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2019 ACR/ARP Annual Meeting

November 8-13, 2019. Atlanta, GA.

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  • Abstract Number: 1007
    Memory ex-Th17 Cells Contribute to Synovial Inflammation in Spondyloarthritis
  • Abstract Number: 2605
    Men and Black Persons Die at Younger Ages from Systemic Sclerosis: A Nationwide Population-based Study
  • Abstract Number: 886
    Mesenchymal Stem Cell Senescence Alleviates Their Chondrogenic and Seno-Suppressive Properties, Contributing to Osteoarthritis Development
  • Abstract Number: 857
    Mesenchymal Stem Cell Therapy Induces FLT3L and CD1c+ Dendritic Cells in Systemic Lupus Erythematosus Patients
  • Abstract Number: 2611
    Mesenchymal Stem Cells in Scleroderma: A Systematic Review
  • Abstract Number: 2543
    Meta-Analysis Examining the Clinical Significance of Monitoring of Hydroxychloroquine Levels in SLE
  • Abstract Number: 2020
    Metabolic Changes Induced by Anti-Malondialdehyde Antibodies Promote Osteoclast Development
  • Abstract Number: 1946
    Metabolic Regulation in Cybrids Obtained from Healthy and Osteoarthritic (OA) Patients: Impaired Metabolic Flexibility in OA Process
  • Abstract Number: 2918
    Metabolic Signatures of Pathogenic T Cells in Medium and Large Vessel Vasculitis
  • Abstract Number: 2324
    Metabolic Syndrome and Early Arthritis: Frequency, Association with Antibodies Profile and Disease Activity
  • Abstract Number: 227
    Metabolomic and Symptom Comparison in Women With/without Fibromyalgia: A Pilot Study
  • Abstract Number: 128
    Metabolomics Analysis Identifies Biomarkers for APS and Suggests a Potential New Pathway Related to APS Pathogenesis
  • Abstract Number: 627
    Metabolomics Screening in Axial Spondyloarthritis: Identifying Potential Biomarkers
  • Abstract Number: 2814
    Methionine Commits Immunometabolism and Epigenetic Regulation of BACH2 Loci in B Cells, Resulting in Biases Toward Plasmablast Differentiation in the Pathogenesis of SLE
  • Abstract Number: 362
    Methods to Efficiently Recruit Minority Patients with Gout for Clinic-Based Registries
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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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