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  • Abstract Number: 714 • 2012 ACR/ARHP Annual Meeting

    Line Blot Assay, a Screening Test for Autoantibodies in Systemic Sclerosis (SSc)

    Kae Takagi1, Yasushi Kawaguchi1, Sayuri Kataoka1, Yuko Ota2, Yuko Okamoto1, Masanori Hanaoka1, Hisae Ichida1, Takahisa Gono1, Yasuhiro Katsumata1 and Hisashi Yamanaka1, 1Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 2Institute of Rheumatology,Tokyo Women's Medical University, Tokyo, Japan

    Background/Purpose: Detection of auto-antibody is informative for diagnosis of SSc. Line blot assay (LBA) provides a quantitative in vitro assay for detecting human IgG class…
  • Abstract Number: 716 • 2012 ACR/ARHP Annual Meeting

    Utility of Novel Patient-Reported Outcome Instruments in Predicting Cardiac Involvement and Pulmonary Hypertension in Patients with Systemic Sclerosis

    Monique E. Hinchcliff1, Mary A. Carns2, Sofia Podlusky2, John Varga3 and Sanjiv J. Shah4, 1Northwestern University, Feinberg School of Medicine, Chicago, IL, 2Department of Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 3Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 4Cardiology, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: Heart involvement in systemic sclerosis (SSc) includes left ventricular systolic and diastolic dysfunction, right ventricular dysfunction, pericardial disease, and pulmonary hypertension. We recently demonstrated…
  • Abstract Number: 717 • 2012 ACR/ARHP Annual Meeting

    Results From a Multi-Tiered Item Collection On Linking Systemic Sclerosis to the International Classification of Functioning, Disability and Health: A EULAR Scleroderma Trials and Research Initiative

    Lesley Ann Saketkoo1, Reuben Escorpizo2, Kevin J. Keen3, Kim Fligelstone4 and Oliver Distler5, 1LSU Scleroderma and Sarcoidosis Patient Care and Research Center, New Orleans, LA, 2ICF Research Branch in cooperation with the WHO Collaborating Centre for the Family of International Classifications in Germany (DIMDI), Nottwil, Switzerland, 3Mathematics and Statistics, University of Northern British Columbia, Prince George, BC, Canada, 4Royal Free Hospital, Scleroderma Unit and Scleroderma Society, London, United Kingdom, 5Department of Rheumatology and Center of Experimental Rheumatology, University Hospital Zurich, Zurich, Switzerland

    Background/Purpose: Systemic Sclerosis (SSc) affects multiple organs with complex combinations of disability. Skin fibrosis, ischemic pain, ulceration, arthritis, joint contractures, myopathy and cardiopulmonary, renal as…
  • Abstract Number: 719 • 2012 ACR/ARHP Annual Meeting

    Biomarkers of Pulmonary Hypertension in Patients with Scleroderma: A Case-Control Study

    Zsuzsanna H. McMahan1, Florian Schoenhoff2, Jennifer van Eyk3, Fredrick M. Wigley4 and Laura K. Hummers4, 1Rheumatology, Johns Hopkins University, Baltimore, MD, 2Department of Cardiovascular Surgery, Berne, Switzerland, 3Johns Hopkins University and Cedars Sinai Medical Center, Los Angeles, CA, 4Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: The objective of this study was to evaluate for an association between various biomarkers and the presence or absence of pulmonary hypertension (PH) in…
  • Abstract Number: 720 • 2012 ACR/ARHP Annual Meeting

    Left-Heart Disease Is a Frequent Cause of Pulmonary Hypertension in Systemic Sclerosis, Is Associated with Increased Levels of MR-ProANP and MR-ProADM but Is Unrelated to Elevated NT-ProBNP Levels: A Retrospective Cohort Analysis

    Lada Miller1, Sandra Chartrand1, Martial Koenig2, Jean-Richard Goulet3, Eric Rich1, Michal Abrahamowicz4, Jean-Luc Senécal1 and Tamara Grodzicky1, 1Rheumatology, Hôpital Notre-Dame du CHUM, Montreal, QC, Canada, 2Internal Medicine, Hôpital Notre-Dame du CHUM, Montréal, QC, Canada, 3Rheumatology, Hôpital Notre-Dame du CHUM, Montréal, QC, Canada, 4Centre Universitaire de Santé McGill (CUSM), Montreal, QC, Canada

