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

Abstracts tagged "Personalized Medicine"

  • Abstract Number: 1342 • 2019 ACR/ARP Annual Meeting

    Identification of Heterogenous Treatment Response Trajectories to anti-IL6 Receptor Treatment in Rheumatoid Arthritis

    Joseph Patrick Michele Blair1, Cecilie Bager 2, Man Hung Eric Tang 2, Morten Karsdal 3, Anne Bay-Jensen 4 and Søren Brunak 5, 1Univeristy of Copenahgen, Copenhagen, Denmark, 2Nordic Bioscience ProScion, Copenhagen, Denmark, 3Nordic Bioscience, Copenhagen, Denmark, 4Nordic Bioscience, Herlev, Denmark, 5Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark, Copenhagen, Hovedstaden, Denmark

    Background/Purpose: Rheumatoid arthritis (RA) is a complex autoimmune disease with a fluctuating course of disease activity and progression. Although treatments have improved substantially in recent…
  • Abstract Number: 1963 • 2019 ACR/ARP Annual Meeting

    Combining Clinical and Candidate Gene Data into a Risk Score for Azathioprine-Associated Leukopenia in Routine Clinical Practice

    Prathima Anandi 1, Alyson Dickson 2, Qiping Feng 1, Wei-Qi Wei 2, William Dupont 2, Dale Plummer 2, Ge Liu 1, Katherine Barker 2, Vivian Kawai 2, Kelly Birdwell 2, Nancy Cox 1, C. Michael Stein 2, Adriana Hung 2 and Cecilia Chung3, 1Vanderbilt University Medical Center, Nashville, 2Vanderbilt University Medical Center, Nashville, TN, 3Vanderbilt University, Nashville, TN

    Background/Purpose: Azathioprine is a widely-used drug for the treatment of rheumatic diseases, inflammatory bowel disease, and for organ transplantation. However, treatment is often limited by…
  • Abstract Number: 2780 • 2019 ACR/ARP Annual Meeting

    Identification of SLE Subgroups at Risk for Poor Outcomes After Hydroxychloroquine Taper or Discontinuation

    Celline C. Almeida-Brasil 1, Evelyne Vinet 2, Christian Pineau 2 and Sasha Bernatsky1, 1Research Institute of the McGill University Health Centre, Montreal, QC, Canada, 2McGill University Health Centre, Montreal, QC, Canada

    Background/Purpose: The risks and benefits of long-term hydroxychloroquine (HCQ) use in systemic lupus erythematosus (SLE), versus tapering or stopping, remain uncertain. We aimed to identify predictors of…
  • Abstract Number: 2915 • 2019 ACR/ARP Annual Meeting

    Machine-learning Classification Identifies a Subset of Patients That Improve on Abatacept via Modulation of a CD28-Related Pathway

    Bhaven Mehta 1, Jennifer Franks 1, Yiwei Yuan 2, Yue Wang 1, Veronica Berrocal 3, Tammara Wood 1, Cathie Spino 4, David Fox 5, Dinesh Khanna 6 and Michael Whitfield7, 1Geisel School of Medicine at Dartmouth, Hanover, NH, 2Geisel School of Medicine at Dartmouth, Hanover, 3Department of Biostatistics, School of Publich Health, University of Michigan, Ann Arbor, MI, 4University of Michigan, Ann Arbor, MI, 5University of Michigan, Ann Arbor, 6Department of Medicine, University of Michigan, Ann Arbor, Michigan, USA, Ann Arbor, 7Department of Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hannover, NH

    Background/Purpose: We analyzed a phase 2 study designed to assess the efficacy of abatacept in patients with diffuse Systemic Sclerosis (SSc). In this work, we…
  • Abstract Number: L08 • 2018 ACR/ARHP Annual Meeting

    High Baseline Serum IL-6 Identifies a Subgroup of Rheumatoid Arthritis Patients with Rapid Joint Damage and Clinical Progression and Predicts Increased Sarilumab Treatment Response

