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Abstracts tagged "Epigenetics"

  • Abstract Number: 767 • 2017 ACR/ARHP Annual Meeting

    Elevated MeCP2 Expression in Diffuse Cutaneous Systemic Sclerosis Dermal Fibroblasts Is Associated with Anti-Fibrotic Effects

    Ye He1, Pei-Suen Tsou2, Dinesh Khanna3 and Amr H Sawalha2, 1Rheumatology, University of Michigan, Ann Arbor, MI, 2Division of Rheumatology, University of Michigan, Ann Arbor, MI, 3University of Michigan, Ann Arbor, MI

    Background/Purpose: Systemic Sclerosis (SSc) is a multisystem autoimmune connective tissue disorder characterized by vascular injury and fibrosis of the skin and internal organs. Methyl-CpG-binding protein…
  • Abstract Number: 903 • 2017 ACR/ARHP Annual Meeting

    Increased Expression of CCN4/WISP1 in Osteoarthritic Articular Cartilage Is Epigenetically Regulated and Disrupts Cartilage Homeostasis

    Martijn H. van den Bosch1, Yolande F. Ramos2, Wouter den Hollander2, Nils Bömer2, Rob G. Nelissen3, Judith V. Bovée4, Peter L. van Lent1, Arjen B. Blom1, Peter M. van der Kraan1 and Ingrid Meulenbelt2, 1Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2Department of Molecular Epidemiology, Leiden University Medical Center, Leiden, Netherlands, 3Department of Orthopedics, Leiden University Medical Center, Leiden, Netherlands, 4Department of Pathology, Leiden University Medical Center, Leiden, Netherlands

    Background/Purpose: Previously, we described increased expression of Wnt-1-induced signaling protein 1 (Wisp1) in murine synovium and cartilage after induction of experimental osteoarthritis (OA) models. WISP1…
  • 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: 1660 • 2017 ACR/ARHP Annual Meeting

    Prolactin Induces an Interferon Signature in Monocytes and Drives IRF1-HAT Interactions

    Yiu Tak Leung1, Lihua Shi2, Kelly Maurer2, Li Song3 and Kathleen E. Sullivan4, 1Temple University, Philadelphia, PA, 2Immunology ARC 1216, The Children's Hospital of Philadelphia, Philadelphia, PA, 3Allergy Immunology, Children's Hospital of Philadelphia, Philadelphia, PA, 4Pediatrics, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Epigenetic changes in systemic lupus erythematosus (SLE) offer a potential explanation for the chronicity of disease. We previously found that interferon regulatory factor-1(IRF1) binding…
  • Abstract Number: 1727 • 2017 ACR/ARHP Annual Meeting

    Genome-Wide DNA Methylation Analysis in Systemic Sclerosis Reveals Hypomethylation of Interferon-Associated Genes in CD4+ and CD8+ T Cells

    Weilin Pu1, Weifeng Ding2, Lei Wang3, Shuai Jiang4, Wenzhen Tu3, Shicheng Guo5, Qingmei Liu6, Yanyun Ma4, Sidi Chen7, Wenyu Wu6, Xiaodong Zhou8, Maureen D. Mayes9, Shervin Assassi9, John D. Reveille9, Li Jin10 and Jiucun Wang10, 1State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences,, State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences and Institutes of Biomedical Sciences, Fudan University, Shanghai, China, Shanghai, China, 2Medical Laboratory Center, Medical Laboratory Center, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, China, Nantong, China, 3Division of Rheumatology, Division of Rheumatology, Shanghai TCM-integrated Hospital, Shanghai, China, Shanghai, China, 4Ministry of Education Key Laboratory of Contemporary Anthropology, School of Life Sciences, Ministry of Education Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China, Shanghai, China, 5Department of Bioengineering, Department of Bioengineering, University of California at San Diego, CA, USA, San Diego, CA, 6Department of Dermatology, Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, China, Shanghai, China, 7State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences and Institutes of Biomedical Sciences,, State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences and Institutes of Biomedical Sciences, Fudan University, Shanghai, China, Shanghai, China, 8Internal Medicine-Rheumatology, University of Texas McGovern Medical School, Houston, TX, 9University of Texas McGovern Medical School, Houston, TX, 10State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences and Institutes of Biomedical Sciences, State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences and Institutes of Biomedical Sciences, Fudan University, Shanghai, China, Shanghai, China

    Background/Purpose: Systemic sclerosis (SSc) is a complex systemic autoimmune disease caused by complicated interaction between genetic, epigenetic and environmental risk factors. Evidence showed epigenetic modifications,…
  • Abstract Number: 1791 • 2017 ACR/ARHP Annual Meeting

