ACR Meeting Abstracts

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  • Abstract Number: 3226 • 2016 ACR/ARHP Annual Meeting

    Maintenance of Clinical Remission and Radiographic Non-Progression with MTX after Completion of 1 Year Initial Treatment with Certolizumab Pegol in Japanese Patients with Early Rheumatoid Arthritis

    Yoshiya Tanaka1, Tatsuya Atsumi2, Kazuhiko Yamamoto3, Tsutomu Takeuchi4, Hisashi Yamanaka5, Naoki Ishiguro6, Katsumi Eguchi7, Akira Watanabe8, Hideki Origasa9, Toshiharu Shoji10, Pauline Ralston11, Désirée van der Heijde12, Nobuyuki Miyasaka13,14 and Takao Koike15, 1University of Occupational and Environmental Health, Kitakyushu, Japan, 2Division of Rheumatology, Endocrinology and Nephrology, Hokkaido University Graduate School of Medicine, Sapporo, Japan, 3The University of Tokyo, Tokyo, Japan, 4Division of Rheumatology, Keio University School of Medicine, Tokyo, Japan, 5Tokyo Women's Medical University, Tokyo, Japan, 6Nagoya University, Nagoya, Japan, 7Department of Rheumatology, Sasebo Chuo Hospital, Sasebo, Japan, 8Tohoku University, Sendai, Japan, 9Division of Biostatistics and Clinical Epidemiology, University of Toyama School of Medicine, Toyama, Japan, 10UCB Pharma, Tokyo, Japan, 11Hays Pharma, London, United Kingdom, 12Leiden University Medical Center, Leiden, Netherlands, 13Department of Medicine and Rheumatology, Tokyo Medical and Dental University, Tokyo, Japan, 14Tokyo Medical and Dental University, Tokyo, Japan, 15Sapporo Medical Center NTT EC, Sapporo, Japan

    Background/Purpose: The efficacy and safety of certolizumab pegol (CZP) treatment in combination with dose-optimized MTX in Japanese MTX-naïve early RA patients (pts) with poor prognostic…
  • Abstract Number: 3227 • 2016 ACR/ARHP Annual Meeting

    Modelling Primary Sjögren’s Syndrome Using Salivary Gland Stem Cells

    Sarah Pringle1, Hendrika Bootsma2, Arjan Vissink3, Fred K.L. Spijkervet4, Robert Coppes5 and Frans G.M. Kroese6, 1Rheumatology and Clinical Immunology, University Medical Centrum Groningen, Groningen, Netherlands, 2Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, The Netherlands, Groningen, Netherlands, 3Department of Oral and Maxillofacial Surgery, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 4Oral and Maxillofacial Surgery, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 5Radiation Oncology and Cell Biology, University Medical Centrum Groningen, Groningen, Netherlands, 6Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands

    Background/Purpose: Primary Sjögren’s Syndrome (pSS) is characterized by lymphocytic infiltration of salivary glands.  Unclear interactions between infiltrating cells and salivary gland ductal cells cause reduced…
  • Abstract Number: 3228 • 2016 ACR/ARHP Annual Meeting

    Specific T Cell and B Cell Distributions Characterize Subgroups of Patients with Primary Sjögren’s Syndrome and Are Associated with Disease Activity and Pro-Inflammatory Cytokine Expression

    Lucas Le Lann1, Quentin Simon1, Christophe Jamin1, Maria Orietta Borghi2, Lorenzo Beretta3, Ricard Cervera4, Alain Saraux5, Divi Cornec1, Rik Lories6, Carlo Chizzolini7, Marta E. Alarcon Riquelme8, Jacques-Olivier Pers1 and on behalf of the PRECISESADS Consortium, 1INSERM ERI29, EA2216, Université de Brest, Labex IGO, CHRU Morvan, Brest, France, 2University of Milan, IRCCS Istituto Auxologico Italiano, Milan, Italy, 3Rheumatology, Milan, Italy, 4Department of Autoimmune Diseases, Institut Clínic de Medicina i Dermatologia, Hospital Clínic de Barcelona, Barcelona, Spain, 5Rheumatology Department, CHU de la Cavale Blanche, Brest Cedex, France, 6Laboratory of Tissue Homeostasis and Disease, Skeletal Biology and Engineering Research Center, KU Leuven and University Hospitals Leuven., Leuven, Belgium, 7University hospital of Geneva, Geneva, Switzerland, 8Centro de Genomica e Investigación Oncológica, Pfizer-University of Granada-Junta de Andalucía, Granada, Spain

