ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 1012 • 2017 ACR/ARHP Annual Meeting

    Analysis of microRNAs in Familial Mediterranean Fever

    Gil Amarilyo1, Nir Pillar2, Ilan Ben-Zvi3, Daphna Weissglas-Volkov2, Jonatan Zalcman2, Liora Harel4, Avi Livneh3 and Noam Shomron2, 1Schneider Children's Medical Center of Israel, Sackler School of Medicine, Tel Aviv University, Petach Tikva, Israel, 2Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel, 3Chaim Sheba Medical Center, Tel Hashomer, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel, 4Schneider Children's Medical Center of Israel, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel

    Background/Purpose: Familial Mediterranean fever (FMF) is thought to be inherited as an autosomal recessive trait. However, there are frequent deviations from this model. The aim…
  • Abstract Number: 1013 • 2017 ACR/ARHP Annual Meeting

    HLA-Class II Associations with ANCA-Associated Vasculitis in the Japanese Population: Different Features from European Populations

    Aya Kawasaki1, Fumio Hirano2, Ken-ei Sada3, Shigeto Kobayashi4, Hidehiro Yamada5, Hiroshi Furukawa1, Kenji Nagasaka6, Takahiko Sugihara7, Kunihiro Yamagata8, Takayuki Sumida9, Shigeto Tohma10, Shoichi Ozaki5, Seiichi Matsuo11, Hiroshi Hashimoto12, Hirofumi Makino13, Yoshihiro Arimura14, Masayoshi Harigai15 and Naoyuki Tsuchiya1, 1Molecular and Genetic Epidemiology Laboratory, University of Tsukuba, Faculty of Medicine, Tsukuba, Japan, 2Departments of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan, 3Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan, 4Department of Internal Medicine, Juntendo University Koshigaya Hospital, Koshigaya, Japan, 5Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan, 6Department of Rheumatology, Ome Municipal General Hospital, Ome, Japan, 7Department of Medicine and Rheumatology, Tokyo Metropolitan Geriatric Hospital, Tokyo, Japan, 8Department of Nephrology, University of Tsukuba, Faculty of Medicine, Tsukuba, Japan, 9Department of Internal Medicine, University of Tsukuba, Faculty of Medicine, Tsukuba, Japan, 10Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara, Japan, 11Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan, 12Juntendo University School of Medicine, Tokyo, Japan, 13Okayama University Hospital, Okayama, Japan, 14First Department of Internal Medicine, Kyorin University School of Medicine, Tokyo, Japan, 15Division of Epidemiology and Pharmacoepidemiology of Rheumatic Diseases, Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan

    Background/Purpose: HLA-class II region harbors the strongest genetic factors for ANCA-associated vasculitis (AAV), and differences in the genetic background of HLA-class II may partly explain…
  • Abstract Number: 1014 • 2017 ACR/ARHP Annual Meeting

    The Rheumatic Disease Data Refinery: A Case Study in Integrative Genomics Reveals Complex IFN Signatures in Therapeutic Studies in SLE

    Jaclyn N Taroni and Casey S. Greene, Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Over the past 15 years, more than 10,000 whole tissue biopsies from patients with rheumatic diseases have been deposited into publicly available gene expression…
  • Abstract Number: 1015 • 2017 ACR/ARHP Annual Meeting

    Key Genes and Pathways between Rheumatoid Arthritis and Osteoarthritis By Integrative Genome-Wide Gene Expression Profiling Analysis

    Rongqiang Zhang1,2, Aimin Yang3, Xiaomei Ren2, Jie Zhang3, Xiaoli Yang4, Qiling Liu2, Na Sun2, Puwei Yuan5 and Yongmin Xiong4, 1School of Public Health, Xi'an Jiaotong University Health Science Center, Key Laboratory of Trace Elements and Endemic Diseases of the National Health and Family Planning Commission, Xi'an 710061, China, Xi'an, China, 2Shaanxi University of Chinese Medicine, Xianyang 712046, China, Xianyang, China, 3School of Public Health, Brown University, Providence, RI 02906, US, Providence, RI, 4School of Public Health, Xi'an Jiaotong University Health Science Center, Key Laboratory of Trace Elements and Endemic Diseases of the National Health and Family Planning Commission, Xi'an 710061, China, Xian, China, 5Shaanxi University of Chinese Medicine, Xianyang 712046, China, XianYang, China

