Belousov Iu B, Glezer M G, Tkhostova E B, Demidova M A
Ter Arkh. 2005;77(10):75-8.
To evaluate a hypotensive effect and metabolic neutrality and safety of ACE inhibitor moexipril in postmenopausal women with arterial hypertension (AH), influence on quality of life.
Thirty two hypertensive postmenopausal women (age 63.1 +/- 0.8 years) received moexipril for 4 months. The history of AH was 10.4 +/- 2.3 years, on the average. After a free of drugs week moexipril was given in a dose 7.5 mg/day with titration to 15 mg in 2 weeks and addition (if the target pressure was not achieved) of hydrochlorothiaside in a dose 12.5 mg. The examination included 24-h monitoring of blood pressure, estimation of microalbuminuria (MAU), endothelial function and blood biochemistry. Initially and after 4 weeks of the treatment quality of life was assessed (scales SF-36 and EuroQol).
The initial level of office BP was 164.33/94.50 mm Hg, in 3 months a target level was achieved (136/84 mm Hg). It persisted for the next month. Moexipril corrected endothelial function and vascular elasticity in all the patients. MAU fell from 28.28 to 8.10 mg/l. Quality of life improved. Lipid and carbohydrate changes were not registered.
Moexipril has a hypotensive and nephroprotective effects, improves endothelial function and quality of life in hypertensive postmenopausal women.
评估血管紧张素转换酶抑制剂莫昔普利对绝经后动脉高血压(AH)女性的降压效果、代谢中性及安全性,以及对生活质量的影响。
32例绝经后高血压女性(年龄63.1±0.8岁)接受莫昔普利治疗4个月。AH病史平均为10.4±2.3年。在停药1周后,给予莫昔普利7.5mg/天的剂量,2周内滴定至15mg,若未达到目标血压则加用(剂量为12.5mg)氢氯噻嗪。检查包括24小时血压监测、微量白蛋白尿(MAU)评估、内皮功能及血液生化检查。在治疗初始及4周后评估生活质量(采用SF-36量表和欧洲五维健康量表)。
初始诊室血压水平为164.33/94.50mmHg,3个月时达到目标水平(136/84mmHg),并在下个月持续保持。莫昔普利改善了所有患者的内皮功能和血管弹性。MAU从28.28mg/l降至8.10mg/l。生活质量得到改善。未发现脂质和碳水化合物的变化。
莫昔普利对绝经后高血压女性具有降压和肾保护作用,可改善内皮功能和生活质量。