Effect of add-on aliskiren to type 1 angiotensin receptor blocker therapy on endothelial function and autonomic nervous system in hypertensive patients with ischemic heart disease

J Clin Hypertens (Greenwich). 2014 Aug;16(8):591-8. doi: 10.1111/jch.12366. Epub 2014 Jul 7.

Abstract

The aim of this study was to evaluate the add-on effect of aliskiren to valsartan on endothelial-dependent vasodilation in hypertensive patients with ischemic heart disease (IHD). After 4 weeks of treatment with 80 mg of valsartan, 28 patients were allocated to either continued treatment with valsartan or an add-on treatment with valsartan plus 150 mg of aliskiren. Aliskiren significantly decreased plasma renin activity, whereas endothelium-dependent vasodilation measured by flow-mediated dilation (FMD) did not change. In contrast, heart rate significantly decreased (73.1 ± 9.8 to 66.3 ± 7.0 beats per minute at baseline and 24 weeks, respectively [P = .009]) and the standard deviation of the R-R intervals (SDNN) significantly increased in the aliskiren group. The add-on aliskiren to valsartan therapy may not improve endothelial functions, although it significantly reduced resting heart rate via regulation of the autonomic nervous system in hypertensive patients with IHD.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Amides / pharmacology*
  • Amides / therapeutic use
  • Angiotensin II Type 1 Receptor Blockers / pharmacology*
  • Angiotensin II Type 1 Receptor Blockers / therapeutic use
  • Antihypertensive Agents / pharmacology*
  • Antihypertensive Agents / therapeutic use
  • Autonomic Nervous System / drug effects*
  • Autonomic Nervous System / physiology
  • Comorbidity
  • Drug Therapy, Combination
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / physiology
  • Female
  • Fumarates / pharmacology*
  • Fumarates / therapeutic use
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Humans
  • Hypertension / drug therapy
  • Hypertension / epidemiology
  • Hypertension / physiopathology*
  • Male
  • Middle Aged
  • Myocardial Ischemia / drug therapy
  • Myocardial Ischemia / epidemiology
  • Myocardial Ischemia / physiopathology*
  • Renin / antagonists & inhibitors
  • Renin / metabolism
  • Tetrazoles / pharmacology*
  • Tetrazoles / therapeutic use
  • Treatment Outcome
  • Valine / analogs & derivatives*
  • Valine / pharmacology
  • Valine / therapeutic use
  • Valsartan
  • Vasodilation / drug effects
  • Vasodilation / physiology

Substances

  • Amides
  • Angiotensin II Type 1 Receptor Blockers
  • Antihypertensive Agents
  • Fumarates
  • Tetrazoles
  • aliskiren
  • Valsartan
  • Renin
  • Valine