    TET1 Is an Important Transcriptional Activator of the Tnfa Locus in Macrophages

    Emmanuel Karouzakis1, Fangfang Sun2, Agnieszka Pajak1, Shuang Ye2, Steffen Gay1, Oliver Distler3 and Michel Neidhart1, 1Center of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Department of Rheumatology, Renji Hospital South Campus, School of Medicine, Shanghai Jiao Tong University, Shanghai, China, 3Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland

    Background/Purpose: Activated macrophages are found in the inflamed and hyperplastic synovial RA tissue. Macrophages are the main producers of high levels of pro-inflammatory cytokines such…
  • Abstract Number: 1925 • 2017 ACR/ARHP Annual Meeting

    TGFβ Promotes Fibrosis By MYST1-Dependent Epigenetic Regulation of Autophagy

    Ariella Zehender1, Neng-Yu Lin2, Adrian Stefanica3, Chih-Wei Chen4, Alina Soare5, Thomas Wohlfahrt6, Simon Rauber6, Christina Bergmann7, Andreas Ramming8, Oliver Distler9, Georg Schett10 and Jörg Distler5, 11Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, 2Department of Internal Medicine III and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 31Department of Internal Medicine 3 – Rheumatology and Immunology, University of Erlangen, Erlangen, Germany, 4Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, Erlangen, Germany, 5Department of Internal Medicine 3 – Rheumatology and Immunology, Universitätsklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Erlangen, Germany, 6Department of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, 7Department of Internal Medicine 3 and Institute for Clinical Immunology, Friedrich-Alexander-University of Erlangen-Nuremberg and University Hospital Erlangen, Erlangen, Germany, 8Department of Internal Medicine 3 – Rheumatology and Immunology, Universitätsklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and University Hospital Erlangen, Erlangen, Germany, 9Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 10Department of Internal Medicine 3 – Rheumatology and Immunology, Department of Internal Medicine 3 and Institute for Clinical Immunology, Friedrich-Alexander-University of Erlangen-Nuremberg and University Hospital Erlangen, Erlangen, Germany

    Background/Purpose: Autophagy (Atg) is catabolic process allowing cells to degrade unnecessary or dysfunctional cellular organelles. Aberrant activation of Atg has been implicated into the pathogenesis…
  • Abstract Number: 2654 • 2017 ACR/ARHP Annual Meeting

    Treatment-Associated DNA Methylation Patterns in Systemic Lupus Erythematosus

    Juliana Imgenberg-Kreuz1,2, Jonas Carlsson Almlöf1, Dag Leonard3, Gunnel Nordmark2, Maija-Leena Eloranta3, Leonid Padyukov4, Iva Gunnarsson4, Elisabet Svenungsson4, Christopher Sjöwall5, Lars Rönnblom2, Ann-Christine Syvänen1 and Johanna K Sandling1,2, 1Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University, Uppsala, Sweden, Uppsala, Sweden, 2Department of Medical Sciences, Section of Rheumatology, Uppsala University, Uppsala, Sweden, Uppsala, Sweden, 3Rheumatology and Science for Life Laboratory, Department of Medical Sciences, Uppsala University, Sweden, Uppsala, Sweden, 4Department of Medicine Solna, Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden, 5Department of Clinical and Experimental Medicine, Rheumatology/AIR, Linköping University, Linköping, Sweden, Linköping, Sweden

    Background/Purpose: DNA methylation has emerged as an important contributing factor in the pathogenesis of systemic lupus erythematosus (SLE). SLE typically requires continuous treatment to control…
  • Abstract Number: 137 • 2017 Pediatric Rheumatology Symposium

    Chromatin Landscapes and Genetic Risk For Juvenile Idiopathic Arthritis

    James Jarvis1, Lisha Zhu2, Lai Ping Wong3, Tao Liu4, Kaiyu Jiang3 and Yanmin Chen3, 1Pediatrics, SUNY Buffalo School of Medicine, Buffalo, NY, 2Biochemistry, University at Buffalo, Buffalo, NY, 3Pediatrics, University at Buffalo, Buffalo, NY, 4Department of Biochemistry, University at Buffalo, Buffalo, NY

    Background/Purpose: The transcriptomes of peripheral blood cells in children with juvenile idiopathic arthritis (JIA) show distinct transcriptional aberrations that suggest impairment of transcriptional regulation. To…
  • Abstract Number: 3119 • 2016 ACR/ARHP Annual Meeting

    Complete Whole Genome Transcriptome, DNA Methylation, and Histone Mark Analysis of Rheumatoid Arthritis (RA) Fibroblast-like Synoviocytes (FLS) Reveals a Distinctive Epigenetic Landscape and Critical Pathogenic Pathways

