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: 1630

A Novel NMR Biomarker of Inflammation (GlycA) Is Elevated in Systemic Lupus Erythematosus

Cecilia P. Chung1, Michelle J. Ormseth2,3, Annette M. Oeser3, Joseph F. Solus3,4, Margery A. Connelly5, James D. Otvos6 and C. Michael Stein3,7, 1Medicine, Vanderbilt University, Nashville, TN, 2Rheumatology, Vanderbilt Medical Center, Nashville, TN, 3Vanderbilt University, Nashville, TN, 4Medicine, Vanderbilt Medical Center, Nashville, TN, 5LipoScience, Inc., Raleigh, NC, 6LipoScience Inc., Raleigh, NC, 7Div of Clinical Pharmacology, Vanderbilt Univ School of Med, Nashville, TN

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: inflammation and systemic lupus erythematosus (SLE)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Title: Systemic Lupus Erythematosus - Clinical Aspects and Treatment: Biomarker, Translational and Nephritis Studies

Session Type: Abstract Submissions (ACR)

Background/Purpose: Nuclear magnetic resonance (NMR) spectra from samples analyzed for lipoproteins also contain a peak (termed GlycA) resulting from glycosylated proteins.  GlycA is not only a novel marker of inflammation but was also associated with coronary heart disease in the MESA study.   Little is known about GlycA in patients with systemic lupus erythematosus (SLE). Therefore, we tested the hypothesis that GlycA concentrations were elevated in patients with SLE and associated with other markers of inflammation.

Methods: We compared concentrations of GlycA in 116 patients with SLE and 83 control subjects, frequency-matched for age, sex, and race. GlycA was detected by NMR, as a signal from methyl group protons on the carbohydrate portions of glycosylated proteins. SLE disease activity index (SLEDAI) and the SLE Collaborating Clinics damage index (SLICC) were calculated. Acute phase reactants [erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)] were measured using standard methods by the hospital clinical laboratory and interleukin-6 (IL-6) using a Lincoplex ELISA assays.     

Results: Patients with SLE had higher concentrations of GlycA [398 (350-445) µmol/L] than control subjects [338 (298-393) µmol/L, p<0.001]. In patients with SLE, concentrations of GlycA were significantly associated with ESR, CRP, IL-6, systolic and diastolic blood pressure. (Table) 

Table: Association of GlycA with disease characteristics

Rho P
ESR 0.43 <0.001
CRP 0.59 <0.001
IL-6 0.27 0.003
Systolic blood pressure 0.23 0.01
Diastolic blood pressure 0.21 0.02
SLEDAI 0.15 0.11
SLICC Damage Index 0.02 0.83

Conclusion: Concentrations of GlycA are higher in patients with SLE than control subjects and are associated with markers of inflammation and blood pressure, but not with SLE disease activity/chronicity scores.


Disclosure:

C. P. Chung,

NIH,

2;

M. J. Ormseth,
None;

A. M. Oeser,
None;

J. F. Solus,
None;

M. A. Connelly,

LipoScience, Inc.,

3;

J. D. Otvos,

LipoScience, Inc,

3;

C. M. Stein,

NIH,

2.

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2014 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/a-novel-nmr-biomarker-of-inflammation-glyca-is-elevated-in-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