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 "ANCA"

  • Abstract Number: 126 • 2016 ACR/ARHP Annual Meeting

    Anti-Neutrophil Cytoplasmic Antibodies (ANCA) in African-American Patients: Disease Associations and Clinical Outcomes in an Urban Cohort

    Philip McCarthy1, Jenna Hudy2, Marie Melville2, Danielle Robson1, John McKinnon2, Sandeep Soman2 and Kathleen Maksimowicz-McKinnon3, 1Michigan State University College of Osteopathic Medicine, East Lansing, MI, 2Henry Ford Hospital, Detroit, MI, 3Rheumatology, Henry Ford Hospital, Detroit, MI

    Background/Purpose: Antineutrophil cytoplasmic antibody-associated vasculitis (AAV) has been most extensively described and studied in non-African-American populations. The significance of and associations with ANCA in African-Americans,…
  • Abstract Number: 1940 • 2016 ACR/ARHP Annual Meeting

    High Prevalence of Inflammatory Heart Disease in Eosinophillic Granulomatosis with Polyangiitis (Churg Strauss) Patients

    Eloi Garcia Vives1, Len Harty2 and David Jayne3, 1Vall d'Hebrón Hospital, Barcelona, Spain, 2Vasculitis & Lupus, Addenbrookes Hospital University of Cambridge, Cambridge, United Kingdom, 3Vasculitis and Lupus Clinic, Addenbrookes Hospital University of Cambridge, Cambridge, United Kingdom

    Background/Purpose: To establish EGPA/Churg Strauss inflammatory heart disease prevalence and develop an algorithm for heart disease screening in EGPA patients. Methods: An audit of all…
  • Abstract Number: 3045 • 2016 ACR/ARHP Annual Meeting

    Immunometabolism in ANCA-Associated Glomerulonephritis

    Peter C. Grayson1, Sean Eddy2, Viji Nair2, Hemang Parikh3, Maja Lindenmeyer4, Laura Mariani2, Huateng Huang2, Wenjun Ju3, Casey Greene5, Clemens Cohen4, Jeffrey Krischer3, Matthias Kretzler2, Peter A. Merkel6 and Felix H. Eichinger2, 1National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Division of Nephrology, University of Michigan, Ann Arbor, MI, 3University of South Florida, Tampa, FL, 4University of Munich, Munich, Germany, 5Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, 6Division of Rheumatology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Mounting an inflammatory response requires immune cells to undergo major changes in metabolism. Mediators such as cytokines can specifically alter the metabolism of different…
  • Abstract Number: 127 • 2016 ACR/ARHP Annual Meeting

    Disease Characteristics and Outcomes in African-American Patients with Antineutrophil Cytoplasmic Antibody-Associated Vasculitis:  a High Risk Group for Poor Outcomes

    Philip McCarthy1, Danielle Robson1, Jenna Hudy2, Marie Melville2, John McKinnon2, Sandeep Soman2 and Kathleen Maksimowicz-McKinnon3, 1Michigan State University College of Osteopathic Medicine, East Lansing, MI, 2Henry Ford Hospital, Detroit, MI, 3Rheumatology, Henry Ford Hospital, Detroit, MI

    Background/Purpose: Antineutrophil antibody-associated vasculitis (AAV) has been most extensively described and studied in non-African American populations. Little is known about the characteristics and outcomes of…
  • Abstract Number: 1941 • 2016 ACR/ARHP Annual Meeting

    Retrospective Survey of Concomitant Autoimmune Diseases and Autoantibodies in a Cohort of Patients with ANCA-Associated Vasculitis (AAV)

    Marta Casal Moura1,2, Sergio Prieto-González2, Georgina Espígol-Frigolé2, Giuseppe Murgia2,3, Marco Alba2, Jose Hernández-Rodríguez2 and Maria C. Cid2, 1Department of Internal Medicine, São João Hospital Center, Porto, Portugal, 2Hospital Clínic. University of Barcelona. IDIBAPS, Vasculitis Research Unit. Department of Autoimmune Diseases, Spain, Barcelona, Spain, 3University Clinic for Visceral Surgery and Medicine Bauchzentrum Bern, Bern, Switzerland

