ACR Meeting Abstracts

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  • Abstract Number: 1794 • ACR Convergence 2020

    Systemic Lupus Erythematosus and Geomagnetic Disturbances: A Time Series Analysis

    George Stojan1, Flavia Giammarino2 and Michelle Petri3, 1Johns Hopkins University, BALTIMORE, MD, 2Deutsche Bank, London, United Kingdom, 3Johns Hopkins University School of Medicine, Baltimore

    Background/Purpose: To examine the influence of solar cycle and geomagnetic effects on SLE disease activity.Methods: The data used for the analysis consisted of 327 observations…
  • Abstract Number: 1795 • ACR Convergence 2020

    Intracellular Homocysteine and Homocysteine Metabolites in Systemic Lupus Erythematosus (SLE)

    George Stojan1, Jessica Li1, Amrita Raj2, Maureen Kane3 and Michelle Petri4, 1Johns Hopkins University, BALTIMORE, MD, 2Johns Hopkins University, Baltimore, 3University of Maryland School of Pharmacy, Baltimore, 4Johns Hopkins University School of Medicine, Baltimore

    Background/Purpose: In SLE, homocysteine has been shown to be a potentially modifiable, independent risk factor for stroke and thrombotic events. All previous epidemiological studies used…
  • Abstract Number: 1796 • ACR Convergence 2020

    A Panel of Urinary Proteins Predicts Active Lupus Nephritis and Response to Rituximab Treatment

    Jennifer Davies1, Emil Carlsson1, Angela Midgley1, Eve Smith1, Ian Bruce2, Michael Beresford1 and Christian Hedrich3, 1Department of Women's and Children's Health, Institute of Life Course and Medical Sciences, Liverpool, England, United Kingdom, 2Centre for Epidemiology Versus Arthritis, The University of Manchester and NIHR Manchester Biomedical Research Centre, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom, 3University of Liverpool, Liverpool, United Kingdom

    Background/Purpose: Approximately 30% of patients with adult-onset systemic lupus erythematosus (SLE) develop lupus nephritis (LN). Presence and/or severity of LN are currently assessed by renal…
  • Abstract Number: 1797 • ACR Convergence 2020

    A Multianalyte Assay Panel (MAP) with Algorithm Containing Cell-Bound Complement Activation Products (CB-CAPs) Is Superior to Anti-dsDNA and Low Serum Complement Levels in Predicting Transition of Probable Lupus to ACR Classified Lupus Within 2 Years

    Rosalind Ramsey-Goldman1, Roberta Vezza Alexander2, Cristina Arriens3, Sonali Narain4, Elena Massarotti5, Daniel J Wallace6, Amit Saxena7, Christopher Collins8, Chaim Putterman9, Kenneth Kalunian10, Armida Sace2, Rowena LaFon2, JoAnne Ligayon2, John Conklin11 and Arthur Weinstein12, 1Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 2Exagen Inc, Vista, CA, 3Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Northwell Health, Great Neck, NY, 5Brigham and Women's Hospital, Boston, MA, 6Cedars-Sinai Medical Center, Beverly Hills, CA, 7NYU School of Medicine, New York, 8MedStar Washington Hospital Center, Washington, DC, 9Albert Einstein College of Medicine, Bronx, NY, 10University of California San Diego, La Jolla, CA, 11Exagen Inc., Vista, CA, 12Loma Linda University and Exagen, Inc, Claremont, CA

    Background/Purpose: We reported previously (Ramsey-Goldman et al., Arthritis Rheumatol 2020) that score > 0.8 of a multianalyte assay panel (MAP) with algorithm predicts fulfillment of…
  • Abstract Number: 1798 • ACR Convergence 2020

    IgE Anti-dsDNA Antibodies in Systemic Lupus Erythematosus Are Associated with Higher Disease Activity at the Baseline and in Longterm Follow-up

    Omer Pamuk1, Zerai Manna2, Rutha Adhanom2, Xiaobai Li3, Mariana Kaplan4 and Sarfaraz Hasni2, 1Rheumatology Fellowship and Training Branch, NIAMS/NIH, Bethesda, MD, 2Lupus Clinical Trials Unit, NIAMS/NIH, Bethesda, MD, 3Biostatistics and Clinical Epidemiology Service, Clinical Center, NIH, Bethesda, MD, 4National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD

