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Additive antiproteinuric effect of combined ACE inhibition and angiotensin II receptor blockade

 

作者: Paolo Ferrari,   Hans-Peter Marti,   Marc Pfister,   Felix Frey,  

 

期刊: Journal of Hypertension  (OVID Available online 2002)
卷期: Volume 20, issue 1  

页码: 125-130

 

ISSN:0263-6352

 

年代: 2002

 

出版商: OVID

 

关键词: nephropathy;proteinuria;hypertension;glomerular filtration rate;irbesartan;fosinopril

 

数据来源: OVID

 

摘要:

BackgroundLimitation of systemic and glomerular hypertension reduces urinary protein excretion and prevents renal function deterioration.ObjectiveTo investigate whether, in hypertensive patients with glomerulonephritis, a combination of an angiotensin converting enzyme inhibitor (ACEI, fosinopril 20 mg/day) with an angiotensin receptor blocker (ARB, irbesartan 150 mg/day) produces a more profound antiproteinuric effect than either drug alone.MethodsTen non-diabetic patients with glomerulonephritis, normal or slightly reduced but stable renal function (creatinine clearance 40–106 ml/min) without immunosuppression were studied. Clinical evaluations, 24 h blood pressure measurements and laboratory tests were performed as follows: (1) without medication (baseline) and in random sequence; (2) ACEI alone; (3) ARB alone; and (4) combination of ACEI + ARB. Each period lasted for 6 weeks, separated by three washout periods of 4 weeks each without therapy.ResultsACEI and ARB alone reduced proteinuria from 7.9±7.1 to 5.3±5.2 and 5.0±4.9 g/24 h (mean±SD), respectively. The combination of ACEI + ARB induced a more remarkable reduction of proteinuria in every patient (to 3.3±3.7 g/24 h) than either drug alone (P= 0.039 by ANOVA). The enhanced antiproteinuric effect of the combined therapy could not be attributed to a more pronounced reduction of 24 h mean arterial pressure (basal, 106±8; ACEI, 97±5; ARB, 98±5; ACEI+ARB, 95±5 mmHg) or creatinine clearance (basal, 77±27; ACEI, 73±31; ARB 80±30; ACEI + ARB, 73±32 ml/min).ConclusionsA combination of ACEI and ARB in patients with glomerulonephritis produces a more profound decrease in proteinuria than either drug alone. This additive antiproteinuric effect is not dependent on changes in blood pressure or creatinine clearance. A long-term controlled study is required to confirm the positive effect of this treatment on the progression of renal function loss.

 

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