    Background/Purpose: Pulmonary hypertension (PH) is a significant cause of morbidity and mortality in systemic sclerosis (SSc). Pulmonary arterial hypertension (PAH) is reportedly the most frequent…
  • Abstract Number: 721 • 2012 ACR/ARHP Annual Meeting

    Measurement of Pulmonary Arteries by Cardiac Magnetic Resonance Imaging: A Simple and Useful Tool for the Detection of Pulmonary Hypertension in Systemic Sclerosis Patients without Overt Cardiac Microvascular Perfusion Defects or Fibrosis

    Sandra Chartrand1, Lada Miller1, Martial Koenig2, Jean-Richard Goulet1, Eric Rich1, Anne S. Chin3, Yves Provost3, Carl Chartrand-Lefebvre3, Pauline Gou1, Jean-Luc Senécal1 and Tamara Grodzicky1, 1Rheumatology, Hôpital Notre-Dame du CHUM, Montréal, QC, Canada, 2Internal Medicine, Hôpital Notre-Dame du CHUM, Montréal, QC, Canada, 3Radiology, Hôtel-Dieu de Montréal du CHUM, Montréal, QC, Canada

    Background/Purpose: Pulmonary hypertension (PH) is a major complication of systemic sclerosis (SSc). We observed that a significant proportion of our SSc patients with PH as…
  • Abstract Number: 722 • 2012 ACR/ARHP Annual Meeting

    Systemic Sclerosis Associated Pulmonary Hypertension – Is Pulmonary Veno-Occlusive Disease As Common As They Say?

    Benjamin E. Schreiber1, Greg Keir2, D. Dobarro3, Clive Handler4, Svetlana Nihtyanova5, Jay Suntharaligam6, Nicola Sverzelatti7, Graham Robinson6, David Hansell8, Athol U. Wells9, Christopher P. Denton10 and John G. Coghlan11, 1Royal Free Hospital NHS Foundation Trust, National Pulmonary Hypertension Service, London, United Kingdom, 2Royal Brompton Hospital, United Kingdom, 3Pulmonary Hypertension, Royal Free Hospital, London, United Kingdom, 4Department of Pulmonary Hypertension, The Royal Free Hospital, London, United Kingdom, 5Department of Rheumatology, Royal Free Hospital, Medical School, London, England, 6Royal United Hospital, Bath, United Kingdom, 7University of Parma, Parma, Italy, 8Royal Brompton Hospital, London, United Kingdom, 9Royal Brompton and Harefield NHS Foundation Trust, Department of Radiology, London, United Kingdom, 10Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, London, United Kingdom, 11National Pulmonary Hypertension Service, The Royal Free Hospital NHS Foundation Trust, London, United Kingdom

    Background/Purpose: Recent reviews have suggested a high prevalence of pulmonary veno-occlusive disease (PVOD) amongst patients with systemic sclerosis (SSc) associated pulmonary hypertension (PH). Interlobular septal…
  • Abstract Number: 723 • 2012 ACR/ARHP Annual Meeting

    Renal Dysfunction and Disease Severity in Scleroderma-Associated Pulmonary Arterial Hypertension

    Stephen C. Mathai1, Laura K. Hummers2 and Virginia D. Steen3, 1Medicine, Johns Hopkins University, Baltimore, MD, 2Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 3Department of Rheumatology, Georgetown University Medical Center, Washington, DC

    Background/Purpose: Renal disease is a common complication of scleroderma (SSc).  Isolated reduction in glomerular filtration rate (GFR), a marker of impaired renal function, can occur…
  • Abstract Number: 724 • 2012 ACR/ARHP Annual Meeting

    Survival, Hospitalization or Need for Combination Therapy At One Year in Patients with Scleroderma-Associated Pulmonary Arterial Hypertension

