Drugs with Blocking Effects on the Renin–Angiotensin–Aldosterone System Do Not Improve Endothelial Dysfunction Long-Term in Hypertensive Patients

Author:

Sozen AB1,Kayacan MS1,Tansel T2,Celebi A3,Kudat H1,Akkaya V1,Erk O1,Hatipoglu I4,Demirel S1

Affiliation:

1. Department of Internal Medicine, Istanbul Faculty of Medicine, University of Istanbul, Istanbul, Turkey

2. Department of Cardiovascular Surgery, Istanbul Faculty of Medicine, University of Istanbul, Istanbul, Turkey

3. Taksim State Hospital, Istanbul, Turkey

4. Department of Pharmacology, Istanbul Faculty of Medicine, University of Istanbul, Istanbul, Turkey

Abstract

In essential hypertension, endothelial dysfunction has been documented many times and correlates with prognosis. The influence of the renin–angiotensin–aldosterone system (RAAS) on endothelial dysfunction has also been studied. The present study investigated the duration of the effects of RAAS-blocking drugs on endothelial function in 44 consecutive, never-treated, outpatients with mild to moderate hypertension. Patients (11 per group) received an angiotensin receptor blocker (ARB; irbesartan 300 mg/day or valsartan 160 mg/day) or an angiotensin-converting enzyme inhibitor (ACEi; fosinopril 10 mg/day or quinapril 20 mg/day). If target blood pressure (< 140/90 mmHg) was not achieved, 12.5 mg/day hydrochlorothiazide was added. Endothelial function, assessed by measuring brachial artery diameter, did not change significantly after 6 weeks, 1 year or 3 years of treatment in any group. Across all groups, endothelium-dependent and-independent vasodilation increased significantly after 6 weeks but, after 1 year, decreased below baseline and was at a similar level after 3 years; groups did not differ significantly. Both ACEi and ARB had similar effects on endothelial function; improvement occurred at the start of treatmentbut was not maintained. Endothelial dysfunction may be a resistant or irreversible feature of hypertension, requiring high doses of antihypertensive drugs and above-average patient compliance.

Publisher

SAGE Publications

Subject

Biochemistry (medical),Cell Biology,Biochemistry,General Medicine

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