ACE inhibitors - Angiotensin II receptor antagonists: A useful combination therapy for ischemic heart disease

16Citations
Citations of this article
51Readers
Mendeley users who have this article in their library.

Abstract

Morbidity and mortality from cardiovascular diseases are still high, even with the use of the best available therapies. There is mounting evidence that excessive renin-angiotensin system activation triggers much of the damaging and progressive nature of cardiovascular and kidney diseases through expression of angiotensin II. Moreover, angiotensin II play a major role in the development of end organ damage through a variety of inflammatory mechanisms. Today, angiotensins-converting enzyme (ACE) inhibitors and angiotensin II receptor antagonists have clearly demonstrated their efficacy in preventing target organ damage and in reducing cardiovascular morbidity and mortality in ischemic heart disease (IHD). Moreover, the development of angiotensin II receptor antagonists has enabled a large gain in tolerability and safety. Several clinical trials have firmly established that these drugs act on the renin-angiotensin system, reducing the incidence of coronary events with monotherapy and combination therapy. In this review we summarize the role mono- and combined therapy of ACE inhibitors and angiotensin II receptor antagonists play in ischemic heart disease. In this respect the review will improve ideas for developing new formulations with combinations of these drugs in the future. © 2010 Mohamed Saleem et al, publisher and licensee Dove Medical Press Ltd.

Cite

CITATION STYLE

APA

Mohamed Saleem, T. S., Bharani, K., & Gauthaman, K. (2010). ACE inhibitors - Angiotensin II receptor antagonists: A useful combination therapy for ischemic heart disease. Open Access Emergency Medicine. Dove Medical Press Ltd. https://doi.org/10.2147/oaem.s10507

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free