Literature DB >> 17378372

Aliskiren, a novel oral renin inhibitor, provides dose-dependent efficacy and placebo-like tolerability in Japanese patients with hypertension.

Toshio Kushiro1, Hiroshige Itakura, Yoshihisa Abo, Hiromi Gotou, Shinji Terao, Deborah L Keefe.   

Abstract

Aliskiren is a novel orally active renin inhibitor for the treatment of hypertension. This study evaluated the antihypertensive efficacy, safety and tolerability of aliskiren in Japanese patients with hypertension. Forty hundred and fifty-five Japanese men and women with a mean sitting diastolic blood pressure of 95-110 mmHg were randomized to receive once-daily double-blind treatment for 8 weeks with aliskiren 75, 150 or 300 mg or placebo. Aliskiren produced significant, dose-dependent reductions in mean sitting diastolic blood pressure (p<0.0005 vs. placebo for each dose) and mean sitting systolic blood pressure (p<0.001 vs. placebo for each dose). The placebo-corrected reductions in mean sitting systolic/diastolic blood pressure were 5.7/4.0, 5.9/4.5 and 11.2/7.5 mmHg in the aliskiren 75, 150 and 300 mg groups, respectively. After 8 weeks' treatment, 27.8%, 47.8%, 48.2% and 63.7% of patients in the placebo and aliskiren 75, 150 and 300 mg groups, respectively, achieved a successful treatment response (diastolic blood pressure <90 mmHg and/or reduced by > or =10 mmHg from baseline; p<0.005 vs. placebo for each dose). Aliskiren treatment was well tolerated, with the incidence of adverse events reported in the active treatment groups (53-55%) being similar to that in the placebo group (50%). This study, which is the first to assess the antihypertensive efficacy and safety of aliskiren in Japanese patients with hypertension, demonstrates that the once-daily oral renin inhibitor aliskiren provides significant, dose-dependent reductions in blood pressure with placebo-like tolerability.

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Year:  2006        PMID: 17378372     DOI: 10.1291/hypres.29.997

Source DB:  PubMed          Journal:  Hypertens Res        ISSN: 0916-9636            Impact factor:   3.872


  26 in total

Review 1.  Aliskiren: the first direct renin inhibitor for hypertension.

Authors:  Anton H van den Meiracker; A H Jan Danser
Journal:  Curr Cardiol Rep       Date:  2007-11       Impact factor: 2.931

Review 2.  First renin inhibitor, aliskiren, for the treatment of hypertension.

Authors:  Darren M Triller; Samuel D Evang; Mina Tadrous; Bong Kyu Yoo
Journal:  Pharm World Sci       Date:  2008-09-18

3.  Efficacy analysis of the renoprotective effects of aliskiren in hypertensive patients with chronic kidney disease.

Authors:  Masanori Abe; Hiroko Suzuki; Kazuyoshi Okada; Noriaki Maruyama; Atsushi Inoshita; Seishiro Baba; Hiroyuki Takashima; Masayoshi Soma
Journal:  Heart Vessels       Date:  2012-05-23       Impact factor: 2.037

4.  The renin angiotensin system and the metabolic syndrome.

Authors:  Chih-Hong Wang; Feng Li; Nobuyuki Takahashi
Journal:  Open Hypertens J       Date:  2010

Review 5.  Aliskiren: a review of its use as monotherapy and as combination therapy in the management of hypertension.

Authors:  Sean T Duggan; Claudine M Chwieduk; Monique P Curran
Journal:  Drugs       Date:  2010-10-22       Impact factor: 9.546

Review 6.  New class of agents for treatment of hypertension: focus on direct renin inhibition.

Authors:  Roberto Fogari; Annalisa Zoppi
Journal:  Vasc Health Risk Manag       Date:  2010-10-05

7.  Oral renin inhibitors in clinical practice: a perspective review.

Authors:  Luca Bonanni; Michele Dalla Vestra
Journal:  Ther Adv Chronic Dis       Date:  2012-07       Impact factor: 5.091

8.  Cardiovascular risk in hypertension - can we ask for more? : focus on aliskiren.

Authors:  Massimo Volpe
Journal:  High Blood Press Cardiovasc Prev       Date:  2013-01-22

Review 9.  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

Review 10.  Nonclassical renin-angiotensin system and renal function.

Authors:  Mark C Chappell
Journal:  Compr Physiol       Date:  2012-10       Impact factor: 9.090

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