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Volume 72, Issue 1, Pages 81-87 (April 2006)


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Effect of rosuvastatin or atorvastatin on urinary albumin excretion and renal function in type 2 diabetic patients

on behalf of the URANUS study investigatorsJonathan SorofaCorresponding Author Informationemail address, Christian Berneb, Annica Siewert-Dellec, Leif Jørgensenc, Philip Sagera

Received 27 June 2005; received in revised form 26 August 2005; accepted 2 September 2005. published online 24 October 2005.

Abstract 

The effect of rosuvastatin or atorvastatin on urinary albumin excretion (UAE) was determined in type 2 diabetic patients. A randomized, double-blind, parallel-group, response-based design compared rosuvastatin 10mg (titrated to 40mg) with atorvastatin 10mg (titrated to 80mg) in type 2 diabetic patients with dyslipidemia, with dose titration to an LDL-C target of <3.0mmol/L. Overnight timed urine collections were obtained at baseline, 8 and 16 weeks to UAE. Glomerular filtration rate (GFR) was determined using the Modification of Diet in Renal Disease formula. Patients with paired, UAE collections of at least 8h duration were analyzed (n=344). No significant change from baseline in UAE was observed for either treatment group or between-treatment groups at 16 weeks, and median UAE for both treatment groups remained within normal limits (rosuvastatin 4.5μg/min, atorvastatin 5.0μg/min). A similar absence of change from baseline was observed for 51 patients with UAE above the normal range at study entry (>20μg/min). No significant change in GFR from baseline after 16 weeks was observed for either treatment group. These data provide reassurance that type 2 diabetic patients can be treated with higher efficacy statins without clinically meaningful effects on urinary albumin excretion.

a Cardiovascular Clinical Research, AstraZeneca LP, C4B-717, 1800 Concord Pike, Wilmington, DE 19803, USA

b Medicinkliniken, Akademiska Sjukhuset, Uppsala, Sweden

c AstraZeneca, Södertälje, Sweden

Corresponding Author InformationCorresponding author. Tel.: +1 302 885 0250; fax: +1 302 885 5450.

PII: S0168-8227(05)00368-2

doi:10.1016/j.diabres.2005.09.004


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