ACR Meeting Abstracts

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Abstracts tagged "Myositis"

  • Abstract Number: 0305 • ACR Convergence 2023

    Prevalence and Clinical Significance of anti-Ro52 Antibodies in Antisynthetase Syndrome

    Javier Narvaez1, Paola Vidal-Montal2, Elena Cañadillas-Sanchez3, Pol Maymó2, Judith Palacios2, Martí Aguilar2, Montserrat Roig2 and Joan Miquel Nolla2, 1Hospital Universitario de Bellvitge, Barcelona, Spain, 2Department of Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain, 3Department of Rheumatology, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain

    Background/Purpose: Antisynthetase syndrome (ASSD) is a systemic autoimmune condition characterized by the positivity of anti-aminoacyl-transfer-RNA synthetases antibodies (ARS) and the occurrence of the classic triad,…
  • Abstract Number: 1162 • ACR Convergence 2023

    Serial Imaging Changes in Skeletal Muscle Composition and Their Association with Clinical Outcomes in Idiopathic Inflammatory Myopathies

    Mamatha Gorijavolu1, Chengappa Kavadichanda1, Ramesh Ananthakrishnan1, Christina Mariaselvam1, Molly Thabah1 and VS Negi2, 1Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India, 2All India Institute of Medical Sciences, Bilaspur, Puducherry, India

    Background/Purpose: Muscle weakness in inflammatory myopathies (IIM) is due to muscle-edema, atrophy and fatty-infiltration among which edema is the predominant cause at baseline. Some IIM…
  • Abstract Number: 1255 • ACR Convergence 2023

    Clinical Characteristics and Disease Outcomes of anti-NXP2 Positive Juvenile Dermatomyositis: A Single Center Cohort

    Sarah Molina1, Dawn Gist2, Marietta De Guzman3, Eyal Muscal4, Jamie Lai2 and Maria Pereira3, 1Baylor College of Medicine - Pediatrics Residency Program, Houston, TX, 2Baylor College of Medicine / Texas Children's Hospital, Houston, TX, 3Baylor College of Medicine, Houston, TX, 4Division of Rheumatology, Department of Pediatrics, Baylor College of Medicine, Houston, TX

    Background/Purpose: Juvenile dermatomyositis (JDM) is a rare idiopathic inflammatory myopathy with clinically heterogeneous presentations that can be categorized by myositis-specific antibodies (MSAs). NXP2 is among…
  • Abstract Number: 1962 • ACR Convergence 2023

    Toll-Like Receptor 7/8 Activation of Immune and Non-Immune Cells in Muscle by RNA-Containing Immune Complexes Can Contribute to Inflammation and the Pathogenesis of Myositis

    Yin Wu1, Aditee Deshpande1, Nicholas Geraci1, Vera Sellers2, Phanindra Velisetty2, David Fiorentino3, Kavita Y. Sarin3 and Andrew Bender1, 1Research Unit – Neurology and Immunology, EMD Serono, Billerica, MA, 2Discovery Technologies, EMD Serono, Billerica, MA, 3Department of Dermatology, Stanford University, Redwood City, CA

    Background/Purpose: Tissue inflammation is a major disease driver in idiopathic inflammatory myopathies (IIM), leading to muscle weakness and, in the case of dermatomyositis (DM), a…
  • Abstract Number: 2576 • ACR Convergence 2023

    Rapid Onset of Response in Adult Dermatomyositis Patients Receiving Anti-interferon β (PF-06823859): Results of a Phase 2, Double-blind, Randomized, Placebo-Controlled Study

    Rohit Aggarwal1, Elena Peeva2, Aaron Mangold3, Abigail Sloan2 and Myron Chu2, 1University of Pittsburgh, Pittsburgh, PA, 2Pfizer, Cambridge, MA, 3Mayo Clinic, Scottsdale, AZ

    Background/Purpose: Interferon (IFN) dysregulation is a key feature in the pathogenesis of Dermatomyositis (DM). PF-06823859 is a potent, selective, humanized IgG1 neutralizing antibody directed against…
  • Abstract Number: 0284 • ACR Convergence 2023

    Phenotyping Calcinosis: A Rare Manifestation of Rare Diseases

    Michele Diomedi1, Federico Fattorini1, Simone Barsotti2, Elenia Laurino1, Chiara Cardelli1, Linda Carli1 and Marta Mosca1, 1Rheumatology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy, 2Internal Medicine, Ospedale di Livorno, Pisa, Italy

