Low-dose ramipril reduces microalbuminuria in type 1 diabetic patients without hypertension: results of a randomized controlled trial
Low-dose ramipril reduces microalbuminuria in type 1 diabetic patients without hypertension: results of a randomized controlled trial. P O'Hare , R Bilbous , T Mitchell , C J O' Callaghan , G C Viberti and Ace-Inhibitor Trial to Lower Albuminuria in Normotensive Insulin-Dependent Subjects...
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Veröffentlicht in: | Diabetes care 2000-12, Vol.23 (12), p.1823-1829 |
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Sprache: | eng |
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Zusammenfassung: | Low-dose ramipril reduces microalbuminuria in type 1 diabetic patients without hypertension: results of a randomized controlled
trial.
P O'Hare ,
R Bilbous ,
T Mitchell ,
C J O' Callaghan ,
G C Viberti and
Ace-Inhibitor Trial to Lower Albuminuria in Normotensive Insulin-Dependent Subjects Study Group
Sir Quentin Hazel Institute of Molecular Medicine, University of Warwick, Gibbet Hill, Coventry, CV47AL, England, U.K.
Abstract
OBJECTIVE: To assess if low (1.25 mg) and/or standard (5 mg) doses of the ACE inhibitor ramipril could prevent progression
of microalbuminuria (incipient diabetic nephropathy) in normotensive type 1 diabetic patients. RESEARCH DESIGN AND METHODS:
This study, using a multicenter randomized placebo-controlled double-blind parallel group, was conducted over 2 years in 28
outpatient diabetic clinics in the U.K. and Ireland. We screened 334 type 1 diabetic patients with suspected microalbuminuria
and normal blood pressure; of these, 140 patients 18-65 years of age with a diagnosis of type 1 diabetes and persistent microalbuminuria,
defined as urinary albumin excretion rate (AER) of 20-200 microg/min, were enrolled in the study. RESULTS: The proportion
of patients progressing to macroalbuminuria was reduced in the ramipril groups but did not reach statistical significance
over 2 years. AER was significantly lower at year 2 in the combined ramipril-treated patients versus placebo (P = 0.013).
More patients on ramipril regressed to normoalbuminuria ( |
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ISSN: | 0149-5992 1935-5548 |
DOI: | 10.2337/diacare.23.12.1823 |