    Robyn T. Domsic1, Lorinda Chung2, Jessica K. Gordon3, Yona Cloonan4, Virginia D. Steen5 and PHAROS Investigators6, 1Medicine - Rheumatology, University of Pittsburgh, Pittsburgh, PA, 2Rheumatology, Stanford Univ Medical Center, Palo Alto, CA, 3Rheumatology, Hospital for Special Surgery, New York, NY, 4Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, 5Department of Rheumatology, Georgetown University Medical Center, Washington, DC, 6Washington, DC, DC

    Background/Purpose: Pulmonary arterial hypertension (PAH) is a leading cause of death in patients with systemic sclerosis (SSc).  Although survival has improved with PAH-specific medications in…
  • Abstract Number: 725 • 2012 ACR/ARHP Annual Meeting

    The Role of Interleukin-23 in Spondyloarthropathy

    Jonathan Sherlock1, Barbara Joyce-Shaikh1, Scott Turner1, Cheng-Chi Chao2, Manjiri Sathe1, Jeff Grein1, Dan Gorman1, Eddie P. Bowman2, Terrill McClanahan1, Jennifer Yearley1, Gerard Eberl3, Christopher D. Buckley4, Robert Kastelein1, Robert Pierce1, Drake LaFace1 and Daniel Cua5, 1Merck, Palo Alto, CA, 2Drug Discovery, Merck, Palo Alto, CA, 3Institut Pasteur, Paris, France, 4Center for Translational Inflammation Research, School of Immunity and Infection, MRC Center for Immune Regulation, Birmingham, United Kingdom, 5Discovery Research, Merck Research Laboratory, Palo Alto, CA

    Background/Purpose: Spondyloarthropathy is characterized by inflammation and bony pathology at the entheseal insertion of tendons to bone.  Recent investigations have converged upon interleukin(IL)-23, demonstrating firstly…
  • Abstract Number: 726 • 2012 ACR/ARHP Annual Meeting

    Dynamic in Vivo Imaging of Th17-Mediated Osteoclastic Bone Resorption in Live Bones by Using Intravital Multiphoton Microscopy

    Junichi Kikuta and Masaru Ishii, Laboratory of Cellular Dynamics, Immunology Frontier Research Center, Osaka University, Osaka, Japan

    Background/Purpose: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by joint synovial inflammation and progressive cartilage/bone destruction. Although various kinds of cell types, such…
  • Abstract Number: 727 • 2012 ACR/ARHP Annual Meeting

    Effects of Odanacatib On BMD and Overall Safety in the Treatment of Osteoporosis in Postmenopausal Women Previously Treated with Alendronate

    Roland Chapurlat1, Sydney Bonnick2, Tobias De Villiers3, Alberto Odio4, Santiago Palacios5, Boyd Scott6, Celine Le Bailly De Tilleghem7, Carolyn DaSilva6, Albert Leung8 and Deborah Gurner6, 1Hôpital Edouard Herriot, Lyon, France, 2Director Osteoporosis Services, Cooper Clinic, Dallas, TX, 3Mediclinic Panorama and Department of Obstetrics & Gynecology, University of Stellenbosch, Cape Town, South Africa, 4Alta California Medical Group, Simi Valley, CA, 5Instituto Palacios, Madrid, Spain, 6Merck Sharp & Dohme Corp., Whitehouse Station, NJ, 7MSD Europe Inc., Brussels, Belgium, 8Clinical Research, Merck Sharp and Dohme Corp., Rahway, NJ

    Background/Purpose: Odanacatib (ODN) is a potent, orally-active cathepsin K inhibitor being developed for the treatment of postmenopausal osteoporosis. This study evaluated the effects of ODN…
  • Abstract Number: 728 • 2012 ACR/ARHP Annual Meeting

    Does the Use of Angiotensin Converting Enzyme Inhibitors Prior to Scleroderma Renal Crisis Affect Prognosis ? – Results of the International Scleroderma Renal Crisis Survey

