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ACR Convergence 2025

October 24-29, 2025. Chicago, Illinois.

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  • Abstract Number: 2655
    Fetal and maternal outcomes in systemic sclerosis and very early diagnosis of systemic sclerosis pregnancies, a national prospective study
  • Abstract Number: 0750
    Fibrinogen as a biomarker in the diagnosis of giant cell arteritis and detection of flares
  • Abstract Number: 0921
    Fibrinogen Co-Modified with Malondialdehyde-Acetaldehyde and Citrulline Promotes Pro-Inflammatory Macrophage Differentiation Through p38 and NF-κB Signaling
  • Abstract Number: 0346
    Fibroblast Growth Factor-23 and Bone Status in Patients with Chronic Kidney Disease Compared to a Healthy Control Group and Its Relationship with Cardiovascular Risk
  • Abstract Number: 1919
    Financial insecurity and discrimination are associated with patient-reported quality of life in patients with SLE
  • Abstract Number: 1850
    First American SLE patients demonstrate enhanced lipid metabolism and B cell activation by high-content proteomic analyses
  • Abstract Number: 1677
    First line anti-TNF therapy in early rheumatoid arthritis is associated with a lower frequency of difficult-to-treat disease at five years and better long-term outcomes compared with usual care
  • Abstract Number: 2653
    First Prospective Evaluation of Recombinant Herpes Zoster Vaccine in Systemic Sclerosis: Immunogenicity, Safety, and Disease Activity Outcomes
  • Abstract Number: 1462
    Five-Year Results of Secukinumab on Minimal Disease Activity (MDA) Components and the Impact of Biologic Treatment Status on Effectiveness and Safety in Patients With Psoriatic Arthritis: Real-World Data From the SERENA Study
  • Abstract Number: 0821
    Flipping The Switch – Classical Complement Activation closely linked to IFN-signalling in Stills Disease
  • Abstract Number: 2080
    Foot laterality does not modify outcome of knee and/or hip osteoarthritis
  • Abstract Number: 0447
    Foot-pressure distribution method for detection of foot joint arthritis in patients with rheumatic diseases
  • Abstract Number: 0059
    Formyl Peptide Receptor 1 (FPR1) Influences Arthritis Severity in a Sex- and Compartment-Specific Manner
  • Abstract Number: 1275
    Fostering connections in Pediatric Rheumatology: A Narrative medicine intervention
  • Abstract Number: 0969
    FOXO1 Mediated Polysialic Acid Dysregulation in Severe Systemic Sclerosis (SSc): A Novel Biomarker and Therapeutic Target?
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Embargo Policy

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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