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Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals
BACKGROUND: Aldose reductase (AR) is the rate-limiting enzyme in the glucose metabolism, which has been implicated in the pathogenesis of diabetic microvascular complications (MVCs). Frequent C-106T polymorphism in the promoter of the AR gene may change the expression of the gene. AIMS: The aim of t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287789/ https://www.ncbi.nlm.nih.gov/pubmed/25593834 http://dx.doi.org/10.4103/2230-8210.131762 |
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author | Rezaee, Majid Reza Sheikh Amiri, Ahmad Ahmadzadeh Hashemi-Soteh, Mohammad Bagher Daneshvar, Fatemeh Emady-Jamaly, Roghaye Jafari, Reza Soleimani, Behyar Haghiaminjan, Hamed |
author_facet | Rezaee, Majid Reza Sheikh Amiri, Ahmad Ahmadzadeh Hashemi-Soteh, Mohammad Bagher Daneshvar, Fatemeh Emady-Jamaly, Roghaye Jafari, Reza Soleimani, Behyar Haghiaminjan, Hamed |
author_sort | Rezaee, Majid Reza Sheikh |
collection | PubMed |
description | BACKGROUND: Aldose reductase (AR) is the rate-limiting enzyme in the glucose metabolism, which has been implicated in the pathogenesis of diabetic microvascular complications (MVCs). Frequent C-106T polymorphism in the promoter of the AR gene may change the expression of the gene. AIMS: The aim of the following study is to study the association between AR C106T genotypes and diabetic MVCs in Iranian population. MATERIALS AND METHODS: We included 206 type 2 diabetic patients categorized into two groups according to the presence or absence of diabetic microangiopathy. The cases of interest were diabetic neuropathy, retinopathy and nephropathy identified during clinical and or laboratory examination. In addition, 114 age- and sex-matched individuals were selected to serve as a control group. AR genotyping was done using an amplification gel electrophoresis. RESULTS: The frequency of CC genotype was specifically higher in subjects with diabetic retinopathy as compared to those without it (53.2% vs. 38.1%, P = 0.030). Patients with diabetic microangiopathy in general; however, did not differ significantly between AR genotype groups. CONCLUSION: The C-106T polymorphism in the AR gene is likely a risk factor for development of only retinal complication of diabetes microvascular in Iranian individuals. |
format | Online Article Text |
id | pubmed-4287789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42877892015-01-15 Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals Rezaee, Majid Reza Sheikh Amiri, Ahmad Ahmadzadeh Hashemi-Soteh, Mohammad Bagher Daneshvar, Fatemeh Emady-Jamaly, Roghaye Jafari, Reza Soleimani, Behyar Haghiaminjan, Hamed Indian J Endocrinol Metab Original Article BACKGROUND: Aldose reductase (AR) is the rate-limiting enzyme in the glucose metabolism, which has been implicated in the pathogenesis of diabetic microvascular complications (MVCs). Frequent C-106T polymorphism in the promoter of the AR gene may change the expression of the gene. AIMS: The aim of the following study is to study the association between AR C106T genotypes and diabetic MVCs in Iranian population. MATERIALS AND METHODS: We included 206 type 2 diabetic patients categorized into two groups according to the presence or absence of diabetic microangiopathy. The cases of interest were diabetic neuropathy, retinopathy and nephropathy identified during clinical and or laboratory examination. In addition, 114 age- and sex-matched individuals were selected to serve as a control group. AR genotyping was done using an amplification gel electrophoresis. RESULTS: The frequency of CC genotype was specifically higher in subjects with diabetic retinopathy as compared to those without it (53.2% vs. 38.1%, P = 0.030). Patients with diabetic microangiopathy in general; however, did not differ significantly between AR genotype groups. CONCLUSION: The C-106T polymorphism in the AR gene is likely a risk factor for development of only retinal complication of diabetes microvascular in Iranian individuals. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4287789/ /pubmed/25593834 http://dx.doi.org/10.4103/2230-8210.131762 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Rezaee, Majid Reza Sheikh Amiri, Ahmad Ahmadzadeh Hashemi-Soteh, Mohammad Bagher Daneshvar, Fatemeh Emady-Jamaly, Roghaye Jafari, Reza Soleimani, Behyar Haghiaminjan, Hamed Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals |
title | Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals |
title_full | Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals |
title_fullStr | Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals |
title_full_unstemmed | Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals |
title_short | Aldose reductase C-106T gene polymorphism in type 2 diabetics with microangiopathy in Iranian individuals |
title_sort | aldose reductase c-106t gene polymorphism in type 2 diabetics with microangiopathy in iranian individuals |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287789/ https://www.ncbi.nlm.nih.gov/pubmed/25593834 http://dx.doi.org/10.4103/2230-8210.131762 |
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