volume 345 issue 12 pages 870-878

The Effect of Irbesartan on the Development of Diabetic Nephropathy in Patients with Type 2 Diabetes

HANS-HENRIK PARVING 1
Hendrik Lehnert 2
Jens Bröchner-Mortensen 3
RAMON GOMIS 4
Steen Andersen 5
Peter Arner 6
Publication typeJournal Article
Publication date2001-09-20
scimago Q1
wos Q1
SJR19.076
CiteScore96.4
Impact factor78.5
ISSN00284793, 15334406
PubMed ID:  11565519
General Medicine
Abstract
Microalbuminuria and hypertension are risk factors for diabetic nephropathy. Blockade of the renin-angiotensin system slows the progression to diabetic nephropathy in patients with type 1 diabetes, but similar data are lacking for hypertensive patients with type 2 diabetes. We evaluated the renoprotective effect of the angiotensin-II-receptor antagonist irbesartan in hypertensive patients with type 2 diabetes and microalbuminuria.A total of 590 hypertensive patients with type 2 diabetes and microalbuminuria were enrolled in this multinational, randomized, double-blind, placebo-controlled study of irbesartan, at a dose of either 150 mg daily or 300 mg daily, and were followed for two years. The primary outcome was the time to the onset of diabetic nephropathy, defined by persistent albuminuria in overnight specimens, with a urinary albumin excretion rate that was greater than 200 microg per minute and at least 30 percent higher than the base-line level.The base-line characteristics in the three groups were similar. Ten of the 194 patients in the 300-mg group (5.2 percent) and 19 of the 195 patients in the 150-mg group (9.7 percent) reached the primary end point, as compared with 30 of the 201 patients in the placebo group (14.9 percent) (hazard ratios, 0.30 [95 percent confidence interval, 0.14 to 0.61; P< 0.001] and 0.61 [95 percent confidence interval, 0.34 to 1.08; P=0.081 for the two irbesartan groups, respectively). The average blood pressure during the course of the study was 144/83 mm Hg in the placebo group, 143/83 mm Hg in the 150-mg group, and 141/83 mm Hg in the 300-mg group (P=0.004 for the comparison of systolic blood pressure between the placebo group and the combined irbesartan groups). Serious adverse events were less frequent among the patients treated with irbesartan (P=0.02).Irbesartan is renoprotective independently of its blood-pressure-lowering effect in patients with type 2 diabetes and microalbuminuria.
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PARVING H. et al. The Effect of Irbesartan on the Development of Diabetic Nephropathy in Patients with Type 2 Diabetes // New England Journal of Medicine. 2001. Vol. 345. No. 12. pp. 870-878.
GOST all authors (up to 50) Copy
PARVING H., Lehnert H., Bröchner-Mortensen J., GOMIS R., Andersen S., Arner P. The Effect of Irbesartan on the Development of Diabetic Nephropathy in Patients with Type 2 Diabetes // New England Journal of Medicine. 2001. Vol. 345. No. 12. pp. 870-878.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1056/NEJMoa011489
UR - https://doi.org/10.1056/NEJMoa011489
TI - The Effect of Irbesartan on the Development of Diabetic Nephropathy in Patients with Type 2 Diabetes
T2 - New England Journal of Medicine
AU - PARVING, HANS-HENRIK
AU - Lehnert, Hendrik
AU - Bröchner-Mortensen, Jens
AU - GOMIS, RAMON
AU - Andersen, Steen
AU - Arner, Peter
PY - 2001
DA - 2001/09/20
PB - Massachusetts Medical Society
SP - 870-878
IS - 12
VL - 345
PMID - 11565519
SN - 0028-4793
SN - 1533-4406
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2001_PARVING,
author = {HANS-HENRIK PARVING and Hendrik Lehnert and Jens Bröchner-Mortensen and RAMON GOMIS and Steen Andersen and Peter Arner},
title = {The Effect of Irbesartan on the Development of Diabetic Nephropathy in Patients with Type 2 Diabetes},
journal = {New England Journal of Medicine},
year = {2001},
volume = {345},
publisher = {Massachusetts Medical Society},
month = {sep},
url = {https://doi.org/10.1056/NEJMoa011489},
number = {12},
pages = {870--878},
doi = {10.1056/NEJMoa011489}
}
MLA
Cite this
MLA Copy
PARVING, HANS-HENRIK, et al. “The Effect of Irbesartan on the Development of Diabetic Nephropathy in Patients with Type 2 Diabetes.” New England Journal of Medicine, vol. 345, no. 12, Sep. 2001, pp. 870-878. https://doi.org/10.1056/NEJMoa011489.