    Background/Purpose: Recent reports indicate that autoreactive anti-dsDNA IgE autoantibodies  and IgE immune complexes and can activate innate and adaptive immunity leading to amplification of lupus…
  • Abstract Number: 1799 • ACR Convergence 2020

    High Fat-Diet as a Catalyst to Lupus Development and Autoimmunity in MRL/lpr Mice

    Hiba Ali1, Juan Meng2, Xuhua Shi2, Linh Hellmers3, Swathi Dhulipala4, Patricia Kachur4, Therese Posas-Mendoza4, Robert Quinet5, William Davis5, Jerald Zakem4, Zongbing You2 and Xin Zhang3, 1Dept. of Rheumatology, Ochsner Medical Center, New Orleans, 2Tulane University Health Science Center, New Orleans, 3Institution of Translational Research, Ochsner Medical Center, New Orleans, 4Dept of Rheumatology, Ochsner Medical Center, New Orleans, 5Dept of Rheumatology, Ochsner Medical Center, New Orleans, LA

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease with features of autoantibodies, skin rash, kidney and other multiple organ involvement. Evidence shows that obesity…
  • Abstract Number: 1800 • ACR Convergence 2020

    Association of Air Pollution with Systemic Lupus Erythematosus Disease Activity in the Central Valley of California

    Mosaab Mohameden1, Ali H.Ali2, Zi Ying Li2, Yabsira Abejie3, Ratnali Jain2 and Candice Reyes Yuvienco4, 1University of Cincinnati College of Medicine, Cincinnati, OH, 2University of California San Francisco Fresno, Fresno, CA, 3Floyd B. Buchanan High School, Fresno, CA, 4University of California San Francisco Fresno, Clovis, CA

    Background/Purpose: Systemic lupus erythematosus (SLE) is a complex multisystem autoimmune disease that affects at least 300,000 people in the United States creating a substantial socioeconomic…
  • Abstract Number: 1801 • ACR Convergence 2020

    An Engineered Extracellular Matrix‐rich Decellularized Substrate Based Podocytes Culture System to Study Intracellular Complement Production and Activation

    Abhigyan Satyam1, Maria Tsokos2 and George Tsokos2, 1Division of Rheumatology & Clinical Immunology/Beth Israel Deaconess Medical Center/Harvard Medical School, boston, 2Division of Rheumatology & Clinical Immunology/Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA

    Background/Purpose: Current technologies do not support long-term cell viability, differentiation and maintenance of podocytes. We developed a biophysical approach, termed macromolecular crowding (MMC), to create…
  • Abstract Number: 1802 • ACR Convergence 2020

    Vitamin D Level: Predictor of SLE Disease Activity in AA Cohort with CLE?

    Ileannette Robledo-Vega1, John Scheinuk2, Emmanuel Pardo2, Ansley Pratt2, Soham Mahato3, Andrew G. Chapple2 and Myriam Guevara4, 1Louisiana State University Health Sciences Center, New Orlenas, LA, 2Louisiana State University, New Orleans, LA, 3LSUHSC School of Public Health, New Orleans, LA, 4Lousiana State University Health Sciences Center, New Orleans, LA

    Background/Purpose: There are few predominant African American (AA) epidemiological studies in Cutaneous Lupus Erythematosus (CLE). The Gilliam classification divides CLE into lupus specific, acute cutaneous…
  • Abstract Number: 1803 • ACR Convergence 2020

    Ability of Innate, Adaptive, and TNF-Superfamily Immune Pathways to Characterize Disease Activity and Inform a Refined Lupus Disease Activity Immune in a Confirmatory Cohort of SLE Patients

    Melissa Munroe1, Wade DeJager2, Susan Macwana2, Ly Tran2, Joel Guthridge2, Eldon Jupe3, Daniele DeFreese3, Ryan Newhardt3, Mohan Purushothaman3, Sanjiv Sharma3, Nancy Redinger2, Teresa Aberle2, Stan Kamp2, Cristina Arriens2, Eliza Chakravarty2, Joan Merrill4 and Judith James5, 1Oklahoma Medical Research Foundation/Progentec Diagnostics, Inc., Oklahoma City, OK, 2Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Progentec Diagnostics, Inc., Oklahoma City, OK, 4Oklahoma Medical Research Foundation, Oklahoma City, 5Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation;Department of Pathology, University of Oklahoma Health Sciences Center;Department of Medicine, University of Oklahoma Health Sciences Center, Edmond, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease driven by complex immune dysregulation, involving altered immune mediators and accumulation of autoantibody (AutoAb) specificities.…
  • Abstract Number: 1804 • ACR Convergence 2020