    Background/Purpose: Anti-neutrophil cytoplasmic antibodies (ANCA) associated vasculitis (AAV) - granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA) and eosinophilic granulomatosis with polyangiitis (EGPA) have heterogenous clinic…
  • Abstract Number: 3046 • 2016 ACR/ARHP Annual Meeting

    Inflammatory Pathways As Shared Molecular Targets Across ANCA-Associated Vasculitis and Nephrotic Syndrome

    Sean Eddy1, Viji Nair1, Hemang Parikh2, Maja Lindenmeyer3, Laura Mariani1, Felix H. Eichinger1, Huateng Huang1, Wenjun Ju2, Casey Greene4, Peter C. Grayson5, Clemens Cohen3, Jeffrey Krischer2, Peter A. Merkel6 and Matthias Kretzler1, 1Division of Nephrology, University of Michigan, Ann Arbor, MI, 2University of South Florida, Tampa, FL, 3University of Munich, Munich, Germany, 4Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, 5National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 6Division of Rheumatology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Clinical trials in rare diseases typically test therapeutic efficacy in one disease defined by a particular clinical phenotype. Improved understanding of the molecular mechanisms…
  • Abstract Number: 978 • 2016 ACR/ARHP Annual Meeting

    A Randomized Clinical Trial of CCX168, an Orally Administered C5aR Inhibitor for Treatment of Patients with ANCA-Associated Vasculitis

    Peter A. Merkel1, John Niles2, Richard Jimenez3, Robert F. Spiera4, Brad H. Rovin5, Andrew Bomback6, Christian Pagnoux7, Antonia Potarca8, Thomas J. Schall9 and Pirow Bekker9, 1Division of Rheumatology, Univ of Pennsylvania; Perelman School of Med, Philadelphia, PA, 2Massachusetts General Hospital, Boston, MA, 3Rheumatology, The Seattle Arthritis Clinic, University of Washington Medicine, Northwest Hospital and Medical Center, Seattle, WA, 4Hospital for Special Surgery, Cornell, New York, NY, 5Ohio State University Medical Center, Columbus, OH, 6Columbia University Medical Center, New York, NY, 7Division of Rheumatology, Mount Sinai Hospital, University Health Network, University of Toronto, Toronto, Canada, Toronto, ON, Canada, 8ChemoCentryx, Inc., Mountain View, CA, 9ChemoCentryx, Mountain View, CA

    Background/Purpose:  Complement 5a (C5a) is involved in the pathogenesis of anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV). CCX168 is an orally administered, small molecule selective inhibitor of…
  • Abstract Number: 1942 • 2016 ACR/ARHP Annual Meeting

    Presentation and Clinical Features of ANCA-Associated Vasculitis in US African Americans: Experience from a Single Center  

    Sebastian Sattui1, Andrew Westfall2 and Angelo L. Gaffo3, 1Tinsley Harrison Internal Medicine Residency Program, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 2Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, 3Medicine, Birmingham VA Medical Center, Birmingham, AL

    Title: Presentation and Clinical Features of ANCA-associated Vasculitis in US African Americans: Experience From a Single Center   Background/Purpose: Little is known about the presentation,…
  • Abstract Number: 3179 • 2016 ACR/ARHP Annual Meeting

    Scale Structure and Measurement Properties of a Disease Specific Patient-Reported Outcome for Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis

