Abstract | AIM: 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. MATERIAL AND METHODS: 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). RESULTS: 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. CONCLUSION:
Moexipril has a hypotensive and nephroprotective effects, improves endothelial function and quality of life in hypertensive postmenopausal women.
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Authors | Iu B Belousov, M G Glezer, E B Tkhostova, M A Demidova |
Journal | Terapevticheskii arkhiv
(Ter Arkh)
Vol. 77
Issue 10
Pg. 75-8
( 2005)
ISSN: 0040-3660 [Print] Russia (Federation) |
PMID | 16320692
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Angiotensin-Converting Enzyme Inhibitors
- Tetrahydroisoquinolines
- moexipril
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Topics |
- Angiotensin-Converting Enzyme Inhibitors
(therapeutic use)
- Female
- Follow-Up Studies
- Humans
- Hypertension
(drug therapy)
- Middle Aged
- Postmenopause
- Quality of Life
- Tetrahydroisoquinolines
(therapeutic use)
- Time Factors
- Treatment Outcome
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