Effect of Disease Activity on Organ Damage Progression in Systemic Lupus Erythematosus: University of Toronto Lupus Clinic Cohort

被引:32
|
作者
Urowitz, Murray B. [1 ]
Gladman, Dafna D. [1 ]
Ibanez, Dominique [1 ]
Su, Jiandong [1 ]
Mursleen, Sara [2 ]
Sayani, Amyn [2 ]
Terres, Jorge Alfonso Ross [2 ,3 ]
Iczkovitz, Sandra [2 ]
机构
[1] Toronto Western Hosp, Ctr Prognosis Studies Rheumat Dis, Toronto, ON, Canada
[2] GlaxoSmithKline Inc, Toronto, ON, Canada
[3] GlaxoSmithKline Inc, Philadelphia, PA USA
关键词
disease activity; systemic lupus erythematosus; COLLABORATING CLINICS/AMERICAN-COLLEGE; MONOCLONAL-ANTIBODY; PHASE-III; INDEX; BELIMUMAB; RECOMMENDATIONS; PREDICTORS; MORTALITY; TIME;
D O I
10.3899/jrheum.190259
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To examine the role of disease activity on organ damage over 5 years in patients with active systemic lupus erythematosus (SLE) despite standard of care. Methods. This analysis of the University of Toronto Lupus Clinic cohort assessed organ damage [measured by Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI)] in patients with active SLE [SLE Disease Activity Index 2000 (SLEDAI-2K) >= 6], using Cox proportional time-independent hazard models. Subgroup analyses were conducted in patients with SLEDAI-2K 6 or 7, 8 or 9, and >= 10 at baseline, and in the overall study population by steroid dose at study entry (< 7.5 vs >= 7.5 mg/day). Results. Among the overall study population (n = 649), SDI progression was observed in 209 (32.2%) patients over the 5-year follow-up period. Mean SDI change in patients with a score > 0 was generally consistent across all SLEDAI-2K subgroups. Multivariable analyses identified age at study start (HR 1.03, P < 0.0001), steroid dose (HR 2.03, P < 0.0001), immunosuppressants (HR 1.44, P = 0.021), and SLEDAI-2K (subgroup analyses HR 1.64-2.03, P = 0.0017 to < 0.0001) as the greatest risk factors for SDI progression, while a study start date after the year 2000 had a protective effect on SDI progression compared with a start date prior to the year 2000 (HR 0.65, P = 0.0004). Conclusion. Patients within the higher SLEDAI-2K subgroups at study entry or receiving high doses of steroids were more likely to have organ damage progression.
引用
收藏
页码:67 / 73
页数:7
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