ACR Meeting Abstracts

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Abstracts tagged "SLE"

  • Abstract Number: 1620 • 2014 ACR/ARHP Annual Meeting

    Antibody to Malondialdehyde-Acetaldehyde Adducts (MAA) As a Potential Biomarker of Inflammation in Systemic Lupus Erythrematosus (SLE)

    Andy Hollins1, Michael Duryee2, Michelene Hearth-Holmes3, Ted R. Mikuls1, Zhixin Zhang4, Kaihong Su5 and Geoffrey M. Thiele6, 1University of Nebraska Medical Center, Omaha, NE, 2Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 3Internal Medicine/Rheumatology Division, University of Nebraska Medical Center, Omaha, NE, 4Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, 5Eppley Cancer Institute, University of Nebraska Medical Center, Omaha, NE, 6Internal Medicine, Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE

    Background/Purpose  Studies have shown that malondialdehyde-acetaldehyde (MAA) is formed as a result of lipid peroxidation of cellular membranes and is capable of binding or adducting…
  • Abstract Number: 686 • 2014 ACR/ARHP Annual Meeting

    Clinicians Approaches to the Management of Background Therapy in SLE Patients in Clinical Remission: Results of an International Survey

    Pintip Ngamjanyaporn1,2, Ian Bruce3, Ben Parker4 and Jamie Sergeant1, 1Institute of Inflammation and Repair School of translation Medicine The University of Manchester, Arthritis Research UK Epidemiology Unit, University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 2Internal Medicine, Mahidol University, Bangkok, Thailand, 3Kellgren Centre for Rheum, Arthritis Research UK Epidemiology Unit, Institution of Inflammation and Repair, University of Manchester, NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester University Hospitals, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 4Institute of Inflammation and Repair School of Translation Medicine The University of Manchester, Arthritis Research UK Epidemiology Unit, University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom

    Background/Purpose: At present there is no consensus on what constitutes a remission in SLE. In particular it is not clear how background therapy should be…
  • Abstract Number: 2837 • 2014 ACR/ARHP Annual Meeting

    Induction of Clinical Remission By Low-Dose Interleukin-2 in Refractory SLE

    Jens Y. Humrich1, Caroline von Spee-Mayer1, Elise Siegert1, Angelika Rose1, Tobias Alexander2, Falk Hiepe1, Andreas Radbruch3, Gerd Burmester4 and Gabriela Riemekasten1, 1Rheumatology and Clinical Immunology, Charité – University Hospital, Berlin, Germany, 2Department of Rheumatology and Clinical Immunology, Charité – University Hospital, Berlin, Germany, 3German Rheumatism Research Centre Berlin (DRFZ), an institute of the Leibniz Association, Berlin, Germany, 4Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology, Berlin, Germany

    Background/Purpose Interleukin-2 (IL-2) is crucial for the growth and survival of regulatory T cells (Treg), and thus for the control of autoimmunity. In previous studies…
  • Abstract Number: 2619 • 2014 ACR/ARHP Annual Meeting

    Low Socioeconomic Status (SES) As Measured By Education Is (not) Associated with Worse Outcome in SLE: Data from the 1000 Canadian Faces of Lupus

    Angela George1, Christine Peschken2, Earl Silverman3, Christian A. Pineau4, C Douglas Smith5, Hector Arbillaga6, Michel Zummer7, Ann Clarke8, Sasha Bernatsky9, Marie Hudson10, Carol A. Hitchon11, Paul R. Fortin12 and Janet E. Pope13, 1Medicine/Rheumatology, University of Western Ontario, London, ON, Canada, 2Medicine & Community Health Sciences, University of Manitoba, Winnipeg, MB, Canada, 3Pediatrics/Rheumatology, Toronto Hospital for Sick Children, U of Toronto, Toronto, ON, Canada, 4Rheumatology, McGill University Health Center, Montreal, QC, Canada, 5The Arthritis Centre, TOH Riverside Campus, Ottawa, ON, Canada, 6Medicine/Rheumatology, Lethbridge Rheumatology practice, Lethbridge, AB, Canada, 7Medicine/Rheumatology, U of Montreal, Montreal, QC, Canada, 8Medicine/Allergy, U of Calgary, Calgary, AB, Canada, 9Clinical Epidemiology, McGill UHC/RVH, Montreal, QC, Canada, 10Medicine/Rheumatology, McGill University, Montreal, QC, Canada, 11Rheumatology, University of Manitoba, Winnipeg, MB, Canada, 12Rheumatology, Laval University, Division of Rheumatology, Centre de Recherche du CHU de Québec and Department of Medicine, Quebec City, QC, Canada, 13St Joseph Health Care, London, ON, Canada

