Division of Nephrology, Phramongkutklao Hospital, Bangkok, Thailand.
The Second Affiliated Hospital of Medical College of Zhejiang University, Hangzhou, Zhejiang, China.
Am J Hypertens. 2017 Nov 6;30(12):1163-1169. doi: 10.1093/ajh/hpx111.
Systolic hypertension is common in elderly patients and remains a challenge to treat effectively. The efficacy and safety of sacubitril/valsartan (LCZ696), a first-in-class angiotensin receptor neprilysin inhibitor, vs. olmesartan was evaluated in elderly Asian patients (≥65 years) with systolic hypertension.
In this randomized, double-blind, 14-week study, patients initially received once-daily sacubitril/valsartan 100 mg or olmesartan 10 mg, increased to sacubitril/valsartan 200 mg or olmesartan 20 mg at week 4. At week 10, for patients with blood pressure (BP) >140/90 mm Hg, the doses were up-titrated to sacubitril/valsartan 400 mg or olmesartan 40 mg. The primary assessment was superiority of sacubitril/valsartan vs. olmesartan in reducing office mean sitting (ms) systolic BP (msSBP) from baseline at week 10. Secondary efficacy assessments included changes from baseline in ms diastolic BP (msDBP), ms pulse pressure (msPP), 24-hour mean ambulatory (ma) BP (maBP), and maPP at week 10; msBP and msPP at weeks 4 and 14.
Overall, 588 patients were randomized (mean age, 70.7 years; baseline msBP, 160.3/84.9 mm Hg; msPP, 75.4 mm Hg). At week 10, sacubitril/valsartan provided superior msSBP reductions vs. olmesartan (22.71 vs. 16.11 mm Hg, respectively; P < 0.001); similarly, reductions from baseline in other BP and PP assessments were significantly greater with sacubitril/valsartan. At week 14, despite more patients requiring up-titration in the olmesartan group, msBP and msPP reductions from baseline were significantly greater with sacubitril/valsartan. Both treatments were generally well-tolerated.
Sacubitril/valsartan is more effective than olmesartan in reducing BP in elderly Asian patients with systolic hypertension.
收缩期高血压在老年患者中很常见,仍然是一种有效的治疗挑战。评估新型血管紧张素受体脑啡肽酶抑制剂沙库巴曲缬沙坦(LCZ696)与奥美沙坦在亚洲老年(≥65 岁)收缩期高血压患者中的疗效和安全性。
在这项随机、双盲、14 周的研究中,患者最初每天接受一次沙库巴曲缬沙坦 100mg 或奥美沙坦 10mg,第 4 周增至沙库巴曲缬沙坦 200mg 或奥美沙坦 20mg。第 10 周时,对于血压(BP)>140/90mmHg 的患者,剂量增加至沙库巴曲缬沙坦 400mg 或奥美沙坦 40mg。主要评估是沙库巴曲缬沙坦优于奥美沙坦,从第 10 周的基线降低诊室平均坐位收缩压(msSBP)。次要疗效评估包括从基线开始的第 10 周的 ms 舒张压(msDBP)、ms 脉压(msPP)、24 小时平均动态(ma)BP(maBP)和 maPP 的变化;第 4 周和第 14 周的 msBP 和 msPP。
共有 588 名患者被随机分组(平均年龄 70.7 岁;基线 msBP 为 160.3/84.9mmHg;msPP 为 75.4mmHg)。第 10 周时,沙库巴曲缬沙坦组提供了优于奥美沙坦组的 msSBP 降低(分别为 22.71mmHg 和 16.11mmHg,P<0.001);同样,沙库巴曲缬沙坦组从基线开始的其他 BP 和 PP 评估的降低也显著更大。第 14 周时,尽管奥美沙坦组有更多的患者需要增加剂量,但沙库巴曲缬沙坦组从基线开始的 msBP 和 msPP 降低仍显著更大。两种治疗方法通常都有良好的耐受性。
在亚洲老年收缩期高血压患者中,沙库巴曲缬沙坦比奥美沙坦更有效地降低血压。