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: 2643

Angiogenic and Antiangiogenic Factors in Patients with Systemic Lupus Erythematosus

Guilherme Ramires de Jesus1, Camila Souto Oliveira2, Flavia Cunha dos Santos3, Nilson Ramires de Jesus3, Luis Cristovao Porto4, Roger A. Levy5 and Evandro Mendes Klumb6, 1Department of Obstetrics, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil, 2Rheumatology, Hospital Universitario Pedro Ernesto, Rio de Janeiro, Brazil, 3Obstetrics, Hospital Universitario Pedro Ernesto, Rio de Janeiro, Brazil, 4Immunology, Hospital Universitario Pedro Ernesto, Rio de Janeiro, Brazil, 5Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil, 6Rheumatology, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Angiogenesis, growth factors and nephritis, Lupus

  • 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: Epidemiology, Women's Health, Cardiovascular and CNS

Session Type: Abstract Submissions (ACR)

Background/Purpose

SLE mainly affects young women and pregnancy in these patients has significant morbidity and mortality. Clinical and laboratory findings in lupus nephritis are similar to those found in patients with preeclampsia (PE), specifically hypertension, proteinuria and edema. It has been proposed the use of angiogenic factors, such as vascular endothelial growth factor (VEGF) and placental growth factor (PlGF), and antiangiogenic factors, as soluble Fms-like tyrosine kinase-1 (sFlt-1), for the differential diagnosis between these two conditions, however available data in the literature about these cytokines in non-pregnant SLE patients are inconsistent. This study was designed to evaluate whether there are differences between serum levels of VEGF, PlGF and sFlt-1 in non-pregnant SLE patients with and without systemic disease activity and whether there are differences in these factors when comparing SLE patients with healthy women.

Methods

54 women with SLE (according to ACR classification criteria) followed at an outpatient clinic of rheumatology were included. They had no other autoimmune disease diagnosed and were divided according to disease activity. 30 patients had inactive disease (mean SLEDAI: 0.7), and 24 had active disease (mean SLEDAI: 11.6). Twenty-three women in this latter group had active nephritis, while 20 patients with inactive disease had history of lupus nephritis. Control group consisted of 34 healthy women who attended a gynecology outpatient clinic.

Results

The mean values of VEGF, PlGF and sFlt-1 of all groups are described on Table 1. Considering the three studied cytokines, the SLE patients had significantly higher mean serum levels than the control group (VEGF: 319.0 + 226.0 x 206.2 + 119.4, p=0.02; PlGF: 42.2 + 54.1 x 13.6 + 21.6, p=0.02; sFlt-1: 107.9 + 49.2 x 70.2 + 95.0, p=0.01). The group of patients with active disease also had significantly higher mean levels of all three factors than controls (VEGF: 331.0 + 216.8 x 206.2 + 119.4, p=0.02; PlGF: 41.2 + 47.3 x 13.6 + 21.6, p=0.02; sFlt-1: 120.5 + 42.4 x 70.2 + 95.0, p=0.02), whereas no statistical difference was found between the group with inactive SLE and the control group. The mean sFlt-1 levels were higher in patients with active SLE than the mean levels of patients with inactive disease (120.5 + 54.9 x 97.8 + 42.4, p=0.02), but there was no significant difference in mean serum of VEGF and PlGF levels between these two groups. 

Conclusion

Patients with active SLE have higher levels of VEGF, PlGF and sFlt-1 than controls. sFlt-1 was also higher in patients with active SLE than patients with inactive SLE. A better understanding of angiogenic and antiangiogenic factors in patients with SLE provided by this study allows the analysis of these cytokines in pregnant woman with SLE and possibly their subsequent application as differential method between PE and lupus nephritis.


Disclosure:

G. Ramires de Jesus,
None;

C. S. Oliveira,
None;

F. C. dos Santos,
None;

N. R. de Jesus,
None;

L. C. Porto,
None;

R. A. Levy,

APS ACTION,

2;

E. M. Klumb,
None.

  • 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/angiogenic-and-antiangiogenic-factors-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