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Abstracts tagged "antiphospholipid syndrome"

  • Abstract Number: 1295 • 2017 ACR/ARHP Annual Meeting

    Pregnancy Outcome in Patients with SLE Compared to Patients with Other Inflammatory Rheumatic Diseases: Real World Data from a Prospective Pregnancy Register

    Rebecca Fischer-Betz1, Christina Bungartz2, Matthias Schneider1, Jutta Richter1, Anja Weiss2, Angela Zink3 and Anja Strangfeld4, 1Policlinic for Rheumatology & Hiller Research Centre for Rheumatology, Heinrich-Heine-University Duesseldorf, Duesseldorf, Germany, 2German Rheumatism Research Center, Berlin, Germany, 3Epidemiology Unit / Rheumatology and Clinical Immunology, German Rheumatism Research Centre (DRFZ) / Charité University Hospital, Berlin, Germany, 4Epidemiology, German Rheumatism Research Center, Berlin, Germany

    Background/Purpose: SLE pregnancies are complicated due to risk for maternal disease exacerbation and potential for fetal and neonatal complications. With careful pre-pregnancy counseling and monitoring…
  • Abstract Number: 2564 • 2017 ACR/ARHP Annual Meeting

    Inhibition of Neutrophil Elastase Protects Against Glomerulonephritis and Thrombosis in a Mouse Model of Lupus

    Gautam Sule1, Levi F. Mazza1, Nayef M. Kazzaz1, Srilakshmi Yalavarthi1, He Meng1 and Jason S. Knight2, 1University of Michigan, Ann Arbor, MI, 2., University of Michigan, Ann Arbor, MI

    Background/Purpose: Neutrophils are potential instigators of autoimmunity and effectors of organ damage in lupus. However, there is presently no consensus as to whether inhibition of…
  • Abstract Number: 2759 • 2017 ACR/ARHP Annual Meeting

    The Risk of Ischaemic Stroke in Primary APS Patients: A Prospective Study

    Massimo Radin1, Karen Schreiber2, Irene Cecchi3, Dario Roccatello4, Maria Jose Cuadrado5 and Savino Sciascia6, 1Department of Clinical and Biological Sciences, Center of Research of Immunopathology and Rare Diseases- Coordinating Center of Piemonte and Valle d’Aosta Network for Rare Diseases, Department of Clinical and Biological Sciences, University of Turin, Italy, Turin, Italy, 2Department of Thrombosis and Haemophilia, Guy's and St Thomas' Hospital, London, United Kingdom., London, United Kingdom, 3Center of Research of Immunopathology and Rare Diseases- Coordinating Center of Piemonte and Valle d’Aosta Network for Rare Diseases, Department of Clinical and Biological Sciences, University of Turin, Italy, Turin, Italy, 4Center of Research of Immunopathology and Rare Diseases- Coordinating Center of Piemonte and Valle d’Aosta Network for Rare Diseases, Department of Clinical and Biological Sciences, University of Turin and S. Giovanni Bo, Turin, Italy, 5St Thomas Hospital, Lupus Research Unit, London, United Kingdom, 6Center of Research of Immunopathology and Rare Diseases- Coordinating Center of Piemonte and Valle d’Aosta Network for Rare Diseases, Department of Clinical and Biological Sciences, University of Turin, Italy, Center of Research of Immunopathology and Rare Diseases- Coordinating Center of Piemonte and Valle d’Aosta Network for Rare Diseases, Department of Clinical and Biological Sciences, University of Turin, Italy, Torino, Italy

    Background/Purpose: The antiphospholipid syndrome(APS)is an autoimmune condition characterized by thrombosis and/or pregnancy morbidity andpersistent positivityfor antiphospholipid antibodies(aPL). The most common neurological manifestation of APS is…
  • Abstract Number: 2761 • 2017 ACR/ARHP Annual Meeting

    Adenosine Receptor Agonism Protects Against Antiphospholipid Antibody-Mediated Netosis and Venous Thrombosis

    Ramadan A. Ali1, He Meng1, Srilakshmi Yalavarthi1, Yogendra Kanthi1 and Jason S. Knight2, 1University of Michigan, Ann Arbor, MI, 2., University of Michigan, Ann Arbor, MI

