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AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients

Introduction: The rennin-angiotensin system (RAS) plays a central role in the regulation of sodium metabolism, vascular tone, blood pressure, renal hemodynamics, and vascular modeling and is activated by hyperglycemiaObjectives: In the present study the influence of AT2R -1332 G:A polymorphism on th...

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Autores principales: Rahimi, Zohreh, Mansouri Zaveleh, Omid, Rahimi, Ziba, Abbasi, Ardeshir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nickan Research Institute 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206021/
https://www.ncbi.nlm.nih.gov/pubmed/25340140
http://dx.doi.org/10.12861/jrip.2013.31
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author Rahimi, Zohreh
Mansouri Zaveleh, Omid
Rahimi, Ziba
Abbasi, Ardeshir
author_facet Rahimi, Zohreh
Mansouri Zaveleh, Omid
Rahimi, Ziba
Abbasi, Ardeshir
author_sort Rahimi, Zohreh
collection PubMed
description Introduction: The rennin-angiotensin system (RAS) plays a central role in the regulation of sodium metabolism, vascular tone, blood pressure, renal hemodynamics, and vascular modeling and is activated by hyperglycemiaObjectives: In the present study the influence of AT2R -1332 G:A polymorphism on the risk of T2DM and its complications in a population from Western Iran has been investigated. Patients and Methods: In a case-control study, 70 individuals with type 2 diabetes mellitus (T2DM) including normo-, micro- and macro-albuminuric patients and 112 healthy subjects from the Kermanshah province were studied to investigate the association between the angiotensin type 2 receptor (AT2R) -1332 G:A variants with the risk of T2DM and its complications. The genotypes of the AT2R were detected using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Analysis of AT2R -1332 G:A polymorphism indicated the absence of association between this polymorphism with T2DM and diabetic nephropathy. Results: Analysis of AT2R -1332 G:A polymorphism indicated the absence of association between this polymorphism with T2DM and diabetic nephropathy. In females with diabetic nephropathy a significantly higher frequency of AA genotype (50%) was detected compared to those without nephropathy (13.3%, p=0.015). The presence of A allele of AT2R was associated with significantly (p=0.029) increased risk of coronary artery disease (CAD) in diabetic patients without nephropathy. Conclusion: Our study indicated an association between the AT2R -1332 G:A polymorphism and the risk of diabetic nephropathy in females only. Also, the A allele was associated with the risk of CAD in those diabetic patients without nephropathy.
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spelling pubmed-42060212014-10-22 AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients Rahimi, Zohreh Mansouri Zaveleh, Omid Rahimi, Ziba Abbasi, Ardeshir J Renal Inj Prev Original Article Introduction: The rennin-angiotensin system (RAS) plays a central role in the regulation of sodium metabolism, vascular tone, blood pressure, renal hemodynamics, and vascular modeling and is activated by hyperglycemiaObjectives: In the present study the influence of AT2R -1332 G:A polymorphism on the risk of T2DM and its complications in a population from Western Iran has been investigated. Patients and Methods: In a case-control study, 70 individuals with type 2 diabetes mellitus (T2DM) including normo-, micro- and macro-albuminuric patients and 112 healthy subjects from the Kermanshah province were studied to investigate the association between the angiotensin type 2 receptor (AT2R) -1332 G:A variants with the risk of T2DM and its complications. The genotypes of the AT2R were detected using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Analysis of AT2R -1332 G:A polymorphism indicated the absence of association between this polymorphism with T2DM and diabetic nephropathy. Results: Analysis of AT2R -1332 G:A polymorphism indicated the absence of association between this polymorphism with T2DM and diabetic nephropathy. In females with diabetic nephropathy a significantly higher frequency of AA genotype (50%) was detected compared to those without nephropathy (13.3%, p=0.015). The presence of A allele of AT2R was associated with significantly (p=0.029) increased risk of coronary artery disease (CAD) in diabetic patients without nephropathy. Conclusion: Our study indicated an association between the AT2R -1332 G:A polymorphism and the risk of diabetic nephropathy in females only. Also, the A allele was associated with the risk of CAD in those diabetic patients without nephropathy. Nickan Research Institute 2013-09-01 /pmc/articles/PMC4206021/ /pubmed/25340140 http://dx.doi.org/10.12861/jrip.2013.31 Text en Copyright © 2013 The Author(s); Published by Nickan Research Institute http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Rahimi, Zohreh
Mansouri Zaveleh, Omid
Rahimi, Ziba
Abbasi, Ardeshir
AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
title AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
title_full AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
title_fullStr AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
title_full_unstemmed AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
title_short AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
title_sort at2r -1332 g:a polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206021/
https://www.ncbi.nlm.nih.gov/pubmed/25340140
http://dx.doi.org/10.12861/jrip.2013.31
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