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The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile

INTRODUCTION: Several polymorphisms have been associated with obesity and type 2 diabetes in different populations. OBJECTIVE: To investigate the frequencies of a genetic polymorphism of vitamin D receptor (FokI and BsmI) in patients with T2D. METHODS: The case–control study was conducted in 138 pat...

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Autores principales: Angel, Bárbara, Lera, Lydia, Márquez, Carlos, Albala, Cecilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968031/
https://www.ncbi.nlm.nih.gov/pubmed/29795525
http://dx.doi.org/10.1038/s41387-018-0038-9
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author Angel, Bárbara
Lera, Lydia
Márquez, Carlos
Albala, Cecilia
author_facet Angel, Bárbara
Lera, Lydia
Márquez, Carlos
Albala, Cecilia
author_sort Angel, Bárbara
collection PubMed
description INTRODUCTION: Several polymorphisms have been associated with obesity and type 2 diabetes in different populations. OBJECTIVE: To investigate the frequencies of a genetic polymorphism of vitamin D receptor (FokI and BsmI) in patients with T2D. METHODS: The case–control study was conducted in 138 patients with T2D and 172 control subjects, men and women (60–79 years old). The genotype and allele frequency determination of VDR polymorphisms were determined in these subjects. RESULTS: The frequency of the C allele of the FokI polymorphism was significantly higher in the T2D group than in healthy subjects (p = 0.025). The frequencies of the BsmI variant were similar in subjects with and without T2D (p = 0.747). Consistent with these data, there was an association of the C allele with T2D (OR = 1.74, 95% CI = 1.003–3.084, p = 0.036), but not the AG + GG variants for BsmI (OR = 1.02, 95% CI = 0.635–1.649, p = 0.916). We can observe a significant association between carrier of the T > C variant of FokI and type 2 diabetes, adjusted for vitamin D, age, obesity (overweight and obesity), seasonality, sex and Homa-IR. Here, we show a significant association between the FokI polymorphisms (TC + CC) and T2D with an odds ratio of 1.9001 (95% CI (1.0970–3.6838), p = 0.041). CONCLUSION: Our study suggests that the C allele (TC + CC) of the VDR-FokI gene is a possible risk factor for T2D in older people living in a community in Santiago de Chile.
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spelling pubmed-59680312018-05-25 The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile Angel, Bárbara Lera, Lydia Márquez, Carlos Albala, Cecilia Nutr Diabetes Article INTRODUCTION: Several polymorphisms have been associated with obesity and type 2 diabetes in different populations. OBJECTIVE: To investigate the frequencies of a genetic polymorphism of vitamin D receptor (FokI and BsmI) in patients with T2D. METHODS: The case–control study was conducted in 138 patients with T2D and 172 control subjects, men and women (60–79 years old). The genotype and allele frequency determination of VDR polymorphisms were determined in these subjects. RESULTS: The frequency of the C allele of the FokI polymorphism was significantly higher in the T2D group than in healthy subjects (p = 0.025). The frequencies of the BsmI variant were similar in subjects with and without T2D (p = 0.747). Consistent with these data, there was an association of the C allele with T2D (OR = 1.74, 95% CI = 1.003–3.084, p = 0.036), but not the AG + GG variants for BsmI (OR = 1.02, 95% CI = 0.635–1.649, p = 0.916). We can observe a significant association between carrier of the T > C variant of FokI and type 2 diabetes, adjusted for vitamin D, age, obesity (overweight and obesity), seasonality, sex and Homa-IR. Here, we show a significant association between the FokI polymorphisms (TC + CC) and T2D with an odds ratio of 1.9001 (95% CI (1.0970–3.6838), p = 0.041). CONCLUSION: Our study suggests that the C allele (TC + CC) of the VDR-FokI gene is a possible risk factor for T2D in older people living in a community in Santiago de Chile. Nature Publishing Group UK 2018-05-25 /pmc/articles/PMC5968031/ /pubmed/29795525 http://dx.doi.org/10.1038/s41387-018-0038-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Angel, Bárbara
Lera, Lydia
Márquez, Carlos
Albala, Cecilia
The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile
title The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile
title_full The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile
title_fullStr The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile
title_full_unstemmed The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile
title_short The association of VDR polymorphisms and type 2 diabetes in older people living in community in Santiago de Chile
title_sort association of vdr polymorphisms and type 2 diabetes in older people living in community in santiago de chile
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968031/
https://www.ncbi.nlm.nih.gov/pubmed/29795525
http://dx.doi.org/10.1038/s41387-018-0038-9
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