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
New York University School of Medicine, Hospital for Joint Diseases, New York, New York 10003, USA.
Arthritis Rheum. 2006 Nov;54(11):3623-32. doi: 10.1002/art.22198.
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.
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.
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.
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.
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。
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。
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。
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。