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  • ACR Meetings

ACR Convergence 2023

November 10-15, 2023. San Diego, CA.

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  • Abstract Number: 1620
    Cardiovascular Risk and Fracture Risk Among Women Initiating Treatment with Romosozumab or Denosumab
  • Abstract Number: 2133
    Cardiovascular Risk Factors Are Associated with Discontinuation of Advanced Therapies Due to Treatment Failure in Rheumatoid Arthritis: Results from the OBRI
  • Abstract Number: 1121
    Cardiovascular Safety of Febuxostat in Patients with Gout or Hyperuricemia: A Systematic Review of Randomized Controlled Trials
  • Abstract Number: 1874
    Cartilage Thickness Measures Are More Responsive Than Cartilage Area Loss Measures: A Comparison of Quantitative and Semi-quantitative Cartilage Assessments from the Osteoarthritis Initiative
  • Abstract Number: 1945
    Case Series of 6 Patients Exhibiting Myositis as a Rheumatologic Adverse Events Related to Cancer Immunotherapy in Two Spanish Hospitals
  • Abstract Number: 2563
    Causal Associations Between Gut Microbiota and Rheumatic Diseases: A Mendelian Randomization Study
  • Abstract Number: 0880
    CD14 Inhibition as a Potential Therapeutic in Post Traumatic OA
  • Abstract Number: 1711
    CD14+ Monocytes Demonstrate a Unique Transcriptional Signature in Macrophage Activation Syndrome, Highlighting a Role for Interferons and Identifying Putative Hemophagocytes in Circulation
  • Abstract Number: 0051
    CD14+CD64+ Classical Monocytes Are the Main Producers of IL-23 at the Enthesis
  • Abstract Number: 0004
    CD22 X CD79b Bispecific Ab Potently Inhibits B Cell Activation and Plasmablast Accumulation
  • Abstract Number: 0079
    CD4 T Cell Repertoire Features in RA Patients with High-risk HLA-DRB1 Alleles
  • Abstract Number: 0800
    CD4+ CD96+ T Cells Are Pathogenic Effector Cells in Giant Cell Arteritis
  • Abstract Number: 1638
    CD40L Inhibition with Dazodalibep Rapidly Reduces Blood Biomarkers of T and B Cell Costimulation in Subjects with Sjögren’s Having High Disease Activity or High Symptom Burden
  • Abstract Number: 2483
    CD68 and Fibrinoid Necrosis Are Synovial Biomarkers of Severity in Early Rheumatoid Arthritis and Are Associated with a Better Response to Methotrexate: Analysis of the UCLouvain Brussels ERA Cohort
  • Abstract Number: 1668
    Cell Specific Molecular Profiling of Scleroderma Associated Interstitial Lung Disease Subtypes
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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 ET on November 14, 2024. 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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