首页> 外文期刊>The American Journal of the Medical Sciences >Low-dose cyclosporine treatment in Chinese nephrotic patients with idiopathic membranous nephropathy: An uncontrolled study with prospective follow-up.
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Low-dose cyclosporine treatment in Chinese nephrotic patients with idiopathic membranous nephropathy: An uncontrolled study with prospective follow-up.

机译:小剂量环孢素治疗中国肾病特发性膜性肾病的患者:一项无控制的前瞻性研究。

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INTRODUCTION: The optimal dose of cyclosporine A (CsA) in treatment of nephrotic proteinuria in idiopathic membranous nephropathy (IMN) remains inconclusive. We evaluated the efficacy and safety of low-dose CsA combined with low-dose prednisone as induction therapy for Chinese nephrotic patients with IMN. METHODS: We conducted a prospective observational cohort study in 18 patients with IMN and nephrotic proteinuria. Twelve patients were refractory to other immunosuppressive therapies. The initial dose of CsA was 1 to 1.5 mg/kg/d combined with 0.15 to 0.50 mg/kg/d prednisone. The dose of CsA was adjusted monthly by 20% to 30% according to efficacy and the 12-hour trough blood concentration (C0) of CsA around 100 ng/mL for 6 months; when proteinuria was <1 g/d, CsA was tapered gradually to a dose of 0.6 to 1 mg/kg/d. RESULTS: Two patients discontinued CsA because of refractory hypertension. The remaining 16 patients had been followed up for 44 +/- 15 weeks. Remission was observed in 11 patients (68.8%: complete remission, 6 and partial remission, 5). The effective dose of CsA for remission was 2.1 +/- 0.4 (1.5-2.5) mg/kg/d, and the mean C0 of CsA was 92.5 +/- 23.5 (58-124) ng/mL. All the 16 patients experienced well-controlled adverse effects, including hypertension (n = 12), hyperuricemia (n = 12), increase of serum creatinine (n = 2), etc. CONCLUSIONS: Low-dose CsA combined with low-dose prednisone was effective and safe as induction therapy in majority of Chinese nephrotic patients with IMN, including those refractory to other immunosuppressive regimens.
机译:简介:环孢素A(CsA)在治疗特发性膜性肾病(IMN)的肾病蛋白尿中的最佳剂量尚无定论。我们评估了低剂量CsA联合低剂量泼尼松作为中国IMN肾病患者的诱导疗法的疗效和安全性。方法:我们对18例IMN和肾病蛋白尿患者进行了一项前瞻性观察队列研究。 12名患者对其他免疫抑制疗法无效。 CsA的初始剂量为1至1.5 mg / kg / d联合泼尼松0.15至0.50 mg / kg / d。根据疗效和CsA的12小时低谷血药浓度(C0)在100 ng / mL附近每月调整CsA剂量6个月至20%至30%;当蛋白尿<1 g / d时,CsA逐渐逐渐降低至0.6至1 mg / kg / d的剂量。结果:两名患者因难治性高血压而中断了CsA治疗。其余16例患者已随访44 +/- 15周。观察到11例患者缓解(68.8%:完全缓解6例和部分缓解5例)。缓解的CsA有效剂量为2.1 +/- 0.4(1.5-2.5)mg / kg / d,CsA的平均C0为92.5 +/- 23.5(58-124)ng / mL。所有16例患者均受到良好控制的不良反应,包括高血压(n = 12),高尿酸血症(n = 12),血清肌酐升高(n = 2)等。结论:低剂量CsA联合低剂量泼尼松对于大多数中国IMN肾病患者,包括那些对其他免疫抑制疗法均无效的患者,作为诱导疗法是有效且安全的。

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