Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Clin Drug Investig. 2011;31(4):237-45. doi: 10.2165/11586510-000000000-00000.
Angiotensin II type 1 (AT1) receptor antagonists (angiotensin receptor blockers [ARBs]) are widely used for the treatment of not only hypertension but also cardiac dysfunction. B-type natriuretic peptide (BNP) is secreted mainly by the cardiac ventricle and plays an important role in the regulation of blood pressure (BP) and body fluid. It has been established that the plasma level of BNP is increased in patients with chronic heart failure in proportion to the severity of cardiac dysfunction. Because cardiac dysfunction is closely associated with a high risk of mortality in patients with diabetes mellitus, early identification and prevention of cardiac dysfunction are important. The objective of this study was to determine the effects of olmesartan medoxomil, a novel ARB, on the plasma level of BNP in hypertensive patients with type 2 diabetes.
This was a preliminary, prospective, observational, open-label study. Sixty-eight type 2 diabetic patients with hypertension (systolic BP [SBP]≥140 mmHg or diastolic BP [DBP]≥90 mmHg) received olmesartan medoxomil 10–20 mg/day for 24 weeks. Plasma levels of BNP, as well as several clinical parameters of glycaemic control and lipid metabolism, were compared before and after 24 weeks of treatment. Another group consisting of 22 age- and body mass index-matched subjects not treated with olmesartan medoxomil was observed for reference purposes.
In the olmesartan medoxomil group, mean±SD SBP decreased from 152.8±16.4 at baseline to 146.8±14.4 mmHg after 24 weeks' treatment (p<0.05); similarly, mean±SD DBP decreased from 85.6±10.5 to 81.3±11.6 mmHg (p<0.05). In 53 subjects in whom plasma levels of BNP could be measured both before and after treatment, mean±SD BNP decreased from 41.3±49.9 to 32.5±36.3 pg/mL (p<0.05). Change in plasma BNP level over the 24-week treatment period in the olmesartan medoxomil group was not correlated with change in SBP or DBP. Multiple regression analysis revealed that change in plasma BNP level was not correlated with baseline value of or change in any other parameters. No other parameters in the olmesartan medoxomil group, and no parameters in the non-olmesartan medoxomil reference group, showed significant changes.
The current preliminary study showed that olmesartan medoxomil treatment might decrease plasma BNP levels, independent of its BP-lowering effect, in hypertensive patients with type 2 diabetes.
血管紧张素 II 型 1(AT1)受体拮抗剂(血管紧张素受体阻滞剂[ARB])不仅广泛用于治疗高血压,也用于治疗心脏功能障碍。B 型利钠肽(BNP)主要由心室分泌,在调节血压(BP)和体液方面发挥重要作用。已经证实,慢性心力衰竭患者的 BNP 血浆水平随着心脏功能障碍的严重程度而增加。由于心脏功能障碍与糖尿病患者的高死亡率密切相关,因此早期识别和预防心脏功能障碍非常重要。本研究的目的是确定新型 ARB——奥美沙坦酯对 2 型糖尿病高血压患者 BNP 血浆水平的影响。
这是一项初步的、前瞻性的、观察性的、开放标签研究。68 例患有高血压(收缩压[SBP]≥140mmHg 或舒张压[DBP]≥90mmHg)的 2 型糖尿病患者接受奥美沙坦酯 10-20mg/天治疗 24 周。在治疗 24 周前后比较 BNP 等血糖控制和脂质代谢的几个临床参数的血浆水平。另一个由 22 名年龄和体重指数匹配且未接受奥美沙坦酯治疗的患者组成的对照组用于参考。
在奥美沙坦酯组中,平均收缩压从基线时的 152.8±16.4mmHg 下降到治疗 24 周后的 146.8±14.4mmHg(p<0.05);同样,平均舒张压从 85.6±10.5mmHg 下降到 81.3±11.6mmHg(p<0.05)。在 53 例可同时测量治疗前后 BNP 血浆水平的患者中,平均 BNP 从 41.3±49.9pg/mL 下降到 32.5±36.3pg/mL(p<0.05)。奥美沙坦酯组治疗 24 周期间 BNP 血浆水平的变化与 SBP 或 DBP 的变化无关。多变量回归分析显示,BNP 血浆水平的变化与基线值或任何其他参数的变化均无关。奥美沙坦酯组的其他参数和非奥美沙坦酯参考组的参数均无显著变化。
本初步研究表明,奥美沙坦酯治疗可能降低 2 型糖尿病高血压患者的 BNP 血浆水平,独立于其降压作用。