    Joanna C. Robson1,2,3, Jill Dawson4, Judy A. Shea5, Helen Doll6, Susan Ashdown7, Renee Borchin8, Ebony Easley9, John T. Farrar10, Don Gebhart11, Katherine Kellom12, Georgia Lanier13, Raashid Luqmani14, Carol A McAlear15, John Mills16, Nataliya Milman17,18,19, Jacqueline Peck7, Gunnar Tomasson20, Peter F. Cronholm9 and Peter A. Merkel21, 1Faculty of Health and Applied Science, University of the West of England, Bristol, United Kingdom, 2Department of Rheumatology, University Hospitals Bristol NHS Trust, Bristol, United Kingdom, 3School of Clinical Sciences, University of Bristol, Bristol, United Kingdom, 4Nuffield Department of Population Health HSRU, University of Oxford, Oxford, United Kingdom, 5Division of General Internal Medicine, University of Pennsylvania, Philadelphia, PA, 6Department of Population Health, University of East Anglia, Norwich, United Kingdom, 7Oxford, Oxford, United Kingdom, 8University of South Florida, Tampa, FL, 9Department of Family Medicine and Community Health, The University of Pennsylvania, Philadelphia, PA, 10University of Pennsylvania, Philadelphia, PA, 11Columbus, Columbus, OH, 12PolicyLab, Children's Hospital of Philadelphia, Philadelphia, PA, United Kingdom, 13NONE, Framingham, MA, 14NDORMS , Rheumathology, Nuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, United Kingdom, 15Penn Vasculitis Center, Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, 16Vasculitis UK, Sheffield, United Kingdom, 17Department of Medicine, University of Ottawa, Ottawa, ON, Canada, 18The Ottawa Hospital, Ottawa, ON, Canada, 19Department of Clinical Epidemiology, Ottawa Hospital Research Institute, Ottawa, ON, Canada, 20Dept of Public Health Sciences, University of Iceland, Reykjavik, IS, 21Division of Rheumatology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose:  Candidate questionnaire items were produced following in-depth qualitative research in the UK, US, and Canada plus cognitive interviews, extensive piloting and independent linguistic and…
  • Abstract Number: 980 • 2016 ACR/ARHP Annual Meeting

    Short-Course Glucocorticoids in ANCA-Associated Vasculitis: A Proof of Concept Study

    Eli Miloslavsky1, John Niles2, Karen Laliberte2, Katherine Cosgrove2 and John H. Stone3, 1Division of Rheumatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 2Department of Medicine, Division of Nephrology, Massachusetts General Hospital, Boston, MA, 3Massachusetts General Hospital Rheumatology Unit, Harvard Medical School, Boston, MA

    Background/Purpose: Despite therapeutic advances in ANCA-associated vasculitis (AAV), patients continue to be exposed to considerable treatment morbidity from long-term glucocorticoid (GC) use.  The optimal duration…
  • Abstract Number: 1943 • 2016 ACR/ARHP Annual Meeting

    Factors Predictive of ANCA-Associated Vasculitis Relapse

    Maxime Samson1, Hervé Devilliers2, Xavier Puéchal3, Christian Pagnoux4, Pascal Cohen3, Luc Mouthon3, Benjamin Terrier5 and Loïc Guillevin3, 1Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 2Department of Internal Medicine and Systemic Diseases, Hôpital François Mitterrand, CHU de Dijon, Dijon, France, 3Department of Internal Medicine, Referral Center for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, Paris, France, 4Division of Rheumatology, Mount Sinai Hospital, University Health Network, University of Toronto, Toronto, Canada, Toronto, ON, Canada, 5National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France

    Background/Purpose:  To identify associations between patients’ clinical and biological characteristics at diagnosis of antineutrophil cytoplasmic antibody-associated vasculitides (AAVs), and their relapse during follow-up. Methods:  Long-term…
  • Abstract Number: 3180 • 2016 ACR/ARHP Annual Meeting

    Utility of Measurements of Urinary Soluble CD163 & MCP-1 in the Identification of Subtle Renal Flares in ANCA-Associated Vasculitis

    Sarah M Moran1, Michelle Ryan1, Paul A. Monach2, David Cuthbertson3, Simon Carette4, Jean Dunne5, Gary S. Hoffman6, Nader A. Khalidi7, Curry L. Koening8, Carol A. Langford9, Carol A. McAlear10, Larry W. Moreland11, Christian Pagnoux4, Philip Seo12, Ulrich Specks13, Antoine G. Sreih14, Steven R. Ytterberg15, Lina Zgaga16, Peter A. Merkel17, Mark A. Little18 and the Vasculitis Clinical Research Consortium, 1Clinical Medicine, Trinity Health Kidney Centre, Dublin, Ireland, 2Rheumatology, Boston University School of Medicine, Boston, MA, 3Biostatistics and Informatics, Department of Pediatrics, University of South Florida, Tampa, FL, 4Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada, 5Immunology Department, St James's Hospital, Dublin, Ireland, 6Rheumatology, Cleveland Clinic, Cleveland, OH, 7McMaster University, St Joseph's Healthcare Hamilton, Hamilton, ON, Canada, 8Rheumatology, University of Utah, Salt Lake City, UT, 9Rheumatic and Immunologic Diseases, Cleveland Clinic, Cleveland, OH, 10University of Pennsylvania, Philadelphia, PA, 11Rheumatology & Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, 12Medicine, Johns Hopkins University, Baltimore, MD, 13Mayo Clinic, Rochester, MN, 14Rheumatology, The University of Pennsylvania, Philadelphia, PA, 15Rheumatology, Mayo Clinic, Rochester, MN, 16Public Health and Primary Care, Trinity College Dublin, Dublin, Ireland, 17Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, 18Clinical Medicine, Trinity College Dublin, Dublin, Ireland

