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Abstracts tagged "scleroderma and systemic sclerosis"

  • Abstract Number: 688 • 2013 ACR/ARHP Annual Meeting

    Minimal Clinically Important Investigations In Systemic Sclerosis

    Jessica Meijs1, Anne A. Schouffoer1, Nina Ajmone Marsan2, Maarten K. Ninaber3 and Tom W.J. Huizinga1, 1Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 2Cardiology, Leiden University Medical Center, Leiden, Netherlands, 3Pulmonology, Leiden University Medical Center, Leiden, Netherlands

    Background/Purpose: The optimal management of Systemic Sclerosis (SSc) is a challenge due to the complexity of early diagnosis and identification of patients who are at…
  • Abstract Number: 674 • 2013 ACR/ARHP Annual Meeting

    Systemic Sclerosis Disease Subset Is a Better Predictor Of Long Term Outcome Than Autoantibody Profile

    Svetlana I. Nihtyanova1, Voon H. Ong2 and Christopher P. Denton3, 1Department of Rheumatology, Royal Free and University College Medical School, London, United Kingdom, 2Department of Rheumatology, The Royal Free and University College Medical School, London, United Kingdom, 3Centre for Rheumatology, Royal Free and University College Medical School, London, United Kingdom

    Background/Purpose: Disease subset has been shown to strongly correlate with survival and risk of organ complications in patients with systemic sclerosis (SSc). Nevertheless evidence in…
  • Abstract Number: 675 • 2013 ACR/ARHP Annual Meeting

    Impact Of Male Sex On Survival In Systemic Sclerosis

    Haseena Hussein1, Peter Lee2, Cathy Chau3 and Sindhu R. Johnson4, 1Medicine, Toronto Scleroderma Research Program, Mount Sinai Hospital, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada, 2Lebovic Bldg, Mt. Sinai Hospital, Toronto, ON, Canada, 3Medicine, Toronto Scleroderma Program, Toronto Western Hospital, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada, 4Medicine, Division of Rheumatology, Toronto Western Hospital, University Health Network Pulmonary Hypertension Programme, Toronto General Hospital, Mount Sinai Hospital and University of Toronto, Toronto, ON, Canada

    Background/Purpose: Systemic sclerosis (SSc) has a female predominance with a female-to-male ratio of 3:1. Sex differences have been seen in many autoimmune diseases; however, little…
  • Abstract Number: 680 • 2013 ACR/ARHP Annual Meeting

    Diastolic Dysfunction Amongst Autoantibody Subgroups Of Patients With Diffuse Scleroderma

    Cory Perugino1, John Stephens2, Colin O'Rourke3 and Soumya Chatterjee4, 1Internal Medicine, Cleveland Clinic, Cleveland, OH, 2Cardiovascular Medicine, Cleveland Clinic, Cleveland, OH, 3Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, 4Rheumatic and Immunologic Ds, Cleveland Clinic, Cleveland, OH

    Background/Purpose: Scleroderma or systemic sclerosis (SSc) is an autoimmune disease characterized by microangiopathy, tissue hypoxia, and fibrosis. At least seven different autoantibodies have been identified…
  • Abstract Number: 2907 • 2013 ACR/ARHP Annual Meeting

    D1398G Variant Of Hepatocyte Growth Factor Receptor – A Potential Biomarker Of Severe Interstitial Lung Disease In African American Scleroderma Patients

    Ilia Atanelishvili1, Tanjina Akter2, Richard M. Silver3 and Galina S. Bogatkevich2, 1Division of Rheumatology & Immunology, Medical University of South Carolina,Charleston,USA, Charleston, SC, 2Department of Rheumatology, Medical University of South Carolina,Charleston,USA, Charleston, SC, 3Div Rheumatology & Immunology, Medical University of South Carolina,Charleston,USA, Charleston, SC

    Background/Purpose: Interstitial lung disease (ILD) is a major complication and leading cause of mortality in scleroderma (SSc, systemic sclerosis). The morbidity and mortality rates in…
  • Abstract Number: 2917 • 2013 ACR/ARHP Annual Meeting

    Mortality, Recurrence, and Hospital Course of Patients With Systemic Sclerosis Related Acute Intestinal Pseudo-Obstruction

    Chris T. Derk1, Nora Sandorfi2, Shivani Purohit3 and Christopher Mecoli4, 1Medicine/Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Division of Rheumatology, Thomas Jefferson Univ Med Coll, Philadelphia, PA, 3Rheumatology Division, Department of Medicine, Rheumatology Division, Department of Medicine, Thomas Jefferson University, Philadelphia, PA, 4Rheumatology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Acute intestinal pseudo-obstruction is a rare gastrointestinal manifestation of SSc with little data existing as to the demographics, clinical course, outcomes and mortality of…
  • Abstract Number: 2739 • 2013 ACR/ARHP Annual Meeting