    Background/Purpose: To determine whether socioeconomic status, as measured by education, impacts disease activity (measured by SLAM-2, SLEDAI-2K) or disease damage (measured by SLICC SDI) in…
  • Abstract Number: 1858 • 2014 ACR/ARHP Annual Meeting

    Standardized Mortality Ratios for Cause-Specific Deaths in Lupus Patients Followed Prospectively at a Single Centre Lupus Clinic

    Barry J. Sheane1, Dominique Ibanez2, Dafna D. Gladman3 and Murray B. Urowitz3, 1Division of Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 3University of Toronto, Toronto Western Hospital, Toronto, ON, Canada

    Background/Purpose Despite the significant improvement in survival rates of patients with systemic lupus erythematosus (SLE) over the last four decades, mortality rates have remained at…
  • Abstract Number: 1310 • 2014 ACR/ARHP Annual Meeting

    Predicting Macrophage Activation Syndrome in Pediatric Systemic Lupus Erythematosus Patients at Diagnosis

    Maya Gerstein1, Roberto Ezequiel Borgia2, Brian Feldman1, Deborah M. Levy3, Sharon Sukhdeo4, Susanne M. Benseler5, Lawrence W.K. Ng1, Mohamed Abdelhaleem6, Earl D. Silverman2 and Linda T Hiraki7, 1Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada, 2Division of Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada, 3Rheumatology, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada, 4Rheumatology, The Hospital For Sick Children, Toronto, ON, Canada, 5Rheumatology, Alberta Children's Hospital, University of Calgary, Calgary, AB, Canada, 6Department of Paediatric Laboratory Medicine, Division of Haematopathology, The Hospital for Sick Children, Toronto, ON, Canada, 7The Hospital for Sick Children, Toronto, ON, Canada

    Background/Purpose It can be difficult to differentiate macrophage activation syndrome (MAS) from active pediatric systemic lupus erythematosus (pSLE). However, this differentiation is in determining correct…
  • Abstract Number: 676 • 2014 ACR/ARHP Annual Meeting

    Response to Rituximab in Patients with Refractory Systemic Lupus Erythematosus (SLE): Results from a National Multicentre Register

