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马来酸氨氯地平与雷米普利在 2 型糖尿病高血压患者中的作用:雷米普利和马来酸氨氯地平在糖尿病肾病保护中的研究(DEMAND)随机临床试验。

Effects of manidipine and delapril in hypertensive patients with type 2 diabetes mellitus: the delapril and manidipine for nephroprotection in diabetes (DEMAND) randomized clinical trial.

机构信息

Mario Negri Institute for Pharmacological Research, Clinical Research Center for Rare Diseases Aldo e Cele Daccò, Ranica, Bergamo, Italy.

出版信息

Hypertension. 2011 Nov;58(5):776-83. doi: 10.1161/HYPERTENSIONAHA.111.174474. Epub 2011 Sep 19.

Abstract

To assess whether angiotensin-converting enzyme inhibitors and third-generation dihydropyridine calcium channel blockers ameliorate diabetic complications, we compared glomerular filtration rate (GFR; primary outcome), cardiovascular events, retinopathy, and neuropathy in 380 hypertensive type 2 diabetics with albuminuria <200 mg/min included in a multicenter, double-blind, placebo-controlled trial (DEMAND [Delapril and Manidipine for Nephroprotection in Diabetes]) and randomized to 3-year treatment with manidipine/delapril combination (10/30 mg/d; n=126), delapril (30 mg/d; n=127), or placebo (n=127). GFR was centrally measured by iohexol plasma clearance. Median monthly GFR decline (interquartile range [IQR]) was 0.32 mL/min per 1.73 m(2) (IQR: 0.16-0.50 mL/min per 1.73 m(2)) on combined therapy, 0.36 mL/min per 1.73 m(2) (IQR: 0.18-0.53 mL/min per 1.73 m(2)) on delapril, and 0.30 mL/min per 1.73 m(2) (IQR: 0.12-0.50 mL/min per 1.73 m(2)) on placebo (P=0.87 and P=0.53 versus combined therapy or delapril, respectively). Similar findings were observed when baseline GFR values were not considered for slope analyses. Albuminuria was stable in the 3 treatment groups. The hazard ratio (95% CI) for major cardiovascular events between combined therapy and placebo was 0.17 (0.04-0.78; P=0.023). Among 192 subjects without retinopathy at inclusion, the hazard ratio for developing retinopathy between combined therapy and placebo was 0.27 (0.07-0.99; P=0.048). Among 200 subjects with centralized neurological evaluation, the odds ratios for peripheral neuropathy at 3 years between combined therapy or delapril and placebo were 0.45 (0.24-0.87; P=0.017) and 0.52 (0.27-0.99; P=0.048), respectively. Glucose disposal rate decreased from 5.8±2.4 to 5.3±1.9 mg/kg per min on placebo (P=0.03) but did not change on combined or delapril therapy. Treatment was well tolerated. In hypertensive type 2 diabetic patients, combined manidipine and delapril therapy failed to slow GFR decline but safely ameliorated cardiovascular disease, retinopathy, and neuropathy and stabilized insulin sensitivity.

摘要

为了评估血管紧张素转换酶抑制剂和第三代二氢吡啶钙通道阻滞剂是否能改善糖尿病并发症,我们比较了肾小球滤过率(GFR;主要结局)、心血管事件、视网膜病变和神经病变,380 例患有白蛋白尿<200mg/min 的 2 型高血压糖尿病患者参与了一项多中心、双盲、安慰剂对照试验(DEMAND[Delapril 和 Manidipine 对糖尿病肾病的保护]),并随机接受 3 年的马尼地平/地尔硫卓联合治疗(10/30mg/d;n=126)、地尔硫卓(30mg/d;n=127)或安慰剂(n=127)治疗。GFR 通过 iohexol 血浆清除率进行中心测量。中位每月 GFR 下降(四分位距[IQR])在联合治疗组为 0.32ml/min/1.73m²(IQR:0.16-0.50ml/min/1.73m²),在地尔硫卓组为 0.36ml/min/1.73m²(IQR:0.18-0.53ml/min/1.73m²),在安慰剂组为 0.30ml/min/1.73m²(IQR:0.12-0.50ml/min/1.73m²)(P=0.87 和 P=0.53,分别与联合治疗或地尔硫卓相比)。当不考虑基线 GFR 值进行斜率分析时,也观察到了类似的发现。3 个治疗组的白蛋白尿均保持稳定。主要心血管事件的危险比(95%CI)在联合治疗与安慰剂之间为 0.17(0.04-0.78;P=0.023)。在 192 例入组时无视网膜病变的受试者中,联合治疗与安慰剂之间发生视网膜病变的危险比为 0.27(0.07-0.99;P=0.048)。在 200 例接受集中神经学评估的受试者中,联合治疗或地尔硫卓与安慰剂相比,3 年后外周神经病变的优势比分别为 0.45(0.24-0.87;P=0.017)和 0.52(0.27-0.99;P=0.048)。安慰剂组的葡萄糖处置率从 5.8±2.4mg/kg/min 降至 5.3±1.9mg/kg/min(P=0.03),而联合或地尔硫卓治疗组未发生变化。治疗耐受性良好。在 2 型高血压糖尿病患者中,马尼地平与地尔硫卓联合治疗未能减缓 GFR 下降,但可安全改善心血管疾病、视网膜病变和神经病变,并稳定胰岛素敏感性。

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