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: 558

Salivary Syndecan-1 Levels Are Associated with Salivary Gland Dysfunction and Immune Dysregulation in Patients with Sjögren’s Syndrome

Eon Jeong Nam1, Jong Wan Kang1, Jung Su Eun1, Na Ri Kim1, Sang Jin Lee1, Keum Hee Sa2, Gi Bum Bae3 and Young Mo Kang4, 1Division of Rheumatology, Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea, Republic of (South), 2Division of Rheumatology, Department of Internal Medicine, Kyungpook National University, Daegu, Korea, Republic of (South), 3Division of Rheumatology, Department of Internal Medicine, Daegu, Korea, Republic of (South), 4Division of Rheumatology, Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Republic of Korea, Daegu, Korea, Republic of (South)

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Sjogren's syndrome and salivary gland

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 5, 2017

Title: Sjögren's Syndrome Poster I: Translational Research

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: Sjögren’s syndrome (SJS) is a chronic autoimmune disorder with lymphocytic infiltration of exocrine and non-exocrine epithelia, in which epithelial cells play a critical role in the initiation and amplification of inflammatory processes. Syndecan-1 (sdc-1), a transmembrane heparan sulfate proteoglycan, is predominantly expressed on epithelial cells and functions primarily as coreceptors through the binding of heparan sulfate chain to a wide range of ligands, such as extracellular matrix components, cytokines, and chemokines. Although ectodomain of sdc-1 is constitutively shed, ectodomain shedding is accelerated in response to diverse pathophysiological conditions and may be related with pathogenesis of SJS. In this study, we investigated the association of sdc-1 levels in plasma and saliva with functional parameters of salivary glands in SJS patients.

Methods: Unstimulated and stimulated salivary flow rates and sdc-1 levels of saliva and plasma were measured in 37 SJS patients and 34 normal controls (NC). We assessed the disease activity indexes, including ESSDAI and ESSPRI, and performed salivary gland scan and serologic markers in SJS patients.

Results: ESSDAI and ESSPRI scores of SJS patients were 3.78 ± 3.33 and 3.95 ± 1.50, respectively. Salivary flow rates in SJS patients and NC were 0.02 ± 0.04 and 0.31 ± 0.20, respectively (p<0.001). While unstimulated salivary flow rates were correlated with ejection fraction (EF) of submandibular glands (r=0.423, p=0.025) in salivary gland scan, stimulated salivary flow rates were associated with EF of parotid glands (r=0.531, p=0.04). Salivary flow rates were inversely associated with ESSPRI scores (r=-0.390, p=0.036) and dryness domain of ESSPRI (r=-0.622 p<0.001) in SJS patients. Plasma and salivary sdc-1 levels were significantly higher in SJS patients than NC (both p<0.001), and inversely correlated with salivary flow rate (plasma, r=-0.515, p<0.001; saliva, r=-0.472, p=0.003). Plasma sdc-1 levels were positively correlated with salivary sdc-1 levels in SJS patients (r=0.632, p<0.001) but not in NC (r=0.217, p=NS). Plasma and salivary sdc-1 levels were related with submandibular gland dysfunction in salivary gland scan. While plasma sdc-1 levels showed an inverse correlation with EF (r=-0.426, p=0.038), salivary sdc-1 levels were inversely correlated with both uptake ratio at 20 minutes (r=-0.526, p=0.017) and EF (r=-0.446, p=0.019). Furthermore, salivary sdc-1 levels were correlated with serum levels of anti-Ro (r=0.397, p=0.030) and -La antibodies (r=0.441, p=0.015) and IgG, although serum level of IgG showed a marginal statistical significance (r=0.331, p=0.074).

Conclusion: Plasma and salivary sdc-1 levels are increased in SJS patients, which is associated with salivary gland dysfunction. In addition, salivary sdc-1 levels may be related with immune dysregulation in pathogenesis of SJS.


Disclosure: E. J. Nam, None; J. W. Kang, None; J. S. Eun, None; N. R. Kim, None; S. J. Lee, None; K. H. Sa, None; G. B. Bae, None; Y. M. Kang, None.

To cite this abstract in AMA style:

Nam EJ, Kang JW, Eun JS, Kim NR, Lee SJ, Sa KH, Bae GB, Kang YM. Salivary Syndecan-1 Levels Are Associated with Salivary Gland Dysfunction and Immune Dysregulation in Patients with Sjögren’s Syndrome [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/salivary-syndecan-1-levels-are-associated-with-salivary-gland-dysfunction-and-immune-dysregulation-in-patients-with-sjogrens-syndrome/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/salivary-syndecan-1-levels-are-associated-with-salivary-gland-dysfunction-and-immune-dysregulation-in-patients-with-sjogrens-syndrome/

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