    Immunochip Analysis Identifies New Susceptibility Loci For Systemic Sclerosis: Implications For Pathogenesis

    Maureen D. Mayes for the US Scleroderma GWAS Group1, Lara Bossini-Castillo for the Spanish Scleroderma Group2, Olga Gorlova3, Jose Ezequiel Martin4, Xiaodong Zhou1, Wei Chen5, Shervin Assassi1, Jun Ying5, John D. Reveille1, Peter K. Gregersen6, Annette T. Lee7, Maria Teruel8, Francisco David Carmona4, Bobby P.C. Koeleman9, Matthew A. Brown and the Immunochip Consortium10, Christopher P. Denton11, Murray Baron for the Canadian Scleroderma Research Group12, Jasper Broen13, T.R.D.J. Radstake13 and Javier Martin4, 1Rheumatology, University of Texas Health Science Center at Houston, Houston, TX, 2Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, Spain, 3Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, 4Immunology, Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Armilla (Granada), Spain, 5Department of Epidemiology, UT M.D. Anderson Cancer Center, Houston, TX, 6Genomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, NY, 7Genomics & Human Genetics, Feinstein Institute for Medical Research, Manhasset, NY, 8Immunology, Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, Spain, 9Department of Medical Genetics, University Medical Center Utrecht, Utrecht, Netherlands, 10Translational Research Institute, University of Queensland Diamantina Institute, Brisbane, Australia, 11Centre for Rheumatology, Royal Free and University College Medical School, London, United Kingdom, 12Rheumatology, Jewish General Hospital, Montreal, QC, Canada, 13Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose : The purpose of this study was to identify SSc risk loci shared with other autoimmune diseases on the Immunochip and to fine-map previously…
  • Abstract Number: 2609 • 2013 ACR/ARHP Annual Meeting

    Dutch Translation and Validation Of The University of California, Los Angeles scleroderma Clinical Trial Consortium Gastrointestinal Tract Instrument 2.0

    Jessica Meijs1, Daisy Pors1, Theodora P.M. Vliet Vlieland2, Tom W.J. Huizinga1 and Annemie J.M. Schuerwegh1, 1Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 2Department of Orthopaedics, Leiden University Medical Center, Leiden, Netherlands

    Background/Purpose: Gastrointestinal tract (GIT) involvement occurs in approximately 90% of the patients with systemic sclerosis (SSc) and leads to a decrease in health-related quality of…
  • Abstract Number: 2582 • 2013 ACR/ARHP Annual Meeting

    Treatment Of Pulmonary Hypertension In Scleroderma Patients With Restricitive Lung Disease.Observations From The Pulmonary Hypertension Assessment and Recognition Of Outcomes In Scleroderma  Cohort

    Virginia D. Steen1 and Robyn T. Domsic2, 1Department of Rheumatology, Georgetown University Medical Center, Washington, DC, 2Medicine - Rheumatology, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: Trials of therapy in  pulmonary  hypertension(PH)  have generally excluded patients with significant interstitial lung disease, but many patients with systemic sclerosis(SSc)  and  PH  have…
  • Abstract Number: 1712 • 2012 ACR/ARHP Annual Meeting

    The Submaximal Heart and Pulmonary Evaluation: A Novel Noninvasive Test to Identify Pulmonary Hypertension in Patients with Systemic Sclerosis

    Elana J. Bernstein1, Jessica K. Gordon2, Robert F. Spiera2, Lisa A. Mandl2 and Evelyn M. Horn3, 1Rheumatology, Columbia University College of Physicians & Surgeons, New York, NY, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Cardiology, New York Presbyterian Hospital/Weill Cornell Medical College, New York, NY

    Background/Purpose: Pulmonary hypertension (PH), defined as a mean pulmonary artery pressure (mPAP) ≥ 25 mmHg on right heart catheterization (RHC), is a leading cause of…
  • Abstract Number: 1505 • 2012 ACR/ARHP Annual Meeting

    Inactivation of Tankyrases Ameliorates Canonical Wnt Signaling and Prevents Experimental Fibrosis

    Alfiya Distler1, Lisa Deloch2, Jingang Huang2, Clara Dees2, Neng Yu Lin2, Christian Beyer3, Oliver Distler4, Georg A. Schett5 and Joerg HW Distler1, 1Department of Internal Medicine III and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 2Department of Internal Medicine 3 and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 3Department of Internal Medicine 3, Department of Internal Medicine 3 and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 4Division of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 5Dept of Medicine 3, Rheumatology and Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany

    Background/Purpose: Systemic sclerosis (SSc) is characterized by aberrant activation of fibroblasts with increased release of extracellular matrix components. Canonical Wnt signaling has recently emerged as…
  • Abstract Number: 1464 • 2012 ACR/ARHP Annual Meeting