    Emily Sutton1, Kath D. Watson2, David A. Isenberg3, Anisur Rahman4, David Jayne5, Caroline Gordon6, Ben Parker7, David P. D'Cruz8, Munther A. Khamashta9, Pamela Lutalo10, Peter Lanyon11, Benjamin Rhodes12, Bridget Griffiths13, Edward M. Vital14, Chee-Seng Yee15, Christopher Edwards16, Mohammed Akil17, Nicola Erb18, Athiveer Prabu19, Asad A. Zoma20, Neil McHugh21, Hazem Youssef22, Lee-Suan Teh23, Michael W. Beresford24 and Ian N. Bruce25, 1University of Manchester, Manchester Academic Health Science Centre, Arthritis Research UK Centre for Epidemiology, Manchester, United Kingdom, 2Arthritis Research UK Centre for Epidemiology, University of Manchester, Manchester, United Kingdom, 3Centre for Rheumatology Research, Rayne Building, 4th Floor, Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom, 4Centre for Rheumatology Research, University College London, London, United Kingdom, 5Vasculitis and Lupus Clinic, Addenbrookes Hospital University of Cambridge, Cambridge, United Kingdom, 6Rheumatology Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom, 7Institute of Inflammation and Repair School of Translation Medicine The University of Manchester, Arthritis Research UK Epidemiology Unit, University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 8Louise Coote Lupus Unit, Guy's and St Thomas' Hospital, London, United Kingdom, 9Lupus Research Unit, The Rayne Institute, St Thomas Hospital, Kings College London School of Medicine, London, United Kingdom, 10Peter Gorer Department of Immunobiology, King's College London School of Medicine, London, United Kingdom, 11Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom, 12Rheumatology, Queen Elizabeth Hospital, Birmingham, United Kingdom, 13Rheumatology, Freeman Hospital, Newcastle Upon Tyne, United Kingdom, 14NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds., United Kingdom, Leeds, United Kingdom, 15Department of Rheumatology, Doncaster and Bassetlaw Hospitals NHS Foundation Trust, Doncaster, United Kingdom, 16Tremona Road, NIHR Wellcome Trust Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom, 17Rheumatology Department, Sheffield South Yorkshire, United Kingdom, 18Rheumatology, Russells Hall Hospital, Dudley, United Kingdom, 19Department of Rheumatology, Worcester Acute Hospitals NHS Trust, Worcester, United Kingdom, 20Rheumatology, Hairmyres Hospital, East Kilbride, United Kingdom, 21Rheumatology, Royal National Hospital, Bath, United Kingdom, 22Department of Rheumatology, NHS Grampian, Aberdeen, United Kingdom, 23Department of Rhuematology, Royal Blackburn Hospital, Blackburn, United Kingdom, 24Alder Hey Children's NHS Foundation Trust Hospital, Institute of Translational Medicine (Child Health), University of Liverpool, Liverpool, United Kingdom, 25Arthritis Research UK Centre for Epidemiology, Centre for Musculoskeletal Research, Institute of Inflammation and repair, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United Kingdom

    Background/Purpose: Published efficacy data for rituximab in SLE are complex with positive single-centre case series and negative randomised controlled trials.  This may be due to…
  • Abstract Number: 2840 • 2014 ACR/ARHP Annual Meeting

    Targeting the RhoA-Rock Pathway to Reverse T Cell Dysfunction in SLE

    Cristina T. Rozo1, Laura Leuenberger2, Kyriakos A. Kirou3, Margaret Robotham1, Sanjay Gupta4, Reena Khianey2, Alessandra B. Pernis4 and Jane E. Salmon2, 1535 East 70th Street, Hospital for Special Surgery, New York, NY, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Hospital for Special Surgery, New York, NY, 4Autoimmunity & Inflammation Research Program, Hospital for Special Surgery, New York, NY

    Background/Purpose Aberrant expansion of TH-17 cells and deregulated production of IL-17 and IL-21 are involved in the pathogenesis of SLE. Production of IL-17 and IL-21…
  • Abstract Number: 2631 • 2014 ACR/ARHP Annual Meeting

    Overall Cause and Cause-Specific Mortality in a Multinational Inception Cohort of SLE

    Murray B. Urowitz1, Dafna D. Gladman1, Nicole Anderson2, Dominique Ibanez3 and Systemic Lupus International Collaborating Clinics (SLICC)4, 1University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, Toronto Western Hospital Research Institute, Toronto, ON, Canada, 3Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 4Toronto Western Hospital, Division of Rheumatology, University of Toronto, Toronto Western Hospital (Coordinating Center), Toronto, ON, Canada

    Background/Purpose: A large multicenter multinational inception cohort was established initially to study risk factors for atherosclerosis (AS) in SLE.   The aim of this study was…
  • Abstract Number: 1828 • 2014 ACR/ARHP Annual Meeting

    Adverse Pregnancy Outcomes in Adolescents and Young Women with Systemic Lupus Erythematosus: A National Estimate

    Nicole Ling1, Isabel E. Allen2, Erica F. Lawson1 and Emily von Scheven3, 1Pediatrics, University of California, San Francisco, San Francisco, CA, 2Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, 3Pediatric Rheumatology, University of California, San Francisco, San Francisco, CA

    Background/Purpose: Pregnant women with SLE have increased risk of adverse outcomes including lupus flare, spontaneous abortion, preeclampsia/eclampsia, premature birth and maternal death, but pregnancy outcomes…
  • Abstract Number: 1294 • 2014 ACR/ARHP Annual Meeting

