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: 2935

Disease Evolution in Late Onset and Early Onset Systemic Lupus Erythematosus (SLE)

Roa'a Al Johani1, Dafna Gladman2, Jiandong Su2 and Murray Urowitz2,3, 1Medicine, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 3Rheumatology, U of Toronto, Toronto Western Hospital, Toronto, ON, Canada

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Systemic lupus erythematosus (SLE)

  • Tweet
  • Email
  • Print
Session Information

Date: Tuesday, November 10, 2015

Title: Systemic Lupus Erythematosus - Clinical Aspects and Treatment Poster Session III

Session Type: ACR Poster Session C

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

Background/Purpose: To compare clinical features, disease activity and outcome in late onset versus early onset SLE over 5 years of follow up.

Methods: Patients with SLE are followed prospectively according to standard protocol and tracked on a computerized database. Patients entering the cohort within one year of diagnosis constitute the inception cohort. Patients with late onset (age at diagnosis ≥ 50 were identified and matched 1:2 based on gender and first clinic visit (+/- 5) years with patients with early disease onset (age at diagnosis 18- 40 years). Groups were compared at baseline and 5-year follow up. Disease activity was measured by the SLE Disease Activity Index (SLEDAI-2K) and Damage was assessed by the Systemic Lupus International Collaborating Clinics/American College of Rheumatology(SLICC/ACR) damage index. All information is collected prospectively in the database.

Results: A total of  86 patients with  late onset disease (84.9% female,81.4% Caucasian ,mean age ±SD 58.05 ± 7.30 ) and  169 patients with early onset disease  (86.4% were female , 71% Caucasian, mean age± SD  27.80 ± 5.90 ) were identified.

Variables

At baseline

5 years

Late

(N= 86)

Early

(N=169)

P value

Late

(N= 86)

Early

(N=169)

P value

 ACR criteria*

4.92 ± 1.05

5.32 ± 1.15

0.001

5.60 ± 1.17

6.31 ± 1.34

0.0001

 SLEDAI-2K score*

4.58 ± 4.68

6.18 ± 6.24

0.006

3.41 ± 4.84

4.09 ± 4.40

0.173

Total SDI*

0.15 ± 0.43

0.17 ± 0.60

0.928

0.98 ± 1.28

0.69 ± 1.16

0.005

SLICC   ≥ 1

9(10.4%)

17(10.1%)

–

43(50.1%)

88(36.1%)

–

IS use

11 (12.8%)

43 (25.4%)

0.001

19 (22.1%)

61 (36.1%)

0.001

Steroid use

60 (69.8%)

102 (60.4%)

0.083

44 (51.2%)

95 (56.2%)

0.340

Average steroids dose in mg/d

22.53 ± 13.07

30.23 ±19.35

0.021

12.58 ± 6.60

15.18±8.51

0.004

* Mean ± SD ; IS= immunosuppressive

At enrollment, late onset SLE had a lower total number of ACR criteria, less renal and neurologic manifestations. Mean SLEDAI-2K scores were lower in late onset SLE, especially renal features  and anti-DNA positivity. Over 5 years, mean SLEDAI-2K scores decreased in both groups, while mean SDI scores increased more significantly in the late onset group ; they developed more cardiovascular, renal and ocular damage , had higher prevalence of hypertension and hypercholesterolemia.

Conclusion: Although late onset SLE group had a milder presentation and less active disease, with the evolution of disease, they developed more organ damage likely a consequence of cardiovascular risk factors and aging.


Disclosure: R. Al Johani, None; D. Gladman, None; J. Su, None; M. Urowitz, None.

To cite this abstract in AMA style:

Al Johani R, Gladman D, Su J, Urowitz M. Disease Evolution in Late Onset and Early Onset Systemic Lupus Erythematosus (SLE) [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/disease-evolution-in-late-onset-and-early-onset-systemic-lupus-erythematosus-sle/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2015 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/disease-evolution-in-late-onset-and-early-onset-systemic-lupus-erythematosus-sle/

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