ACR Meeting Abstracts

ACR Meeting Abstracts

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  • Abstract Number: 2812 • 2017 ACR/ARHP Annual Meeting

    Healthcare Resource Utilization and Costs in Patients with Systemic Lupus Erythematosus before and after Initiating Treatment with Intravenous Belimumab: A US Claims Database Analysis

    Christopher F Bell1, Julie Priest2,3, Marni Stott-Miller4, Hong Kan5, Justyna Amelio6, Xue Song7, Brendan Limone7, Virginia Noxon7 and Karen H. Costenbader8, 1GSK US Value, Evidence and Outcomes, Research Triangle Park, NC, 2GSK US Value, Evidence and Outcomes (at the time of Study)*, Research Triangle Park, NC, 3US Health Outcomes Durham, *ViiV Healthcare (Present), Durham, NC, 4GSK Real World Evidence & Epidemiology, Uxbridge, United Kingdom, 5Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 6GSK Real World Evidence & Epidemiology, Stevenage, United Kingdom, 7Truven Health Analytics, an IBM company, Ann Arbor, MI, 8Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA

    Background/Purpose: Belimumab, an inhibitor of B lymphocyte stimulator, is approved in adults with active, autoantibody-positive systemic lupus erythematosus (SLE) receiving standard of care. There is…
  • Abstract Number: 2813 • 2017 ACR/ARHP Annual Meeting

    Interferon-Induced APOL1 over-Expression Causes Autophagic Dysfunction and Mitochondrial Stress in Risk Variant-Carrying Endothelial Cells

    Ashira Blazer1, Sara Rasmussen2, Androo Markham3, Shilpi Mehta-Lee4, Jill P. Buyon4 and Robert M. Clancy2, 1Division of Rheumatology, NYU School of Medicine, New York, NY, 2Department of Medicine, Division of Rheumatology, NYU School of Medicine, New York, NY, 3Medicine, NYU School of Medicine, New York, NY, 4NYU School of Medicine, New York, NY

    Background/Purpose: In SLE Apolipoprotein L1 (APOL1) risk variants (RV) associate with cardiovascular and end stage renal disease. APOL1 induction initially promotes cellular maintenance through autophagy;…
  • Abstract Number: 2814 • 2017 ACR/ARHP Annual Meeting

    Interferon-β Production By B Cells Promotes B Cell Survival and Is Strongly Associated with Active Disease in African Americans with SLE

    Jennie Hamilton1, Qi Wu2, PingAr Yang3, Bao Luo4, Shanrun Liu5, Jun Li6, Ignacio Sanz7, W. Winn Chatham8, Hui-Chen Hsu2 and John D. Mountz9, 1Medicine/Division of Clinical Immunology and Rhematology, University of Alabama at Birmingham, Birmingham, AL, 2Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 3Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 5Biochemistry & Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL, 6Medicine, University of Alabama at Birmingham, Birmingham, AL, 7Rheumatology and Lowance Center for Human Immunology, Emory University School of Medicine and Lowance Center for Human Immunology, Atlanta, GA, 8Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 9University of Alabama at Birmingham, Department of Medicine, Birmingham, AL

    Background/Purpose: Plasmacytoid dendritic cells are considered the main source of pathogenic IFN in SLE. However, recent work found that elevated serum type I IFN protein…
  • Abstract Number: 2815 • 2017 ACR/ARHP Annual Meeting

    Pathological Roles By Siglec and Type I Interferons for the Development of Autoimmune Congenital Heart Block

    Robert M. Clancy1, Marc Halushka2 and Jill P. Buyon1, 1NYU School of Medicine, New York, NY, 2Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Given that diseases associated with anti-SSA/Ro such as SLE and Sjögren’s syndrome associate with an upregulation of type I interferons, recent attention has focused…
  • Abstract Number: 2816 • 2017 ACR/ARHP Annual Meeting

    Prediction of Connective Tissue Disease in an at-Risk Cohort Using a Novel Interferon Stimulated Gene Expression Score

    Md Yuzaiful Md Yusof1,2, Yasser M El-Sherbiny1,3, Antonios Psarras1, Elizabeth M.A. Hensor1,4, Adewonuola Alase1, Alaa Mohamed1, Miriam Wittmann1,4, Paul Emery1,4 and Edward M Vital1,4, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 2NIHR Leeds Biomedical Research Unit, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom, 3Clinical Pathology dept., School of Medicine, Mansoura University, Mansoura, Egypt, 4NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom

    Prediction of connective tissue disease in an at-risk cohort using a novel interferon stimulated gene expression scoreBackground/Purpose: A period of ANA positivity and other immune…
  • Abstract Number: 2817 • 2017 ACR/ARHP Annual Meeting

    Expression Patterns of Interferon Induced Genes in Newborns Exposed to Ro/SSA Autoantibodies in Utero

