical Parameters and Standard Treatment

    Amelia Chiara Trombetta1, Vanessa Smith2, Emanuele Gotelli1, Massimo Ghio1, Sabrina Paolino1, Carmen Pizzorni3, Amber Vanhaecke4, Barbara Ruaro5, Alberto Sulli3 and Maurizio Cutolo3, 1Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino, Genoa, Italy, Genoa, Italy, 2Faculty of Internal Medicine, Ghent University, Ghent, Belgium, 3Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, IRCCS Policlinico San Martino, University of Genoa, Genoa, Italy, Genoa, Italy, 4Department of Rheumatology, Ghent University Hospital, Ghent University, Ghent, Belgium, Gent, Belgium, 5Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genoa, Genoa, Italy, Genoa, Italy

    Vitamin D Deficiency In Systemic Sclerosis Patients: Relations With Multiple Clinical Parameters and Standard TreatmentBackground/Purpose : In SSc patients, low 25-hydroxyvitamin D (25(OH)D) serum concentrations have…
  • Abstract Number: 2889 • 2017 ACR/ARHP Annual Meeting

    Aminaphtone Ameliorates Clinical Symptoms and Increases Skin Blood Perfusion in Patients with Both Primary and Secondary Raynaud Phenomenon: A Six-Month Open Study

    Alberto Sulli1, Maurizio Cutolo2, Carmen Pizzorni2, Sabrina Paolino2, Elisa Alessandri2, Emanuele Gotelli2 and Barbara Ruaro2, 1Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino, Genoa, Italy, Genova, Italy, 2Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino, Genoa, Italy, Genoa, Italy

    Background/Purpose: Current treatments for Raynaud's phenomenon (RP) have limited efficacy, which was mainly demonstrated by physician/patient reported outcomes. Aminaphtone is a vasoactive drug recently suggested…
  • Abstract Number: 2069 • 2016 ACR/ARHP Annual Meeting

    Dipeptidyl-Peptidase-4 (DPP4) Positive Fibroblast Subpopulation Promotes Fibrosis and Are a Molecular Target for Treatment of Fibrosis

    Alina Soare1,2, Simon Rauber3, Thomas Wohlfahrt1, Clara Dees4, Ruifang Liang4, Yun Zhang1, Chih-Wei Chen1, Andreas Ramming5, Oliver Distler6, Carina Mihai7, Georg Schett4 and Joerg HW Distler4, 1Department of Internal Medicine 3 and Institute for Clinical Immunology, Department of Internal Medicine 3 and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 2Carol Davila University of Medicine and Pharmacy, Internal Medicine and Rheumatology Department, Cantacuzino Clinical Hospital, Bucharest, Romania, 3Department of Internal Medicine 3, Rheumatology and Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 4Department of Internal Medicine 3 – Rheumatology and Immunology, Universitätsklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Erlangen, Germany, 5Department of Internal Medicine 3, Rheumatology and Immunology, Department of Internal Medicine 3, Rheumatology and Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 6Center of Experimental Rheumatology, University Hospital Zurich, Zurich, Switzerland, 7Department of Internal Medicine and Rheumatology, Carol Davila University of Medicine and Pharmacy, Cantacuzino Hospital, Bucharest, Romania

    Background/Purpose:  Dipeptidyl-peptidase-4 (DPP4) has been recently shown to identify a distinct dermal lineage with intrinsic fibrogenic potential and its targeted inhibition leads to reduced scar…
  • Abstract Number: 2888 • 2016 ACR/ARHP Annual Meeting

    Usefulness of Bosentan in the Prevention of Pulmonary Hypertension in Patients with Systemic Sclerosis

    Ivan Castellví1, Carmen Pilar Simeón2, Monica Paola Sarmiento1, Alfredo Guillen2, Cesar Diaz-Torné3, Josep Maria De Llobet Zubiaga1, Jordi Casademont4 and Vicent Fonollosa2, 1Rheumatology, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain, 2Internal Medicine, Hospital Universitari Vall d'Hebron, Barcelona, Spain, 3Rheumatology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain, 4Internal Medicine, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain

    Background/Purpose:  Systemic sclerosis (SSc) is a systemic autoimmune disease in which the damage of microcirculation is critical to develop the disease. In SSc, vascular complications…
  • Abstract Number: 2913 • 2016 ACR/ARHP Annual Meeting

    Four Year Effects of Combined Bosentan and Iloprost Treatment on Nailfold Absolute Capillary Number, Fingertip Blood Perfusion and Clinical Status, in Systemic Sclerosis Patients

    Amelia Chiara Trombetta1, Carmen Pizzorni2, Barbara Ruaro3, Sabrina Paolino3, Alberto Sulli2, Vanessa Smith4 and Maurizio Cutolo3, 1Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, Genoa, Italy, Genova, Italy, 2Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, IRCCS A.O.U. San Martino-IST, University of Genova, Genoa, Italy, Genova, Italy, 3Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, IRCCS A.O.U. San Martino-IST, University of Genova, Genoa, Italy, Genoa, Italy, 4Department of Rheumatology, Ghent University Hospital, Ghent University, Ghent, Belgium

    Background/Purpose:  In systemic sclerosis (SSc), microvascular damage progresses from capillary dilation to capillary loss and reactive angiogenesis, as detectable by nailfold videocapillaroscopy (NVC) [1]. The…
  • Abstract Number: 3247 • 2016 ACR/ARHP Annual Meeting

    Safety and Efficacy of Belimumab with Background Mycophenolate for Early Diffuse Cutaneous Systemic Sclerosis: A Randomized, Placebo Controlled, Pilot Trial

    Jessica K. Gordon1, Eliza Pelrine2, Yuo-Yu Lee3, Cynthia Magro4, Elana J. Bernstein5, Horatio F. Wildman6 and Robert F. Spiera1, 1Rheumatology, Hospital for Special Surgery, New York, NY, 2Hospital for Special Surgery, New York, NY, 3Epidemiology and Biostatistics, Hospital for Special Surgery, New York, NY, 4Pathology, Weill Cornell Medical College, New York, NY, 5Department of Medicine, Division of Rheumatology, Columbia University, New York, NY, 6Dermatology, Weill Cornell Medical College, New York, NY

    Background/Purpose: Abnormalities of B cell function are part of the pathogenesis of systemic sclerosis (SSc), and B-lymphocyte stimulator (BLyS) is increased in the serum and…
  • Abstract Number: 1896 • 2016 ACR/ARHP Annual Meeting

    Efficacy of Pulmonary Arterial Hypertension-Specific Drugs Combination Therapy in Survival of Patients with Pulmonary Arterial Hypertension Associated with Systemic Sclerosis and Other Connective Tissue Diseases

    Sumiaki Tanaka1, Yu Matsueda1, Gakuro Abe2, Jun Okada3 and Shunsei Hirohata1, 1Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Kanagawa, Japan, 2Kitasato University School of Medicine, Sagamihara, Japan, 3Nutritional management, Kitasato Junior Collage of health and Hygienic Sciences, Minami-Uonuma, Japan

    Background/Purpose: Survival of patients with pulmonary arterial hypertension (PAH) associated with connective tissue disease (CTD), especially systemic sclerosis (SSc), is poorer than that of patients…
  • Abstract Number: 848 • 2015 ACR/ARHP Annual Meeting

    Nitroglycerin Patch Application in Systemic Sclerosis: Evaluation By Laser Doppler Imaging

    Georgiana Bentea, Aurelien Wauters, Jean-Claude Wautrecht and Elie Cogan, Erasme Hospital, Brussels, Belgium

    Background/Purpose: Systemic sclerosis (SSc) is a complex autoimmune disease, commonly associated with Raynaud phenomenon (RP). The aim of this study was to characterize the microvascular…
  • Abstract Number: 1879 • 2015 ACR/ARHP Annual Meeting

    Immunosuppressive “Routine”� Treatment of SSc Patients with Limited Cutaneous Involvement and Interstitial Lung Disease

    Dörte Huscher1, Sabine Adler2, Elise Siegert3, Giuseppina Abignano4, Yannick Allanore5, Jerome Avouac6, Kerstin Becker7, Laszlo Czirjak8,9, Francesco Del Galdo10, Christopher P. Denton11, Oliver Distler12, Ivan Foeldvari13, Beata Garay-Toth14, Serena Guiducci15, Veronika K. Jaeger16, Veronika Lóránd9, Marco Matucci-Cerinic17, Britta Maurer18, Ulf Müller-Ladner19, Svetlana I. Nihtyanova20, Ingo H. Tarner21, Gabriele Valentini22, Serena Vettori23, Ulrich A. Walker24 and Gabriela Riemekasten25, 1Charité-University Hospital and German Rheumatism Research Centre, Berlin, Germany, 2Rheumatology, Immunology, Allergology, University Hospital Bern, Bern, Switzerland, 3Rheumatology and Clinical Immunology, Charité – University Hospital, Berlin, Berlin, Germany, 4Clinical and Experimental Medicine, Second University of Naples, Napoli, Italy, 5Department of Rheumatology A, Paris Descartes University, Cochin Hospital, Paris, France, 6Paris Descartes University, Rheumatology A department, Cochin Hospital, Paris, France, 7Rheumatology and Clinical Immunology, Charité University Hospital, Berlin, Germany, 8Rheumatology, Pecs, Hungary, 9Rheumatology and Immunology Medical School, University of Pécs, Pécs, Hungary, 10Scleroderma Group, Leeds Institute of Molecular Medicine, Leeds, United Kingdom, 11Rheumatology and Connective Tissue Diseases, University College London, London, United Kingdom, 12Department of Rheumatology, Research of Systemic Autoimmune Diseases, University Hospital Zurich, Zurich, Switzerland, 13Hamburger Zentrum für Kinder-und Jugendrheumatologie, Hamburg, Germany, 14FESCA, Budapest, Hungary, 15Rheumatology, University of Florence, Florence, Italy, 16Department of Rheumatology, University Hospital Basel, Basel, Switzerland, 17Dept of Medicine/Div of Rheum, University of Florence, Firenze, Italy, 18r, University Hospital Zurich, Zurich, Switzerland, 19Internal Medicine and Rheumatology, Justus-Liebig-University of Giessen, Kerckhoff-Klinik, Bad Nauheim, Germany, 20Rheumatology, UCL Division of Medicine, London, United Kingdom, 21Rheumatology and Clinical Immunology, Justus-Liebig-University of Giessen, Kerckhoff-Klinik, Bad Nauheim, Germany, 22Internal and Experimental Medicine, Rheumatology Unit, Second University of Naples, Naples, Italy, 23Department of Internal and Experimental Medicine, Rheumatology Unit, Second University of Naples, Naples, Italy, 24Rheumatology, Systemic Sclerosis, Basel, Switzerland, 25Clinic of Rheumatology, University of Luebeck, Lübeck, Germany

    Background/Purpose: Interstitial lung disease (ILD) represents one of the most frequent causes of death in systemic sclerosis (SSc) patients. Yet, there are no approved drugs…
  • 1
  • 2
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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 ET on November 14, 2024. 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.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology