Literature DB >> 18625162

Direct renin inhibition: an analysis of possible benefits.

Brian K Dockery1, John D Bisognano.   

Abstract

The US Food and Drug Administration's approval in March 2007 of aliskiren, the first commercially available direct renin inhibitor, for the treatment of hypertension met with great enthusiasm. Clinical trials have demonstrated it to be as effective as other commonly prescribed antihypertensive agents with few side effects. Preclinical studies in genetically manipulated rats have shown it to be effective in reversing angiotensin II-induced cardiac and renal damage. Despite the notable absence of human clinical data for this agent, many clinicians have touted aliskiren as the ideal agent to achieve additional suppression of the renin-angiotensin-aldosterone system (RAAS) as a means to reduce the morbidity and mortality of chronic diseases of the cardiovascular and renal systems. Clinical studies are ongoing and future studies are planned to prove its effectiveness in several chronic diseases known to be related to RAAS activation.

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Year:  2008        PMID: 18625162     DOI: 10.1007/s11906-008-0058-2

Source DB:  PubMed          Journal:  Curr Hypertens Rep        ISSN: 1522-6417            Impact factor:   5.369


  43 in total

1.  Limitation of excessive extracellular matrix turnover may contribute to survival benefit of spironolactone therapy in patients with congestive heart failure: insights from the randomized aldactone evaluation study (RALES). Rales Investigators.

Authors:  F Zannad; F Alla; B Dousset; A Perez; B Pitt
Journal:  Circulation       Date:  2000-11-28       Impact factor: 29.690

2.  Efficacy and safety of combined use of aliskiren and valsartan in patients with hypertension: a randomised, double-blind trial.

Authors:  Suzanne Oparil; Steven A Yarows; Samir Patel; Hui Fang; Jack Zhang; Andrew Satlin
Journal:  Lancet       Date:  2007-07-21       Impact factor: 79.321

3.  Structure of recombinant human renin, a target for cardiovascular-active drugs, at 2.5 A resolution.

Authors:  A R Sielecki; K Hayakawa; M Fujinaga; M E Murphy; M Fraser; A K Muir; C T Carilli; J A Lewicki; J D Baxter; M N James
Journal:  Science       Date:  1989-03-10       Impact factor: 47.728

4.  Functional evidence for a role of vascular chymase in the production of angiotensin II in isolated human arteries.

Authors:  V Richard; S Hurel-Merle; E Scalbert; G Ferry; F Lallemand; J P Bessou; C Thuillez
Journal:  Circulation       Date:  2001-08-14       Impact factor: 29.690

5.  Renal vascular responses to renin inhibition with zankiren in men.

Authors:  N D Fisher; N Hollenberg
Journal:  Clin Pharmacol Ther       Date:  1995-03       Impact factor: 6.875

Review 6.  Clinical pharmacokinetics and efficacy of renin inhibitors.

Authors:  G A Rongen; J W Lenders; P Smits; T Thien
Journal:  Clin Pharmacokinet       Date:  1995-07       Impact factor: 6.447

7.  Aliskiren, an oral renin inhibitor, provides dose-dependent efficacy and sustained 24-hour blood pressure control in patients with hypertension.

Authors:  Byung-Hee Oh; Jerry Mitchell; James R Herron; Jenny Chung; Mahmudul Khan; Deborah L Keefe
Journal:  J Am Coll Cardiol       Date:  2007-03-20       Impact factor: 24.094

Review 8.  Aliskiren: a review of its use in the management of hypertension.

Authors:  James E Frampton; Monique P Curran
Journal:  Drugs       Date:  2007       Impact factor: 9.546

9.  Evidence of a partial escape of renin-angiotensin-aldosterone blockade in patients with acute myocardial infarction treated with ACE inhibitors.

Authors:  C Borghi; S Boschi; E Ambrosioni; G Melandri; A Branzi; B Magnani
Journal:  J Clin Pharmacol       Date:  1993-01       Impact factor: 3.126

10.  Renin increases mesangial cell transforming growth factor-beta1 and matrix proteins through receptor-mediated, angiotensin II-independent mechanisms.

Authors:  Y Huang; S Wongamorntham; J Kasting; D McQuillan; R T Owens; L Yu; N A Noble; W Border
Journal:  Kidney Int       Date:  2006-01       Impact factor: 18.998

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