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硫唑嘌呤与小剂量泼尼松联合治疗系统性红斑狼疮时病情复发及长期预后的预测因素

Predictors of flares and long-term outcome of systemic lupus erythematosus during combined treatment with azathioprine and low-dose prednisolone.

作者信息

Oelzner P, Abendroth K, Hein G, Stein G

机构信息

Clinic of Internal Medicine IV, Friedrich Schiller University Jena, Germany.

出版信息

Rheumatol Int. 1996;16(4):133-9. doi: 10.1007/BF01419725.

Abstract

Many patients with systemic lupus erythematosus (SLE) receive long-term treatment with azathioprine and prednisolone to control disease activity. In a retrospective study we evaluated the efficacy of combined treatment with azathioprine (2 mg/kg body weight/d) and low-dose prednisolone (7-12 mg/d) and the predictors of disease flares during this therapy regimen in 61 patients with SLE. We found three predictors of flares: renal disease, persistence of dsDNA antibodies for at least 1 year after the beginning of treatment and reduction in azathioprine dosage to below 2 mg/kg/d. The occurrence of flares was significantly associated with a higher rate of disease-related death. Furthermore, the persistence of dsDNA antibodies for at least 2 years was associated with progression of renal disease. We concluded that suppression of production of dsDNA antibodies with high avidity is a suitable parameter to determine efficacy of treatment and long-term outcome during combined therapy with azathioprine and low-dose prednisolone in SLE.

摘要

许多系统性红斑狼疮(SLE)患者接受硫唑嘌呤和泼尼松龙的长期治疗以控制疾病活动。在一项回顾性研究中,我们评估了硫唑嘌呤(2毫克/千克体重/天)和低剂量泼尼松龙(7 - 12毫克/天)联合治疗的疗效,以及61例SLE患者在此治疗方案期间疾病复发的预测因素。我们发现了三个复发预测因素:肾脏疾病、治疗开始后双链DNA(dsDNA)抗体持续存在至少1年以及硫唑嘌呤剂量降至2毫克/千克/天以下。疾病复发的发生与疾病相关死亡的较高发生率显著相关。此外,dsDNA抗体持续存在至少2年与肾脏疾病进展相关。我们得出结论,在SLE患者中,用硫唑嘌呤和低剂量泼尼松龙联合治疗期间,抑制高亲和力dsDNA抗体的产生是确定治疗疗效和长期预后的合适参数。

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