CJASN
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Published ahead of print on September 27, 2006
Clinical Journal of the American Society of Nephrology
© 2006 American Society of Nephrology
doi: 10.2215/CJN.01270406
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
CJN.01270406v1
1/6/1293    most recent
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Uribarri, J.
Right arrow Articles by Tuttle, K. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Uribarri, J.
Right arrow Articles by Tuttle, K. R.


IN-DEPTH REVIEWS

Advanced Glycation End Products and Nephrotoxicity of High-Protein Diets

Jaime Uribarri * and Katherine R. Tuttle {dagger}1

*Division of Nephrology, Department of Medicine, Mount Sinai School of Medicine, New York, New York; and {dagger}Providence Medical Research Center, Sacred Heart Medical Center, University of Washington School of Medicine, Spokane, Washington


1 To whom correspondence should be addressed. E-mail: ktuttle{at}this.org.


   Abstract

The popularity of high-protein diets has surged recently as obesity has become more and more common in the United States and other developed nations. In view of the high prevalence of type 2 diabetes and chronic kidney disease among obese people, it is important to understand potential effects of high-protein diets on the kidney. The hypothesis that high-protein diets are nephrotoxic because of their excessive dietary advanced glycation end product (AGE) content and an increased amino acid load that enhances AGE formation in situ was explored. This review discusses the following evidence: (1) High-protein diets are deleterious to the kidney; (2) AGE are metabolic mediators of kidney damage; (3) dietary protein-derived AGE contribute to proinflammatory and pro-oxidative processes in diabetes and kidney disease; and (4) dietary protein-derived AGE produce functional and structural abnormalities that are involved in kidney damage. Future research should consider dietary AGE as a potential therapeutic target for kidney disease in obesity, diabetes, and perhaps other causes of chronic kidney disease.




This article has been cited by other articles:


Home page
NDT PlusHome page
Y. W. J. Sijpkens, N. C. Berkhout-Byrne, and T. J. Rabelink
Optimal predialysis care
NDT Plus, October 1, 2008; 1(suppl_4): iv7 - iv13.
[Abstract] [Full Text] [PDF]


Home page
Diabetes Spectr.Home page
P. Weber
Nutritional Challenges of a Dual Diagnosis: Chronic Kidney Disease and Diabetes
Diabetes Spectr, January 1, 2008; 21(1): 26 - 29.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2006 by the American Society of Nephrology.