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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (9)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Losito, A.
Right arrow Articles by Jeffery, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Losito, A.
Right arrow Articles by Jeffery, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrol Dial Transplant (2002) 17: 2184-2188
© 2002 European Renal Association-European Dialysis and Transplant Association

Polymorphism of renin–angiotensin system genes in dialysis patients—association with cerebrovascular disease

Attilio Losito1,, Kamini Kalidas2, Stefania Santoni1, Luigi Ceccarelli1 and Steve Jeffery2

1 UO Nefrologia e Dialisi, Policlinico Monteluce, Perugia, Italy and 2 Medical Genetics Unit, St. George's Hospital Medical School, London, UK

Background. Polymorphisms of genes of the renin–angiotensin system (RAS) have been found in association with cerebrovascular and cardiovascular diseases in the general population. In dialysis patients, RAS gene polymorphisms have been studied in combination and separately and have yielded conflicting results.

Methods. In this study we have analysed, in 160 dialysis patients, the distribution of the following genetic polymorphisms: M235T and T174M of the angiotensinogen gene, A1166C of the angiotensin II type 1 receptor gene and the insertion/deletion (I/D) of the ACE gene. The association of these polymorphisms with cerebrovascular and cardiovascular diseases was also tested. Healthy blood donors and hospital staff (169) were the control group for the distribution of the polymorphisms.

Results. The distribution of the polymorphisms in dialysis patients as a whole did not differ significantly from that of healthy controls. However, for patients with severe cerebrovascular disease, 70% carried the D allele compared with 52% of patients without cerebrovascular disease (P=0.035). We also found that the degree of carotid artery stenosis was significantly correlated with the presence of the ACE ‘D’ allele in subjects on dialysis (P=0.0348).

Conclusions. The distribution of RAS genes in dialysis patients is similar to that of the normal population. The presence of the D allele of ACE gene is associated with cerebrovascular disease and the degree of carotid artery stenosis. We postulate that the ACE gene polymorphism is a risk factor for cerebrovascular disease in dialytic patients.

Keywords: dialysis; genes; polymorphism; renin–angiotensin

Correspondence and offprint requests to: Dr Attilio Losito, UO Nefrologia e Dialisi, Policlinico Monteluce, I-06122 Perugia, Italy. Email: atlosito{at}tin.it


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
Ther Adv Cardiovasc DisHome page
H. Suzuki
Therapeutic efficacy of renin--angiotensin blockade in patients receiving dialysis
Therapeutic Advances in Cardiovascular Disease, October 1, 2009; 3(5): 397 - 405.
[Abstract] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
T. A. Manolio, E. Boerwinkle, C. J. O'Donnell, and A. F. Wilson
Genetics of Ultrasonographic Carotid Atherosclerosis
Arterioscler Thromb Vasc Biol, September 1, 2004; 24(9): 1567 - 1577.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
J. L. Hansen, S. Haunso, M. R. Brann, S. P. Sheikh, and D. M. Weiner
Loss-of-Function Polymorphic Variants of the Human Angiotensin II Type 1 Receptor
Mol. Pharmacol., March 1, 2004; 65(3): 770 - 777.
[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.