Addition of 300 mg Irbesartan to usual antihypertensive therapy in type 1 diabetic nephropathy induced a 37% mean reduction in albuminuria (95% CI 20-49, P<0.001).
RCT (n=21)
Double-blind
Randomized crossover
Does irbesartan added to ACE inhibitors and diuretics reduce albuminuria and blood pressure in type 1 patients with diabetic nephropathy?
Dual blockade of the renin-angiotensin system with irbesartan added to ACE inhibitors significantly reduces albuminuria and blood pressure in type 1 diabetic nephropathy, though potassium monitoring is required.
Effect estimate: 37% reduction (95% CI 20-49)
Absolute Event Rate: 996% vs 1574%
p-value: p=<0.001
BACKGROUND: Albuminuria and hypertension are predictors of poor renal and cardiovascular outcome in patients with diabetes. Approximately 30% of type 1 patients with diabetic nephropathy (DN) have albuminuria >1 g/day, and blood pressure >135 and/or >85 mmHg despite antihypertensive therapy with recommended doses of ACE inhibitor (ACEI) and diuretics. We tested the effect of dual blockade of the renin-angiotensin system (RAS) in these patients. METHODS: We performed a randomised double blind crossover trial with 2 months treatment with Irbesartan 300 mg o.d. and placebo added on top of previous antihypertensive treatment. We included 21 type 1 patients with DN responding insufficiently to ACEI and diuretics, as defined above. At the end of each treatment period, albuminuria, 24-h blood pressure and glomerular filtration rate (GFR) were measured. RESULTS: Addition of 300 mg Irbesartan to the patients' usual antihypertensive therapy induced a mean reduction in albuminuria of 37% (95% CI 20-49, P<0.001); from 1574 mg/24 h (95% CI 1162-2132) to 996 mg/24 h (95% CI 699-1419), a reduction in 24-h blood pressure of 8 mmHg systolic (95% CI -2 to 18) and 5 mmHg diastolic (95% CI 1-9) (P=0.11 and 0.01, respectively) (from placebo, mean (SE) 146 (4)/80 (2) mmHg). GFR remained unchanged. Serum potassium increased (mean 4.3 to 4.6 mmol/l, P=0.02). Intervention to reduce serum potassium was needed in two patients with GFR <35 ml/min/1.73 m(2). Otherwise the dual blockade with Irbesartan was safe and well tolerated. CONCLUSIONS: Dual blockade of the RAS may offer additional renal and cardiovascular protection in type 1 patients with DN responding insufficiently to conventional antihypertensive therapy, including recommended doses of ACEI and diuretics.
Peter Karl Jacobsen (Sat,) conducted a rct in Type 1 diabetic nephropathy (n=21). Irbesartan vs. Placebo was evaluated on Albuminuria (mg/24 h) (37% reduction, 95% CI 20-49, p=<0.001). Addition of 300 mg Irbesartan to usual antihypertensive therapy in type 1 diabetic nephropathy induced a 37% mean reduction in albuminuria (95% CI 20-49, P<0.001).
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