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: 613

Serum Level of Syndecan-1 Is Associated with Disease Activity in Patients with Systemic Lupus Erythematosus

In-Woon Baek1, Ki-Jo Kim2, Ji-Young Kim3, Su-Jung Park3, Chong-Hyeun Yoon4, Wan-Uk Kim5 and Chul Soo Cho6, 1Internal medicine, Catholic University of Korea, Callege of Medicine, Seoul, South Korea, 2Internal Medicine, College of Medicine, Catholic University of Korea, Seoul, South Korea, 3Internal Medicine, Research Institute of Bone & Joint Diseases, Catholic University of Korea, Seoul, South Korea, 4Internal Medicine, Uijeongbu St. Mary's Hospital, The Catholic University of Korea, Uijeongbu, South Korea, 5Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea, 6St Marys Hospital, Seoul, South Korea

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Systemic lupus erythematosus (SLE)

  • Tweet
  • Email
  • Print
Session Information

Title: Systemic Lupus Erythematosus: Clinical Aspects

Session Type: Abstract Submissions (ACR)

Background/Purpose: Syndecan-1(SDC1), a transmemebrane heparan-sulfate glycoprotein, is predominantly expressed by plasma cells and is a receptor for a proliferation-inducing ligand (APRIL). SDC-1 is readily shed and release into plasma under certain pathologic conditions and remains biologically active to affect cellular behaviour of plasma cells. Plasma cells are effector cells producing pathogenic autoantibodies in systemic lupus erythematosus (SLE). The purpose of this study are to evaluate serum SDC1 concentration and to determine association between its levels and certain clinical manifestation in patients with SLE.

Methods: Serum samples from 127 patients with SLE and 24 normal healthy controls were assayed for SDC1 and APRIL by enzyme linked immunosorbent assay. Medical records were thoroughly reviewed for clinical features and serologic values. Disease activity was assessed using the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI).

Results: Serum SDC1 levels were significantly elevated in patients with SLE compared to controls (61.2 ± 6.5 versus 31.4 ± 4.5 ng/ml, P<0.001). The level was correlated positively with anti-double stranded DNA (dsDNA) antibody titer and SLEDAI score (r=0.263, P=0.004, and g=0.231, P=0.012, respectively), but negatively with C3 and CH50 levels associated with the presence of active proteinuria (>0.5 gm/day) in SLE patients with lupus nephritis. Moreover, serum SDC1 levels had significant correlation with level of APRIL, which was known as surrogate marker of disease activity (r=0.507, P=0.001).

Conclusion: Serum SDC1 levels are elevated and correlated with markers of disease activity in patients with SLE, suggesting that serum SDC1 could be used as a potential marker of disease activity in patients with SLE.


Disclosure:

I. W. Baek,
None;

K. J. Kim,
None;

J. Y. Kim,
None;

S. J. Park,
None;

C. H. Yoon,
None;

W. U. Kim,
None;

C. S. Cho,
None.

  • Tweet
  • Email
  • Print

« Back to 2012 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/serum-level-of-syndecan-1-is-associated-with-disease-activity-in-patients-with-systemic-lupus-erythematosus/

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