    Background/Purpose: Idiopathic inflammatory myopathies (IIMs) are rare systemic autoimmune disorders, with a pleiotropic clinical picture, specifically characterized from the inflammatory involvement of striate muscles. Calcinosis…
  • Abstract Number: 0306 • ACR Convergence 2023

    Fitbit Is a Valid and Reliable Physical Activity Monitor in Idiopathic Inflammatory Myopathy

    Akanksha Sharma1, shiri keret2, Raisa Lomanto Silva3, Tanya Chandra4, Joel Levin5, Siamak Moghadam-Kia3, Chester V. Oddis6 and Rohit Aggarwal6, 1UPMC Mercy Hospital, Pittsburgh, PA, 2Bnai Zion, Atlit, Israel, 3University of Pittsburgh Medical Center, Pittsburgh, PA, 4Georgetown University Hospital, Washington, DC, 5University of Pittsburgh, Katz Graduate School, Pittsburgh, PA, 6University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: Idiopathic inflammatory myopathies (IIM, myositis) are a systemic autoimmune disease leading to debilitating muscle weakness and significant limitations in daily activities. Physical activity monitor…
  • Abstract Number: 1168 • ACR Convergence 2023

    Evaluation of Agreement Between Functional and Radiological Changes in Idiopathic Inflammatory Myositis (IIM) Associated Interstitial Lung Disease (ILD)

    Sonali Narain1, Can Hu2, Michael Liu1, Himanshu Vashistha1, Kourosh Shargani3 and Galina Marder1, 1Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, 2Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Fort Lee, NJ, 3Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Manhasset, NY

    Background/Purpose: ILD is a major cause of morbidity and mortality in IIM. The diagnosis and progression of ILD often relies on high resolution computed tomography…
  • Abstract Number: 1622 • ACR Convergence 2023

    Myositis-associated Autoantibodies in Juvenile Myositis Are Associated with Severe Disease Features and Mortality

    Matthew Sherman1, Payam Noroozi Farhad2, Katherine Pak3, Iago Pinal-Fernandez3, Kakali Sarkar2, Megan Neely4, Ira Targoff5, Frederick Miller6, Andrew Mammen7 and Lisa Rider8, 1NIAMS/NIH, Washington, DC, 2Environmental Autoimmunity Group, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, 3National Institutes of Health, Bethesda, MD, 4Department of Biostatistics and Bioinformatics, Duke University, Durham, NC, 5Veterans Affairs Medical Center, University of Oklahoma Health Sciences Center, and Oklahoma Medical Research Foundation, Oklahoma City, OK, 6NIH, NIEHS, Chapel Hill, NC, 7NIH, Bethesda, MD, 8NIEHS, NIH, Bethesda, MD

    Background/Purpose: Myositis-associated autoantibodies (MAAs), such as anti-Ro52 autoantibodies (Abs), have been found to be associated with interstitial lung disease (ILD) and worse prognosis in the…
  • Abstract Number: 1963 • ACR Convergence 2023

    Effect of JAK-STAT Inhibition by Baricitinib and Tofacitinib on Disease Phenotype in a Mouse Model of Myositis

    Rita Spathis, Sabrina Narvesen, Deeva Robles Kuriplach, Karen Huang, Teja Sundar, Daniel Shulman, Elizabeth Bagley, Kanneboyina Nagaraju and Melissa Morales, Binghamton University, Johnson City, NY

    Background/Purpose: Dysregulation of the interferon (IFN) pathway plays a major role in the pathophysiology of autoimmune myositis. Upregulation of type 1 IFN stimulated genes (an…
  • Abstract Number: 2578 • ACR Convergence 2023

    Machine Learning Identifies New Sporadic Inclusion Body Myositis Endotypes Associated with Unique Autoantibody Profiles

    Jenny Wei1, Mark Tarnopolsky2, Marie Hudson3, Ross Mitchell4, Katherine Buhler5, Antoine Dufour6, Luiz de Almeida6, Paul R. Fortin7, Eric Boilard8, Yann Becker8, Erin Hatcher2, Mei Feng Zhang6, Marvin Fritzler6 and May Choi6, 1University of Toronto, Toronto, ON, Canada, 2McMaster University, Hamilton, ON, Canada, 3McGill University, Montréal, QC, Canada, 4University of Alberta, Edmonton, AB, Canada, 5University of Calgary; Cumming School of Medicine, Calgary, AB, Canada, 6University of Calgary, Calgary, AB, Canada, 7Centre ARThrite - CHU de Québec - Université Laval, Quebec City, QC, Canada, 8Université Laval, Quebec City, QC, Canada

