Yusuf Salim, Diener Hans-Christoph, Sacco Ralph L, Cotton Daniel, Ounpuu Stephanie, Lawton William A, Palesch Yuko, Martin Reneé H, Albers Gregory W, Bath Philip, Bornstein Natan, Chan Bernard P L, Chen Sien-Tsong, Cunha Luis, Dahlöf Björn, De Keyser Jacques, Donnan Geoffrey A, Estol Conrado, Gorelick Philip, Gu Vivian, Hermansson Karin, Hilbrich Lutz, Kaste Markku, Lu Chuanzhen, Machnig Thomas, Pais Prem, Roberts Robin, Skvortsova Veronika, Teal Philip, Toni Danilo, VanderMaelen Cam, Voigt Thor, Weber Michael, Yoon Byung-Woo
Population Health Research Institute, McMaster University, Hamilton, ON, Canada.
N Engl J Med. 2008 Sep 18;359(12):1225-37. doi: 10.1056/NEJMoa0804593. Epub 2008 Aug 27.
Prolonged lowering of blood pressure after a stroke reduces the risk of recurrent stroke. In addition, inhibition of the renin-angiotensin system in high-risk patients reduces the rate of subsequent cardiovascular events, including stroke. However, the effect of lowering of blood pressure with a renin-angiotensin system inhibitor soon after a stroke has not been clearly established. We evaluated the effects of therapy with an angiotensin-receptor blocker, telmisartan, initiated early after a stroke.
In a multicenter trial involving 20,332 patients who recently had an ischemic stroke, we randomly assigned 10,146 to receive telmisartan (80 mg daily) and 10,186 to receive placebo. The primary outcome was recurrent stroke. Secondary outcomes were major cardiovascular events (death from cardiovascular causes, recurrent stroke, myocardial infarction, or new or worsening heart failure) and new-onset diabetes.
The median interval from stroke to randomization was 15 days. During a mean follow-up of 2.5 years, the mean blood pressure was 3.8/2.0 mm Hg lower in the telmisartan group than in the placebo group. A total of 880 patients (8.7%) in the telmisartan group and 934 patients (9.2%) in the placebo group had a subsequent stroke (hazard ratio in the telmisartan group, 0.95; 95% confidence interval [CI], 0.86 to 1.04; P=0.23). Major cardiovascular events occurred in 1367 patients (13.5%) in the telmisartan group and 1463 patients (14.4%) in the placebo group (hazard ratio, 0.94; 95% CI, 0.87 to 1.01; P=0.11). New-onset diabetes occurred in 1.7% of the telmisartan group and 2.1% of the placebo group (hazard ratio, 0.82; 95% CI, 0.65 to 1.04; P=0.10).
Therapy with telmisartan initiated soon after an ischemic stroke and continued for 2.5 years did not significantly lower the rate of recurrent stroke, major cardiovascular events, or diabetes. (ClinicalTrials.gov number, NCT00153062.)
中风后长期降低血压可降低复发性中风的风险。此外,在高危患者中抑制肾素 - 血管紧张素系统可降低包括中风在内的后续心血管事件的发生率。然而,中风后不久使用肾素 - 血管紧张素系统抑制剂降低血压的效果尚未明确确立。我们评估了中风后早期开始使用血管紧张素受体阻滞剂替米沙坦进行治疗的效果。
在一项涉及20332例近期发生缺血性中风患者的多中心试验中,我们将10146例患者随机分配接受替米沙坦(每日80毫克),10186例患者接受安慰剂。主要结局是复发性中风。次要结局是主要心血管事件(心血管原因死亡、复发性中风、心肌梗死或新发或恶化的心力衰竭)和新发糖尿病。
从中风到随机分组的中位间隔时间为15天。在平均2.5年的随访期间,替米沙坦组的平均血压比安慰剂组低3.8/2.0毫米汞柱。替米沙坦组共有880例患者(8.7%)发生后续中风,安慰剂组有934例患者(9.2%)发生后续中风(替米沙坦组的风险比为0.95;95%置信区间[CI]为0.86至1.04;P = 0.23)。替米沙坦组有1367例患者(13.5%)发生主要心血管事件,安慰剂组有1463例患者(14.4%)发生主要心血管事件(风险比为0.94;95%CI为0.87至1.01;P = 0.11)。替米沙坦组1.7%的患者和安慰剂组2.1%的患者发生新发糖尿病(风险比为0.82;95%CI为0.65至1.04;P = 0.10)。
缺血性中风后不久开始使用替米沙坦治疗并持续2.5年,并未显著降低复发性中风、主要心血管事件或糖尿病的发生率。(临床试验注册号,NCT00153062。)