    Rizi Ai1, Deepa Hammaker2, David L. Boyle3, Andre ‎ Wildberg4, Keisuke Maeshima2, Emmanuele Palescandolo5, Vinod Krishna5, Bryan Linggi6, Radu Dobrin5, John W. Whitaker7, Wei Wang8 and Gary Firestein9, 1Chemistry and Biochemistry, UC San Diego, La Jolla, CA, 2Division of Rheumatology, Allergy and Immunology, UCSD School of Medicine, La Jolla, CA, 3Division of Rheumatology, Allergy and Immunology, University of California, San Diego, La Jolla, CA, 4Chemistry and Biochemistry, UNIVERSITY OF CALIFORNIA SAN DIEGO, LA JOLLA, CA, 5Janssen Pharmaceuticals, Spring House, PA, 6janssen Pharmaceuticals, Spring House, PA, 7Janssen Pharmaceuticals, La Jolla, CA, 8Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA, 9Medicine, UCSD, La Jolla, CA

    Background/Purpose: RA FLS display a unique aggressive phenotype with a distinctive DNA methylation profile that marks genes involved with cytokine signaling, cell recruitment, and matrix…
  • Abstract Number: 3120 • 2016 ACR/ARHP Annual Meeting

    RA Net: A Systems Biology Approach to Identify Genes Regulating Pathogenic Pathways in Rheumatoid Arthritis (RA) Fibroblast-like Synoviocytes (FLS)

    Wei Wang1, RIchard Ainsworth2, Richard Stein2, Rizi Ai3 and Gary Firestein4, 1Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA, 2UC San Diego, La Jolla, CA, 3Chemistry and Biochemistry, UC San Diego, La Jolla, CA, 4Medicine, UCSD, La Jolla, CA

    Background/Purpose: Rheumatoid arthritis (RA) remains a significant unmet need despite improved therapy. Defining the interlaced nature of gene regulation and disease pathogenesis using integrative systems…
  • Abstract Number: 647 • 2016 ACR/ARHP Annual Meeting

    Genomic and Epigenetic Bioinformatics Demonstrate Dual TNF-α and IL17A Target Engagement By ABT-122, and Suggest Mainly TNF-α–Mediated Relative Target Contribution to Drug Response in MTX-IR Rheumatoid Arthritis Patients

    Robert W. Georgantas III1, Melanie Ruzek2, Justin Wade Davis1, Feng Hong1, Elizabeth Asque1, Kenneth Idler1, Heikki T. Mansikka1, Benoit Guerette1 and Jeffrey F. Waring1, 1AbbVie Inc., North Chicago, IL, 2Immunology Discovery, AbbVie, Worcester, MA

    Background/Purpose: ABT-122 is a dual variable domain (DVD-Ig) biologic which inhibits TNF-α and IL17A. In a 12-wk phase 2 study (NCT02141997) in MTX-IR patients (pts)…
  • Abstract Number: 1093 • 2016 ACR/ARHP Annual Meeting

    DNA Methylation Defines Joint Specific Differences in Synovial Fibroblasts  from OA and RA Patients

    Emmanuel Karouzakis1, Mojca Frank Bertoncelj2, Kerstin Klein1, Christoph Kolling3, Renate E. Gay1, Steffen Gay1 and Caroline Ospelt1, 1Center of Experimental Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 3Schulthess Clinic, Zurich, Switzerland

    Background/Purpose: Recent studies revealed epigenetic changes in DNA methylation associated with rheumatoid arthritis (RA) synovial fibroblasts (SF). In addition, we have shown that SF exhibit…
  • Abstract Number: 1566 • 2016 ACR/ARHP Annual Meeting

    Histone Lysine Methylation and STAT3 Differentially Regulate Constitutive and IL-6-Induced MMPs Gene Activation in Rheumatoid Arthritis Synovial Fibroblasts

    Yasuto Araki1,2, Takuma Tsuzuki Wada2,3, Yoshimi Aizaki1,2, Kazuhiro Yokota1, Hiroshi Kajiyama1, Yu Funakubo Asanuma1, Kojiro Sato1, Hiromi Oda4 and Toshihide Mimura1,2, 1Department of Rheumatology and Applied Immunology, Faculty of Medicine, Saitama Medical University, Saitama, Japan, 2Project Research Division, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan, 3Department of Rheumatology and Applied Immunology, Faculty of Medicine, Saitama Medical University, Iruma, Japan, 4Orthopedic Surgery, Faculty of Medicine, Saitama Medical Univeristy, Morohongo Moroyama, Japan

    Background/Purpose:  Rheumatoid arthritis (RA) is a chronic inflammatory autoimmune disease that causes progressive joint destruction. In spite of the modern medications, including biologic reagents, it…
  • Abstract Number: 1665 • 2016 ACR/ARHP Annual Meeting

    Validation of Germ Line Epigenetic Variants Associated with Psoriatic Disease

    Remy Pollock1, Laila Zaman1, Vinod Chandran2 and Dafna D Gladman3, 1University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 3University of Toronto, Toronto, ON, Canada

    Background/Purpose:  Heritable epigenetic phenomena may play a role in the parent-of-origin effect observed in psoriasis and psoriatic arthritis (PsA). A previous epigenome-wide association study (EWAS)…
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