ACR Meeting Abstracts

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Abstracts tagged "Systemic sclerosis"

  • Abstract Number: 1044 • 2019 ACR/ARP Annual Meeting

    TGF-β Isoforms Modulate the RNA Cargo of Extracellular Vesicles (Exosomes) Isolated from Cultured Normal Human Lung Microvascular Endothelial Cells: A Mechanistic Link Between Endothelial Cell Dysfunction and the Establishment of a Profibrotic Phenotype in SSc?

    Peter Wermuth1 and Sergio Jimenez 1, 1Jefferson Institute of Molecular Medicine and Division of Connective Tissue Diseases, Thomas Jefferson University, Philadelphia, PA, Philadelphia, PA

    Background/Purpose: Extracellular vesicles (EV) are a diverse assortment of lipid bilayer-bound vesicles of various sizes and origin. Exosomes are a subset of EV arising from…
  • Abstract Number: 1629 • 2019 ACR/ARP Annual Meeting

    Significance of Abnormal Nailfold Videocapillarscopy Among Patients with Raynaud’s Phenomenon And/or Suspected Connective Tissue Disease: A Cross-Sectional Single-Center US Experience

    Yasser Radwan1, Tina Gunderson 2, Cynthia Crowson 3, Alicia Hinze 1, Kevin Moder 4, Floranne Ernste 4, Shreyasee Amin 4, Uma Thanarajasingam 2, Thomas Osborn 1, Kenneth Warrington 4, Paul Wennberg 4 and Ashima Makol 1, 1Mayo Clinic Minnesota, rochester, MN, 2Mayo Clinic, Rochester, MN, 3Mayo Clinic Rochester, Rochester, 4Mayo Clinic Rochester, rochester, MN

    Background/Purpose: Nailfold videocapillaroscopy (NVC) is a simple, non-invasive & highly sensitive tool to evaluate structural abnormalities of the microcirculation in vivo and considered a key…
  • Abstract Number: 1656 • 2019 ACR/ARP Annual Meeting

    Health-Related Quality of Life in Patients with Systemic Sclerosis-Associated Interstitial Lung Disease (SSc-ILD): Impact of Lung Function on Patient-Reported Outcomes in a Randomized Phase III Trial

    Michael Kreuter 1, Anna Maria Hoffmann-Vold 2, Marco Matucci-Cerinic 3, Lesley Saketkoo 4, Kristin Highland5, Hilary Wilson 6, Margarida Alves 7, Nils Schoof 6 and Toby Maher 8, 1Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik, University of Heidelberg, Member of the German Center for Lung Research, Germany, Germany, Germany, 2Department of Rheumatology, Oslo University Hospital, Oslo, Norway, Oslo, Norway, 3University of Florence, Department of Medicine, Florence, Italy, Florence, Italy, 4New Orleans Scleroderma and Sarcoidosis Patient Care and Research Center, New Orleans; Tulane University School of Medicine, University Medical Center – Comprehensive Pulmonary Hypertension Center, USA, New Orleans, 5Cleveland Clinic, Cleveland, Ohio, USA, Cleveland, OH, 6Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany, 7Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany, Ingelheim am Rhein, Germany, 8National Heart and Lung Institute, Imperial College London, UK and National Institute for Health Research Clinical Research Facility, Royal Brompton Hospital, London, UK, London, United Kingdom

    Background/Purpose: SSc-ILD is a major cause of morbidity and mortality in patients with systemic sclerosis. A subset of patients with SSc-ILD show a decline in…
  • Abstract Number: 2598 • 2019 ACR/ARP Annual Meeting

    Different Treatment Backgrounds Do Not Influence Aminaphtone Efficacy in Primary and Secondary Raynaud’s Phenomenon

    Alberto Sulli1, Federica Goegan 2, Emanuele Gotelli 2, Massimo Patane' 3, Carmen Pizzorni 3, Sabrina Paolino 3, Elisa Alessandri 4 and Barbara Ruaro 5, 1Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS Ospedale Policlinico San Martino, Genoa, Italy, Genoa, Italy, 2Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Genoa, Italy, 3Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic Hospital, Genoa, Italy, Genoa, Italy, 4Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic Hospital, Genoa, Italy, Genova, 51 Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS Ospedale Policlinico San Martino, Genoa, Italy; 2 Cardinal Ferrari Centre, S. Stefano Rheabilitation, Fontanellato (Parma), Italy, Genoa, Italy

    Background/Purpose: Aminaphtone treatment improves clinical symptoms of Raynaud's phenomenon (RP) and increases peripheral blood perfusion (BP) in patients with either primary or secondary RP (1-2).The…
  • Abstract Number: 2747 • 2019 ACR/ARP Annual Meeting

    Identification of Naturally Presented Peptides of the Autoantigen Topoisomerase-I Reveals a Common Pathogenic Mechanism in Patients with Systemic Sclerosis

    Eleni Tiniakou1, Andrea Fava 2, Zsuzsanna McMahan* 3, Tara Gurh 4, Robert O'Meally 4, Ami Shah 5, Frederick Wigley 3, Robert Cole 4, Francesco Boin 6 and Erika Darrah 1, 1Johns Hopkins University, Baltimore, MD, 2Johns Hopkins University School of Medicine, Baltimore, MD, 3Johns Hopkins University, Division of Rheumatology, Baltimore, 4Johns Hopkins University, Baltimore, 5Johns Hopkins Hospital, Baltimore, MD, 6UCSF, San Francisco, CA

    Background/Purpose: Autoimmune responses to DNA topoisomerase-I (TOP1) are found in a subset of patients with scleroderma at high risk for interstitial lung disease (ILD) and…
  • 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: 729 • 2019 ACR/ARP Annual Meeting

    Modelled Patient Level Skin Score Trajectory Predicts Risk of Death or Major Organ-Based Complications in Diffuse Cutaneous Systemic Sclerosis

    Svetlana Nihtyanova1, Emma Derrett-Smith 1, Carmen Fonseca 1, Voon Ong 2 and Christopher Denton 3, 1UCL Medical School, Royal Free Campus, London, United Kingdom, 2UCL Medical School, Royal Free Campus, London, 3University College London Division of Medicine, Centre for Rheumatology and Connective Tissue Diseases, London, UK, London, United Kingdom

    Background/Purpose: For most patients with diffuse cutaneous systemic sclerosis (dcSSc), skin thickness improves over time, especially with background immunosuppressive treatment. This has reduced confidence in…
  • Abstract Number: 1046 • 2019 ACR/ARP Annual Meeting

    The Effect of Nintedanib versus Mycopheolate Mofetil in the FRA2 Mouse Model of Systemic Sclerosis Associated Interstitial Lung Disease

    Thuong Trin-Minh 1, Yun Zhang 2, Jörg Distler 3 and Lutz Wollin4, 1University Erlangen-Nuremberg, Erlangen-Nuremburg, Germany, 2University Erlangen-Nuremberg, Erlangen, Germany, 3Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, Erlangen, Germany, 4oehringer Ingelheim, Biberach, Germany

    Background/Purpose: Interstitial lung disease (ILD) is a key driver of mortality in patients with systemic sclerosis (SSc). In lack of approved treatment it constitutes a…
  • Abstract Number: 1630 • 2019 ACR/ARP Annual Meeting

    Contribution of Chest Wall Muscle Atrophy to Decline of Forced Vital Capacity in Patients with Systemic Sclerosis-associated Interstitial Lung Disease

    Takashi Nawata1, Mikito Suzuki 2, Yuichiro Shirai 3 and Masataka Kuwana 3, 11. Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan. 2. Department of Medicine and Clinical Science, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan, Tokyo, Japan, 2Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, Tokyo, Japan, 3Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan, Bunkyo-ku, Tokyo, Japan

    Background/Purpose: Interstitial lung disease (ILD) is the leading causes in patients with systemic sclerosis (SSc). Forced vital capacity (FVC) is routinely used for assessment of…
  • Abstract Number: 1657 • 2019 ACR/ARP Annual Meeting

    Sarcopenia in Systemic Sclerosis

    Iván Dario Remolina Rincón1, Maria Alak 2, Graciela Alsina 3, Pedro Quevedo 2, Mariano Rivero 4 and Damian Duartes 5, 1Hospital Británico, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina, 2Hospital Britanico de Buenos Aires, Ciudad Autonoma de Buenos Aires, Ciudad Autonoma de Buenos Aires, Argentina, 3Consultorios Pampa, Ciudad Autonoma de Buenos Aires, Ciudad Autonoma de Buenos Aires, Argentina, 4Hospital Británico, Buenos Aires, Buenos Aires, Argentina, 5Hospital Británico, Ciudad Autonoma de Buenos Aires, Ciudad Autonoma de Buenos Aires, Argentina

    Background/Purpose: Gastrointestinal tract involvement in systemic sclerosis (SSc) occurs in almost all patients varying in severity and affecting motility, digestion, absorption and excretion. These abnormalities…
  • Abstract Number: 2599 • 2019 ACR/ARP Annual Meeting

    Body Composition and Nailfold Videocapillaroscopy Patterns in a Cohort of Systemic Sclerosis Patients

    Tomatis Veronica 1, Sabrina Paolino 2, Alberto Sulli3, Emanuele Gotelli 4, Andrea Casabella 5, Francesco Cattelan 6, Schenone Carlotta 1, Carmen Pizzorni 2, Elisa Alessandri 7 and Maurizio Cutolo 8, 1Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic Hospital, Genoa, Italy, Genova, Liguria, Italy, 2Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic Hospital, Genoa, Italy, Genoa, Italy, 3Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS Ospedale Policlinico San Martino, Genoa, Italy, Genoa, Italy, 4Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Genoa, Italy, 51 Research Laboratory and Academic Division of the Clinical Rheumatology Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic Hospital, Genoa, Italy, Genoa, Italy, 6Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, IRCCS Polyclinic Hospital San Martino, University of Genoa, Genoa, Italy, 7Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS San Martino Polyclinic Hospital, Genoa, Italy, Genova, 8Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, IRCCS Ospedale Policlinico San Martino, Genoa, Italy, Genoa, Italy

    Background/Purpose: Systemic sclerosis (SSc) is a chronic autoimmune disease, characterized by microvascular damage and progressive fibrosis. Among clinical complications, abnormal body composition and sarcopenia have been reported…
  • Abstract Number: 2748 • 2019 ACR/ARP Annual Meeting

    Cracking a Novel Profibrotic Molecular Mechanism: lncRNA H19X and DDIT4L Crosstalk

    Elena Pachera1, Shervin Assassi 2, Gloria Salazar 3, Mojca Frank-Bertoncelj 4, Jörg Distler 5, Gabriela Kania 6 and Oliver Distler 7, 1Center of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, Zurich, Zurich, Switzerland, 2Division of Rheumatology and Clinical Immunogenetics, University of Texas McGovern Medical School, Houston, Texas, USA, Houston, TX, 3University of Texas McGovern Medical School, Houston, 4University Hospital Zürich, Zürich, Switzerland, 5Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, Erlangen, Germany, 6Centre of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 7Dept. of Rheumatology, University Hospital Zürich, Zürich, Switzerland, Zürich, Switzerland

    Background/Purpose: Long noncoding RNAs (lncRNAs) are an emerging class of noncoding transcripts involved in the regulation of gene expression in health and disease. LncRNAs function…
  • 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: 731 • 2019 ACR/ARP Annual Meeting

    A Systemic Review of Factors Associated with Systemic Sclerosis-associated Pulmonary Arterial Hypertension (SSc-PAH)

    Yuxuan Jiang 1, Matthew Turk 1 and Janet Pope2, 1University of Western Ontario, London, ON, Canada, 2Western University, London, ON, Canada

    Background/Purpose: Pulmonary arterial hypertension (PAH) in systemic sclerosis (SSc) is a lethal complication affecting approximately 8-15% of patients. Screening methods including echocardiography and pulmonary function…
  • Abstract Number: 1047 • 2019 ACR/ARP Annual Meeting

    CXCL4-L1 Levels Are Elevated in Systemic Sclerosis Patients and Correlate with Pulmonary Arterial Hypertension and Capillaroscopic Indices of Vascular Damage

    Vasiliki Kalliopi Bournia1, Markos Patsouras 2, Nikolaos Vlachoyiannis 3, Athanasios Tzioufas 4, Petros Sfikakis 5 and Panagiotis Vlachoyiannopoulos 6, 11st Department of Propaedeutic and Internal Medicine, Medical School, National and Kapodistrian University of Athens, Athens, Greece, Athens, Greece, 2Department of Pathophysiology, Medical School, National and Kapodistrian University of Athens, Greece, Athens, 31st Department of Propaedeutic and Internal Medicine, Medical School, National and Kapodistrian University of Athens, Athens, Greece, Athens, 4Department of Pathophysiology, Athens School of Medicine, National and Kapodistrian University of Athens, Athens, Greece, Athens, Greece, 5Joint Rheumatology Programme, National & Kapodistrian University of Athens Medical School, Athens, Greece, Athens, Greece, 6University General Hospital of Athens “Laiko”, Athens, Greece

    Background/Purpose: Recent findings have implicated CXCL4 in the pathogenesis of systemic sclerosis (SSc), while also indicating a potential role of this chemokine as a biomarker…
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