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Abstract Number: 2090

Evaluation of Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) vs. SLEDAI-2K Glucocorticoids (SLEDAI-2KG) on Patient Health-Related Quality of Life (HRQoL) in Systemic Lupus Erythematosus (SLE)

Alan Cheng1, Vibeke Strand2, Jiandong Su3, Nicole Anderson3, Lee S Simon4 and Zahi Touma3, 1Michael G. DeGroote School of Medicine, McMaster University, Schroeder Arthritis Institute, Krembil Research Institute, University Health Network, University of Toronto, Toronto, ON, Canada, 2Stanford University School of Medicine, Stanford, CA, 3Schroeder Arthritis Institute, Krembil Research Institute, University Health Network and University of Toronto, Toronto, ON, Canada, 4SDG LLC, West Newton, MA

Meeting: ACR Convergence 2022

Keywords: Disease Activity, Patient reported outcomes, SF36

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Session Information

Date: Monday, November 14, 2022

Title: SLE – Diagnosis, Manifestations, and Outcomes Poster III: Outcomes

Session Type: Poster Session D

Session Time: 1:00PM-3:00PM

Background/Purpose: Systemic Lupus Erythematosus Disease Activity Index-2000 (SLEDAI-2K) Glucocorticoid Index (SLEDAI-2KG) is a novel valid index able to measure disease activity while accounting for prednisone usage. Previous studies examining disease activity and Health-related quality of life (HRQoL) have been inconsistent, with most finding no association between the two. Given that SLE patients report lower HRQoL compared to the general population, establishing a better understanding between disease activity and its impact on HRQoL may improve patients’ health outcomes.

This study had 2 aims:

1) Ascertain the association of the novel index, SLEDAI-2KG with the 36-Item Short Form Survey (SF-36), and
2) Compare the performances of the SLEDAI-2K and SLEDAI-2KG in determining poor HRQoL based on normative Canadian population data.

Methods: This is a single centre cross-sectional retrospective analysis of 1357 patients treated from 1994 to 2020. Data from SLEDAI-2K, SLEDAI-2KG and SF-36 at the first visit in the cohort were analysed. Descriptive statistics were used to describe patients’ baseline characteristics.

Aim 1: We hypothesised that SLEDAI-2K and SLEDAI-2KG would have none to low correlations with SF-36 domains but that SLEDAI-2KG would show better correlations. Spearman correlations were determined between disease activity indices and SF-36 domains.

Aim 2: Age and gender (A/G) matched SF-36 scores based on Canadian population norms were determined and HRQOL was then categorized as below or equal to or above Canadian norms. Univariate logistic regressions were performed using either SLEDAI-2K or SLEDAI-2KG as the sole independent variable to evaluate the association with normative scores.

Results: 1357 SLE patients (88.5% female) were included in the study. Mean age and duration of SLE at the 1st visit were 38.0 ± 13.6 and 8.5 ± 5.2 years respectively. 854 (62.9%) patients were treated with prednisone at mean doses of 12.0 ± 11.6 mg/day (Table 1). SLEDAI-2KG scores were in general 2 points higher than SLEDAI-2K scores (6.5 ± 5.9 and 4.5 ± 4.7 respectively).

There were weak negative correlations (r < 0.3) with both SLEDAI-2K and SLEDAI-2KG and the 8 SF-36 domain and physical (PCS) and mental (MCS) component summary scores, ranging from -0.06 to -0.12 and -0.07 to -0.20 respectively. Correlation coefficients of SLEDAI-2KG with SF-36 were approximately double those of SLEDAI-2K but remained < 0.3.

When dichotomizing SF-36 scores based on Canadian A/G matched norms, the majority of patients reported scores less than (54.0-88.0%) normative values across all SF-36 domains, PCS and MCS, with exception of the Role Emotional domain (43.9%) (Table 2).

In univariate analyses, an increase of 1 in the SLEDAI-2KG score was associated with higher odds of SF-36 scores less than Canadian norms compared with SLEDAI-2K (14-47% vs. 10-30% respectively) (Table 3).

Conclusion: Both SLEDAI-2K and SLEDAI-2KG scores weakly correlated with SF-36. SLEDAI-2KG, compared with SLEDAI-2K, was more likely to identify SLE patients with poorer HRQoL across all SF-36 domains. These results might serve as a more comprehensive guide for determining disease prognosis and treatment decisions to improve HRQoL in SLE.

Supporting image 1

Table 1: Spearman correlations between two SLEDAI total scores and eight SF36 domain and two component scores

Supporting image 2

Table 2: Percentage of patients reporting SF_36 domain scores lower than Canadian age/gender matched norms

Supporting image 3

Table 3: Univariate Logistic regression to identify patients lower than Canadian norm by gender/age standardized for SF_36 domains


Disclosures: A. Cheng, None; V. Strand, AbbVie, Amgen, AstraZeneca, Bayer, Bristol-Myers Squibb(BMS), Boehringer-Ingelheim, Chemocentryx, Celltrion, Genentech/Roche, Gilead, GlaxoSmithKlein(GSK), Inmedix, Janssen, Kiniksa, Merck/MSD, Novartis, Pfizer, Regeneron Pharmaceuticals, Rheos, R-Pharma, Samsung, Sandoz, Sanofi, Scipher, Setpoint, Spherix, Aria, Bioventus, Blackrock, Equilium, Glenmark, Horizon, Kypha, Lilly, MiMedx, Sorrento, Tonix, Priovant; J. Su, None; N. Anderson, None; L. Simon, None; Z. Touma, None.

To cite this abstract in AMA style:

Cheng A, Strand V, Su J, Anderson N, Simon L, Touma Z. Evaluation of Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) vs. SLEDAI-2K Glucocorticoids (SLEDAI-2KG) on Patient Health-Related Quality of Life (HRQoL) in Systemic Lupus Erythematosus (SLE) [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/evaluation-of-systemic-lupus-erythematosus-disease-activity-index-2000-sledai-2k-vs-sledai-2k-glucocorticoids-sledai-2kg-on-patient-health-related-quality-of-life-hrqol-in-systemic-lupus-erythe/. Accessed .
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