Wright Jackson T, Bakris George, Greene Tom, Agodoa Larry Y, Appel Lawrence J, Charleston Jeanne, Cheek DeAnna, Douglas-Baltimore Janice G, Gassman Jennifer, Glassock Richard, Hebert Lee, Jamerson Kenneth, Lewis Julia, Phillips Robert A, Toto Robert D, Middleton John P, Rostand Stephen G
Case Western Reserve University, Department of Medicine, University Hospitals of Cleveland and the Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, OH 44106-5014, USA.
JAMA. 2002 Nov 20;288(19):2421-31. doi: 10.1001/jama.288.19.2421.
Hypertension is a leading cause of end-stage renal disease (ESRD) in the United States, with no known treatment to prevent progressive declines leading to ESRD.
To compare the effects of 2 levels of blood pressure (BP) control and 3 antihypertensive drug classes on glomerular filtration rate (GFR) decline in hypertension.
Randomized 3 x 2 factorial trial with enrollment from February 1995 to September 1998.
A total of 1094 African Americans aged 18 to 70 years with hypertensive renal disease (GFR, 20-65 mL/min per 1.73 m(2)) were recruited from 21 clinical centers throughout the United States and followed up for 3 to 6.4 years.
Participants were randomly assigned to 1 of 2 mean arterial pressure goals, 102 to 107 mm Hg (usual; n = 554) or 92 mm Hg or less (lower; n = 540), and to initial treatment with either a beta-blocker (metoprolol 50-200 mg/d; n = 441), an angiotensin-converting enzyme inhibitor (ramipril 2.5-10 mg/d; n = 436) or a dihydropyridine calcium channel blocker, (amlodipine 5-10 mg/d; n = 217). Open-label agents were added to achieve the assigned BP goals.
Rate of change in GFR (GFR slope); clinical composite outcome of reduction in GFR by 50% or more (or > or =25 mL/min per 1.73 m2) from baseline, ESRD, or death. Three primary treatment comparisons were specified: lower vs usual BP goal; ramipril vs metoprolol; and amlodipine vs metoprolol.
Achieved BP averaged (SD) 128/78 (12/8) mm Hg in the lower BP group and 141/85 (12/7) mm Hg in the usual BP group. The mean (SE) GFR slope from baseline through 4 years did not differ significantly between the lower BP group (-2.21 [0.17] mL/min per 1.73 m2 per year) and the usual BP group (-1.95 [0.17] mL/min per 1.73 m2 per year; P =.24), and the lower BP goal did not significantly reduce the rate of the clinical composite outcome (risk reduction for lower BP group = 2%; 95% confidence interval [CI], -22% to 21%; P =.85). None of the drug group comparisons showed consistent significant differences in the GFR slope. However, compared with the metoprolol and amlodipine groups, the ramipril group manifested risk reductions in the clinical composite outcome of 22% (95% CI, 1%-38%; P =.04) and 38% (95% CI, 14%-56%; P =.004), respectively. There was no significant difference in the clinical composite outcome between the amlodipine and metoprolol groups.
No additional benefit of slowing progression of hypertensive nephrosclerosis was observed with the lower BP goal. Angiotensin-converting enzyme inhibitors appear to be more effective than beta-blockers or dihydropyridine calcium channel blockers in slowing GFR decline.
在美国,高血压是终末期肾病(ESRD)的主要病因,尚无已知的预防导致ESRD的病情逐渐恶化的治疗方法。
比较两种血压(BP)控制水平和三类抗高血压药物对高血压患者肾小球滤过率(GFR)下降的影响。
1995年2月至1998年9月进行的随机3×2析因试验。
从美国21个临床中心招募了1094名年龄在18至70岁之间患有高血压肾病(GFR为20 - 65 mL/(min·1.73 m²))的非裔美国人,并随访3至6.4年。
参与者被随机分配到两个平均动脉压目标之一,即102至107 mmHg(常规目标;n = 554)或92 mmHg及以下(较低目标;n = 540),并初始接受β受体阻滞剂(美托洛尔50 - 200 mg/d;n = 441)、血管紧张素转换酶抑制剂(雷米普利2.5 - 10 mg/d;n = 436)或二氢吡啶类钙通道阻滞剂(氨氯地平5 - 10 mg/d;n = 217)中的一种进行治疗。添加开放标签药物以达到指定的血压目标。
GFR的变化率(GFR斜率);GFR从基线水平降低50%或更多(或≥25 mL/(min·1.73 m²))、ESRD或死亡的临床综合结局。指定了三项主要治疗比较:较低血压目标与常规血压目标;雷米普利与美托洛尔;氨氯地平与美托洛尔。
较低血压组达到的平均(标准差)血压为128/78(12/8)mmHg,常规血压组为141/85(12/7)mmHg。从基线到4年,较低血压组(每年-2.21[0.17]mL/(min·1.73 m²))和常规血压组(每年-1.95[0.17]mL/(min·1.73 m²);P = 0.24)的平均(标准误)GFR斜率无显著差异,较低血压目标并未显著降低临床综合结局的发生率(较低血压组风险降低2%;95%置信区间[CI],-22%至21%;P = 0.85)。药物组之间的比较在GFR斜率方面均未显示出一致的显著差异。然而,与美托洛尔组和氨氯地平组相比,雷米普利组在临床综合结局方面的风险降低分别为22%(95%CI,1% - 38%;P = 0.04)和38%(95%CI,14% - 56%;P = 0.004)。氨氯地平组和美托洛尔组在临床综合结局方面无显著差异。
较低血压目标并未观察到对减缓高血压性肾硬化进展有额外益处。血管紧张素转换酶抑制剂在减缓GFR下降方面似乎比β受体阻滞剂或二氢吡啶类钙通道阻滞剂更有效。