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Persistent Disease Activity Remains a Burden for Patients with Systemic Lupus Erythematosus
Christine A Peschken1,2, Yishu Wang3,4, Michal Abrahamowicz3,4
1From the Departments of Internal Medicine and Community Health Sciences, University of Manitoba, Winnipeg; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec; University of Western Ontario and St. Joseph's Health Care London, London; Hospital for Sick Children, Toronto; University of Toronto, Toronto; Medical Affairs, GlaxoSmithKline Inc., Mississauga, Ontario; CH Maisonneuve-Rosemont, Montreal; BC Children's Hospital, Vancouver, British Columbia; McGill University Health Centre, Montreal, Quebec; Jewish General Hospital, Lady Davis Institute and McGill University, Montreal, Quebec; IWK Health Centre and Dalhousie University, Halifax, Nova Scotia; University of Ottawa, Ottawa, Ontario; Division of Rheumatology, Arthritis Research Canada, University of British Columbia; Rheumatology Clinic, Calgary, Alberta; Montreal Children's Hospital, McGill University Health Centre, Montreal; Division of Rheumatology, Department of Medicine, CHU de Québec-Université Laval, Quebec City, Quebec, Canada; GlaxoSmithKline Inc., King of Prussia, Pennsylvania, USA. christine.peschken@umanitoba.ca.
Objective:
Persistent systemic lupus erythematosus (SLE) disease activity is associated with increased morbidity and mortality. In a multicenter cohort of patients with prevalent SLE, we described persistence, patterns, and predictors of change in disease activity over time.
Methods:
Based on SLE Disease Activity Index (SLEDAI)-2K scores at cohort entry, patients were classified into 4 groups: low (score < 4; LOW), moderate (4 to < 6; MOD), moderately high (6 to ≤ 10; MHIGH), and very high (> 10; VHIGH). Multivariable linear and longitudinal mixed linear regression models were used to identify predictors of change over time in SLEDAI-2K.
Results:
There were 2019 participants, with declining followup data over 5 years (1326, 580, 274, 186, and 148 patients, respectively). At cohort entry, mean (± SD) age was 42 (± 17) years, disease duration 11 (± 10) years, and 90% were female. The 4 groups included 44% LOW (n = 891), 20% MOD (n = 400), 22% MHIGH (n = 442), and 14% VHIGH (n = 286); therefore, 36% had clinically important SLE activity. The proportion of patients in the LOW group at entry who moved to a higher activity level varied from 30% (167/557) at 1 year, to 49% (41/83) at 3 years, and 54% (30/56) at 5 years. Among 181 patients with MOD to VHIGH entry activity and 3 years of followup, 116 (64.1%) remained active. In all analyses, only higher SLEDAI-2K at cohort entry remained a significant predictor of higher SLEDAI-2K in subsequent years.
Conclusion:
Higher SLEDAI-2K at study entry was the single major independent predictor of higher SLEDAI-2K over time, reflecting frequent persistence of active disease, even in patients with longstanding disease. This highlights gaps in the optimal treatment of SLE.
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