    Comparison of Baseline Characteristics of the Combined Response Index for Systemic Sclerosis (CRISS) Cohort to Patients Enrolled in Clinical Trials of Diffuse Systemic Sclerosis

    Heather Gladue1, Daniel Furst2, Veronica Berrocal3, James R. Seibold4, Peter A. Merkel5, Maureen D. Mayes6, Kristine Phillips7, Robert W. Simms8, Shervin Assassi9, Philip J. Clements10, Paul Maranian11 and Dinesh Khanna12, 1University of Michigan, Ann Arbor, MI, 2David Geffen School of Medicine, Div of Rheumatology, University of California at Los Angeles, Los Angeles, CA, 3Div of Rheumatology, University of Michigan, Ann Arbor, MI, 4Scleroderma Research Consultants LLC, Avon, CT, 5University of Pennsylvania, Philadelphia, PA, 6Rheumatology, University of Texas Health Science Center at Houston, Houston, TX, 7Rheumatology, University of Michigan Medical School, Ann Arbor, MI, 8Rheumatology, Boston University School of Medicine, Boston, MA, 9Rheumatology, Univ of Texas Health Science Houston, Houston, TX, 10University of California, Los Angeles, Department of Medicine, Los Angeles, CA, 11Division of Rheumatology, UCLA Medical School, Los Angeles, CA, 12Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI

    Background/Purpose: Randomized clinical trials (RCTs) of treatment of diffuse systemic sclerosis (dcSSc) would benefit from a composite index that predicted efficacy better than current standard…
  • Abstract Number: 1470 • 2012 ACR/ARHP Annual Meeting

    Clinical Features Associated with Anti-Th/to in Non-Scleroderma Patients – Sine Scleroderma?

    Ann D. Chauffe1, Minoru Satoh1, Angela Ceribelli2, Edward K.L. Chan2, Yi Li1, Eric S. Sobel3, Westley H. Reeves4 and Michael R. Bubb1, 1Medicine, University of Florida, Gainesville, FL, 2Oral Biology, University of Florida, Gainesville, FL, 3Medicine/Div of Rheumatology, University of Florida, Gainesville, FL, 4Rheumatology & Clinical Imm, University of Florida, Gainesville, FL

    Background/Purpose: Autoantibodies in scleroderma (systemic sclerosis, SSc) such as anti-topoisomerase I (Scl-70), RNA polymerase III, centromere, U3RNP/fibrillarin, and Th/To are associated with a unique subset…
  • Abstract Number: 853 • 2012 ACR/ARHP Annual Meeting

    Systemic Sclerosis Classification Criteria: Developing Methods for Multi-Criteria Decision Analysis

    Sindhu R. Johnson1, Raymond P. Naden2, Jaap Fransen3, Frank H.J. van den Hoogen4, Janet E. Pope5, Murray Baron6, Alan G. Tyndall7, Marco Matucci-Cerinic8 and Dinesh Khanna on behalf of ACR/EULAR Classification Criteria SSc9, 1Dept of Rheumatology, Toronto Western Hospital, Toronto, ON, Canada, 2Auckland City Hospital, Auckland, New Zealand, Austria, 3Rheumatic Diseases, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands, 4Rheumatology, Rheumatology Centre Sint Maartenskliniek and Radboud university medical center, Ubbergen (Nijmegen), Netherlands, 5Medicine/Rheumatology, St. Joseph Health Care London, University of Western Ontario, London, ON, Canada, 6Pavillion A, Rm 216, Lady David Institute for Medical Research and Jewish General Hospital, Montreal, QC, Canada, 7Rheumatology, University of Basel, Basel, Switzerland, 8Medicine, Univ Florence, Firenze, Italy, 9Div of Rheumatology, University of Michigan, Ann Arbor, MI

    Background/Purpose: Classification criteria for systemic sclerosis (SSc) are being developed. Twenty-three candidate criteria have been identified, but need to be reduced. The objectives of this…
  • Abstract Number: 711 • 2012 ACR/ARHP Annual Meeting

    Myopathy Is a Poor Prognostic Feature in Systemic Sclerosis: Results From the Canadian Scleroderma Research Group

    MIchelle Jung1, Murray Baron2, Marie Hudson3, Ashley Bonner4, Janet E. Pope5 and Canadian Scleroderma Research Group6, 1Western University, London, ON, Canada, 2Pavillion A, Rm 216, Lady David Institute for Medical Research and Jewish General Hospital, Montreal, QC, Canada, 3Jewish General Hospital, McGill University, Montreal, QC, Canada, 4McMaster University, Hamilton, ON, Canada, 5Medicine/Rheumatology, St. Joseph Health Care London, University of Western Ontario, London, ON, Canada, 6Montreal, QC, Canada

    Background/Purpose: Myopathy / myositis is associated with more severe systemic scleroderma (SSc).  The aim of this study was to determine such clinical information from the…
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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.

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