    Background/Purpose : The goal of the IMI PRECISESADS project is to reclassify individuals affected by systemic autoimmune diseases (SADs) into clusters of molecular, instead of…
  • Abstract Number: 3229 • 2016 ACR/ARHP Annual Meeting

    Bone Morphogenetic Protein 6 Receptor Inhibition Restores Salivary Gland Function in a Mouse Model of Primary Sjögren’s Syndrome

    Hongen Yin1, Lovika Kalra1, Arif Karim1, Zhennan Lai1, Maria Guimaro1, Lauren Aber1, Bill Swaim1, Sandra Afione1, Alexandria Voigt2, Cuong Nguyen3, Paul Yu4, Donald Bloch5 and John A. Chiorini1, 1Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, 2Department of Pathology and Infectious Diseases, University of Florida, Gainesville, FL, 3Department of Pathology and Infectious Diseases, University of Florida, Bethesda, MD, 4Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 5Center for Immunology and Inflammatory Diseases and the Division of Rheumatology, Allergy, and Immunology of the Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA

    Background/Purpose:   Methods:   Results: Elevated BMP6 was found in 63/80 (78.8%) of pSS patients examined in this study. In humans, ALK2 and ALK3 receptors…
  • Abstract Number: 3230 • 2016 ACR/ARHP Annual Meeting

    Genome-Wide Association Study Identifies Novel Sjögren’s Syndrome Risk Loci in the Regions of NAB1, TYK2, and PTTG1-mir146a

    Christopher J. Lessard1, Indra Adrianto1, John Ice1, Astrid Rasmussen2, Kiely Grundahl3, Jennifer A. Kelly4, R. Hal Scofield1, Simon Bowman5, Susan Lester6, Per Eriksson7, Maija-Leena Eloranta8, Johan G. Brun9, Lasse G. Goransson10, Erna Harboe10, Marika Kvarnström11, Michael T. Brennan12, James Chodosh13, Raj Gopalakrishnan14, Andrew J.W. Huang15, Pamela Hughes16, David M. Lewis17, Michael D. Rohrer18, Donald U. Stone19, Nelson L. Rhodus20, Barbara M. Segal21, Lida Radfar22, A. Darise Farris23, Joel M. Guthridge24, Patrick M. Gaffney1, Judith A. James1, John B. Harley25, Lars Rönnblom8, Juan-Manuel Anaya26, Deborah S. Cunninghame-Graham27, Timothy J. Vyse28, Ilias Alevizos29, Xavier Mariette30, Roald Omdal10, Marie Wahren-Herlenius31, Torsten Witte32, Roland Jonsson33, Maureen Rischmueller34, Lindsey A. Criswell35, Courtney G. Montgomery1, Wan-Fai Ng36, Gunnel Nordmark37 and Kathy L. Sivils1, 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, USA, Oklahoma City, OK, 3Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma CIty, OK, 4Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 5Department of Rheumatology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom, 6Queen Elizabeth Hospital, University of Adelaide, Adelaide, Australia, 7University Hospital, Rheumatology clinic, Linköping, Sweden, 8Uppsala University, Department of Medical Sciences, Rheumatology and Science for Life Laboratory, Uppsala, Sweden, 9Department of Rheumatology, Haukeland University Hospital, Bergen, Norway, 10Clinical Immunology Unit, Department of Internal Medicine, Stavanger University Hospital, Stavanger, Norway, 11Karolinska Institutet, Stockholm, Sweden, 12Department of Oral Medicine, Carolinas Medical Center, Charlotte, NC, 13Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 14Diagnostic and Biological Sciences, Division of Oral Pathology, University of Minnesota School of Dentistry, Minneapolis, MN, 15Washington University,, St Louis, MO, 16Division of Oral and Maxillofacial Surgery, Department of Developmental and Surgical Science, University of Minnesota School of Dentistry, Minneapolis, MN, 17Department of Oral and Maxillofacial Pathology, University of Oklahoma College of Dentistry, Oklahoma City, OK, 18Hard Tissue Research Laboratory, University of Minnesota School of Dentistry, Minneapolis, MN, 19Dean McGee Eye Institute, Oklahoma City, OK, 20Department of Diagnostic and Biological Sciences, University of Minnesota School of Dentistry, Minneapolis, MN, 21Division of Rheumatology, University of Minnesota Medical School, Minneapolis, MN, 22Oral Diagnosis and Radiology Department, University of Oklahoma College of Dentistry, Oklahoma City, OK, 23Arthritis & Immunology Program, Oklahoma Medical Research Foun, Oklahoma City, OK, 24Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 25Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Childrens Hospital, Cincinnati, OH, 26Center for Autoimmune Diseases Research (CREA). School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia., Bogotá, Colombia, 27Department of Medical and Molecular Genetics, King's College London, London, United Kingdom, 28Division of Immunology, Infection and Inflammatory Disease, King’s College London, London, United Kingdom, 29Sjögren's Syndrome Clinic, National Institute of Dental and Craniofacial Research, Bethesda, MD, 30Institut National de la Santé et de la Recherche Médicale, Université Paris-Sud, AP-HP, Hôpitaux Universitaires Paris-Sud, Paris, France, 31Department of Medicine, Solna, Unit of Experimental Rheumatology, Karolinska Institutet, and Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden, 32Department of Clinical Immunology and Rheumatology, Hannover Medical School, Hannover, Germany, 33Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway, 34Rheumatology, University of Adelaide, Adelaide, Australia, 35Division of Rheumatology, UCSF, San Francisco, CA, 36Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom, 37Rheumatology, Department of Medical Sciences, Uppsala University, Sweden, Uppsala, Sweden