    Gudny Ella Thorlacius1, Malin Hedlund1, Margarita Ivanchenko1, Vijole Ottosson1, Amina Ossoinak1, Linda Lagnefeldt1, Lars Rönnblom2, Sven-Erik Sonesson3, Maija-Leena Eloranta4 and Marie Wahren-Herlenius1, 1Unit of Experimental Rheumatology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden, 2Department of Medical Sciences, Section of Rheumatology, Uppsala University, Uppsala, Sweden, Uppsala, Sweden, 3Pediatric Cardiology Unit, Department of Women´s and Children´s Health, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden, 4Rheumatology and Science for Life Laboratory, Department of Medical Sciences, Uppsala University, Sweden, Uppsala, Sweden

    Background/Purpose: Women with Sjögren’s syndrome and autoantibodies against Ro/SSA are at risk for pregnancy complications, including neonatal lupus erythematosus (NLE) and a congenital heart block…
  • Abstract Number: 2818 • 2017 ACR/ARHP Annual Meeting

    Gene Expression Analysis Demonstrates That Multiple Type 1 Interferons Are Involved in Lupus Pathogenesis

    Michelle Catalina1, Prathyusha Bachali2, Sushma Madamanchi1, Amrie Grammer1 and Peter Lipsky1, 1Ampel BioSolutions LLC, Charlottesville, VA, 2Ampel BioSolutions LLC, Charlottesville, MA

    Background/Purpose: A role for interferon (IFN) in lupus pathogenesis has been inferred from the prominent IFN gene signature (IGS) found in lupus peripheral blood. However,…
  • Abstract Number: 2819 • 2017 ACR/ARHP Annual Meeting

    Association of Socioeconomic Status with Osteoarthritis-Induced Disability Progression

    Divya Narayanan1, Rebecca J. Cleveland2, Joanne M. Jordan3, Eric Seaberg4 and Leigh F. Callahan1, 1Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 2Thurston Arthritis Research Center, University of North Carolina School of Medicine, Chapel Hill, NC, 3Thurston Arthritis Research Center, University of North CArolina at Chapel Hill, Chapel Hill, NC, 4Bloomberg School of Public Health, Johns Hopkins Unviersity, Baltimore, MD

    Background/Purpose: Osteoarthritis (OA) is the number one chronic condition of the joints. Social determinants associated with disability progression due to OA are largely unknown. Efforts…
  • Abstract Number: 2820 • 2017 ACR/ARHP Annual Meeting

    Disease Activity By the Sledai in Lupus Patients Who Self Report Sleep Disturbance and Sleep Impairment Using the Patient-Reported Outcomes Measurement Information System Instruments

    Teresa Aberle1, Rufei Lu2, Sarah Cioli3, Stan Kamp1, Wade DeJager1, Stephen Apel4, Cristina Arriens5, Eliza Chakravarty6, Aikaterini Thanou1, Joel M. Guthridge7, Joan T. Merrill8 and Judith A. James9, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Arthritis and Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Oklahoma Medical Research Foundation, Oklahoma City, OK, 5Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 6Oklahoma Medical research af, Edmond, OK, 7Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, OKC, OK, 8Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 9Arthritis & Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Lupus patients commonly report sleep dysfunction, which is associated with upregulation of inflammatory cytokines in healthy people. Studies exploring relationships between self-reported sleep dysfunction…
  • Abstract Number: 2821 • 2017 ACR/ARHP Annual Meeting

    A Multidisciplinary Telemedicine Program for Identification of Spondyloarthritis in Medically Underserviced Communities

    Christopher Hawke1, Laura Passalent1, Nigil Haroon2, Robert D Inman3 and Y. Raja Rampersaud4, 1Allied Health, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, Toronto Western Hospital, University of Toronto, Spondylitis Clinic, Toronto, ON, Canada, 3Department of Immunology, University of Toronto, Toronto, ON, Canada, 4Arthritis Program, Krembil Research Institute, University Health Network, Torotno, ON, Canada

    Background/Purpose: Early diagnosis is critical for optimal management of patients with inflammatory arthritis. Axial spondyloarthritis (AxSpA) has the longest delay in diagnosis among inflammatory joint…
  • Abstract Number: 2822 • 2017 ACR/ARHP Annual Meeting

    A Randomized Controlled Effectiveness Trial of the Enhance-Fitness® Physical Activity Program in People with Arthritis

    Dina L. Jones1, Jennifer L. Eicher1, Hannah M. Ludwick2 and Kayéromi D. Gomez3, 1Orthopaedics, West Virginia University, Morgantown, WV, 2Biostatistics, West Virginia University, Morgantown, WV, 3Office of Research, University of Illinois College of Medicine at Rockford, Rockford, IL

    Background/Purpose: EnhanceFitness® (EF) is an evidence-based, community-delivered intervention for older adults; however, its effectiveness in people with arthritis is unknown. The purpose of this pragmatic,…
  • Abstract Number: 2823 • 2017 ACR/ARHP Annual Meeting