    Background/Purpose: We have previously reported that antiphospholipid antibodies (aPL) activate neutrophils and thereby exaggerate neutrophil extracellular trap release (NETosis), which potentially contributes to the thrombotic…
  • Abstract Number: 2762 • 2017 ACR/ARHP Annual Meeting

    Study of 60 Patients with Intrauterine Fetal Deaths Related to Antiphospholipid Syndrome

    Mériem Belhocine1, Laetitia Coutte2, Nicolas Martin Silva3, Nathalie Morel4, Gaelle Guettrot-Imbert4, Romain Paule4, Michel Dreyfus5, Micaela Fredi6, Odile Souchaud-Debouverie7, Jean Charles Piette8, Veronique Le Guern4 and Nathalie Costedoat-Chalumeau1, 1Service de médecine interne Pôle médecine, Hôpital Cochin, Centre de référence maladies auto-immunes et systémiques rares de l’île de France, Paris, France, 2Department of Internal Medicine, Department of Internal Medicine, Cochin University Hospital, paris, France, 3Department of Internal Medicine, Department of Internal Medicine, University Hospital Center of Caen, Caen, France, 4Department of Internal Medicine, Department of Internal Medicine, Cochin University Hospital, Paris, France, 5Department of Gynecology and Obstetrics, Department of Gynecology and Obstetrics, University Hospital Center of Caen, Caen, France, 6Department of Rheumatology and Clinical Immunology, Rheumatology and Clinical Immunology, Rheumatology and Clinical Immunology, Spedali Civili of Brescia, Brescia, Italy, 7Department of Internal Medicine, Department of Internal Medicine, Poitiers University Hospital, Poitiers, France, 8Department of Internal Medicine, Department of Internal Medicine, University Hospital Pitié-Salpétrière, Paris, France

    Background/Purpose: The antiphospholipid syndrome (APS) is defined by a combination of arterial and/or venous thrombosis, pregnancy morbidity, and persistent antiphospholipid antibodies. There is a real…
  • Abstract Number: 1059 • 2016 ACR/ARHP Annual Meeting

    Quality of Life in Patients with Antiphospholipid Syndrome Is Related to Disease Burden and Anticoagulant Therapy

    Gabriela Hernandez-Molina1, Itzel Gonzalez-Pérez2, Carlos Pacheco2 and Antonio R. Cabral3, 1Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico City, Mexico, 2Immunology and Rheumatology, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico, 3Department of Medicine. Division of Rheumatology, The Ottawa Hospital.University of Ottawa, Ottawa, ON, Canada

    Background/Purpose:  Few studies have reported impaired health related quality of life (HRQoL) in patients with primary antiphospholipid syndrome (APS); however the causes of this outcome…
  • Abstract Number: 1060 • 2016 ACR/ARHP Annual Meeting

    Antiphospholipid Antibodies and Related Clinical Events Following Infection in Children: A Systematic Review of Case Reports

    Noha Abdel-Wahab1, Maria A. Lopez-Olivo2 and Maria Suarez-Almazor3, 1Section of Rheumatology and Clinical Immunology, Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA. Rheumatology and Rehabilitation Department, Assiut University Hospitals, Assiut, Egypt, Houston, TX, 2Section of Rheumatology and Clinical Immunology, Department of General Internal Medicine,The University of Texas MD Anderson Cancer Center, Houston, Texas, USA,, Houston, TX, 3Section of Rheumatology and Clinical Immunology, Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA., Houston, TX

    Background/Purpose: A systematic review of case reports to summarize existing evidence in the literature regarding the association of APS and infection during childhood. Our aims…
  • Abstract Number: 1062 • 2016 ACR/ARHP Annual Meeting

    Non-Conventional Antiphospholipid Antibodies in Patients with Clinical Obstetrical APS: Prevalence and Pregnancies Treatment Efficacy

