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: 2694

Performance of Anti-Scl-70 Antibody Testing By Multiple-Bead, Enzyme-Linked Immunosorbent Assay, and Immunodiffusion in a University Setting

Kate Homer1, Jeffery Warren2, Dmitry Karayev3, Puja P. Khanna4, Amber Young5, Vivek Nagaraja5, Allan L. Metzger6 and Dinesh Khanna5, 1Department of Internal Medicine, Rheumatology Division, Scleroderma Program, University of Michigan, Ann Arbor, MI, 2Department of Pathology, University of Michigan, Ann Arbor, MI, 3RDL Reference Laboratory, Santa Monica, CA, 4University of Michigan, Ann Arbor, MI, 5Division of Rheumatology, Department of Internal Medicine, University of Michigan Scleroderma Program, University of Michigan, Ann Arbor, MI, 6RDL Reference Laboratory, Los Angeles, CA

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: Enzyme-Linked Immunoabsorbant Assays (ELISA) and systemic sclerosis

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

Date: Tuesday, October 23, 2018

Title: Systemic Sclerosis and Related Disorders – Clinical Poster III

Session Type: ACR Poster Session C

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

Background/Purpose: The gold standard for anti-Scl-70 antibody testing in systemic sclerosis (SSc) uses immunodiffusion (ID) techniques, but enzyme-linked immunosorbent assay (ELISA) and multi-bead technology are often used to save time and cost. There is concern that using this methodology results in an increase in false positive results. Our aim was to assess the performance of the multi-bead, ELISA, and ID testing methods.

Methods: We conducted a retrospective study of patients whose extractable nuclear antigen-10 (ENA-10) autoantibody panel tested positive for the anti-Scl-70 antibody by multi-bead technology during a one-year period. All samples positive by multi-bead were sent to a reference laboratory to be reflexed for ELISA, and all anti-Scl-70 antibodies positive by ELISA were further tested by ID. Clinical data was reviewed by a rheumatologist and assessed for presence of SSc, internal organ involvement, and other connective tissue disease (CTD).

Results: Approximately 9500 extractable nuclear antigen-10 (ENA-10) panels were ordered by physicians at the at our institution between August 2016 and August 2017. Of these, 129 patients were positive for the anti-Scl-70 antibody by multi-bead assay, 51 were positive by ELISA, and 21 were positive by ID. On chart review of the patients who were positive by multi-bead assay, 33 (25.6%) had SSc and 9 (7.0%) had diffuse cutaneous SSc (dcSSc). Twenty-four (18.6%) had other CTDs, with 72 (55.8%) presenting with no evidence of CTD (Table). Of the 51 patients who were positive by multi-bead and ELISA, 23 (45.1%) had a diagnosis of SSc and 8 (15.7%) had dcSSc. Eight (15.7%) were diagnosed with other CTDs. For the 21 patients who were positive by multi-bead, ELISA and ID, 19 (90.5%) were diagnosed with SSc and 8 (38.1%) had dcSSc. We found that 25.6% of patients positive by multi-bead, 45.1% positive by ELISA, and 90.5% positive by ELISA and ID had SSc.

Conclusion: Multi-bead assays have a high rate of false positive results for the anti-Scl-70 antibody in patients without clinical evidence of SSc. A stepwise approach of confirmation of positive multi-bead results using both ELISA and ID greatly improves the predictive value of antibody testing for the diagnosis of SSc.

Table: Relative frequency of anti-Scl-70 antibody in patients diagnosed with systemic sclerosis, diffuse cutaneous systemic sclerosis and other connective tissue diseases

Total

n (%)

SSc

n (%)

Diffuse Cutaneous SSc

n (%)

Other CTDs

n (%)

Anti-Scl-70 positive by multi-bead

129 (100)

33 (25.6)

9 (7.0)

24 (18.6)

Anti-Scl-70 Negative by ELISA

78 (60.5)

10 (12.8)

1 (1.3)

16 (20.5)

Anti-Scl-70 Positive by multi-bead + ELISA

51 (39.5)

23 (45.1)

8 (15.7)

8 (15.7)

Anti-Scl-70 Negative by ID (positive by multi-bead + ELISA)

30 (58.8)

4 (13.3)

0 (0)

6 (20.0)

Anti-Scl-70 Positive by multi-bead, ELISA and ID

21 (41.2)

19 (90.5)

8 (38.1)

1 (4.8)


Disclosure: K. Homer, None; J. Warren, None; D. Karayev, RDL Reference Laboratory, 3; P. P. Khanna, AstraZeneca, 2,SOBI, 2,Ironwood, 2; A. Young, T32-AR007080-38, 2; V. Nagaraja, None; A. L. Metzger, RDL Reference Laboratory, 4; D. Khanna, Eicos Sciences, 1,Pfizer, Inc., 2,Horizon, 2,BMS, 2,Actelion, 5,Bayer, 5,Bayer, 2,Corbus, 5,Cytori, 5,EMD Serono, 5,Genentech, Inc., 5,Sanofi-Aventis, 5,GSK, 5,Boehringer Ingelheim, 5.

To cite this abstract in AMA style:

Homer K, Warren J, Karayev D, Khanna PP, Young A, Nagaraja V, Metzger AL, Khanna D. Performance of Anti-Scl-70 Antibody Testing By Multiple-Bead, Enzyme-Linked Immunosorbent Assay, and Immunodiffusion in a University Setting [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/performance-of-anti-scl-70-antibody-testing-by-multiple-bead-enzyme-linked-immunosorbent-assay-and-immunodiffusion-in-a-university-setting/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2018 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/performance-of-anti-scl-70-antibody-testing-by-multiple-bead-enzyme-linked-immunosorbent-assay-and-immunodiffusion-in-a-university-setting/

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