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1.
Kidney Int Suppl ; (83): S77-85, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12864880

ABSTRACT

The leading cause of end-stage renal disease (ESRD) is diabetic nephropathy. Interventions that prevent or palliate renal disease have a positive impact by improving patient care and diminishing healthcare costs. The following review summarizes clinical trals that evaluated treatment in various patient populations including Type 2 diabetic patients with microalbuminuria, subjects with proteinuric non-diabetic nephropathies, and Type 1 and Type 2 diabetic patients with overt nephropathy. These clinical trials have demonstrated that agents directly affecting the renin-angiotensin-aldosterone system provide renal protection beyond that attributable to blood pressure control.


Subject(s)
Angiotensin II Type 2 Receptor Blockers , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Antihypertensive Agents/therapeutic use , Diabetic Nephropathies/drug therapy , Kidney Failure, Chronic/prevention & control , Clinical Trials as Topic , Humans
2.
J Clin Pharmacol ; 43(6): 591-603, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12817522

ABSTRACT

The pharmacokinetics and pharmacodynamics of 7 days of treatment with losartan 50 mg/hydrochlorothiazide 12.5 mg were evaluated in 14 patients with normal renal function and in 12 patients with mild to moderate renal impairment. The efficacy of losartan 50 mg/hydrochlorothiazide 12.5 mg titrated to losartan 100 mg/hydrochlorothiazide 25 mg was examined in 32 hypertensive patients with mild to moderate renal impairment who were treated for 12 weeks. Safety was assessed in both studies by the incidence of adverse experiences. After 7 days of treatment, the AUC for losartan, E-3174, and hydrochlorothiazide was slightly higher in patients with mild to moderate renal impairment, but the reduction in blood pressure (BP) after 7 days was not different between the two groups. The final (week 12) mean reductions in trough sitting diastolic and systolic BP were 15.0 +/- 7.1 mmHg (p < 0.01) and 20.8 +/- 16.7 mmHg (p < 0.01), respectively. There were no observed increases in drug-related adverse experiences in either study. Overall, the combination of losartan/hydrochlorothiazide was effective in lowering blood pressure and was well tolerated in patients with mild to moderate renal impairment.


Subject(s)
Antihypertensive Agents , Hydrochlorothiazide , Hypertension , Losartan , Renal Insufficiency/complications , Antihypertensive Agents/adverse effects , Antihypertensive Agents/pharmacokinetics , Antihypertensive Agents/therapeutic use , Area Under Curve , Drug Administration Schedule , Drug Therapy, Combination , Female , Half-Life , Humans , Hydrochlorothiazide/adverse effects , Hydrochlorothiazide/pharmacokinetics , Hydrochlorothiazide/therapeutic use , Hypertension/complications , Hypertension/drug therapy , Hypertension/metabolism , Losartan/adverse effects , Losartan/pharmacokinetics , Losartan/therapeutic use , Male , Metabolic Clearance Rate , Middle Aged , Renal Insufficiency/metabolism , Safety
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