    Background/Purpose: Sporadic inclusion body myositis (sIBM) is a subset of autoimmune inflammatory myopathies (AIM) that is often challenging to diagnose. The objective of this study…
  • Abstract Number: 0287 • ACR Convergence 2023

    6-Minute Walk Distance Associates with Physiologic Measures and Physician/Patient Reported Outcomes in Myositis Related Interstitial Lung Disease

    Sangmee Bae1, Fereidoun Abtin2, Grace Kim3, Daniela Markovic4, Siamak Moghadam-Kia5, Chester V. Oddis6, Lila Pourzand2, Didem Saygin6, Daniel Sullivan7, Koichi Yamaguchi8, Donald Tashkin3, Christina Charles-Schoeman9, Jonathan Goldin3 and Rohit Aggarwal6, 1UCLA Rheumatology, Los Angeles, CA, 2UCLA Radiological Sciences, Los Angeles, CA, 3University of California Los Angeles, Los Angeles, CA, 4UCLA Department of Medicine Statistics Core, Los Angeles, CA, 5University of Pittsburgh Medical Center, Pittsburgh, PA, 6University of Pittsburgh, Pittsburgh, PA, 7UCLA Pulmonology, Pittsburgh, PA, 8University of Pittsburgh Medical Center Rheumatology, Pittsburgh, PA, 9UCLA Medical Center, Santa Monica, CA

    Background/Purpose: The 6 minute walk distance (6MWD) provides a global evaluation of sub-maximal exercise capacity that is easily performed and highly reproducible, and is used…
  • Abstract Number: 0664 • ACR Convergence 2023

    Quantitative Hand Held Dynamometry to Assess Muscle Strength in Scleroderma Associated Myopathy

    Julie Paik1, Christopher Mecoli2, Anshula Nallapati1, Ami Shah3, Fred Wigley4, Zsuzsanna McMahan5 and Laura Hummers1, 1Johns Hopkins University, Baltimore, MD, 2Johns Hopkins University School of Medicine, Baltimore, MD, 3Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Ellicott City, MD, 4Department of Rheumatology, Johns Hopkins Medicine, Baltimore, MD, 5Johns Hopkins Rheumatology, Lutherville, MD

    Background/Purpose: Manual muscle strength testing can be challenging in SSc associated myopathy (SSc-AM) due to contractures or skin tightening. Since there is currently no validated…
  • Abstract Number: 1169 • ACR Convergence 2023

    All-cause Mortality and Risk Factors for Death in a Large Multi-center Prospective Registry Cohort of Idiopathic Inflammatory Myositis in China

    Liying Peng1, Peng Yin2, Mucong Li3, Qian Wang4, Yanhong wang1, Shuang Zhou4, chanyuan wu4, Jiuliang zhao1, Dong xu5, Mengtao Li3 and xiaofeng Zeng4, 1Peking Union Medical College, Beijing, China, 2Chinese Center for Disease Control and Prevention, Beijing, China, 3Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, 4Department of Rheumatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, 5Peking Union Medical College Hospital, Beijing, China

    Background/Purpose: Our study depicted the mortality and independent risk factors of IIM patients in a large multi-center prospective registry cohort in China. Methods: Patients registered…
  • Abstract Number: 1927 • ACR Convergence 2023

    Manifestations, Management and Outcomes of Interstitial Lung Disease Associated with Anti-synthetase Syndrome: A Systematic Literature Review

    Koushan Kouranloo1, Mrinalini Dey2, Veronica Yioe3, Lisa G Spencer3 and Caroline V Cotton4, 1Rheumatology & Internal Medicine Trainee- Surrey, UK. Education fellow University of Liverpool, Liverpool, United Kingdom, 2Queen Elizabeth Hospital, London, United Kingdom; University of Liverpool, Liverpool, United Kingdom, 3Liverpool Regional Lung Disease Service, Aintree Hospital, Lower Lane, Liverpool, United Kingdom, 4Department of rheumatology, Liverpool University NHS Foundation Trust, Liverpool, United Kingdom

    Background/Purpose: Anti-synthetase syndrome (ASS) is a chronic autoimmune inflammatory condition, characterized by myositis, interstitial lung disease (ILD), arthritis, Raynaud's phenomenon and mechanic's hands. This systematic…
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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.

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