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从环孢素微乳剂转换为他克莫司免疫预防可改善接受治疗但血脂仍持续异常的心脏移植受者的胆固醇水平:加拿大他克莫司与环孢素微乳剂多中心随机试验

Conversion from cyclosporine microemulsion to tacrolimus-based immunoprophylaxis improves cholesterol profile in heart transplant recipients with treated but persistent dyslipidemia: the Canadian multicentre randomized trial of tacrolimus vs cyclosporine microemulsion.

作者信息

White Michel, Haddad Haissam, Leblanc Marie-Hélène, Giannetti Nadia, Pflugfelder Peter, Davies Ross, Isaac Debra, Burton Jeffrey, Chan Michael, Azevedo Eduardo, Howlett Jonathan, Ignaszewski Andrew, Busque Stéphane, Cantarovich Marcello, Ferguson Ralph, Genest Jacques, Ross Heather

机构信息

Research Center of Montreal Heart Institute, Montreal, Quebec.

出版信息

J Heart Lung Transplant. 2005 Jul;24(7):798-809. doi: 10.1016/j.healun.2004.05.023.

Abstract

BACKGROUND

Tacrolimus improves lipid profile in renal and liver transplant recipients. The impact of conversion from cyclosporine microemulsion (Neoral) to tacrolimus (Prograf) in a large randomized study of stable heart transplant recipients with treated but persistent mild dyslipidemia is reported.

METHODS

One hundred twenty-nine long-term (>or=12 months) cyclosporine microemulsion-treated heart transplant recipients with low-density lipoprotein cholesterol >2.5 mmol/liter and/or a total cholesterol/high-density lipoprotein cholesterol ratio >4 were recruited for the study. Complete lipid profile was assessed before (baseline) and after 6 months of treatment with either cyclosporine microemulsion maintenance (n=64) or tacrolimus conversion (n=65).

RESULTS

At 6 months, tacrolimus-converted patients exhibited a greater decrease in total cholesterol (from 5.51 +/- 0.16 to 4.88 +/- 1.22 mmol/liter [tacrolimus], vs 5.61 +/- 1.36 to 5.38 +/- 0.87 mmol/liter [cyclosporine]; p = 0.0078). This decrease in cholesterol was caused largely by a decrease in low-density lipoprotein cholesterol (-0.41 +/- 0.54 [tacrolimus] vs -0.13 +/- 0.55 [cyclosporine]; p=0.0018). There were no changes in high-density lipoprotein cholesterol and triglyceride levels, but apolipoprotein B therapy was reduced in tacrolimus-converted vs cyclosporine-maintained patients (p=0.0003). By 6 months, 23.7% of tacrolimus- vs 6.7% of cyclosporine-treated patients met the target lipid levels for high-risk patients (p=0.0094). Conversion from cyclosporine to tacrolimus resulted in decreases in blood urea nitrogen, creatinine, and uric acid without any changes in glucose, HbA(1C), and insulin levels.

CONCLUSIONS

Conversion from cyclosporine microemulsion- to tacrolimus-based immunoprophylaxis resulted in decreased cholesterol, apolipoprotein B, urea, creatinine, and uric acid without any clinically evident perturbation of glucose metabolism in stable heart transplant recipients with treated but persistent mild dyslipidemia.

摘要

背景

他克莫司可改善肾移植和肝移植受者的血脂情况。本文报告了一项针对接受治疗但仍存在持续性轻度血脂异常的稳定心脏移植受者的大型随机研究中,从环孢素微乳剂(新山地明)转换为他克莫司(普乐可复)的影响。

方法

招募了129名长期(≥12个月)接受环孢素微乳剂治疗的心脏移植受者,其低密度脂蛋白胆固醇>2.5 mmol/L和/或总胆固醇/高密度脂蛋白胆固醇比值>4,参与本研究。在接受环孢素微乳剂维持治疗(n = 64)或他克莫司转换治疗(n = 65)6个月之前(基线)和之后,评估完整的血脂情况。

结果

6个月时,转换为他克莫司治疗的患者总胆固醇下降幅度更大(从5.51±0.16降至4.88±1.22 mmol/L[他克莫司组],相比之下,环孢素组从5.61±1.36降至5.38±0.87 mmol/L;p = 0.0078)。胆固醇的下降主要是由于低密度脂蛋白胆固醇的降低(-0.41±0.54[他克莫司组] vs -0.13±0.55[环孢素组];p = 0.0018)。高密度脂蛋白胆固醇和甘油三酯水平没有变化,但转换为他克莫司治疗的患者与维持环孢素治疗的患者相比,载脂蛋白B水平降低(p = 0.0003)。到6个月时,他克莫司治疗组23.7%的患者与环孢素治疗组6.7%的患者达到了高危患者的血脂目标水平(p = 0.0094)。从环孢素转换为他克莫司导致血尿素氮、肌酐和尿酸降低,而血糖、糖化血红蛋白(HbA1C)和胰岛素水平没有变化。

结论

在接受治疗但仍存在持续性轻度血脂异常的稳定心脏移植受者中,从环孢素微乳剂转换为他克莫司进行免疫预防可降低胆固醇、载脂蛋白B、尿素、肌酐和尿酸,且未对葡萄糖代谢产生任何临床上明显的干扰。

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