The effect of moderate-dose corticosteroids in preventing severe flares in patients with serologically active, but clinically stable, systemic lupus erythematosus - Findings of a prospective, randomized, double-blind, placebo-controlled trial

被引:102
作者
Tseng, Chung-E
Buyon, Jill P.
Kim, Mimi
Belmont, H. Michael
Mackay, Meggan
Diamond, Betty
Marder, Galina
Rosenthal, Pamela
Haines, Kathleen
Ilie, Virginia
Abramson, Steven B.
机构
[1] NYU, Sch Med, New York, NY USA
[2] Yeshiva Univ, Albert Einstein Coll Med, Bronx, NY USA
[3] Long Isl Jewish Hlth Syst, New Hyde Pk, NY USA
来源
ARTHRITIS AND RHEUMATISM | 2006年 / 54卷 / 11期
关键词
COMPLEMENT SPLIT PRODUCTS; DISEASE-ACTIVITY; VASCULAR INJURY; ACTIVATION PRODUCTS; PREDICTIVE VALUE; DNA ANTIBODIES; UP-REGULATION; ANTI-DSDNA; LONG-TERM; SLE;
D O I
10.1002/art.22198
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Serial measurements of anti-doublestranded DNA (anti-dsDNA) and complement are routine in the management of systemic lupus erythematosus (SLE), but their utility as biomarkers in preemptive treatment to prevent flares remains a subject of controversy. We hypothesized that concomitant elevation of anti-dsDNA and C3a can predict SLE activity in patients with stable or inactive disease and that short-term treatment with corticosteroids can avert flares. Methods. In this prospective, randomized, double-blind, placebo-controlled trial, 154 patients were evaluated monthly for up to 18 months, with measurements of C3a, C3, C4, CH50, and anti-dsDNA levels. Patients who remained clinically stable but showed serologic evidence of an SLE flare (elevation of both the anti-dsDNA level by 25% and the C3a level by 50% over the previous 1-2 monthly visits) were randomized to receive either prednisone or placebo therapy at a dosage of 30 mg/day for 2 weeks, 20 mg/day for 1 week, and 10 mg/day for 1 week. Results. Forty-one patients (21 randomized to prednisone and 20 randomized to placebo) experienced a serologic flare. Analysis of severe flares occurring <= 90 days from randomization revealed that 6 occurred in patients taking placebo and none occurred in patients taking prednisone (P = 0.007). Severe flares resulted in an increase in the prednisone dosage to > 40 mg/day and/or the addition of an immunosuppressive agent. Furthermore, improvement in scores on the Systemic Lupus Erythematosus Disease Activity Index, decreased levels of anti-dsDNA antibodies, and increased levels of C4 occurred 1 month after initiation of prednisone treatment. Conclusion. These preliminary data support our hypothesis that in a subset of clinically stable SLE patients with a combination of elevated C3a and anti-dsDNA levels, short-term corticosteroid therapy may avert a severe flare.
引用
收藏
页码:3623 / 3632
页数:10
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