    Background/Purpose: Sjögren’s syndrome (SS) is a complex autoimmune disease with both environmental and genetic factors contributing to pathophysiology. The goal of this genome-wide association study…
  • Abstract Number: 3231 • 2016 ACR/ARHP Annual Meeting

    miR200b-5p Expression in Minor Salivary Glands (MSG): A Possible Predictor of Lymphoma Development in Sjögren’s Syndrome (SS)?

    Efstathia K. Kapsogeorgou1, Aristea Papageorgiou1, Michael Voulgarelis2 and Athanasios G. Tzioufas3, 1Department of Pathophysiology, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece, 2Pathophysiology, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece, 3School of Medicine, Pathophysiology Department, National and Kapodistrian University of Athens, Athens, Greece

    Background/Purpose:  The miRNAs of the miR-200 family are critical regulators of oncogene and tumor suppressor genes. A preliminary study of several miRNAs in the MSGs…
  • Abstract Number: 3232 • 2016 ACR/ARHP Annual Meeting

    Decreased Expression of Micro-RNA 130a and Micro-RNA 708 in Type-1 Classical Dendritic Cells of Patients with Primary SS Indicates Their Dysregulation

    Maarten R. Hillen1,2, Sofie L.M. Blokland1,2, Elena Chouri1,2, Ana Lopes1,2, Aike A. Kruize2, Marzia Rossato1,2, Timothy R.D.J. Radstake1,2 and Joel A.G. van Roon1,2, 1Laboratory of Translational Immunology, UMC Utrecht, Utrecht, Netherlands, 2Department of Rheumatology & Clinical Immunology, UMC Utrecht, Utrecht, Netherlands

    Background/Purpose:  cDespite the fact that especially cDC1s are candidate key players in the activation of local T and B-cells in pSS, they have rarely been…
  • Abstract Number: 3233 • 2016 ACR/ARHP Annual Meeting

    Determinants of Pain, Fatigue, Physical Function and Social Participation in SLE Patients, Measured with Patient Reported Outcomes Measurement Information System (PROMIS®) Computerized Adaptive Tests

    Shanthini Kasturi1, Jayme C. Burket2, Jessica Berman1, Kyriakos A. Kirou1, Alana B. Levine1, Lisa R. Sammaritano1 and Lisa Mandl1, 1Rheumatology, Hospital for Special Surgery, New York, NY, 2Healthcare Research Institute, Hospital for Special Surgery, New York, NY