    Background/Purpose: Prior work has shown that urinary soluble CD163 (usCD163) displays excellent biomarker characteristics for detection of active renal vasculitis using samples from patients with…
  • Abstract Number: 999 • 2016 ACR/ARHP Annual Meeting

    Utility of Neutrophil CD64 Expression & sTREM-1 in Distinguishing Bacterial Infection from Disease Flare in SLE and ANCA Associated Vasculitis

    Sajal Ajmani, Harshit Singh, Saurabh Chaturvedi, Mohit kumar Rai and Vikas Agrawal, Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India

    Background/Purpose: Fever is a common presenting manifestation of systemic lupus erythematosus (SLE) and ANCA associated vasculitis (AAV). Treating physician is challenged to differentiate between disease…
  • Abstract Number: 1944 • 2016 ACR/ARHP Annual Meeting

    Disease Activity, Glucocorticoid Exposure, and Rituximab Determine Body Composition Changes during Induction Treatment of ANCA-Associated Vasculitis

    Zachary Wallace1, Eli Miloslavsky2, Sebastian H. Unizony3, Na Lu4, Gary S. Hoffman5, Cees G.M. Kallenberg6, Carol A. Langford7, Peter A. Merkel8, Paul A. Monach9, Philip Seo10, Robert F. Spiera11, Eugene William St.Clair12, Paul Bruntetta13, Matthew Cascino14, Hyon K. Choi15 and John H. Stone3, 1Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Boston, MA, 2Division of Rheumatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 3Massachusetts General Hospital Rheumatology Unit, Harvard Medical School, Boston, MA, 4Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 5Rheumatology, Cleveland Clinic, Cleveland, OH, 6Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 7Rheumatic and Immunologic Diseases, Cleveland Clinic, Cleveland, OH, 8Division of Rheumatology, Univ of Pennsylvania; Perelman School of Med, Philadelphia, PA, 9Rheumatology, Boston University School of Medicine, Boston, MA, 10Medicine, Johns Hopkins University, Baltimore, MD, 11Hospital for Special Surgery, Cornell, New York, NY, 12Rheumatology and Immunology, Duke University, Durham, NC, 13Genentech, Inc., South San Francisco, CA, 14University of California-San Francisco, San Francisco, CA, 15Rheumatology, Allergy and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, MA

    Background/Purpose: ANCA-associated vasculitis (AAV) treatment includes high dose glucocorticoids (GCs), which are associated with increased body-mass index (BMI), a complication abhorred by patients and associated…
  • Abstract Number: 1215 • 2016 ACR/ARHP Annual Meeting

    Interferon Signature Genes Are Differentially Expressed Between Microscopic Polyangiitis and Systemic Lupus Erythematosus Peripheral Blood Transcriptomes

    Aya Kawasaki1, Daisuke Tsukui2, Yuya Kondo3, Yoshitaka Kimura2, Kurumi Asako2, Hiroshi Furukawa1, Hajime Kono2, Takayuki Sumida4 and Naoyuki Tsuchiya1, 1Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan, 2Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan, 3Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan, 4Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

    Background/Purpose:  Interferon (IFN) signature has been established in the peripheral blood of the patients with systemic lupus erythematosus (SLE) by transcriptome analyses, indicating a role…
  • « Previous Page
  • 1
  • …
  • 13
  • 14
  • 15
  • 16
  • 17
  • …
  • 20
  • 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