    Anita Boyapati1, Jérôme Msihid2, Sergio Schwartzman3, Ernest Choy4, Mark C. Genovese5, Gerd R. Burmester6, Gordon Lam7, Toshio Kimura1, Jonathan Sadeh8 and Neil M.H. Graham1, 1Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 2Sanofi Chilly-Mazarin, Chilly-Mazarin, NJ, France, 3Hospital for Special Surgery, New York, NY, 4CREATE Center, Cardiff University School of Medicine, Cardiff, Great Britain, 5Division of Immunology & Rheumatology, Stanford University, Stanford, CA, 6Charité-Universitätsmedizin Berlin, Free University and Humboldt University of Berlin, Berlin, Germany, 7Atrium Health, Charlotte, NC, 8Sanofi, Bridgewater, NJ

    Background/Purpose: Clinical application of biomarkers to predict response to therapy is the next frontier in RA.  Despite the key role of IL-6 in RA, the…
  • Abstract Number: 919 • 2018 ACR/ARHP Annual Meeting

    A Machine Learning Classifier for Assigning Individual Patients with Systemic Sclerosis to Intrinsic Molecular Subsets

    Jennifer Franks1, Viktor Martyanov1, Guoshuai Cai2, Yue Wang3, Tammara A. Wood1 and Michael L. Whitfield4, 1Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 2Environmental Health Sciences, Arnold School of Public Health at University of South Carolina, Columbia, SC, 3Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 4Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hanover, NH

    Background/Purpose: High-throughput gene expression profiling of skin biopsies from patients with systemic sclerosis (SSc) has identified four “intrinsic” gene expression subsets conserved across multiple cohorts…
  • Abstract Number: 1494 • 2018 ACR/ARHP Annual Meeting

    Predictors of Persistence to Methotrexate Treatment in RA – Assessment of Different Modelling Approaches

    Helga Westerlind1, Mateusz Maciejewski2, Thomas Frisell3, Scott Jelinsky4, Daniel Ziemek5 and Johan Askling1, 1Unit of Clinical Epidemiology, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden, 2Systems Immunology, Inflammation & Immunology,, Pfizer, Cambridge, MA, 3Clinical Epidemiology Unit, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden, 4Inflammation and Immunology, Pfizer Research and Development, Cambridge, MA, 5Systems Immunology, Inflammation & Immunology,, Pfizer, Berlin, Germany

    Background/Purpose: As a step towards personalized medicine, we seek to identify patients with new-onset RA who are likely to remain well on MTX monotherapy. Patients…
  • Abstract Number: 1876 • 2018 ACR/ARHP Annual Meeting

    Machine Learning Classification of Peripheral Blood Gene Expression Identifies a Subset of Patients with Systemic Sclerosis Most Likely to Show Clinical Improvement in Response to Hematopoietic Stem Cell Transplant

    Jennifer Franks1, Viktor Martyanov2, Tammara A. Wood2, Leslie Crofford3, Lynette Keyes-Elstein4, Daniel E. Furst5, Ellen Goldmuntz6, Maureen D. Mayes7, Peter McSweeney8, Richard Nash8, Keith Sullivan9 and Michael L. Whitfield10, 1Geisel School of Medicine at Dartmouth, Hanover, NH, 2Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 3Division of Rheumatology and Immunology, Vanderbilt University Medical Center, Nashville, TN, 4Rho, Inc, Chapel Hill, NC, 5University of California Los Angeles, Los Angeles, CA, 6NIAID, NIH, Bethesda, MD, 7Rheumatology, University of Texas McGovern Medical School, Houston, TX, 8Colorado Blood Cancer Institute, Denver, CO, 9Duke University Medical Center, Durham, NC, 10Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hanover, NH

    Background/Purpose: The SCOT (Scleroderma: Cyclophosphamide or Transplantation) trial (Sullivan K. et al, 2018) demonstrated the clinical benefit of hematopoietic stem cell transplant (HSCT) compared to…
  • Abstract Number: 2048 • 2018 ACR/ARHP Annual Meeting

    In Vitro Proof-of-Concept of Pathobiology-Guided Therapy in Immune Mediated Inflammatory Arthritis

    Morten Aagaard Nielsen1, Bent Deleuran2,3 and Tue Wenzel Kragstrup2,3,4, 1Of Biomedicine, Aarhus University, Aarhus, Denmark, 2Department of Biomedicine, Aarhus University, Aarhus, Denmark, 3Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark, 4Randers Regional Hospital, Randers, Denmark

