- Abstract Number: 1906 • ACR Convergence 2025 - The incidence and mortality of connective tissue diseases in England: a population-level cohort study from 2012 to 2023Background/Purpose: The reported incidence and mortality of connective tissue diseases (CTDs) in England has been inconsistent in the literature. Our objective was to describe current…
- Abstract Number: 1206 • ACR Convergence 2025 - Overexpression of lymphotoxin in autophagy-deficient mice as model for inclusion body myositisBackground/Purpose: Inclusion body myositis (IBM) is a progressive muscle disorder characterized by inflammation and degeneration with altered proteostasis. To better understand the interrelationship between these…
- Abstract Number: 0866 • ACR Convergence 2025 - Immunoglobulin from sera of patients with myositis can passively enter cultured human endothelial cellsBackground/Purpose: Most patients with inflammatory myopathies have autoantibodies to intracellular proteins. We previously showed that immunoglobulin colocalizes with its cognate autoantigen in muscle biopsies from…
- Abstract Number: 0294 • ACR Convergence 2025 - Clinical relevance of low titer positive myositis-specific autoantibodies and myositis-associated autoantibodies in patients with an underlying malignancy.Background/Purpose: The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of autoimmune connective tissue diseases that often present with multisystem involvement. Autoantibodies such as myositis-specific…
- Abstract Number: 2076 • ACR Convergence 2025 - Nutritional Discourse in Online Myositis Communities: A Reddit Analysis of Patient-led DiscussionsBackground/Purpose: The intersection of nutrition and autoimmune myopathies represents a significant yet understudied domain in rheumatological care. We conducted a meticulous analysis of online myositis…
- Abstract Number: 1775 • ACR Convergence 2025 - Study Of Type -1 Interferon Gene Signature Markers In Muscle Biopsy Samples Of Patients With IIMBackground/Purpose: Idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of autoimmune diseases primarily affecting skeletal muscle, with potential involvement of other organs. They are classified…
- Abstract Number: 1205 • ACR Convergence 2025 - Real-time MRI for assessment of swallowing impairment in inclusion body myositis and oculopharyngeal muscular dystrophy.Background/Purpose: Swallowing dysfunction -dysphagia- is a frequent and debilitating symptom in neuromuscular disorders, leading to malnutrition, cachexia, aspiration pneumonia and death. Identification of the underlying…
- Abstract Number: 0864 • ACR Convergence 2025 - Immunophenotyping Reveals Upregulated IL-9R on Circulating T and B Cells in DermatomyositisBackground/Purpose: Idiopathic inflammatory myopathies (IIM), or myositis, comprise a group of autoimmune diseases with significant morbidity, yet the pathogenesis of myositis remains incompletely understood. In…
- Abstract Number: 0293 • ACR Convergence 2025 - Presence of Anti-cN-1A (Mup44, NT5c1A) IgG is Specific for Sporadic Inclusion Body MyositisBackground/Purpose: Sporadic inclusion body myositis (sIBM) is an autoimmune disease manifesting with muscle degeneration, inflammatory infiltrates and inclusion vacuoles. Diagnosis of sIBM is hampered by…
- Abstract Number: 2075 • ACR Convergence 2025 - Ferritin trends differentiate anti-MDA5 Dermatomyositis from anti-Jo1 Antisynthetase SyndromeBackground/Purpose: Serum ferritin (FERR) is a recognized marker of immune activation and a key laboratory feature of anti-MDA5 Dermatomyositis (DM). It has been increasingly studied…
- Abstract Number: 1663 • ACR Convergence 2025 - Tocilizumab for acute exacerbation of rheumatic disease-related interstitial lung disease: A prospective real-world studyBackground/Purpose: Acute exacerbation (AE) of rheumatic disease-related interstitial lung disease (RD-ILD) is a severe and potentially life-threatening condition, while there remains no clear consensus of…
- Abstract Number: 1203 • ACR Convergence 2025 - Rituximab in Treatment Refractory vs Treatment Naive Anti-Signal Recognition Particle (SRP) Myositis – A Case SeriesBackground/Purpose: Anti-Signal Recognition Particle (Anti-SRP) Myositis is a form of Polymyositis. Available consensus guidelines recommend initial combination therapy of high dose corticosteroids and Methotrexate and…
- Abstract Number: 0863 • ACR Convergence 2025 - Myeloid Dendritic Cell Subsets Characterize Muscle of Inclusion Body Myositis Patients and Correlate with KLRG1+ and TBX21+ CD8+ T cellsBackground/Purpose: Although inclusion body myositis (IBM) is an inflammatory myopathy, there are no effective immunomodulating agents, underlying the need for better understanding of its pathogenesis.…
- Abstract Number: 0292 • ACR Convergence 2025 - Patterns and Predictors of Longitudinal Trajectories of Pain in Individuals with Inflammatory MyopathiesBackground/Purpose: Idiopathic inflammatory myopathies (IIM) have historically been considered a disease of painless weakness. However, recent studies indicate that most patients with IIM experience pain…
- Abstract Number: 2073 • ACR Convergence 2025 - Cell-free DNA as a Potential Marker of Muscle Involvement and Treatment Response in MyositisBackground/Purpose: Idiopathic inflammatory myopathies (IIM) are characterized by inflammatory muscle injury. Circulating cell-free DNA (cfDNA), including nuclear (cfnDNA) and mitochondrial (cfmtDNA) DNA, has been shown…
- « Previous Page
- 1
- 2
- 3
- 4
- 5
- …
- 34
- Next Page »