    ARSENE MEKINIAN1, Marie Charlotte Bourrienne2, LIONEL CARBILLON3, AMELIE BENBARA4, SYLVIE CHOLLET MARTIN5, AHMED TIGAIZIN3, Francois Montestruc6, Olivier Fain7 and Pascale Nicaise-Roland8, 1SAINT ANTOINE HOSPITAL, PARIS, France, 2Unité Fonctionnelles d'Immunologie « Autoimmunité et Hypersensibilités », AP-HP, Hôpital Bichat-Claude Bernard, Paris, paris, France, 3JEAN VERDIER HOSPITAL, BONDY, France, 4JEAN VERDIER HOSPITAL, PARIS, France, 5UNITE HYPERSENSIBILITE, PARIS, France, 6exystat, PARis, France, 7Internal Medicine Department, Saint Antoine Hospital, Paris, France, 8Immunology Department, Bichat Claude-bernard, Universitary Hospital, APHP, Paris, France

    Background/Purpose: To describe the prevalence of non-conventional APL in patients with obstetrical APS pregnancy adverse outcome without conventional APL and the impact of treatment on…
  • Abstract Number: 1068 • 2016 ACR/ARHP Annual Meeting

    Recurrence of  Thrombosis Despite Negativization of Antiphospholipid Antibodies in Primary Antiphospholipid Syndrome. a Follow-up to 5 Years

    Gabriela Medina1, Eduardo Briones-Garcia2, Pilar Cruz-Dominguez3, Oscar I Florez-Durante4, Olga-Lidia Vera-Lastra5, Miguel A. Saavedra6 and Luis J. Jara7, 1Clinical research unit, Hospital de Especialidades Centro Medico La Raza,IMSS, Mexico City, Mexico, 2Direction of Education and Research, Clinical Research Unit, Mexico, Mexico, 3Research Division, Hospital de Especialidades, Centro Médico La Raza, IMSS, Mexico, Mexico, 4Clinical researh Unit, Escuela Nacional de Ciencias Biológicas Instituto Politécnico Nacional, Mexico, Mexico, 5Rheumatology, Inst Mexicano Seguro Social, Mexico City, Mexico, 6Rheumatology, Centro Médico Nacional La Raza IMSS, México, Mexico, 7Direction of education and research, Hospital de Especialidades Centro Medico La Raza, Mexico City, Mexico

    Background/Purpose: In some antiphospholipid syndrome (APS) patients, the antiphospholipid antibodies (aPL) becomes persistently negative. Discontinuation of anticoagulation has been proposed, however the long term follow-up…
  • Abstract Number: 1071 • 2016 ACR/ARHP Annual Meeting

    Anti-β2GP-I-Domain 3 and Aps/PT-IgG Antibodies Identify Primary APS Patients with Both Thrombotic and Hematological Manifestations

    Diego Hernández-Ramírez1, Gabriela Hernandez-Molina2, Carlos Núñez-Álvarez3, Miguel Astudillo-Angel4, Carlos Pacheco1, Elizabeth Olivares-Martínez1 and Antonio R. Cabral5, 1Immunology and Rheumatology, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico, 2Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico City, Mexico, 3Immunology and Rheumatology, Instituto Nacional de Ciencias Medicas y Nutricion S.Z., Mexico city, Mexico, 4Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico, 5Department of Medicine. Division of Rheumatology, The Ottawa Hospital.University of Ottawa, Ottawa, ON, Canada

    Background/Purpose: Thrombocytopenia and hemolytic anemia (HA) are considered non-criteria clinical manifestations by the Sydney revised criteria for APS. These features can precede, follow a thrombotic…
  • Abstract Number: 1072 • 2016 ACR/ARHP Annual Meeting

    Antiphospholipid Syndrome Alliance for Clinical Trials & International Networking Registry Analysis: Cardiovascular Risk Factors Among Different Groups of Antiphospholipid Antibody-Positive Patients

    Ozan Unlu1, Doruk Erkan2, Maria Tektonidou3 and On Behalf of APS ACTION .4, 1Barbara Volcker Center for Women and Rheumatic Diseases, Hospital for Special Surgery, Weill Cornell Medicine, New York, NY, 2Rheumatology, Hospital for Special Surgery- Weill Cornell Medicine, New York, NY, 3First Department of Internal Medicine, School of Medicine, National University of Athens, Athens, Greece, 4., New York, NY