    Background/Purpose: Rheumatoid arthritis (RA) and Osteoarthritis (OA) are two most common types of joint diseases with lots of similar symptoms, and their pathological mechanisms remain…
  • Abstract Number: 1016 • 2017 ACR/ARHP Annual Meeting

    The Genetic Biomarkers to Predicting Response of TNF Inhibitors Treatment in Rheumatoid Arthritis

    So-Young Bang1, Youngho Park2, Kwangwoo Kim3, Young Bin Joo4, Soo-Kyung Cho5, Chan-Bum Choi1, Yoon-Kyoung Sung2, Tae-Hwan Kim2, Jae-Bum Jun1, Dae-Hyun Yoo1, Hye-Soon Lee6 and Sang-Cheol Bae7, 1Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South), 2Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South), 34Department of Biology, Kyung Hee University, Seoul, Korea, Republic of (South), 4Internal Medicine, Department of Rheumatology, St. Vincent's Hospital, The Catholic University of Korea, Suwon, Gyeonggido, Korea, Republic of (South), 5Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South), 6Hanyang University Guri Hospital, Gyeonggi-do, Korea, Republic of (South), 7Department of Rhematology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea, Republic of (South)

    Background/Purpose: Although pharmacogenetic studies of TNF inhibitors (TNFi) response presented the estimates of high heritability, only few loci with suggestive weak association as biomarkers for…
  • Abstract Number: 1017 • 2017 ACR/ARHP Annual Meeting

    Investigation of Differential Methylation As a Potential Biomarker of Methotrexate Response in Patients with Rheumatoid Arthritis

    Nisha Nair1, Darren Plant2,3, Suzanne M Verstappen1, John D Isaacs4, Ann W. Morgan5, Kimme L. Hyrich6, Anne Barton7 and Anthony G. Wilson8, 1Arthritis Research UK Centre of Genetics and Genomics and Centre of Epidemiology, Manchester, United Kingdom, 2Arthritis Research UK Centre for Genetics and Genomics, The University of Manchester, Manchester, United Kingdom, 3NIHR Manchester Musculoskeletal BRU, Central Manchester Foundation Trust and University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom, 4Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, United Kingdom, 5NIHR-Leeds Musculoskeletal Biomedical Research Unit, Leeds, United Kingdom, 6National Institute of Health Research Manchester Musculoskeletal Biomedical Research Centre, Central Manchester NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom, 7Arthritis Research UK, Centre for Genetics and Genomics, Centre for Musculoskeletal Research, Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, United Kingdom, 8UCD School of Medicine and Medical Science, Conway Institute, University College Dublin, Dublin, Ireland

    Background/Purpose: Methotrexate (MTX) is the first-line disease modifying anti-rheumatic drug for the treatment of rheumatoid arthritis (RA). However, many patients do not respond adequately or…
  • Abstract Number: 1018 • 2017 ACR/ARHP Annual Meeting

    Comprehensive Identification of Differentially Methylated Regions Associated with Systemic Sclerosis in Dermal Fibroblasts from African-American Patients

    Paula S. Ramos1,2, Willian da Silveira3, E. Starr Hazard3, Ilia Atanelishvili4, Robert C. Wilson5, Jim C. Oates1, Galina S. Bogatkevich4 and Gary Hardiman1,2,3, 1Department of Medicine, Medical University of South Carolina, Charleston, SC, 2Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, 3Center for Genomic Medicine, Medical University of South Carolina, Charleston, SC, 4Division of Rheumatology and Immunology, Department of Medicine, Medical University of South Carolina, Charleston, SC, 5Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC

    Background/Purpose: The etiology and reasons underlying the ethnic disparities in systemic sclerosis (SSc) remain unknown. African-Americans are disproportionally affected by SSc, yet dramatically underrepresented in…
  • Abstract Number: 1019 • 2017 ACR/ARHP Annual Meeting

    Molecular Profiling of RA Patients Suggests a Differential Involvement of Adaptive and Innate Cell Populations in Response to Anti-TNF Treatment

    Victor Farutin1, Thomas Prod'homme1, Kevin McConnell1, Nathaniel Washburn1, Patrick Halvey1, Jamey Guess1, Nur Sibel Gunay1, Jan Hillson2, Carol J. Etzel3, Katherine C. Saunders3, Dimitrios A. Pappas3,4, Anthony Manning1, Leona Ling1 and Ishan Capila1, 1Research, Momenta Pharmaceuticals, Inc., Cambridge, MA, 2Clinical Research, Momenta Pharmaceuticals, Inc., Cambridge, MA, 3Corrona, LLC, Southborough, MA, 4Columbia University, New York, NY

    Background/Purpose: Despite the success of anti-TNF therapies in RA, ~ 30 % of patients are non-responders. Several studies have focused on understanding the biology underlying…
  • Abstract Number: 1020 • 2017 ACR/ARHP Annual Meeting

    The Inflammatory and Proliferative Synovial Lesion in Post-Infectious Lyme Arthritis Results from Impaired Wound Healing

    Robert Lochhead1,2, David Ordonez-Del Valle1,2, Klemen Strle2,3, Sheila Arvikar1,2, John Aversa4 and Allen Steere1,2, 1Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, BOSTON, MA, 2Department of Medicine, Harvard Medical School, BOSTON, MA, 3Department of Immunology and Inflammatory Diseases, Massachusetts General Hospital, BOSTON, MA, 4School of Medicine, Yale University, New Haven, CT

    Background/Purpose: Lyme arthritis (LA) is initially triggered by Borrelia burgdorferi infection, but in some patients, the synovitis persists despite 2-3 months of antibiotic therapy and…
  • Abstract Number: 1021 • 2017 ACR/ARHP Annual Meeting

    GWAS of Gout in Patients with Hyperuricemia Identified Many Possible New Candidate Risk Alleles

    Jing Cui1, Zhi Zhang1, Elizabeth Karlson2 and Daniel H. Solomon2, 1Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Brigham and Women's Hospital and Harvard Medical School, Boston, MA

    Background/Purpose:  Virtually all gout patients have high levels of uric acid in the blood (hyperurincemia, HU), but approximately 80% of patients with HU will never…
  • Abstract Number: 1022 • 2017 ACR/ARHP Annual Meeting

    A Personalized Medicine Approach to Improve the Prediction of Azathioprine-Induced Pancreatic Injury: Preliminary Results

    Tyler Reese1, Savannah Hurt2, Rany Octaria2, Alyson Dickson2, Prathima Anandi2, Vivian Kawai2, Kelly Birdwell2, Adriana Hung2, C. Michael Stein3, QiPing Feng2 and Cecilia P. Chung3, 1Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, 2Vanderbilt University Medical Center, Nashville, TN, 3Medicine, Vanderbilt University Medical Center, Nashville, TN

    Background/Purpose: Azathioprine (AZA) is used to treat rheumatic diseases and to prevent transplant rejection. There is marked variability in toxicity to azathioprine; one such toxicity…
  • Abstract Number: 1023 • 2017 ACR/ARHP Annual Meeting

    The Autoimmune Discovery Ichip Distinguishes Healthy Individuals (HC) from Those with SLE, Rheumatoid Arthritis (RA), Scleroderma (SSc), Sjogren’s Syndrome (SS), and the Anti-Phospholipid Syndrome (APS)

