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Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients

AIMS: The aldose reductase (AR) gene, a rate-limiting enzyme of the polyol pathway, has been investigated as a candidate gene in determining susceptibility to diabetic microangiopathy. However, the association of the AR gene with diabetic macroangiopathy has not been investigated. Therefore, the pre...

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Autores principales: Watarai, A, Nakashima, E, Hamada, Y, Watanabe, G, Naruse, K, Miwa, K, Kobayashi, Y, Kamiya, H, Nakae, M, Hamajima, N, Sekido, Y, Niwa, T, Oiso, Y, Nakamura, J
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1619898/
https://www.ncbi.nlm.nih.gov/pubmed/16911628
http://dx.doi.org/10.1111/j.1464-5491.2006.01946.x
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author Watarai, A
Nakashima, E
Hamada, Y
Watanabe, G
Naruse, K
Miwa, K
Kobayashi, Y
Kamiya, H
Nakae, M
Hamajima, N
Sekido, Y
Niwa, T
Oiso, Y
Nakamura, J
author_facet Watarai, A
Nakashima, E
Hamada, Y
Watanabe, G
Naruse, K
Miwa, K
Kobayashi, Y
Kamiya, H
Nakae, M
Hamajima, N
Sekido, Y
Niwa, T
Oiso, Y
Nakamura, J
author_sort Watarai, A
collection PubMed
description AIMS: The aldose reductase (AR) gene, a rate-limiting enzyme of the polyol pathway, has been investigated as a candidate gene in determining susceptibility to diabetic microangiopathy. However, the association of the AR gene with diabetic macroangiopathy has not been investigated. Therefore, the present study was conducted to determine whether genetic variations of AR may determine susceptibility to diabetic macroangiopathy. METHODS: There were 378 Type 2 diabetic patients enrolled in this study. A single nucleotide polymorphism in the promoter region (C-106T) was genotyped and the AR protein content of erythrocytes measured by ELISA. RESULTS: There were no significant differences in genotypic or allelic distribution in patients with or without ischaemic heart diseases, but there was a significant increase in the frequency of the CT + TT genotype and T allele in patients with stroke (P = 0.019 and P = 0.012). The erythrocyte AR protein content was increased in patients with the CT and TT genotype compared with those with the CC genotype. After adjustment for age, duration of diabetes, body mass index, systolic blood pressure, HbA(1c), and serum creatinine, triglycerides, and total cholesterol in multivariate logistic-regression models, the association between this AR genotype and stroke remained significant. CONCLUSIONS: Our results suggest that the CT or TT genotype of the AR gene might be a genetic marker of susceptibility to stroke in Type 2 diabetic patients. This observation might contribute to the development of strategies for the prevention of stroke in Type 2 diabetic patients.
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spelling pubmed-16198982006-11-03 Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients Watarai, A Nakashima, E Hamada, Y Watanabe, G Naruse, K Miwa, K Kobayashi, Y Kamiya, H Nakae, M Hamajima, N Sekido, Y Niwa, T Oiso, Y Nakamura, J Diabet Med Original Articles AIMS: The aldose reductase (AR) gene, a rate-limiting enzyme of the polyol pathway, has been investigated as a candidate gene in determining susceptibility to diabetic microangiopathy. However, the association of the AR gene with diabetic macroangiopathy has not been investigated. Therefore, the present study was conducted to determine whether genetic variations of AR may determine susceptibility to diabetic macroangiopathy. METHODS: There were 378 Type 2 diabetic patients enrolled in this study. A single nucleotide polymorphism in the promoter region (C-106T) was genotyped and the AR protein content of erythrocytes measured by ELISA. RESULTS: There were no significant differences in genotypic or allelic distribution in patients with or without ischaemic heart diseases, but there was a significant increase in the frequency of the CT + TT genotype and T allele in patients with stroke (P = 0.019 and P = 0.012). The erythrocyte AR protein content was increased in patients with the CT and TT genotype compared with those with the CC genotype. After adjustment for age, duration of diabetes, body mass index, systolic blood pressure, HbA(1c), and serum creatinine, triglycerides, and total cholesterol in multivariate logistic-regression models, the association between this AR genotype and stroke remained significant. CONCLUSIONS: Our results suggest that the CT or TT genotype of the AR gene might be a genetic marker of susceptibility to stroke in Type 2 diabetic patients. This observation might contribute to the development of strategies for the prevention of stroke in Type 2 diabetic patients. Blackwell Publishing Ltd 2006-08 /pmc/articles/PMC1619898/ /pubmed/16911628 http://dx.doi.org/10.1111/j.1464-5491.2006.01946.x Text en © 2006 The Authors. Journal compilation © 2006 Diabetes UK https://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Watarai, A
Nakashima, E
Hamada, Y
Watanabe, G
Naruse, K
Miwa, K
Kobayashi, Y
Kamiya, H
Nakae, M
Hamajima, N
Sekido, Y
Niwa, T
Oiso, Y
Nakamura, J
Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients
title Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients
title_full Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients
title_fullStr Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients
title_full_unstemmed Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients
title_short Aldose reductase gene is associated with diabetic macroangiopathy in Japanese Type 2 diabetic patients
title_sort aldose reductase gene is associated with diabetic macroangiopathy in japanese type 2 diabetic patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1619898/
https://www.ncbi.nlm.nih.gov/pubmed/16911628
http://dx.doi.org/10.1111/j.1464-5491.2006.01946.x
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