    Impact of the Kynurenine/Tryptophan Pathway on Cognitive Dysfunction and Depression in Systemic Lupus Erythematosus

    Erik Anderson1, Joanna Fishbein2, Joseph Hong2, Julien Roeser3, Richard Furie4, Cynthia Aranow2, Bruce Volpe2, Betty Diamond5 and Meggan Mackay6, 1Feinstein Institutes for Medical Research, New York, NY, 2Feinstein Institutes for Medical Research, Manhasset, NY, 3Charles River Laboratories, South San Francisco, CA, 4Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, 5Northwell Health, Manhasset, NY, 6Feinstein Institute for Medical Research, Manhasset, NY

    Background/Purpose: Tryptophan (TRP) is metabolized to kynurenine (KYN), quinolonic acid [QA, a N-methyl D-aspartate receptor (NMDAR) agonist] and kynurenic acid (KA, an NMDAR antagonist). KYN/TRP…
  • Abstract Number: 1805 • ACR Convergence 2020

    Longitudinal Analysis of IFN Status and Disease Characteristics in SLE

    Melissa Northcott1, Alberta Hoi2, Rachel Koelmeyer3 and Eric Morand4, 1Medicine, School of Clinical Sciences at Monash Health, Monash University, Melbourne, Victoria, Australia, 2Monash University, Melbourne, Victoria, Australia, 3Monash University, Clayton, Victoria, Australia, 4Medicine, School of Clinical Sciences at Monash Health, Monash University, Melbourne, Australia

    Background/Purpose: The type 1 interferon (IFN) cytokine family is key to the pathogenesis of SLE, evidenced by the expression of IFN stimulated genes (ISGs) in…
  • Abstract Number: 1806 • ACR Convergence 2020

    The Association of Interferon-α with Kynurenine/Tryptophan Pathway Activation in Systemic Lupus Erythematosus

    Erik Anderson1, Ying Jin2, Sara Goodwin2, Julien Roeser3, Richard Furie4, Cynthia Aranow5, Bruce Volpe5, Betty Diamond6 and Meggan Mackay7, 1Feinstein Institutes for Medical Research, New York, NY, 2Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 3Charles River Laboratories, South San Francisco, CA, 4Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, 5Feinstein Institutes for Medical Research, Manhasset, NY, 6Northwell Health, Manhasset, NY, 7Feinstein Institute for Medical Research, Manhasset, NY

    Background/Purpose: Type I IFN contributes to SLE pathogenesis and stimulates the kynurenine/tryptophan (KYN/TRP) pathway, producing elevated quinolinic acid (QA) levels relative to kynurenic acid (KA)…
  • Abstract Number: 1807 • ACR Convergence 2020

    The Extent of Tubulointerstitial Inflammation in Lupus Nephritis Identifies Two Distinctive Subgroups: Impact on Inflammation Characteristics and Prognosis in Patients with Lupus Nephritis

    Sang Jin Lee1, Eon Jeong Nam1, Man-Hoon Han2 and Yong Jin Kim2, 1Department of Internal Medicine, Kyungpook National University Hospital,, Daegu, Republic of Korea, 2Department of Pathology, Kyungpook National University Hospital,, Daegu, Republic of Korea

    Background/Purpose: Lupus nephritis is common clinical manifestation and contributes significantly to mortality in systemic lupus erythematosus (SLE). Recently several studies has been reported that severity of…
  • Abstract Number: 1808 • ACR Convergence 2020

    Erythrocyte Complement Receptor 1 (ECR1) and Erythrocyte Bound C4d (EC4d) Associate with Adverse Pregnancy Outcomes and Preeclampsia in Pregnant Women with Systemic Lupus Erythematosus (SLE)

    Jill Buyon1, John Conklin2, Michael Golpanian1, JoAnne Ligayon3, Thierry Dervieux4, Peter Izmirly1, H. Michael Belmont1, Jane Salmon5 and Roberta Vezza Alexander3, 1New York University, New York, NY, 2Exagen Inc., Vista, CA, 3Exagen Inc, Vista, CA, 4Exagen Inc, San Diego, CA, 5Hospital for Special Surgery, New York, NY

    Background/Purpose: Despite improvement in management and outcomes of pregnancies complicated by SLE, the risk of adverse events and preeclampsia (PE) continues to exceed that of…
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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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