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他克莫司与环孢素治疗儿童激素抵抗型肾病综合征的疗效及安全性:一项随机对照试验

Efficacy and safety of tacrolimus versus cyclosporine in children with steroid-resistant nephrotic syndrome: a randomized controlled trial.

作者信息

Choudhry Swati, Bagga Arvind, Hari Pankaj, Sharma Sonika, Kalaivani Mani, Dinda Amit

机构信息

Division of Nephrology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.

出版信息

Am J Kidney Dis. 2009 May;53(5):760-9. doi: 10.1053/j.ajkd.2008.11.033. Epub 2009 Mar 5.

Abstract

BACKGROUND

To examine whether tacrolimus is more effective and safe than cyclosporine (CsA) in inducing remission in patients with steroid-resistant nephrotic syndrome (SRNS).

STUDY DESIGN

Randomized controlled trial, nonblind, parallel group.

SETTINGS & PARTICIPANTS: Tertiary-care hospital; 41 consecutive patients with idiopathic SRNS, estimated glomerular filtration rate greater than 60 mL/min/1.73 m(2), and histological characteristics showing minimal change disease, focal segmental glomerulosclerosis, or mesangioproliferative glomerulonephritis were randomly assigned to treatment with tacrolimus (n = 21) or CsA (n = 20).

INTERVENTION

Tacrolimus (0.1 to 0.2 mg/kg/d) or CsA (5 to 6 mg/kg/d) for 1 year; cotreatment with alternate-day prednisolone and enalapril.

OUTCOMES

Patients achieving complete remission (urinary protein-creatinine ratio < 0.2 g/g and serum albumin > or = 2.5 g/dL) or partial remission (urinary protein-creatinine ratio, 0.2 to 2 g/g, and serum albumin > or =2.5 g/dL) at 6 and 12 months; time to remission; proportion with relapses; side effects.

RESULTS

No patient was lost to follow-up. After 6 months of therapy, remission occurred in 18 (85.7%) and 16 patients (80%) treated with tacrolimus and CsA, respectively (relative risk [RR], 1.07; 95% confidence interval [CI], 0.81 to 1.41). Rates of remission at 12 months were also similar (RR, 1.14; 95% CI, 0.84 to 1.55). The proportion of patients who experienced relapse was significantly greater in those receiving CsA compared with tacrolimus (RR, 4.5; 95% CI, 1.1 to 18.2; P = 0.01). The decrease in blood cholesterol levels was greater with tacrolimus compared with CsA (difference in mean values, 45.1 mg/dL; 95% CI, 19.1 to 71.2). Persistent nephrotoxicity necessitating stoppage of medicine was seen in 4.7% and 10% patients, respectively. Cosmetic side effects (hypertrichosis and gum hypertrophy) were significantly more frequent in CsA-treated patients (P < 0.001).

LIMITATIONS

Single-center study, small sample size, and short duration of follow-up.

CONCLUSIONS

Tacrolimus or CsA in combination with low-dose steroids show similar efficacy in inducing remission in patients with SRNS. Therapy with tacrolimus is a promising alternative to CsA in view of the lower risk of relapses and lack of cosmetic side effects.

摘要

背景

探讨他克莫司在诱导激素抵抗型肾病综合征(SRNS)患者缓解方面是否比环孢素(CsA)更有效且更安全。

研究设计

随机对照试验,非盲法,平行组。

研究地点与参与者

三级医疗中心;41例连续性特发性SRNS患者,估计肾小球滤过率大于60 mL/min/1.73 m²,组织学特征显示为微小病变肾病、局灶节段性肾小球硬化或系膜增生性肾小球肾炎,被随机分配接受他克莫司治疗(n = 21)或CsA治疗(n = 20)。

干预措施

他克莫司(0.1至0.2 mg/kg/d)或CsA(5至6 mg/kg/d)治疗1年;联合隔日泼尼松龙和依那普利治疗。

观察指标

患者在6个月和12个月时达到完全缓解(尿蛋白肌酐比<0.2 g/g且血清白蛋白≥2.5 g/dL)或部分缓解(尿蛋白肌酐比为0.2至2 g/g且血清白蛋白≥2.5 g/dL);缓解时间;复发比例;副作用。

结果

无患者失访。治疗6个月后,接受他克莫司和CsA治疗的患者分别有18例(85.7%)和16例(80%)出现缓解(相对危险度[RR],1.07;95%置信区间[CI],0.81至1.41)。12个月时的缓解率也相似(RR,1.14;95%CI,0.84至1.55)。与他克莫司相比,接受CsA治疗的患者复发比例显著更高(RR,4.5;95%CI,1.1至18.2;P = 0.01)。与CsA相比,他克莫司使血胆固醇水平下降幅度更大(均值差异,45.1 mg/dL;95%CI,19.1至71.2)。分别有4.7%和10%的患者出现持续性肾毒性而需要停药。CsA治疗的患者出现美容方面的副作用(多毛症和牙龈增生)明显更频繁(P < 0.001)。

局限性

单中心研究,样本量小,随访时间短。

结论

他克莫司或CsA联合小剂量激素在诱导SRNS患者缓解方面疗效相似。鉴于复发风险较低且无美容方面的副作用,他克莫司治疗是CsA的一个有前景的替代方案。

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