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: 0552

The Impact of Antiphospholipid Antibodies on Future Atherosclerotic Cardiovascular Disease Risk in Systemic Lupus Erythematosus

YuFang Ding1, Can Huang2, Jiuliang zhao3, Qian Wang1, Xinping Tian3, Mengtao Li3 and xiaofeng Zeng1, 1Department of Rheumatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, 2Peking Unoin Medical College Hospital, Beijing, China, 3Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China

Meeting: ACR Convergence 2023

Keywords: Atherosclerosis, Stroke, Systemic lupus erythematosus (SLE)

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 12, 2023

Title: (0543–0581) SLE – Diagnosis, Manifestations, & Outcomes Poster I

Session Type: Poster Session A

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

Background/Purpose: Patients with systemic lupus erythematosus (SLE) suffered from an increasing risk of cardiovascular diseases (23·3 events per 1000 patient-years). Antiphospholipid antibodies (aPLs), including anticardiolipin antibodies (aCL), anti-????2 glycoprotein I antibodies (aβ2GPI), and lupus anticoagulant (LA), increase the risk of thrombotic events in antiphospholipid syndrome, but the impact of aPLs on SLE patients was not yet determined. In this multi-center prospective study, we aimed to determine the association between aPLs and future atherosclerotic cardiovascular disease (ASCVD) risk in SLE.

Methods: Seven aPL isotypes (aCL IgG/IgM/IgA, aβ2GPI IgG/IgM/IgA, and LA) were measured based on international guidelines at SLE diagnosis and during follow-up. Clinical manifestations, disease activity status and organ damage were collected. Future ASCVD events were defined as new onset nonfatal myocardial infarction, nonfatal stroke, coronary or peripheral artery revascularization, or cardiovascular death.

Results: Among the 1573 recruited SLE patients, 525 (33.4%) had positive aPLs. LA had the highest prevalence (324 [20.6%]), followed by aCL IgG (249 [15.8%]), aβ2GPI IgG (199 [12.7%]), aCL IgA (58 [3.7%]), aβ2GPI IgM (83 [5.3%]), aβ2GPI IgA (58 [3.7%]), aCL IgM (92 [5.8%]). 116 (7.37%) patients developed ASCVD during the mean follow-up of 4.51±2.32 years and 92 patients were aPLs positive. In univariate Cox regression analysis, both aPLs (HR=7.81, 95% CI, 5.00-12.24, p< 0.001) and traditional risk factors of cardiovascular disease were associated with future ASCVD events (Table 1). Kaplan-Meier plots suggested a potential trend towards ASCVD in positive versus negative aPLs antibodies. More importantly, anticoagulant or antiplatelet therapy can reduce ASCVD risk in SLE patients with positive aPLs (HR=0.57, 95% CI,0.25-0.93, P=0.026) (Figure 1). In multiple Cox regression analysis, aCL IgG (HR=1.95, 95% CI, 1.25-3.00, p=0.003), aCL IgM (HR=1.83, 95% CI, 1.03-3.20, p=0.039), and LA (HR=5.13, 95% CI 3.23-8.20, p< 0.001) positivity remained independently associated with ASCVD; traditional risk factors for ASCVD, including smoking, gender, age and hypertension, also play an independent role in SLE patients (Figure 2).

Conclusion: SLE patients with positive aPLs, especially positive aCL IgG/IgM and LA, warrant more care and surveillance of future ASCVD events during follow-up. Antithrombotic therapy has a protective effect on future ASCVD.

Supporting image 1

Table 1. Proportion of ASCVD in SLE patients with different isotypes of aPLs

Supporting image 2

Figure 1. Cumulative probability of ASCVD in patients with or without aPLs (A), aβ2-GPI IgG antibody (B), aβ2-GPI IgM antibody (C), aβ2-GPI IgA antibody (D), aCL IgG antibody (E), aCL IgM antibody (F), aCL IgA antibody (G), and LA (H). (I) Cumulative probability of ASCVD in aPLs negative patients, aPLs positive patients with anticoagulant or antiplatelet therapy, and aPLs positive patients without anticoagulant or antiplatelet therapy.

Supporting image 3

Figure 2. Risk factors of ASCVD in SLE patients.


Disclosures: Y. Ding: None; C. Huang: None; J. zhao: None; Q. Wang: None; X. Tian: None; M. Li: None; x. Zeng: None.

To cite this abstract in AMA style:

Ding Y, Huang C, zhao J, Wang Q, Tian X, Li M, Zeng x. The Impact of Antiphospholipid Antibodies on Future Atherosclerotic Cardiovascular Disease Risk in Systemic Lupus Erythematosus [abstract]. Arthritis Rheumatol. 2023; 75 (suppl 9). https://acrabstracts.org/abstract/the-impact-of-antiphospholipid-antibodies-on-future-atherosclerotic-cardiovascular-disease-risk-in-systemic-lupus-erythematosus/. Accessed .
  • Tweet
  • Email
  • Print

« Back to ACR Convergence 2023

ACR Meeting Abstracts - https://acrabstracts.org/abstract/the-impact-of-antiphospholipid-antibodies-on-future-atherosclerotic-cardiovascular-disease-risk-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