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Establishing a new option for target-organ protection: rationale for ARB plus ACE inhibitor combination therapy.
Cohn, Jay N; Goldman, Jesse M.
Affiliation
  • Cohn JN; Rasmussen Center for Cardiovascular Disease Prevention, Cardiovascular Division, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA. cohnx001@tc.umn.edu
Am J Hypertens ; 21(3): 248-56, 2008 Mar.
Article in En | MEDLINE | ID: mdl-18219303
ABSTRACT
Activation of the renin-angiotensin system (RAS) plays an important role in the promotion of cardiovascular disease and target-organ damage, mediated in part by hypertension. Combination therapy targeting RAS activation may reduce target-organ damage and provide superior blood pressure (BP) control; combining angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) represents one possible approach. In monotherapy studies, both ACE inhibitors and ARBs have demonstrated similar positive effects on BP and on RAS-related target-organ damage, including nephropathy and congestive heart failure. Studies of combination therapy, most of which involved addition of an ARB to existing ACE inhibitor therapy, have demonstrated benefits among patients with congestive heart failure and renal disease. However, variances in study design and populations, dosing and titration methods, and clinical end points, in addition to inherent differences between agents, limit the ability to reach clinically meaningful conclusions about the value of dual RAS inhibition. Trials designed to document such efficacy are currently underway.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Angiotensin-Converting Enzyme Inhibitors / Angiotensin II Type 1 Receptor Blockers / Hypertension Type of study: Etiology_studies Limits: Humans Language: En Journal: Am J Hypertens Journal subject: ANGIOLOGIA Year: 2008 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Angiotensin-Converting Enzyme Inhibitors / Angiotensin II Type 1 Receptor Blockers / Hypertension Type of study: Etiology_studies Limits: Humans Language: En Journal: Am J Hypertens Journal subject: ANGIOLOGIA Year: 2008 Document type: Article Affiliation country: Estados Unidos