Jerums G, Allen T J, Campbell D J, Cooper M E, Gilbert R E, Hammond J J, Raffaele J, Tsalamandris C
Department of Medicine, University of Melbourne, Austin & Repatriation Medical Centre, Heidelberg 3084, VIC, Australia.
Am J Kidney Dis. 2001 May;37(5):890-9. doi: 10.1016/s0272-6386(05)80003-4.
The aim of this study is to compare the efficacy of an angiotensin-converting enzyme inhibitor with a dihydropyridine calcium channel blocker in preventing progression to macroalbuminuria and/or a decline in renal function in normotensive patients with type 1 diabetes and microalbuminuria. Forty-two patients were randomized to treatment with either perindopril, slow-release nifedipine, or placebo. In the first 3 months, drug dosage was titrated to achieve a decrease in diastolic blood pressure of at least 5 mm HG: Thirty-three patients had a minimum of 24 months' data, and 25 patients were followed up beyond 36 months (mean, 67 +/- 4 months). Patients were studied every 3 months and at the end of the treatment period; those who remained normotensive discontinued therapy and were followed up for an additional 3 months. Baseline geometric mean albumin excretion rates (AERs) were as follows: perindopril, 66 microg/min; nifedipine, 59 microg/min; and placebo, 66 microg/min. During the first 3 years, 7 of the perindopril-treated but none of the placebo or nifedipine-treated patients reverted to normoalbuminuria (P < 0.01). Median AERs at 3 years of treatment in each group were 23 microg/min for perindopril, 122 microg/min for nifedipine, and 112 microg/min for placebo patients (P < 0.01). In patients with more than 3 years' follow-up, median AERs decreased by 45% in the first year and then stabilized in the perindopril group, but increased by 17.6% in the nifedipine group and 27.6% in the placebo group (P < 0.03) in the first year, then increased progressively. In these same patients, there was a significant decline in glomerular filtration rate in the nifedipine group (-7.8 +/- 1.8 mL/min/1.73 m(2)/y), but not in the other two groups (perindopril, -1.0 +/- 1.2 mL/min/1.73 m(2)/y; placebo, -1.3 +/- 1.1 mL/min/1.73 m(2)/y; P = 0.004). At the end of the study, cessation of treatment for 3 months was associated with a doubling of AERs in the perindopril-treated group, but no change in the other two groups (P < 0.001). In conclusion, long-term perindopril therapy is more effective than nifedipine or placebo in delaying the progression of diabetic nephropathy and reducing AER to the normoalbuminuric range (<20 microg/min) in normotensive patients with type 1 diabetes and microalbuminuria.
本研究旨在比较血管紧张素转换酶抑制剂与二氢吡啶类钙通道阻滞剂在预防1型糖尿病合并微量白蛋白尿的血压正常患者进展为大量白蛋白尿和/或肾功能下降方面的疗效。42例患者被随机分为培哚普利、缓释硝苯地平或安慰剂治疗组。在最初3个月,调整药物剂量以使舒张压至少降低5 mmHg:33例患者有至少24个月的数据,25例患者随访超过36个月(平均67±4个月)。每3个月及治疗期末对患者进行研究;仍血压正常的患者停止治疗并额外随访3个月。基线几何平均白蛋白排泄率(AER)如下:培哚普利组为66μg/min;硝苯地平组为59μg/min;安慰剂组为66μg/min。在最初3年,培哚普利治疗组中有7例患者恢复为正常白蛋白尿,而安慰剂组和硝苯地平治疗组均无(P<0.01)。每组治疗3年时的AER中位数分别为:培哚普利组23μg/min,硝苯地平组122μg/min,安慰剂组112μg/min(P<0.01)。在随访超过3年的患者中,培哚普利组AER中位数在第1年下降45%,随后稳定;而硝苯地平组在第1年增加17.6%,安慰剂组增加27.6%(P<0.03),随后逐渐增加。在这些相同患者中,硝苯地平组肾小球滤过率显著下降(-7.8±1.8 mL/min/1.73 m²/y),而其他两组无下降(培哚普利组,-1.0±1.2 mL/min/1.73 m²/y;安慰剂组,-1.3±1.1 mL/min/1.73 m²/y;P=0.004)。研究结束时,培哚普利治疗组停药3个月与AER翻倍相关,而其他两组无变化(P<0.001)。总之,在延缓1型糖尿病合并微量白蛋白尿的血压正常患者糖尿病肾病进展以及将AER降低至正常白蛋白尿范围(<20μg/min)方面,长期培哚普利治疗比硝苯地平和安慰剂更有效。