Aggressive antihypertensive strategies based on hydrochlorothiazide,candesartan or lisinopril decrease left ventricular mass and improve arterial compliance in patients with type II diabetes mellitus and hypertension

A.M. Spoelstra-de Man, F.J. van Ittersum, M.T. van Meeteren-Schram, O. Kamp, R.A. van Dijk, R.G. IJzerman, J.W. Twisk, C.B. Brouwer, C.D.A. Stehouwer

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18 Citations (Scopus)

Abstract

We investigated the effects of aggressive antihypertensive therapy based on hydrochlorothiazide, candesartan or lisinopril on left ventricular mass (LVM) index and arterial stiffness in hypertensive type II diabetic individuals. Seventy hypertensive type II diabetic individuals were treated with three antihypertensive strategies in a randomized, double-blind, double-dummy design. Blood pressure was titrated to levels below 130/85 mm Hg or a decrease in systolic pressure of 10% with a diastolic pressure below 85 mm Hg. After titration, patients were treated for 12 months. Mean blood pressures were 157/93, 151/94 and 149/93 mm Hg at baseline in the hydrochlorothiazide (n = 24), candesartan (n = 24) and lisinopril (n = 22) groups, and 135/80, 135/82 and 131/80 mm Hg after titration. About 70% reached target blood pressures, with the median use of three antihypertensive drugs. Left ventricular mass index and all estimates of arterial stiffness showed significant improvement after 12 months: that is, LVM index (-11 g/m
Original languageEnglish
Pages (from-to)599-611
Number of pages12
JournalJournal of human hypertension
Volume20
Issue number8
DOIs
Publication statusPublished - Aug 2006

Keywords

  • Adult
  • Aged
  • Antihypertensive Agents/pharmacology
  • Benzimidazoles/pharmacology
  • Blood Pressure/drug effects
  • Compliance
  • Diabetes Mellitus, Type 2/complications
  • Diastole/drug effects
  • Double-Blind Method
  • Humans
  • Hydrochlorothiazide/pharmacology
  • Hypertension/complications
  • Lisinopril/pharmacology
  • Middle Aged
  • Organ Size/drug effects
  • Systole/drug effects
  • Tetrazoles/pharmacology
  • Ventricular Function, Left/drug effects

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