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Serum adiponectin predicts all-cause mortality and end stage renal disease in patients with type I diabetes and diabetic nephropathy.

Authors :
Jorsal, Anders
Tarnow, Lise
Frystyk, Jan
Lajer, Maria
Flyvbjerg, Allan
Parving, Hans-Henrik
Vionnet, Nathalie
Rossing, Peter
Source :
Kidney International. Sep2008, Vol. 74 Issue 5, p649-654. 6p. 4 Charts, 1 Graph.
Publication Year :
2008

Abstract

Adiponectin levels are increased in patients with type I diabetes especially in the presence of microangiopathy. Here we determined the predictive value of serum adiponectin levels and 8 adiponectin gene polymorphisms for mortality, cardiovascular events and end-stage renal disease in type I diabetic patients. This prospective, observational follow-up study of type I diabetics consisted of 438 patients with overt diabetic nephropathy that were compared to 440 type I patients with normal albumin excretion. These two groups were followed an average of 8 years and generally matched for gender, age and duration of diabetes. Cox regression analysis of 373 patients showed a covariate-adjusted hazard ratio for all-cause mortality of 1.46 for a change of one standard deviation in log10 of serum adiponectin. There was no association with cardiovascular events; however, serum adiponectin levels predicted end stage renal disease in a covariate-adjusted analysis. Two of eight gene polymorphisms, found in the 878 patients, were associated with increased serum adiponectin levels but none of the polymorphisms were associated with a renal or cardiovascular outcome. These studies show that high serum adiponectin levels predict mortality and progression to end stage renal disease in type I diabetic patients.Kidney International (2008) 74, 649–654; doi:10.1038/ki.2008.201; published online 21 May 2008 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00852538
Volume :
74
Issue :
5
Database :
Academic Search Index
Journal :
Kidney International
Publication Type :
Academic Journal
Accession number :
33869400
Full Text :
https://doi.org/10.1038/ki.2008.201