ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 349

Galectin-3 in the Systemic Circulation Is Increased in Newly Diagnosed Rheumatoid Arthritis and Is Associated with Anti-CCP and Bone Marrow Edema

Saida Farah Issa1, Anne Friesgaard Christensen2, Hanne M. Lindegaard1, Merete Lund Hetland3, Kim Hoerslev-Petersen4, Kirsten Junker5, Kristian Stengaard-Pedersen6, Tine Lottenburger2, Torkell Ellingsen1, Ib Hansen7, Jens Kristian Pedersen1, Ulrik B. Lauridsen8, Anders Svendsen9, Ulrik Tarp6, Jan Pødenphant10, Mikkel Østergaard11 and Peter Junker1, 1Department of Rheumatology, Odense University Hospital, Odense, Denmark, 2Department of Rheumatology, Vejle Hospital, Vejle, Denmark, 3DANBIO, Center for Rheumatology and Spine Diseases, Glostrup Univ Hospital, Glostrup, Denmark, 4Rheumatology, Research Unit at King Christian X Hospital for Rheumatic Diseases, Graasten, Denmark, 5Institute of Molecular Medicine, Cardiovascular & Renal Research, University of Southern Denmark, Odense, Denmark, 6Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark, 7Rheumatology, Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark, 8Department of Rheumatology, Copenhagen Center for Arthritis Research, Center for Rheumatology and Spine Diseases, Glostrup Hospital, Glostrup, Denmark, 9University of Southern Denmark, The Danish Twin Registry, Epidemiology, Institute of Public Health, Odense, Denmark, 10Department of Rheumatology, Copenhagen University Hospital at Gentofte, Gentofte, Denmark, 11Center for Rheumatology and Spine Diseases, Glostrup Hospital, Copenhagen Center for Arthritis Research, Center for Rheumatology and Spine Diseases, Glostrup Hospital, Glostrup, Denmark

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: galectin, inflammation and rheumatoid arthritis (RA)

  • Tweet
  • Email
  • Print
Session Information

Title: Rheumatoid Arthritis - Clinical Aspects: Novel Biomarkers and Other Measurements of Disease Activity

Session Type: Abstract Submissions (ACR)

Background/Purpose: Galectin-3 (Gal-3), a 26kD beta-galactoside binding protein, has been implicated as a pro-inflammatory mediator in animal arthritis and rheumatoid arthritis (RA) in humans. Thus, Gal-3 is overexpressed by fibroblast-like synoviocytes in the rheumatoid synovium, particularly upon adhesion to cartilage components. Moreover, Gal-3 is increased in serum in animal arthritis and in serum and synovial fluid in patients with long-standing RA as compared with osteoarthritis and healthy individuals.

The aims of this investigation were to quantify the serum level of Gal-3 in a large cohort of patients with newly diagnosed RA before treatment, and to study possible associations with clinical, serological and imaging findings.

Methods: One hundred and sixty DMARD naïve patients with RA of recent onset were included (the CIMESTRA cohort)(1).  One hundred and nineteen volunteer blood donors served as healthy controls. Variables included demographics, clinical disease measures (Disease Activity Score in 28 joints-DAS28, Health Assessment Questionnaire-HAQ, Visual Analog Scales– patients global assessment, pain and physicians assessment), autoantibody status and MRI of the non-dominant wrist. Gal-3 was measured by ELISA (R&D)

Results: Gal-3 was significantly increased in RA patients, 4.49 ug/L (95% CI 4.17;4.81) compared with healthy controls, 3.96 ug/L (3.70;4.22; p = 0.02).

Gal-3 correlated positively with Capsular Reactive Protein (CRP), Erythrocyte Sedimentation Rate(ESR), and HAQ, but not with joint counts, DAS28 or rheumatoid nodules (table 1.a). Stratification according to autoantibody seropositivity and smoking showed that Gal-3 was significantly higher in seropositive than in seronegative RA, particularly in smokers (table 1.b). A similar pattern was observed in IgM-RF only and IgM-RF+anti-CCP positive subsets (p = 0.01 and p = 0.03). There was no association between Gal-3 and anti-ccp titer. By contrast, Gal-3 was positively correlated with bone marrow edema in patients (p = 0.03).

 

Conclusion : In this study we show that Gal-3 is increased in DMARD naïve patients with RA of recent onset. The associations with autoantibody seropositivity and bone marrow edema provide additional evidence for a role of Gal-3 in the RA disease pathway and hence that Gal-3 has potential as a seromarker for synovial pathology in RA.

Acknowledgements: We would like to thank The Danish Rheumatism Association for financial support.

References

1.       HETLAND, M. L. et al. Arthritis Rheum. 2006, 54, 1401-9.


Disclosure:

S. F. Issa,
None;

A. F. Christensen,
None;

H. M. Lindegaard,
None;

M. L. Hetland,
None;

K. Hoerslev-Petersen,
None;

K. Junker,
None;

K. Stengaard-Pedersen,
None;

T. Lottenburger,
None;

T. Ellingsen,
None;

I. Hansen,
None;

J. K. Pedersen,
None;

U. B. Lauridsen,
None;

A. Svendsen,
None;

U. Tarp,
None;

J. Pødenphant,
None;

M. Østergaard,

Abbott/Abbvie, Centocor, Merck, Schering-Plough,,

2,

Abbott/Abbvie, BMS, Boehringer-Ingelheim, Eli-Lilly, Centocor, GSK, Janssen, Merck, Mundipharma, Novo, Pfizer, Schering-Plough, Roche UCB, and Wyeth.,

5;

P. Junker,
None.

  • Tweet
  • Email
  • Print

« Back to 2014 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/galectin-3-in-the-systemic-circulation-is-increased-in-newly-diagnosed-rheumatoid-arthritis-and-is-associated-with-anti-ccp-and-bone-marrow-edema/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology