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  • Abstract Number: 763 • 2015 ACR/ARHP Annual Meeting

    Lupus-Related SNPs and Risk of Diffuse Large B-Cell Non-Hodgkin Lymphoma

    Sasha Bernatsky1,2, John Spinelli3, Patrick M. Gaffney4, Karin E Smedby5, Rosalind Ramsey-Goldman6, Sophia Wang7 and Ann E. Clarke8, 1Rheum/Clin. Epid., McGill MUHC/RVH, Montreal, QC, Canada, 2Clinical Epidemiology, Research Institute of the McGill University Health Centre, McGill University, Montreal, QC, Canada, 3School of Population and Public Health, University of British Columbia, Vancouver, QC, Canada, 4Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 5Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden, 6Fsm # M300, Northwestern University, Chicago, IL, 7Division of Cancer Etiology, Department of Population Sciences, Beckman Research Institute, Duarte, CA, 8Immunology/Epidemiology, Montreal General Hospital, Montreal, QC, Canada

    Background/Purpose: The determinants behind the increased risk of non-Hodgkin Lymphoma (NHL) in systemic lupus (SLE) are unclear. The most common type of NHL in SLE…
  • Abstract Number: 764 • 2015 ACR/ARHP Annual Meeting

    Gastrointestinal Adverse Events of Azathioprine in Daily Clinical Practice: Independent of Thiopurine Methyltransferase Activity

    Eun Young Ahn1, Hyun Mi Kwon1, Sung-Hwan Park2, Yeong Wook Song1 and Kichul Shin3, 1Division of Rheumatology, Department of Internal Medicine, Seoul National University Hospital, Seoul, South Korea, 2Division of Rheumatology, Department of Internal Medicine, Seoul St. Mary's Hospital, Seoul, South Korea, 3Division of Rheumatology, Department of Internal Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, South Korea

    Background/Purpose: Azathioprine (AZA) is a commonly used immunosuppressive agent for a number of systemic rheumatic diseases. Although it is regarded to be relatively safe to…
  • Abstract Number: 765 • 2015 ACR/ARHP Annual Meeting

    Clinical Improvements in Systemic Lupus Erthematosus Are Correlated to Cellular and Soluble Biomarkers in Classical Complement Pathway

    Chaim Putterman1, Jill P. Buyon2, Richard Furie3, Rosalind Ramsey-Goldman4, Kenneth Kalunian5, John Conklin6, Tyler O'Malley7, Derren Barken8 and Thierry Dervieux7, 1Division of Rheumatology, Albert Einstein College of Medicine, Bronx, NY, 2NYU School of Medicine, New York, NY, 3NSLIJHS, Lake Success, NM, 4Northwestern University Feinberg School of Medicine, Chicago, IL, 5UCSD School of Medicine, La Jolla, CA, 61261 Liberty Way Suite C, Exagen Diagnostics, Vista, CA, 7Research and Development, Exagen Diagnostics, Vista, CA, 8Exagen Diagnostics, Vista, CA

    Background/Purpose : There is a need to identify biomarkers that track disease response in systemic lupus erythematosus (SLE).  The value of various biomarkers in monitoring…
  • Abstract Number: 766 • 2015 ACR/ARHP Annual Meeting

    Clinical and Immunological Characteristics of 150 Systemic Lupus Erythematosus Patients in Urban Jamaica

    Keisha Maloney1, Trevor Ferguson2 and Karel De Ceulaer3, 1Department of Medicine,, University of the West Indies, Kingston 7, Jamaica, 2Epidemiology Research Unit, Tropical Medicine Research Institute, University of the West Indies, Kingston 7, Jamaica, 3Internal Medicine, University of the West Indies, Kgn 7, Jamaica

    Background/Purpose: Epidemiological studies in systemic lupus erythematosus (SLE) have been reported in the literature in many countries and ethnic groups. Although SLE in Jamaica has…
  • Abstract Number: 767 • 2015 ACR/ARHP Annual Meeting

    Estimating the Pre-Test Probability of Systemic Lupus Erythematosus By Utilizing Anti-Double Stranded DNA and Cell Bound Complement Activation Products Testing from Rheumatology Based Practices in the United States

    Stuart L. Silverman1, Derren Barken2, John Conklin3, Claudia Ibarra4 and Thierry Dervieux5, 1OMC Clinical Research Center, Beverly Hills, CA, 2Exagen Diagnostics, Vista, CA, 31261 Liberty Way Suite C, Exagen Diagnostics, Vista, CA, 4Clinical Laboratory, Exagen Diagnostics, Vista, CA, 5Research and Development, Exagen Diagnostics, Vista, CA

    Background/Purpose : Clinicians are aware that the interpretation of any clinical diagnostic test and post-test probability of disease is highly influenced by pre-test probability or…
  • Abstract Number: 768 • 2015 ACR/ARHP Annual Meeting

    The Lupus Foundation of America Rapid Evaluation of Activity in Lupus (LFA-REAL) Instrument Correlates Between Trained Clinical Investigators and Clinicians

