|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Benefits of Candesartan added to ACE inhibitor in inhibition of progression of nephropathy A study assessed if adding Candesartan ( Atacand ) to ACE ( angiotensin-converting enzyme ) inhibitors would delay progression of nephropathy in hypertensive patient with non-diabetic renal disease. Candesartan cilexetil is an angiotensin II receptor antagonist ( ARB ). The study involved 90 hypertensive patients with chronic renal insufficiency, who had urinary protein excretion exceeding 1.0g/d despite treatment with ACE inhibitors. They were randomised to ACE inhibitor, either Benazepril ( Lotensin ) 2.5 to 10 mg daily or Trandolapril ( Mavik ) 2 to 4 mg daily, plus Candesartan ( 2 to 12 mg/d ), or to control group ( ACE inhibitors only ). The target blood pressure was 130/80 mmHg or less and the primary outcome was the changes in serum creatinine and the reduction of proteinuria. The mean duration of follow-up was 3.1 years. At years 2 and 3, systolic and diastolic blood pressure were reduced from 140/84 to 129/78 mmHg in the Candesartan group and from 135/85 to 130/80 mmHg in the control group ( p < 0.01 from baseline in both groups ). Serum creatinine increased from 3.02 to 3.38 mg/dl ( 267-299 micromol/L ) in the Candesartan group versus 3.00 to 4.48 mg/dl ( 265-396 micromol/L ) in the ACE inhibitor group ( p < 0.01 at year 3 in ACE inhibitor group ). The level of proteinuria declined in each group ( p < 0.05 ), the degree of reduction was greater in the Candesartan than in the control group ( p < 0.01 ). Pretreatment proteinuria correlated significantly with decline of renal function in both groups, whereas reduction of proteinuria negatively correlated with decline in renal function in the Candesartan group. The authors conclude “ Candesartan plus an ACE inhibitor was effective in slowing the progression of renal insufficiency in hypertensive patients with non-diabetic renal disease through reduction of proteinuria.” Source: Clinical Journal of the American Society of Nephrology, 2006 XagenaMedicine2006 « Home | Stampa articolo | Invia E-mail |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
© XAGENA 2010 - P.IVA: 04454930969 - REA: 1748680 - Tutti i diritti riservati |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||