    Preliminary Comparison of Patient-Centered Weight Loss Programs Starting before Versus after Knee Replacement

    Christine Pellegrini1,2, Rowland W. Chang3, Dorothy D. Dunlop4, David Conroy1,5, Julia (Jungwha) Lee6, Linda VanHorn6, Bonnie Spring1 and Kenzie Cameron7, 1Northwestern University Feinberg School of Medicine, Chicago, IL, 2Exercise Science, University of South Carolina's Arnold School of Public Health, Columbia, SC, 3Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 4Center for Healthcare Studies, Northwestern University Feinberg School of Medicine, Chicago, IL, 5Kinesiology, The Pennsylvania State University, University Park, PA, 6Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 7General Internal Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: Most patients risk gaining weight in the years after knee replacement, adding further concern to a population that is mostly overweight/obese prior to surgery.…
  • Abstract Number: 2824 • 2017 ACR/ARHP Annual Meeting

    Sleep and Depression Mediate the Relationship between Pain and Cognitive Dysfunction in Lupus Patients

    Teresa A. Lillis1, Vanessa Tirone1, Stacy Weinberg2, Nisarg Gandhi3, Ailda Nika4, Winston Sequeira4, Stevan E. Hobfoll1, Joel A. Block2 and Meenakshi Jolly4, 1Behavioral Sciences, Rush University Medical Center, Chicago, IL, 2Division of Rheumatology, Rush University Medical Center, Chicago, IL, 3Rush University Medical Center, Chicago, IL, 4Rheumatology, Rush University Medical Center, Chicago, IL

    Background/Purpose: Cognitive Dysfunction (CD) is seen among 20-80% of patients with Systemic Lupus Erythematosus (SLE) and adversely affects their quality of life and productivity. Pain,…
  • Abstract Number: 2825 • 2017 ACR/ARHP Annual Meeting

    A Possible Environmental Origin for a Proportion of the Genetic Risk of Rheumatoid Arthritis and Systemic Lupus Erythematosus

    John B. Harley1, Xiaoting Chen1, Mario Pujato2, Daniel Miller1, Avery Maddox1, Carmy Forney3, Albert Magnusen3, Arthur Lynch1, Kashish Chetal4, Masashi Yukawa5, Artem Barski6, Nathan Salomonis4, Kenneth Kaufman7, Leah C. Kottyan8 and Matthew Weirauch9, 1Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2Center of Autoimmune Genomics and Etiology (CAGE), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 3Center of Autoimmune Genomics and Etiology (CAGE), Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 4Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 5Divisions of Allergy and Immunology and Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 6Divisions of Allergy and Immunology and Bioinformatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 7Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Children's Hospital Medical Center; US Department of Veterans Affairs Medical Center, Cincinnati, OH, 8Center for Autoimmune Genomics and Etiology (CAGE), Division of Allergy and Immunology, Cincinnati Children's Hospital, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 9Center for Autoimmune Genomics and Etiology (CAGE) and Divisions of Biomedical Informatics and Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

    Background/Purpose: Nearly 150 genetic loci are convincingly associated with lupus (SLE) or rheumatoid arthritis (RA) and underlie their incompletely understood mechanisms of pathogenesis. Since 90%…
  • Abstract Number: 2826 • 2017 ACR/ARHP Annual Meeting

    Fine-Mapping Identifies Causal Variants for RA and T1D in DNASE1L3, Sirpg, MEG3, TNFAIP3 and CD28/CTLA4 Loc

    Harm-Jan Westra1, Marta Martinez-Bonet2, Suna Onengut3, Annette Lee4, Yang Luo1, Nikola Teslovich1, Jane Worthington5, Javier Martín6, TWJ Huizinga7, Lars Klareskog8, Solbritt Rantapää Dahlqvist9, Wei-Min Chen3, Aaron Quinlan10, John Todd11, Stephen Eyre5, Peter Nigrovic2, Peter Gregersen4, Stephen Rich3 and Soumya Raychaudhuri12, 1Division of Genetics and Rheumatology, Department of Medicine, Harvard Medical School, Boston, MA, 2Division of Rheumatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 3Department of Public Health Sciences, University of Virginia, Charlottesville, VA, 4The Feinstein Institute for Medical Research, Northwell Health, Manhasset, NY, 5Arthritis Research UK Centre for Genetics and Genomics, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United Kingdom, 6Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, PTS-Granada, Granada, Spain, 7Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 8Dept. of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, 9University of Umeå, Umeå, Sweden, 10Department of Human Genetics, University of Utah, Salt Lake City, UT, 11JDRF/Wellcome Trust Diabetes and Inflammation Laboratory, Wellcome Trust Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom, 12Division of Medicine and Rheumatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA

    Background/Purpose: While genome-wide association studies have identified risk loci for rheumatoid arthritis and other autoimmune diseases, in very few instances have causal variants driving risk…
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