    Background/Purpose: Poor SLE outcomes have been associated with certain clinical and socio-demographic characteristics, but the determinants of patient reported outcomes (PROs) in SLE are unknown.…
  • Abstract Number: 3234 • 2016 ACR/ARHP Annual Meeting

    Prevalence and Metric of Depression and Anxiety in Lupus: A Systematic Review and Meta-Analys

    Ahmed Moustafa1, Mohamed Hassanein2, Lihi Eder3, Joan E. Wither4, William Fung5, Panayiotis Lambiris6 and Zahi Touma4, 1Medicine, Western University, London, ON, Canada, 2Michigan State University, East Lansing, MI, 3Medicine, University of Toronto, Women's College Hospital, Toronto, ON, Canada, 4Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 5Medicine, University of Toronto, Toronto, ON, Canada, 6University Health Network, Toronto, ON, Canada

    Background/Purpose:  To systematically review the literature on the: 1) prevalence of depression and anxiety in SLE patients and 2) metrics of depression and anxiety.  …
  • Abstract Number: 3235 • 2016 ACR/ARHP Annual Meeting

    Long-Term Impact of Belimumab on Health-Related Quality of Life and Fatigue in Patients with Systemic Lupus Erythematosus: Up to 7 Years of Treatment Exposure

    Vibeke Strand1, Pam Berry2, Sulabha Ramachandran2 and James Fettiplace3, 1Stanford University School of Medicine, Palo Alto, CA, 2GSK, Philadelphia, PA, 3GSK, Uxbridge, Middlesex, United Kingdom

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder that causes long-term organ damage over time and impairment in health-related quality of life (HRQoL).…
  • Abstract Number: 3236 • 2016 ACR/ARHP Annual Meeting

    Socio-Demographic and Clinical Factors Influencing Generic and Disease-Specific Quality of Life in Patients with Systemic Lupus Erythematosus: Results of a Prospective Multicenter Study

    Hervé Devilliers1, Jean-François Besancenot1, Sylvain Audia2, Bernard Bonnotte3, Francois Maurier4, Christiane Broussolle5, Nadine Magy-Bertrand6, Denis Wahl7, Jean-Loup Pennaforte8, Thierry Martin9, Olivier Aumaître10, Gilles Blaison11, Geraldine Muller1, Alexis Mathian12, Christine Binquet13 and Zahir Amoura14, 1Department of Internal Medicine and Systemic Diseases, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 2Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, CHU de Dijon; INSERM, UMR1098, University of Bourgogne Franche-Comté, FHU INCREASE, Dijon, France, 3Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 4Department of Internal Medicine, HP Metz Belle Isle Hospital, Metz, France, 5Internal medicine department, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Lyon, France, 6CHU Jean-Minjoz, Service de médecine interne et immunologie clinique, Besançon, France, 7CHU de Nancy, Vascular Medicine Division and Regional Competence Centre For Rare Vascular And Systemic Autoimmune Diseases; and UMR_S U1116 Research Unit, Nancy, France, 8Internal Medicine, Internal medicine departement, CHU de Reims, Reims, France, 9Internal medicine and clinical immunology departement, Strasbourg University Hospital, Strasbourg, France, 10CHU Pitié-Salpêtrière - Department of Internal Medicine 2. Referal center for SLE/APS, Paris, France, 11Internal medicine departement, Colmar Hospital, Colmar, France, 12Hôpital Pitié-Salpêtrière, AP-HP, UPMC Univ Paris 06 & French National Reference Center For Systemic Lupus and Antiphospholipid Syndrome, Paris, France, 13INSERM, CIC 1432, Clinical Epidemiology Unit, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 14Department of Internal Medicine 2. Referal center for SLE/APS, Hôpital Pitié-Salpêtrière, AP-HP, UPMC Univ Paris 06 & French National Reference Center For Systemic Lupus and Antiphospholipid Syndrome, Paris, France

    Background/Purpose: To describe demographic, socio-economic and lupus-related factors associated with health-related quality of life (HRQOL) in systemic lupus erythematosus (SLE), as measured by 2 generic…
  • Abstract Number: 3237 • 2016 ACR/ARHP Annual Meeting

