机构地区:[1]中南大学湘雅二医院器官移植中心,长沙410011
出 处:《中南大学学报(医学版)》2007年第1期59-62,共4页Journal of Central South University :Medical Science
摘 要:目的:探讨他克莫司(FK506)替换环孢素A(CsA)治疗慢性移植肾肾病(CAN)的有效性及安全性。方法:根据是否以FK506替换CsA,将73例CAN患者分成两组,CsA组30例,维持原免疫抑制方案(CsA、霉酚酸酯及泼尼松联用)不变,采用替换方案的FK506组43例,除将CsA转换成FK506外,其他用药同CsA组。两组均随访1年以上,监测血清肌酐(SCr)、肾小球滤过率(GFR)、24h尿蛋白定量、血脂[包括总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白(LDL)、高密度脂蛋白(HDL)]等生化指标的变化情况,并观察随访期间药物的毒副作用。结果:转换治疗12个月后,FK506组SCr显著低于CsA组[分别为(194.8±42.5)μmol/Lvs.(245.4±52.8)μmol/L,P<0.01],FK506组GFR显著高于CsA组[(50.14±3.92)mL/(min.1.73m2)vs.(40.58±2.49)mL/(min.1.73m2),P<0.01];FK506组24h尿蛋白定量显著低于CsA组[(2.0±0.5)gvs.(3.9±0.7)g,P<0.01];FK506组除HDL外,TC,TG,LDL均显著低于CsA组[(5.19±0.73)mmol/Lvs.(6.94±1.37)mmol/L;(1.86±0.84)mmol/Lvs.(3.14±1.38)mmol/L;(3.03±0.71)mmol/Lvs.(3.82±0.89)mmol/L,P<0.01];FK506组震颤发生率较CsA组高(P<0.01),但高血压发生率显著低于CsA组(P<0.05)。结论:FK506转换治疗后,肾功能减退得到延缓,蛋白尿降低,血脂代谢得到改善,FK506可以有效延缓CAN进展。Objective To investigate the feasibility and safety of substituting tacrolimus ( FK506 ) for cyclosporin A ( CsA ) on delaying the pace of renal dysfunction in patients with biopsyproven chronic allograft nephropathy (CAN). Methods Seventy-three renal transplantation patients with CAN proved by allograft biopsy were collected in this study. Patients were randomly divided into 2 groups. Patients were either converted to FK506 ( FK506 group, n = 43 ) or remained on their initial CsA-based immunosuppression (CsA group, n = 30 ). The clinical data at study entry and after 12 months including blood urea nitrogen ( BUN ) , serum creatinine ( SCr ) , glomerular filtration rate ( GFR ) , 24-hour urine protein excretion, serum total cholesterol ( TC ) , triglyceride ( TG ) , low density lipoprotein (LDL)and the side effects of calcineurin inhibitors were monitored during a follow-up of over 12 months. Results Twelve months later, the level of SCr was statistically reduced and GFR levels were obviously elevated in the FK506 group as compared with CsA group [ (194.8 ±42.5 ) μmol/L vs. ( 245. 4 ± 52. 8 ) μmol/L and ( 50. 14 ± 3. 92 ) mL/( min · 1. 73 m^2 ) vs. (40.58 ± 2.49 ) mL/( min · 1.73 m^2 ) , P 〈 0.01 ]. Quantity of 24-hour urine protein excretion in the FK506 group was (2.020.5) g which is significantly lower than (3.9 ±0.7) g in the CsA group ( P 〈 0.01 ). TC, TG, and LDL levels remained unchanged in the CsA group, while those were statistically reduced in the FK506 group respectively [ ( 5. 19 ± 0. 73 ) mmol/L vs. (6.94±1.37) mmol/L,(1.86 ±0.84) mmol/L vs. (3. 14 ±1.38) mmol/L,(3.03 ±0.71) mmol/L vs. (3.82 ±0.89) mmol/L,P 〈 0.01]. Tremor obviously increased (P 〈0.01 ) and hypertension obviously decreased ( P 〈 0.05 ) in the FK506 group compared with the CsA group. Conclusion FK506 treatment can greatly improve the proteinuria and hyperlipidemia. Conversion from CsA to FK506 is an
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