Hahn B H, Kantor O S, Osterland C K
Ann Intern Med. 1975 Nov;83(5):597-605. doi: 10.7326/0003-4819-83-5-597.
A prospective, randomized drug trial compared prednisone (60 mg per day initially) to azathioprine (3 to 4 mg/kg of body weight - day initially) plus prednisone in 24 patients with life-threatening systemic lupus erythematosus. Each group contained patients matched for age, sex, disease duration, previous therapy, and clinical and laboratory features of lupus erythematosus. During a mean follow-up period of 18 to 24 months, there were no significant differences between the two groups in number of deaths, renal or extrarenal manifestations of disease, serum complement levels, DNA antibodies, antinuclear antibody titers, lupus erythematosus cells, or Coombs' antibodies. There was no convincing evidence of a steroid-sparing effect of azathioprine. Side effects attributable to steroids were equally common in both groups; infections were not increased in the combination therapy group. Azathioprine was hepatotoxic in doses of 200 mg daily or more. Azathioprine was not a useful adjunct to corticosterolds in short-term therapy of a small number of patients with severe systemic lupus.
一项前瞻性随机药物试验,将24例患有危及生命的系统性红斑狼疮的患者分为两组,一组初始剂量为泼尼松(每日60毫克),另一组初始剂量为硫唑嘌呤(3至4毫克/千克体重·日)加泼尼松。每组患者在年龄、性别、病程、既往治疗以及红斑狼疮的临床和实验室特征方面相匹配。在平均18至24个月的随访期内,两组在死亡人数、疾病的肾脏或肾外表现、血清补体水平、DNA抗体、抗核抗体滴度、红斑狼疮细胞或库姆斯抗体方面均无显著差异。没有令人信服的证据表明硫唑嘌呤有激素节省作用。两组中由类固醇引起的副作用同样常见;联合治疗组的感染并未增加。硫唑嘌呤每日剂量达200毫克或更高时具有肝毒性。在少数重症系统性红斑狼疮患者的短期治疗中,硫唑嘌呤并非皮质类固醇的有用辅助药物。