    Anca Askanase1, Teja Kapoor2, Cynthia Aranow3, Karen H. Costenbader4, Jennifer Grossman5, Diane L. Kamen6, S. Sam Lim7, Mimi Kim8, Paola Daly9,10, Leslie M. Hanrahan11 and Joan T. Merrill12, 1NYU School of Medicine, New York, NY, 2Columbia University, New York, NY, 3Feinstein Institute for Medical Research, Mahasset, NY, 4Rheumatology, Immunology & Allergy, Brigham & Women's Hospital, Boston, MA, 5Rheumatology, UCLA, LA, CA, 6Medicine, Medical University of South Carolina, Charleston, SC, 7Emory University School of Medicine, Atlanta, GA, 8Biostatistics and Research Design Resource, Albert Einstein Coll Med, Bronx, NY, 9Lupus Foundation of America, Washington DC, DC, 10Lupus Foundation of America, Washington, DC, 11Lupus Fnd of America, Washington, DC, 12Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose:   Current SLE disease activity measures, such as SLEDAI and BILAG, can be challenging to score and interpret, making them impractical for use in…
  • Abstract Number: 769 • 2015 ACR/ARHP Annual Meeting

    Evaluation of Soluble Alpha-Klotho in Neuropsychiatric Systemic Lupus Erythematosus

    Kunihiro Ichinose1, Takeshi Ushigusa2, Masataka Umeda1, Tomohiro Koga2, Atsushi Kawakami2 and Shuntaro Sato3, 1Department of Immunology and Rheumatology, Nagasaki University, Nagasaki, Japan, 2Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 3Clinical Research Center, Nagasaki University Hospital, Nagasaki, Japan

    Evaluation of Soluble alpha-Klotho in Neuropsychiatric Systemic Lupus ErythematosusABSTRACTBackground/Purpose: Neuropsychiatric systemic lupus erythematosus (NPSLE) is a serious complication in SLE that presents a variety of…
  • Abstract Number: 770 • 2015 ACR/ARHP Annual Meeting

    Circulating Levels of iC3b and C3 Correlate with Sledai-2K Responder Index-50 (S2K RI-50) Disease Activity Scores: The Castle (Complement Activation Signatures in Systemic Lupus Erythematosus) Study

    Alfred Kim1, Vibeke Strand2, Nancy Mathis1, Deepali Sen3, Jonathan Miner3, Elizabeth Schramm1, Robin Bruchas4, Nick Staten4, Paul Olson4, Chad Stiening4 and John Atkinson1, 1Rheumatology, Washington University School of Medicine, Saint Louis, MO, 2Adjunct, Division of Immunology / Rheumatology, Stanford University, Palo Alto, CA, 3Division of Rheumatology, Washington University School of Medicine, Saint Louis, MO, 4Kypha, Inc., Saint Louis, MO

    Background/Purpose: A major unmet need in SLE is the identification of a biomarker that consistently tracks with disease activity. One current approach is measuring complement…
  • Abstract Number: 771 • 2015 ACR/ARHP Annual Meeting

    Convergent Validity of New Disease Assessment Instruments in Systemic Lupus Erythematosus in Relation to Sledai-2K

    Christopher Collins1, W. Winn Chatham2, Howard Busch3, Norman B. Gaylis4, Emily Hautamaki5 and Siva Narayanan6, 1MedStar Washington Hospital Center, Washington, DC, 2Medicine/Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Science & Research Institute, Jupiter, FL, 4Arthritis & Rheumatic Disease Specialties, Aventura, FL, 5Ipsos Healthcare, Washington, DC, 6Global Evidence, Value and Access, Ipsos Healthcare, Washington, DC

    Background/Purpose: Current validated disease assessment instruments (DAIs) in systemic lupus erythematosus (SLE) such as SLEDAI-2K and BILAG, require disease expertise and/or involve complex scoring systems,…
  • Abstract Number: 772 • 2015 ACR/ARHP Annual Meeting

    Post-Phlebotomy Stability of Soluble and Cellular Forms of Complement Activation: Implications in SLE Diagnostic Assays

    John Conklin1, Basil Jones2, Tyler O'Malley3, Duncan Poling4, JoAnne Ligayon5, Leilani Wolover6, Ying Qu7, Claudia Ibarra8, Puja Chitkara9 and Thierry Dervieux3, 11261 Liberty Way Suite C, Exagen Diagnostics, Vista, CA, 2Exagen Diagnostics, Vista, CA, 3Research and Development, Exagen Diagnostics, Vista, CA, 4Research and Development, Exagen Diagnostics Inc., Vista, CA, 5Flow Cytometry, Exagen Diagnostics Inc., Vista, CA, 6Research and Development, Exagen Diagnostics, Inc., Vista, CA, 7Exagen Diagnostic Inc, Vista, CA, 8Clinical Laboratory, Exagen Diagnostics, Vista, CA, 9Rheumatology, Center For Arthritis and Rheumatologic Excellence, Chula Vista, CA

    Background/Purpose: Deregulation and activation of the classical complement system is known to be associated with systemic lupus erythematosus (SLE). As such, several investigators have proposed…
  • Abstract Number: 773 • 2015 ACR/ARHP Annual Meeting

