Document Detail


Dual blockade of the renin-angiotensin-aldosterone system: beyond the ACE inhibitor and angiotensin-II receptor blocker combination.
MedLine Citation:
PMID:  19661925     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The renin-angiotensin-aldosterone system (RAAS), an important regulator of blood pressure as well as fluid and electrolyte balance, plays an important role in the pathophysiology of cardiovascular and kidney diseases. Blockade of the RAAS with angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin-II (ANG-II) receptor blockers (ARBs) lowers blood pressure, decreases morbidity and mortality in patients with chronic heart failure, and decreases proteinuria and the rate of decline in renal function in patients with chronic kidney disease. Although these drugs are highly effective and are widely used in the management of cardiovascular and kidney diseases, current treatment regimens with ACEIs and ARBs may not completely suppress the RAAS. Combinations of ACEIs and ARBs have been shown to be superior to either agent alone for some, but certainly not all, composite cardiovascular and kidney outcomes. With the growing appreciation of the role of aldosterone in the pathogenesis of cardiorenal diseases and the recent approval of the direct renin inhibitor (DRI), aliskiren, additional combination strategies have emerged that may offer novel ways to more fully suppress the RAAS. This review examines what is presently known about ACEI/ARB combination therapy and explores alternative combination strategies that include DRIs and mineralocorticoid receptor blockers (MRBs).
Authors:
Andrew S Bomback; Robert Toto
Related Documents :
7043495 - Evening primrose oil, a dietary prostaglandin precursor, diminishes vascular reactivity...
2839205 - Potent depressor action of leumorphin, a kappa-opioid agonist, in conscious rats.
8315515 - Slow developing pressor effect of angiotensin ii and vascular structure.
393505 - Effects of an angiotensin ii antagonist; [sarcosine 1, isoleucine 8] angiotensin ii, on...
16960515 - Moderate resistance training and vascular health in overweight women.
11525235 - Effects of cardiac glycosides on 24-h ambulatory blood pressure in healthy volunteers a...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2009-08-06
Journal Detail:
Title:  American journal of hypertension     Volume:  22     ISSN:  1941-7225     ISO Abbreviation:  Am. J. Hypertens.     Publication Date:  2009 Oct 
Date Detail:
Created Date:  2009-09-24     Completed Date:  2010-01-14     Revised Date:  2011-06-30    
Medline Journal Info:
Nlm Unique ID:  8803676     Medline TA:  Am J Hypertens     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1032-40     Citation Subset:  IM    
Affiliation:
Department of Medicine, Division of Nephrology, Columbia University College of Physicians and Surgeons, New York, New York, USA. asb68@columbia.edu
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Aldosterone / metabolism
Amides / therapeutic use
Angiotensin II Type 1 Receptor Blockers / therapeutic use*
Angiotensin-Converting Enzyme Inhibitors / therapeutic use*
Antihypertensive Agents / therapeutic use*
Cardiovascular Diseases / drug therapy
Dose-Response Relationship, Drug
Drug Therapy, Combination
Fumarates / therapeutic use
Humans
Kidney Diseases / drug therapy
Receptors, Mineralocorticoid / agonists
Renin-Angiotensin System / drug effects*
Chemical
Reg. No./Substance:
0/Amides; 0/Angiotensin II Type 1 Receptor Blockers; 0/Angiotensin-Converting Enzyme Inhibitors; 0/Antihypertensive Agents; 0/Fumarates; 0/Receptors, Mineralocorticoid; 0/aliskiren; 52-39-1/Aldosterone

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Heritability of blood pressure responses to cold pressor test in a Chinese population.
Next Document:  Compound ion salt, a novel low-sodium salt substitute: from animal study to community-based populati...