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特立氟胺治疗特发性膜性肾病伴肾病综合征的疗效。

Effect of prolonged tacrolimus treatment in idiopathic membranous nephropathy with nephrotic syndrome.

机构信息

Department of Nephrology, Second Hospital of Jilin University, Changchun, China.

出版信息

Pharmacology. 2013;91(5-6):259-66. doi: 10.1159/000348570. Epub 2013 May 7.

Abstract

OBJECTIVE

Tacrolimus has been used for idiopathic membranous nephropathy (IMN) therapy, but most patients who achieved remission showed a high relapse rate when tacrolimus was withdrawn after 6-12 months of therapy. We proposed that a prolonged therapeutic course should help reduce the relapse rate.

METHODS

A total of 42 patients with nephrotic syndrome caused by IMN were randomly divided into short-term (n = 20) and long-term (n = 22) groups. All patients received initial treatment with tacrolimus and prednisone for 6 months, and afterward only the long-term patient group was tapered with low-dose tacrolimus until 24 months.

RESULTS

Over 85% of the patients achieved proteinuria reduction, serum albumin improvement and serum lipid recovery; the probability of remission in both groups was over 80% at 6 months. The remission rate was steady at over 80% after 12 and 24 months in the long-term group, but only 50 and 45%, respectively, in the short-term group. Nine patients (45%) relapsed in the short-term group after tacrolimus withdrawal, while not a single patient suffered recurrence in the long-term group. The concentration of tacrolimus remained similar between the two groups at 5-8 ng/ml during the initial 6 months, and was significantly decreased at 12 months compared to 6 months (p < 0.05), along with reduction of oral administration in the long-term group.

CONCLUSION

Combined therapy of tacrolimus with prednisone can relieve IMN significantly; prolonged tacrolimus treatment at a low blood concentration can alleviate the illness persistently, with a low recurrence rate and gratifying safety.

摘要

目的

他克莫司已用于特发性膜性肾病(IMN)的治疗,但大多数患者在治疗 6-12 个月后停用他克莫司时显示出高复发率。我们提出延长治疗疗程有助于降低复发率。

方法

共有 42 例特发性膜性肾病引起的肾病综合征患者随机分为短期组(n = 20)和长期组(n = 22)。所有患者均接受初始治疗,即他克莫司联合泼尼松治疗 6 个月,此后仅长期组患者以低剂量他克莫司逐渐减量至 24 个月。

结果

超过 85%的患者蛋白尿减少、血清白蛋白改善和血脂恢复;两组患者在 6 个月时的缓解率均超过 80%。长期组在 12 个月和 24 个月时的缓解率稳定在 80%以上,而短期组分别为 50%和 45%。短期组有 9 例(45%)患者在停用他克莫司后复发,而长期组无一例复发。在最初的 6 个月内,两组患者他克莫司浓度均保持在 5-8ng/ml 之间相似,而在 12 个月时与 6 个月相比显著降低(p <0.05),同时长期组的口服剂量减少。

结论

他克莫司联合泼尼松治疗可显著缓解特发性膜性肾病;低血浓度延长他克莫司治疗可持久缓解病情,复发率低,安全性好。

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