    Chaim Putterman1, Armando Gabrielli2, Alexandra Balbir-Gurman3, Pennina Safer4, Keren Jakobi-Brook4, Rachel Sorek4, Ilana Gluzman4, Steve Wallace5 and Irun R. Cohen4,6, 1Division of Rheumatology, Albert Einstein College of Medicine, Bronx, NY, USA, Bronx, NY, 2Istituto di Clinica Medica dell'Università di Ancona, Ancona, Italy, Ancona, Italy, 3Rheumatology Unit, Rambam Health Care Campus, Rappaport Faculty of Medicine, Technion, Haifa, Israel, Haifa, Israel, 4ImmunArray Ltd., Rehovot, Israel, Rehovot, Israel, 5ImmunArray Inc., VA, USA, Richmond, VA, 6Weizmann Institute of Science, Rehovot, Israel, Rehovot, Israel

    Background/Purpose: Current serological tests are not sufficiently accurate in differentiating between HC and those with autoimmune rheumatic diseases. We developed the iCHIP antigen microarray to…
  • Abstract Number: 1024 • 2017 ACR/ARHP Annual Meeting

    High-Throughput Proteomic Profiling Identifies Dysregulated Proteins in Neonatal-Onset Multisystem Inflammatory Disease (NOMID) That Respond to IL-1blocking Treatment

    Megha Garg1,2, Brian Sellers3, Adriana Almeida de Jesus4, Angélique Biancotto5, Foo Cheung6 and Raphaela Goldbach-Mansky4, 1National Institutes of Arthritis, Musculoskletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Translational Autoinflammatory Disease Studies, NIH/NIAID, Bethesda, MD, 3Center for Human Immunology, Autoimmunity and Inflammation, NIH/NHLBI, Bethesda, MD, 4Translational Autoinflammatory Disease Studies (TADS), Laboratory of Clinical Investigation and Microbiology (LCIM), NIAID/NIH, Bethesda, MD, 5Center for Human Immunology, Autoimmunity and Inflammation (CHI), NHLBI, NIH, Bethesda, MD, 6Center for Human Immunology Autoimmunity and Inflammation (CHI), NHLBI, NIH, Bethesda, MD

    Background/Purpose: Neonatal-onset multisystem inflammatory disease (NOMID) is an IL- 1 mediated autoinflammatory disease caused by a gain-of-function mutations in NLRP3that results in constitutive activation of…
  • Abstract Number: 1025 • 2017 ACR/ARHP Annual Meeting

    Submetabolome Profiling with Differential Chemical Isotope Labeling Liquid Chromatography Mass Spectrometry and a Universal Metabolome Standard Reveals a Metabolite Profile with 99% Accuracy for Rheumatoid Arthritis

    Walter P. Maksymowych1, Derrick Blackmore2, Roman Eisner3, Liang Li4 and Zaeem Siddiqi2, 1Department of Medicine, University of Alberta, Edmonton, AB, Canada, 2Medicine, University of Alberta, Edmonton, AB, Canada, 3City of Edmonton, Edmonton, AB, Canada, 4Chemistry, University of Alberta, Edmonton, AB, Canada

    Background/Purpose: Early diagnosis of rheumatoid arthritis (RA) is hampered by suboptimal accuracy of currently available serological biomarkers. Recent advancements in metabolomic profiling include dansylation liquid…
  • Abstract Number: 1026 • 2017 ACR/ARHP Annual Meeting

    Gene Expression Analysis Reveals Common Pathways of Tissue Pathogenesis in Lupus Organ Involvement

    Amrie Grammer1, Sarah Heuer1, Robert Robl1, Adam Labonte1, Prathyusha Bachali1, Sushma Madamanchi1 and Peter E. Lipsky2, 1AMPEL BioSolutions and RILITE Research Institute, Charlottesville, VA, 2AMPEL BioSolutions, LLC, Charlottesville, VA

    Background/Purpose: Lupus is a prototypic autoimmune disease characterized by B cell hyperactivity, autoantibody formation and resultant tissue damage. The mechanisms underlying tissue pathology in lupus…
  • « Previous Page
  • 1
  • …
  • 1271
  • 1272
  • 1273
  • 1274
  • 1275
  • …
  • 2425
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology