Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose: The Medical Outcome Survey Short Form 36 (SF-36) is one of the most widely used tools for measuring patient reported outcomes. In cross-sectional studies, there has been no correlation between QoL and disease activity or damage. The aim of this study is to assess QoL over time in the first 5 years of a multinational multicenter cohort.
Methods: An inception cohort of SLE patients from 31 centres in 12 countries has been assembled according to a standardized protocol between 2000 and 2013 to study the risk factors for atherosclerosis. Patients enter the cohort within 15 months of SLE diagnosis (≥4 ACR criteria). Clinical and laboratory features of SLE and comorbidities are gathered in a standardized protocol at yearly intervals. In addition patients complete the SF-36 at yearly intervals. Only patients who had 5 years of follow up and who had a minimum of 5 completed questionnaires were included in this analysis. The outcomes assessed include the 8 health domains of SF-36, in addition to physical component scores (PSC) and mental component scores (MCS) for each patient. In order to test for change in SF-36 domains over the 5 year period, GEE models were run separately for each of the 8 domains and the 2 composite scores. Each model adjusted for repeated measures by patients. Domains were also compared for gender, age, ethnicity and active disease (SLEDAI-2K ≥ 6) at enrolment.
Results: 485 patients (90.1% female) with 5 or more SF-36 evaluations were included. The disease duration at enrolment was 5.3 ± 4.1 months and the mean age at diagnosis was 35.8 ± 13.2 years. The race/ethnicity distribution was as follows: 57% Caucasian, 15% Black, 16% Asian, 8% Hispanic and 4% other. All 8 domains, in addition to MCS and PCS showed improvement that was statistically significant in the first 2 years of follow-up. No significant improvement was noted in any of the 8 domains or composite scores from years 3-5.
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Using Visits in Years 0, 1 and 2 only
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Using Visits in Years 2, 3, 4 and 5 only
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Yearly increase
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95% CI
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P value
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Yearly increase
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95% CI
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P value
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Physical Function
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3.86
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2.69, 5.04
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<0.0001 |
0.20
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-0.40, 0.80
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0.51
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Role Physical
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7.98
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5.64, 10.32
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<0.0001 |
0.35
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-0.92, 1.63
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0.59
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Bodily Pain
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3.15
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1.87, 4.43
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<0.0001 |
0.28
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-0.46, 1.02
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0.46
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General Health
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2.21
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1.24, 3.19
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<0.0001 |
0.18
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-0.38, 0.75
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0.53
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Vitality
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3.09
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2.03, 4.15
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<0.0001 |
-0.04
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-0.64, 0.57
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0.90
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Social Function
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5.02
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3.67, 6.37
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<0.0001 |
0.15
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-0.60, 0.90
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0.70
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Role Emotional
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4.71
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2.50, 6.92
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<0.0001 |
0.28
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-1.04, 1.60
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0.68
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Mental Health
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2.41
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1.48, 3.33
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<0.0001 |
0.19
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-0.32, 0.70
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0.46
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PCS
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1.70
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1.18, 2.22
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<0.0001 |
0.09
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-0.19, 0.38
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0.53
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MCS
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1.39
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0.83, 1.95
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<0.0001 |
0.06
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-0.26, 0.38
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0.73
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Baseline domain scores range from 44.2-70.7 and PCS and MCS scores were 39.4 and 44.9. In year 2 domain scores range from 52.4-71.6 and PCS and MCS scores were 42.8 and 47.7.
Generally higher values of SF-36 scores are associated with male gender, younger age and Hispanic and Asian ethnicities. Levels of disease activity were not associated with SF-36.
Conclusion: Unlike late stage lupus where QoL is stable, in patients with early disease (within the first 2 years) all domains improve. Therefore SF-36 may be used as an outcome measure for improvement in the first two years of SLE.
Disclosure:
M. B. Urowitz,
None;
D. Ibanez,
None;
N. Anderson,
None;
D. D. Gladman,
None;
S. L. SLICC,
None.
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ACR Meeting Abstracts - https://acrabstracts.org/abstract/changes-in-quality-of-life-in-the-first-5-years-of-disease-in-the-systemic-lupus-erythematosus-international-collaborating-clinics-slicc-cohort/