    Background/Purpose: Traditional cardiovascular disease (CVD) risk factors increase the risk of thrombotic clinical manifestations in antiphospholipid antibody (aPL)-positive patients.  The prevalence of CVD risk factors…
  • Abstract Number: 1962 • 2016 ACR/ARHP Annual Meeting

    Antiphospholipid Syndrome Neutrophils Are Characterized By Overexpression of P-Selectin Glycoprotein Ligand 1, a Potential Therapeutic Target

    Jason S Knight1, Patrick S. Coit1, He Meng1, Srilakshmi Yalavarthi1, Paul Renauer1, Robert C Grenn1, Levi F Mazza1, Hui Wang2, Daniel T Eitzman2 and Amr H Sawalha1, 1Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI

    Background/Purpose:  Treatment of the thrombotic manifestations of antiphospholipid syndrome (APS) primarily focuses on inhibiting clotting pathways. In an effort to identify upstream inflammatory targets that…
  • Abstract Number: 1965 • 2016 ACR/ARHP Annual Meeting

    Antiphospholipid Syndrome Alliance for Clinical Trials & International Networking Registry Analysis: First and Recurrent Thrombosis Risk after 720 Patient-Years of Follow-up

    Ozan Unlu1, W. David Branch2, Paul R. Fortin3, Maria Gerosa4, Guillermo J. Pons-Estel5, Maria Tektonidou6, Amaia Ugarte7, Doruk Erkan8 and On Behalf of APS ACTION .9, 1Barbara Volcker Center for Women and Rheumatic Diseases, Hospital for Special Surgery, Weill Cornell Medicine, New York, NY, 2Obstetrics and Gynecology, University of Utah and Intermountain Healthcare, Salt Lake City, UT, 3Medicine, CHU de Québec - Université Laval, Québec, QC, Canada, 4University of Milan, Istituto Ortopedico Gaetano Pini, Milano, Italy, 5Department of Autoimmune Diseases, Institut Clínic de Medicina i Dermatologia, Hospital Clínic de Barcelona, Barcelona, Spain, 6First Department of Internal Medicine, School of Medicine, National University of Athens, Athens, Greece, 7Hospital Universitario Cruces, Biscay, Spain, 8Rheumatology, Hospital for Special Surgery- Weill Cornell Medicine, New York, NY, 9., New York, NY

    Background/Purpose: APS ACTION Registry was created to study the natural course of disease over 10 years in persistently antiphospholipid antibody (aPL)-positive patients. Previously, based on…
  • Abstract Number: 2086 • 2016 ACR/ARHP Annual Meeting

    Hexagonal Phase Phospholipid Neutralization Assay Is the Most Sensitive but Least Specific Among Nine Tests for Detecting APS in SLE or Non-SLE Patients

    Katalin Banki1, Phillip Aleksiejuk2, Jessica Patel2 and Andras Perl3, 1Clinical Pathology, SUNY Upstate Medical University, Syracuse, NY, 2Internal Medicine, SUNY Upstate Medical University, Syracuse, NY, 3Department of Medicine, Upstate Medical University, Syracuse, NY

    Background/Purpose: Antiphospholipid antibody syndrome (APS) is an autoimmune, hypercoagulable state which may elicit thrombosis and pregnancy loss.  Although several tests exist to guide diagnosis of…
  • Abstract Number: 2087 • 2016 ACR/ARHP Annual Meeting

    A Type I Interferon Signature in Monocytes and Decreased Levels of Circulating Plasmacytoid Dendritic Cells in Patients with Primary Antiphospholipid Syndrome

    Lucas L. van den Hoogen1, Ruth D.E. Fritsch-Stork2, Marjan A. Versnel3, Ronald H.W.M. Derksen4, Joel A.G. van Roon5,6 and Timothy R.D.J. Radstake5,6, 1Rheumatology and Clinical Immunology, Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 2Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 3Immunology, Erasmus Medical Center, Rotterdam, Netherlands, 4Departments of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 5Laboratory of Translational Immunology, UMC Utrecht, Utrecht, Netherlands, 6Department of Rheumatology & Clinical Immunology, UMC Utrecht, Utrecht, Netherlands

    Background/Purpose: In several autoimmune diseases, most notably in systemic lupus erythematosus (SLE), a type I interferon (IFN) signature has been described. This signature is thought…
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