    Responsiveness and Its Magnitude in the 36-Item Short Form Health Survey and the Lupus Quality of Life Questionnaire in Patients with Active Disease

    Stephanie Nantes1, Jiandong Su2 and Zahi Touma3, 1University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 3Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada

    Background/Purpose: SF-36 and LupusQoL are Health-Related Quality-of-Life (HRQoL) questionnaires used in SLE. We determined: (1) concurrent construct validity of SF-36 and LupusQoL against disease activity…
  • Abstract Number: 3238 • 2016 ACR/ARHP Annual Meeting

    Depression Symptoms throughout the Lifespan in a Low-Income, Minority Cohort of Lupus Patients: Who Is at Risk?

    Tamar Rubinstein1, Noa Schwartz2, Nicole Jordan3, Rebecca Lois4, Dawn Wahezi5,6, Ruth E K Stein7,8 and Chaim Putterman2, 1Division of Pediatric Rheumatology, Albert Einstein College of Medicine, Children's Hospital at Montefiore, Bronx, NY, 2Division of Rheumatology, Albert Einstein College of Medicine, Bronx, NY, 3Montefiore Medical Center, New York, NY, 4Psychiatry and Pediatrics, Albert Einstein College of Medicine, Children's Hospital at Montefiore, Bronx, NY, 5Pediatric Rheumatology, Albert Einstein College of Medicine, Bronx, NY, 6Pediatric Rheumatology, The Children's Hospital at Montefiore, Bronx, NY, 7Pediatrics, Children's Hospital at Montefiore, Bronx, NY, 8Pediatrics, Albert Einstein College of Medicine, Bronx, NY

      Background/Purpose: Depression is commonly seen in lupus, but widely varying prevalence rates have been reported. This may be due to different demographics and characteristics…
  • Abstract Number: 3239 • 2016 ACR/ARHP Annual Meeting

    Expression of IFN-Regulated Genes in Autoantibody Exposed Babies in Utero

    Malin Hedlund1, Gudny-Ella Thorlacius1, Margarita Ivanchenko1, Vijole Ottosson1, Amina Ossoinak1, Linda Lagnefeldt1, Joanna Tingstrom1, Alexander Espinosa1, Lars Rönnblom2, Maija-Leena Eloranta2, Sven-Erik Sonesson1 and Marie Wahren-Herlenius3, 1Department of Medicine, Solna, Unit of Experimental Rheumatology, Karolinska Institutet, and Karolinska University Hospital, Stockholm, Stockholm, Sweden, 2Uppsala University, Department of Medical Sciences, Rheumatology and Science for Life Laboratory, Uppsala, Sweden, 3Department of Medicine, Solna, Unit of Experimental Rheumatology, Karolinska Institutet, and Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden

    Background/Purpose: Ro/SSA autoantibodies and an IFN signature are commonly present in women with Sjögren’s syndrome and SLE. During pregnancy, the autoantibodies are transported across the…
  • Abstract Number: 3240 • 2016 ACR/ARHP Annual Meeting

    Interferon Kappa Is a Novel Type I IFN That Drives Cutaneous Inflammation in Systemic Lupus

    Jasmine Stannard1, Tamra J. Reed2, Emily Myers3, Lori Lowe4, Mrinal Sarkar4, Xianying Xing5, Celine C. Berthier6, Johann Gudjonsson4 and J. Michelle Kahlenberg7, 1Int. Medicine/Rheumatology, University of Michigan, Ann Arbor, MI, 2Internal Medicine, Rheumatology, University of Michigan, Ann Arbor, MI, 3Internal Medicine, Rheumatology, Georgetown University, Washington, DC, 4Dermatology, University of Michigan, Ann Arbor, MI, 5Dermatology, University of Michigan, University of Michigan, Ann Arbor, MI, 6Nephrology, Division of Nephrology, University of Michigan Medical Center, Ann Arbor, MI, 7Internal Medicine, Division of Rheumatology, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI

    Background/Purpose: Cutaneous lupus erythematosus (CLE) lesions are disfiguring, scarring, difficult to treat, and affect up to 70% of patients with systemic lupus erythematosus (SLE). Type…
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