    Background/Purpose: Immune mediated inflammatory arthritis are very heterogeneous diseases including rheumatoid arthritis (RA), psoriatic arthritis (PsA) and spondyloarthritis (SpA). The available biological and targeted synthetic…
  • Abstract Number: 1672 • 2017 ACR/ARHP Annual Meeting

    Cytokines and Autoantibody Cluster-Interaction in Systemic Lupus Erythematosus. a Systems Medicine Approach

    Julian Barahona-Correa, Yovana Pacheco, Diana M. Monsalve, Manuel Rojas, Yhojan Rodríguez, Juliana Saavedra, Mónica Rodríguez-Jiménez, Ruben Mantilla, Carolina Ramírez-Santana, Nicolás Molano-González and Juan-Manuel Anaya, Center for Autoimmune Diseases Research (CREA), School of Medicine and Health Sciences, Universidad del Rosario, Bogota, Colombia

    Background/Purpose: Evidence supports the existence of different sub-phenotypes and the pivotal role of cytokines and autoantibodies in systemic lupus erythematosus (SLE). Cytokines interact in a…
  • Abstract Number: 2429 • 2017 ACR/ARHP Annual Meeting

    Towards Precision Medicine in Rheumatoid Arthritis (RA): Trans-Ethnic Analysis and Prioritization of SNPs in the AFF3 Locus

    Vincent A. Laufer1, Maria I. Danila2, Richard J. Reynolds3, Leah C. Kottyan4, Kenneth Kaufman5, John B. Harley6, Carl D Langefeld7, Donna Arnett8 and S. Louis Bridges Jr.9, 1Division of Clinical Rheumatology and Immunology, University of Alabama at Birmingham, Birmingham, AL, 2University of Alabama at Birmingham, Birmingham, AL, 3Medicine, University of Alabama at Birmingham, Birmingham, AL, 4Center for Autoimmune Genomics and Etiology (CAGE), Division of Allergy and Immunology, Cincinnati Children's Hospital, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 5Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Children's Hospital Medical Center; US Department of Veterans Affairs Medical Center, Cincinnati, OH, 6Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 7Wake Forest University, Winston Salem, NC, 8University of Kentucky College of Public Health, Lexington, KY, 9Clinical Immunology & Rheum, Univ of Alabama, Birmingham, AL

    Background/Purpose: Genetic variants in AFF3 have been associated with RA, including in our GWAS and ImmunoChip analyses of African-Americans (610 RA; 1543 controls). Likewise, an…
  • Abstract Number: 2600 • 2017 ACR/ARHP Annual Meeting

    Plasma Cell and T-Cell Activity Downregulation during MMF Therapy in SLE May be Necessary for Successful Immunosuppression

    Cristina Arriens1, Rufei Lu2, Teresa Aberle2, Stan Kamp2, Wade DeJager2, Melissa E. Munroe2, Eliza Chakravarty1, Katherine Thanou2, Joan T. Merrill3, Joel M. Guthridge4 and Judith A. James3, 1Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, OKC, OK

    Background/Purpose: MMF is a key therapy for moderate to severe SLE. MMF inhibits inosine monophosphate dehydrogenase, an enzyme needed in nucleotide synthesis required for lymphocyte…
  • Abstract Number: 166 • 2017 ACR/ARHP Annual Meeting

    Integrative Systems Biology Approach Identifies Key Transcription Factors and Novel Rheumatoid Arthritis (RA) and Individualized Therapeutic Targets

    RIchard Ainsworth1, Kai Zhang2, Gary S. Firestein3 and Wei Wang4, 1UC San Diego, La Jolla, CA, 2UCSD School of Engineering, San Diego, CA, 3Medicine, University of California San Diego, La Jolla, CA, 4Chemistry and Biochemistry, UC San Diego, La Jolla, CA

    Background/Purpose: The search for novel targets in RA requires novel computational methods and in silicosystems to identify non-obvious pathways that account for the diversity of…
  • 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: 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…
  • 1
  • 2
  • 3
  • 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