    Clinical Evaluation of Patients with Positive Antibodies to Extractable Nuclear Antigens but Negative ANA

    Megan L. Krause1, Michael Ettore2, Melissa R. Snyder3, Cynthia S. Crowson4 and Kevin G. Moder1, 1Rheumatology, Mayo Clinic, Rochester, MN, 2Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 3Laboratory Medicine, Mayo Clinic, Rochester, MN, 4Health Sciences Research, Mayo Clinic, Rochester, MN

    Background/Purpose: In the setting of a negative ANA, antibodies to extractable nuclear antigens (ENA) should be correspondingly negative, but alternative clinical scenarios occasionally arise.  This…
  • Abstract Number: 774 • 2015 ACR/ARHP Annual Meeting

    Anti-Nuclear Antibodies Have High Sensitivity for Systemic Lupus Erythematosus: Results of a Systematic Literature Review and Meta-Regression of Diagnostic Data

    Nicolai Leuchten1, Ralph Brinks2, Annika Hoyer3, Monika Schoels4, Martin Aringer1, Sindhu R. Johnson5, David I. Daikh6, Thomas Dorner7, George Bertsias8 and on behalf of the SLE Classification Criteria Steering Committee, 1Medicine III, University Medical Center and Faculty of Medicine at the TU Dresden, Dresden, Germany, 2Hiller Center for Research in Rheumatology, Duesseldorf, Germany, 3Institute for Biometry and Epidemiology, German Diabetes Center, Duesseldorf, Germany, 42nd Department of Medicine, Hietzing Hospital, Vienna, Austria, 5Dept of Rheumatology, Toronto Western and Mt. Sinai Hospitals, University of Toronto, Toronto, ON, Canada, 6Rheumatology, UCSF/VA Medical Center, San Francisco, CA, 7Charité University Medicine Berlin, Berlin, Germany, 8Rheumatology, Clinical Immunology, and Allergy, University of Crete, Heraklion, Greece

    Background/Purpose: EULAR and ACR have jointly funded a project to improve existing SLE classification criteria, aiming at earlier and more accurate classification of the disease.…
  • Abstract Number: 775 • 2015 ACR/ARHP Annual Meeting

    Identification of Candidate Items for Revised Classification Criteria for Systemic Lupus Erythematosus

    Gabriela Schmajuk1, Bimba F. Hoyer2, Martin Aringer3, Sindhu R. Johnson4, Thomas Dorner5, David I. Daikh6 and SLE Classification Criteria Steering Committee, 1San Francisco VA Medical Center, University of California, San Francisco, San Francisco, CA, 2Charité University Medicine, Department of Medicine/Rheumatology and Clinical Immunology and German Rheumatism Research Centre Berlin (DRFZ), Berlin, Germany, 3Rheumatology, Medicine III, University Clinical Center, Technical University Dresden, Dresden, Germany, 4Dept of Rheumatology, Toronto Western and Mt. Sinai Hospitals, University of Toronto, Toronto, ON, Canada, 5Charité – Universitätsmedizin, Berlin, Germany, 6Rheumatology, UCSF/VA Medical Center, San Francisco, CA

    Background/Purpose: EULAR and ACR have jointly funded a project to improve existing classification criteria for SLE; this abstract reports on the early phase of this…
  • Abstract Number: 776 • 2015 ACR/ARHP Annual Meeting

    Sensitivity of Antinuclear Antibody By Immunofluorescence Testing for Detection of Anti-Ro/SSA Antibodies

    Ivan Alcantara-Arreola1, Nina Tello-Winniczuk2 and Alejandro Diaz-Borjon3, 1Hospital Angeles Lomas, Huixquilucan, Mexico, 2Division of Internal Medicine / Rheumatology, Hospital Angeles Lomas, Huixquilucan, Mexico, 3Med/Div of Rheumatology, Hospital Angeles Lomas, Huixquilucan, Mexico

    Background/Purpose: A positive ANA test is a diagnostic criterion for several rheumatic diseases, although it may appear in other autoimmune disorders and healthy individuals. An…
  • Abstract Number: 777 • 2015 ACR/ARHP Annual Meeting

    SLE-KeyTM Rule-out Test to Assess Lupus in Anti-Nuclear Antibody Positive Subjects Using the Immunarray iCHIP®

    D. Scott Batty1, I.R. Cohen2, Chaim Putterman3, Nicole Jordan4, Keren Jakobi5, Rachel Sorek5, Yakov Blumenstein5, Pennina Safer5 and David Pisetsky6, 1ImmunArray Inc., Richmond, VA, 2Weizmann Institute of Science, Rehovot, Israel, 3Division of Rheumatology, Albert Einstein College of Medicine, Bronx, NY, 4Montefiore Medical Center, New York, NY, 5ImmunArray LTD, Rehovot, Israel, 6Duke University Medical Center and Durham VAMC, Durham, NC

    Background/Purpose: SLE is associated with a broad spectrum of autoantibodies, but currently there is no single serologic test to diagnose SLE definitively.  Diagnosis is thus…
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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 CT on October 25. 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].

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