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替米沙坦、雷米普利或二者联用对高血管风险人群的肾脏结局影响(ONTARGET研究):一项多中心、随机、双盲、对照试验

Renal outcomes with telmisartan, ramipril, or both, in people at high vascular risk (the ONTARGET study): a multicentre, randomised, double-blind, controlled trial.

作者信息

Mann Johannes F E, Schmieder Roland E, McQueen Matthew, Dyal Leanne, Schumacher Helmut, Pogue Janice, Wang Xingyu, Maggioni Aldo, Budaj Andrzej, Chaithiraphan Suphachai, Dickstein Kenneth, Keltai Matyas, Metsärinne Kaj, Oto Ali, Parkhomenko Alexander, Piegas Leopoldo S, Svendsen Tage L, Teo Koon K, Yusuf Salim

机构信息

Schwabing General Hospital, and KfH Kidney Centre, Ludwig Maximilians University Munchen, Germany.

出版信息

Lancet. 2008 Aug 16;372(9638):547-53. doi: 10.1016/S0140-6736(08)61236-2.

Abstract

BACKGROUND

Angiotensin receptor blockers (ARB) and angiotensin converting enzyme (ACE) inhibitors are known to reduce proteinuria. Their combination might be more effective than either treatment alone, but long-term data for comparative changes in renal function are not available. We investigated the renal effects of ramipril (an ACE inhibitor), telmisartan (an ARB), and their combination in patients aged 55 years or older with established atherosclerotic vascular disease or with diabetes with end-organ damage.

METHODS

The trial ran from 2001 to 2007. After a 3-week run-in period, 25 620 participants were randomly assigned to ramipril 10 mg a day (n=8576), telmisartan 80 mg a day (n=8542), or to a combination of both drugs (n=8502; median follow-up was 56 months), and renal function and proteinuria were measured. The primary renal outcome was a composite of dialysis, doubling of serum creatinine, and death. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00153101.

FINDINGS

784 patients permanently discontinued randomised therapy during the trial because of hypotensive symptoms (406 on combination therapy, 149 on ramipril, and 229 on telmisartan). The number of events for the composite primary outcome was similar for telmisartan (n=1147 [13.4%]) and ramipril (1150 [13.5%]; hazard ratio [HR] 1.00, 95% CI 0.92-1.09), but was increased with combination therapy (1233 [14.5%]; HR 1.09, 1.01-1.18, p=0.037). The secondary renal outcome, dialysis or doubling of serum creatinine, was similar with telmisartan (189 [2.21%]) and ramipril (174 [2.03%]; HR 1.09, 0.89-1.34) and more frequent with combination therapy (212 [2.49%]: HR 1.24, 1.01-1.51, p=0.038). Estimated glomerular filtration rate (eGFR) declined least with ramipril compared with telmisartan (-2.82 [SD 17.2] mL/min/1.73 m(2)vs -4.12 [17.4], p<0.0001) or combination therapy (-6.11 [17.9], p<0.0001). The increase in urinary albumin excretion was less with telmisartan (p=0.004) or with combination therapy (p=0.001) than with ramipril.

INTERPRETATION

In people at high vascular risk, telmisartan's effects on major renal outcomes are similar to ramipril. Although combination therapy reduces proteinuria to a greater extent than monotherapy, overall it worsens major renal outcomes.

摘要

背景

已知血管紧张素受体阻滞剂(ARB)和血管紧张素转换酶(ACE)抑制剂可降低蛋白尿。二者联合使用可能比单独使用任一药物更有效,但目前尚无关于肾功能比较性变化的长期数据。我们研究了雷米普利(一种ACE抑制剂)、替米沙坦(一种ARB)及其联合用药对55岁及以上患有已确诊动脉粥样硬化性血管疾病或伴有终末器官损害的糖尿病患者的肾脏影响。

方法

该试验从2001年持续至2007年。在为期3周的导入期后,25620名参与者被随机分配至每日服用10mg雷米普利组(n = 8576)、每日服用80mg替米沙坦组(n = 8542)或两种药物联合组(n = 8502;中位随访时间为56个月),并对肾功能和蛋白尿进行测量。主要肾脏结局是透析、血清肌酐翻倍和死亡的复合指标。分析采用意向性分析。本研究已在ClinicalTrials.gov注册,注册号为NCT00153101。

结果

在试验期间,784名患者因低血压症状而永久停止随机治疗(联合治疗组406例,雷米普利组149例,替米沙坦组229例)。替米沙坦组(n = 1147 [13.4%])和雷米普利组(1150 [13.5%];风险比[HR] 1.00,95%可信区间0.92 - 1.09)的复合主要结局事件数量相似,但联合治疗组增加(1233 [14.5%];HR 1.09,1.01 - 1.18,p = 0.037)。次要肾脏结局,即透析或血清肌酐翻倍,替米沙坦组(189 [2.21%])和雷米普利组(174 [2.03%];HR 1.09,0.89 - 1.34)相似,联合治疗组更常见(212 [2.49%]:HR 1.24,1.01 - 1.51,p = 0.038)。与替米沙坦(-2.82 [标准差17.2] mL/min/1.73m²对-4.12 [17.4],p < 0.0001)或联合治疗(-6.11 [17.9],p < 0.0001)相比,雷米普利组估算肾小球滤过率(eGFR)下降最少。替米沙坦组(p = 仅0.004)或联合治疗组(p = 0.001)的尿白蛋白排泄增加少于雷米普利组。

解读

在血管风险高的人群中,替米沙坦对主要肾脏结局的影响与雷米普利相似。虽然联合治疗比单一治疗能更大程度地降低蛋白尿,但总体上会使主要肾脏结局恶化。

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