Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Gæde, P.
Right arrow Articles by Pedersen, O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gæde, P.
Right arrow Articles by Pedersen, O.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrol Dial Transplant (2003) 18: 539-542
© 2003 European Renal Association-European Dialysis and Transplant Association

Impact of low-dose acetylsalicylic acid on kidney function in type 2 diabetic patients with elevated urinary albumin excretion rate

Peter Gæde, Henrik Post Hansen, Hans-Henrik Parving and Oluf Pedersen

Steno Diabetes Center, Gentofte, Copenhagen, Denmark

Background. Low-dose treatment with acetylsalicylic acid (ASA) is widely recommended to type 2 diabetic patients as primary prevention against cardiovascular disease. High-dose treatment with cyclooxygenase inhibitors reduces urinary albumin excretion rate (AER) in type 1 diabetic patients with micro- or macroalbuminuria. Whether a similar effect on AER exists during low-dose ASA treatment, which may confound the diagnosis and monitoring of micro- and macroalbuminuria in type 2 diabetic patients, remains to be elucidated.

Methods. In a randomized, double-blind, crossover trial, 31 type 2 diabetic patients with elevated levels of AER (>30 mg/24 h) were, in random order, given ASA (150 mg/day) for 4 weeks followed by placebo for 4 weeks with a 2 week washout period or vice versa. At the end of each treatment period AER, glomerular filtration rate (GFR), blood pressure (BP), transcapillary escape rate (TERalb) of albumin and haemoglobin A1c (HbA1c) were measured.

Results. The following variables remained unchanged (mean (95% CI) unless otherwise noted) (ASA vs placebo, paired Student's t-test): AER (201 (119–341) vs 205 (124–340) mg/24 h (geometric mean, 95% CI); P=0.78), GFR (103 (94–111) vs 102 (93–110) ml/min; P=0.58), systolic BP (151 (146–158) vs 152 (146–158) mmHg; P=0.68), diastolic BP (87 (83–91) vs 87 (82–91) mmHg; P=0.88), TERalb (6.3 (5.7–6.9) vs 5.9 (5.1–6.7); P=0.45) and HbA1c (8.6 (8.1–9.0) vs 8.5 (8.1–9.0) %; P=0.60).

Conclusions. Low-dose treatment with 150 mg ASA daily does not have any impact on AER or GFR in type 2 diabetic patients with micro- or macroalbuminuria. Consequently, the widely recommended prescription of low-dose ASA as a primary and secondary prevention strategy against cardiovascular disease in these patients does not confound the diagnosis or monitoring of micro- or macroalbuminuria.

Keywords: acetylsalicylic acid; albuminuria; glomerular filtration rate; randomized trial; type 2 diabetes mellitus; urinary albumin excretion rate

Correspondence and offprint requests to: Peter Gæde, MD, Steno Diabetes Center, Niels Steensens Vej 2, DK-2820 Gentofte, Copenhagen, Denmark. Email: p.gaede{at}dadlnet.dk


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Diabetes CareHome page
E. G. Camargo, L. S. Weinert, J. Lavinsky, J. L. Gross, and S. P. Silveiro
The Effect of Aspirin on the Antiproteinuric Properties of Enalapril in Microalbuminuric Type 2 Diabetic Patients: A randomized, double-blind, placebo-controlled study
Diabetes Care, July 1, 2007; 30(7): e66 - e66.
[Full Text] [PDF]


Home page
Diabetes CareHome page
J. L. Gross, M. J. de Azevedo, S. P. Silveiro, L. H. Canani, M. L. Caramori, and T. Zelmanovitz
Diabetic Nephropathy: Diagnosis, Prevention, and Treatment
Diabetes Care, January 1, 2005; 28(1): 164 - 176.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.