    Marie Hudson1, Murray Baron2, Solene Tatibouet1, Daniel Furst3, Dinesh Khanna4 and International Scleroderma Renal Crisis Study Investigaots5, 1Jewish General Hospital, McGill University, Montreal, QC, Canada, 2Pavillion A, Rm 216, Lady David Institute for Medical Research and Jewish General Hospital, Montreal, QC, Canada, 3David Geffen School of Medicine, Div of Rheumatology, University of California at Los Angeles, Los Angeles, CA, 4Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 5Montreal

    Background/Purpose: Scleroderma renal crisis (SRC) is an infrequent but life-threatening complication of systemic sclerosis (SSc). The outcome of SRC has improved considerably since the advent…
  • Abstract Number: 729 • 2012 ACR/ARHP Annual Meeting

    Apolipoprotein L1 Risk Variants Underlie Racial Disparities in Lupus Nephritis-Induced End-Stage Renal Disease

    Robert P. Kimberly1, Barry I. Freedman2, Carl D. Langfeld3, Devin Absher4, Kelly K. Andringa1, Daniel Birmingham5, Elizabeth E. Brown6, Mary E. Comeau7, Karen H. Costenbader8, Lindsey A. Criswell9, Jeffrey C. Edberg10, John B. Harley11, Judith A. James12, Diane L. Kamen13, Joan T. Merrill14, Timothy B. Niewold15, Neha Patel16, Michelle Petri17, Rosalind Ramsey-Goldman18, Jane E. Salmon19, Mark Segal20, Kathy Moser Sivils12, Betty P. Tsao21, Bruce A. Julian1 and Lupus Nephritis-ESRD Consortium22, 1Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 2Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 3Department of Biostatistics, Wake Forest University Health Sciences, Winston-Salem, NC, 4HudsonAlpha Institute for Biotechnology, Huntsville, AL, 5Medicine, Ohio State University Medical Center, Columbus, OH, 6University of Alabama at Birmingham, Birmingham, AL, 7Wake Forest University Health Sciences, Winston-Salem, NC, 8Rheumatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 9Department of Medicine, University of California, San Francisco, Rosalind Russell Medical Research Center for Arthritis, San Francisco, CA, 10Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 11Division of Rheumatology and The Center for Autoimmune Genomics & Etiology, University of Cincinnati, Cincinnati Children's Hospital Medical Center; US Department of Veterans Affairs Medical Center, Cincinnati, OH, 12Oklahoma Medical Research Foundation, Oklahoma City, OK, 13Department of Medicine, Arthritis & Clinical Immunology Program, Oklahoma Medical Research Foundation, Charleston, SC, 14Clinical Pharmacology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 15Section of Rheumatology and Gwen Knapp Center for Lupus and Immunology Research, University of Chicago, Chicago, IL, 16Rheumatology, SUNY Downstate Medical Center, Brooklyn, NY, 17Johns Hopkins University School of Medicine, Baltimore, MD, 18Medicine/Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 19Rheumatology, Hospital for Special Surgery, New York, NY, 20Medicine/Nephrology, University of Florida, Gainesville, FL, 21Medicine/Rheumatology, UCLA School of Medicine, Los Angeles, CA, 22Medicine, Birmingham, AL

    Background/Purpose: The G1 and G2 coding variants in the apolipoprotein L1 gene (APOL1;  G1: a compound missense allele (glycine-342/methionine-384) and G2: an in-frame deletion (deletion…
  • Abstract Number: 730 • 2012 ACR/ARHP Annual Meeting

    Disease Modifying Effect of Strontium Ranelate in Experimental Dog Osteoarthritis: Inhibition of Major Catabolic Pathways

    Jean-Pierre Pelletier1, Mohit Kapoor2, Daniel Lajeunesse2, Hassan Fahmi3 and Johanne Martel-Pelletier1, 1Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Montreal, QC, Canada, 2Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Notre-Dame Hospital, Montreal, QC, Canada, 3Pharmacology, Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Montreal, QC, Canada

    Background/Purpose: To assess the disease modifying (DMOA) effect of strontium ranelate (SrRan) under therapeutic conditions on the progression of structural changes and on the major…
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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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