Superior effect of an angiotensin-converting enzyme inhibitor over a diuretic for reducing aortic systolic pressure
- PMID: 17414675
- DOI: 10.1097/HJH.0b013e3280ac1533
Superior effect of an angiotensin-converting enzyme inhibitor over a diuretic for reducing aortic systolic pressure
Abstract
Background: In recent studies, benefit has been shown for angiotensin-converting enzyme (ACE) inhibitors and calcium antagonists over a beta-blocker in hypertension, through a greater reduction in aortic than brachial systolic and pulse pressure. No data are available on diuretics, even though these are the preferred initial treatment of patients with mild hypertension.
Methods: In this study, 101 patients with mild essential hypertension were randomly assigned to an 8-week period of monotherapy with enalapril 10 mg a day or indapamide 2.5 mg a day. Central as well as brachial systolic, augmented, and pulse pressure were determined using SphygmoCor, as in the REASON and CAFE trials.
Results: Enalapril and indapamide reduced brachial systolic, diastolic, mean and pulse pressure to the same extent, and the heart rate was unchanged. Although there was no difference in brachial pressure with enalapril and indapamide, enalapril caused a greater fall in estimated aortic systolic, and pulse pressures. The augmentation index, an index of wave reflection, fell from 33.7 to 28.3% with enalapril but was unchanged with indapamide.
Conclusion: Results infer a reduction in wave reflection with enalapril, causing a fall in aortic pressure augmentation, and a corresponding fall in aortic systolic and pulse pressure. These were not apparent from brachial cuff measurements. Results show that a diuretic, like a beta-blocker agent, is not as effective a therapy as an ACE inhibitor in reducing aortic systolic and pulse pressure, and that the difference is not attributable to a change in heart rate.
Comment in
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Bashing diuretics or failure of surrogate endpoint?J Hypertens. 2007 May;25(5):949-50. doi: 10.1097/HJH.0b013e32813a32a0. J Hypertens. 2007. PMID: 17414656 No abstract available.
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