    Gender Differences in the Lupus Nephritis Biomarkers in Children

    Khalid Abulaban1, Hermine Brunner2, Michael Bennett3, Shannen L. Nelson4, Jun Ying5 and Prasad Devarajan3, 1Pediatric Rheumatology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 2Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 3Nephrology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 4Rheumatology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 5University of Cincinnati, Cincinnati, OH

    Background/Purpose:  Lupus nephritis (LN) is frequently associated with a poor long-term prognosis. The non-invasive traditional measures of LN (LN-TM) currently used to monitor LN have…
  • Abstract Number: 674 • 2014 ACR/ARHP Annual Meeting

    A Novel Strategy to  Identify and Evaluate Approved Drugs and Treatments for Repositioning As Therapies for Systemic Lupus Erythematosus (SLE)

    Peter E. Lipsky, Matthew Ryals, Jacob Smearman, Victoria Soler and Amrie Grammer, AMPEL BioSolutions, Charlottesville, VA

    Background/Purpose: Development of new SLE treatments has been slow with only one new treatment approved in the past half century. One way to increase the…
  • Abstract Number: 2841 • 2014 ACR/ARHP Annual Meeting

    Identifying Novel Lupus Severity Risk Variants through Identification of Alleles with High Ethnic Variability Worldwide

    Belinda A. Waltman1, Kimberly E. Taylor2, Julio Molineros3, Sarah French4, Joanne Nitiham1, Jennifer Kelly3, Adam Adler5, Judith A. James3, Swapan Nath6, Marta Alarcon-Riquelme3,7 and Lindsey A. Criswell1, 1Medicine, University of California, San Francisco, Rosalind Russell / Ephraim P. Engleman Rheumatology Research Center, San Francisco, CA, 2Department of Medicine, University of California, San Francisco, Rosalind Russell / Ephraim P. Engleman Rheumatology Research Center, San Francisco, CA, 3Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4School of Medicine, University of California, San Francisco, Rosalind Russell / Ephraim P. Engleman Rheumatology Research Center, San Francisco, CA, 5Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 6Oklahoma Medical Research Foundation, Oklahoma City, OK, 7GENYO. Center for Genomics and Oncological Research, Granada, Spain

    Background/Purpose: Substantial epidemiologic evidence demonstrates that SLE disproportionately affects minority patients in terms of incidence, prevalence, and disease severity. European ancestry has been associated with…
  • Abstract Number: 2623 • 2014 ACR/ARHP Annual Meeting

    Treatment Patterns and Resource Utilization of Systemic Lupus Erythematosus Patients Newly Initiating Standard of Care: United States Commercial and Medicare Supplemental Claims Analysis

    Shonda A Foster1, Emily Durden2, Brett Maiese2, Sarah Al Sawah1 and Kathleen Solotkin1, 1Eli Lilly and Company, Indianapolis, IN, 2Truven Health Analytics, Bethesda, MD

    Background/Purpose: Currently, there is not a standard treatment algorithm for the management of Systemic Lupus Erythematosus (SLE); however, there are medications that may be considered…
  • Abstract Number: 1813 • 2014 ACR/ARHP Annual Meeting

    DNA Sensors Regulate Inflammation in a Model of Autoimmune Arthritis

    Rebecca Baum1, Shruti Sharma2, Sudesh Pawaria3, Susan Carpenter4, Katherine A. Fitzgerald5, Ann Marshak-Rothstein6 and Ellen M. Gravallese7, 1Cell Biology, University of Massachusetts Medical School, Worcester, MA, 2Department of Medicine - Infectious Diseases Division, University of Massachusetts Medical School, Worcester, MA, 3Department of Medicine, University of Massachusetts Medical School, Worcester, MA, 4University of California, San Francisco, San Francisco, CA, 5Department of Medicine, Division of Infectious Diseases and Immunology, University of Massachusetts Medical School, Worcester, MA, 6Department of Medicine, Division of Rheumatology, University of Massachusetts Medical School, Worcester, MA, 7Department of Medicine, Division of Rheumatology, UMass Memorial Medical Center, Worcester, MA

    Background/Purpose: Innate immune sensors such as cytosolic DNA sensors and toll-like receptors (TLRs) detect viral or bacterial DNA, resulting in production of proinflammatory cytokines and…
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