首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Factors associated with progression of interstitial fibrosis in renal transplant patients receiving tacrolimus and mycophenolate mofetil.
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Factors associated with progression of interstitial fibrosis in renal transplant patients receiving tacrolimus and mycophenolate mofetil.

机译:与接受他克莫司和霉酚酸酯治疗的肾移植患者间质纤维化进展有关的因素。

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BACKGROUND: We recently reported a randomized study in renal transplant patients (RTP) receiving tacrolimus, mycophenolate mofetil, and prednisone in which patients who had early protocol biopsies (PBx) derived no benefit compared with controls (no PBx) at 6 months, likely due to the low prevalence of subclinical rejection. We report on the follow-up of these patients to 24 months at which time a repeat PBx and tests of renal function were performed. METHODS: Of the 240 RTP randomized, 22 were excluded for a protocol violation. Approximately 75% of the remaining 218 (111 PBx and 107 controls) completed the study. RESULTS: At 24 months, graft function was excellent with a mean creatinine clearance of approximately 74 mL/min and negligible proteinuria; however, the prevalence of interstitial fibrosis and tubular atrophy (IF/TA)-ci + ct more than or equal to 2-increased from approximately 3% at baseline to up to 40% to 50%. By logistic regression analysis, the only independent positive correlate of IF/TA was transplantation with a deceased donor. However, by post hoc analysis, use of angiotensin-II-converting enzyme inhibitors or angiotensin II receptor blockers was negatively correlated with both the prevalence of IF/TA at 24 months and its progression between 6 and 24 months in RTP that had paired biopsies. CONCLUSIONS: A regimen of tacrolimus, mycophenolate mofetil, and prednisone results in excellent renal function at 24 months posttransplant but with a progressive increase in IF/TA. A potential inhibitory effect of angiotensin-II-converting enzyme inhibitor/angiotensin II receptor blockers on IF/TA is suggested that requires confirmation in a randomized study.
机译:背景:我们最近报道了接受他克莫司,霉酚酸酯和强的松治疗的肾移植患者(RTP)的一项随机研究,其中在6个月时进行早期活检(PBx)的患者与对照组(无PBx)相比无益处导致亚临床排斥反应的发生率较低。我们报告了这些患者的随访情况,直至24个月,然后进行了重复的PBx和肾功能测试。方法:在随机分配的240个RTP中,有22个因违反协议而被排除在外。其余218位(111 PBx和107位对照)中约有75%完成了研究。结果:24个月时,移植物功能良好,平均肌酐清除率约为74 mL / min,蛋白尿可忽略不计;然而,间质纤维化和肾小管萎缩(IF / TA)-ci + ct的患病率大于或等于2,从基线时的约3%增加到40%至50%。通过逻辑回归分析,IF / TA的唯一独立正相关是已故供体的移植。然而,通过事后分析,使用血管紧张素II转换酶抑制剂或血管紧张素II受体阻滞剂与IF / TA在24个月时的流行率以及在已配对活检的RTP中6到24个月的进展均呈负相关。结论:他克莫司,霉酚酸酯和强的松的治疗方案在移植后24个月时具有出色的肾功能,但IF / TA逐渐升高。提示血管紧张素II转换酶抑制剂/血管紧张素II受体阻滞剂对IF / TA的潜在抑制作用需要在随机研究中得到证实。

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