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中等剂量皮质类固醇对血清学活动但临床稳定的系统性红斑狼疮患者预防严重病情发作的影响:一项前瞻性、随机、双盲、安慰剂对照试验的结果

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.

作者信息

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

机构信息

New York University School of Medicine, Hospital for Joint Diseases, New York, New York 10003, USA.

出版信息

Arthritis Rheum. 2006 Nov;54(11):3623-32. doi: 10.1002/art.22198.

Abstract

OBJECTIVE

Serial measurements of anti-double-stranded 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 <or=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.

摘要

目的

抗双链DNA(抗dsDNA)和补体的系列检测是系统性红斑狼疮(SLE)管理中的常规项目,但其作为预防病情复发的抢先治疗生物标志物的效用仍存在争议。我们假设抗dsDNA和C3a同时升高可预测病情稳定或无活动的SLE患者的疾病活动,且短期使用皮质类固醇治疗可避免病情复发。

方法

在这项前瞻性、随机、双盲、安慰剂对照试验中,对154例患者进行长达18个月的每月评估,检测C3a、C3、C4、CH50和抗dsDNA水平。临床保持稳定但出现SLE病情复发血清学证据(在之前1 - 2次每月访视中抗dsDNA水平升高25%且C3a水平升高50%)的患者被随机分为接受泼尼松或安慰剂治疗,剂量为30mg/天,共2周,20mg/天,共1周,10mg/天,共1周。

结果

41例患者(21例随机接受泼尼松治疗,20例随机接受安慰剂治疗)出现血清学病情复发。对随机分组后<或=90天内发生的严重病情复发进行分析发现,6例发生在服用安慰剂的患者中,服用泼尼松的患者未发生(P = 0.007)。严重病情复发导致泼尼松剂量增加至>40mg/天和/或加用免疫抑制剂。此外,在开始泼尼松治疗1个月后,系统性红斑狼疮疾病活动指数评分改善、抗dsDNA抗体水平降低以及C4水平升高。

结论

这些初步数据支持我们的假设,即在一部分C3a和抗dsDNA水平升高的临床稳定SLE患者中,短期皮质类固醇治疗可能避免严重病情复发。

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