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  lüll Direct renin inhibition: focus on aliskiren Pool JLJ Manag Care Pharm  2007[Oct]; 13 (8 Suppl B): 21-33BACKGROUND: Despite the availability of many effective, well-tolerated drugs, a  significant proportion of treated hypertensive patients still have uncontrolled  high blood pressure (BP) and thus face serious morbidity and mortality. The  renin-angiotensin aldosterone system (RAAS) is a key target for BP control and  for cardiovascular and renal protection. Renin controls the rate-limiting step in  the RAAS cascade and hence is the optimal target for RAAS suppression. Aliskiren  is the first direct renin inhibitor (DRI) to be approved by the U.S. Food and  Drug Administration and the European Medicines Agency for treating hypertension.  OBJECTIVE: To provide an overview of the pharmacology, pharmacokinetics,  preclinical, and clinical efficacy and safety data on the DRI aliskiren. RESULTS:  Approximately 70% of essential hypertension is associated with elevated renin  levels. Aliskiren is a potent and highly specific inhibitor of renin, with oral  bioavailability of 2.6% and an elimination half-life of 40 hours, making it  suitable for once-daily oral administration. Aliskiren dose-dependently reduced  BP, inhibited plasma renin activity (PRA), attenuated renal damage in animal  models, and showed efficient and longer- lasting blockade of the RAAS in  normotensive human subjects compared with other RAAS inhibitors. The clinical  efficacy and safety of aliskiren have been evaluated both as monotherapy and in  combination with other antihypertensive agents in phase II and phase III trials  of patients with mild to severe hypertension. When used as monotherapy, aliskiren  led to significant dose-dependent reductions in BP from baseline that were  greater than those obtained with placebo and comparable with those achieved with  an angiotensin II receptor blocker (ARB). The combination of aliskiren with a  diuretic, a calcium channel blocker (CCB), an angiotensin-converting enzyme  inhibitor (ACEI), or an ARB generally had greater and longer-lasting BP-lowering  efficacy than did single agents alone. Aliskiren also countered the reactive  increase in PRA caused by diuretic, CC B, ACEI, and ARB therapy. Once-daily  treatment with aliskiren was well tolerated. CONCLUSIONS: As a DRI, aliskiren  blocks the RAAS more completely than do other current downstream RAAS inhibitors.  When used once daily, aliskiren is a safe and effective antihypertensive agent  that can be used as monotherapy or in combination with other agents to provide  additional options to improve BP control.|Amides/adverse effects/pharmacology/*therapeutic use[MESH]|Animals[MESH]|Antihypertensive Agents/*therapeutic use[MESH]|Drug Therapy, Combination[MESH]|Fumarates/adverse effects/pharmacology/*therapeutic use[MESH]|Humans[MESH]|Hypertension/*drug therapy[MESH]|Renin/*antagonists & inhibitors[MESH] |