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Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men

BACKGROUND: Genome-wide association studies have been used extensively to identify genetic variants linked to metabolic syndrome (MetS), but most of them have been conducted in non-Asian populations. This study aimed to evaluate the association between MetS and previously studied single nucleotide p...

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Autores principales: Son, Ki Young, Son, Ho-Young, Chae, Jeesoo, Hwang, Jinha, Jang, SeSong, Yun, Jae Moon, Cho, BeLong, Park, Jin Ho, Kim, Jong-Il
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568070/
https://www.ncbi.nlm.nih.gov/pubmed/26365620
http://dx.doi.org/10.1186/s12944-015-0111-5
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author Son, Ki Young
Son, Ho-Young
Chae, Jeesoo
Hwang, Jinha
Jang, SeSong
Yun, Jae Moon
Cho, BeLong
Park, Jin Ho
Kim, Jong-Il
author_facet Son, Ki Young
Son, Ho-Young
Chae, Jeesoo
Hwang, Jinha
Jang, SeSong
Yun, Jae Moon
Cho, BeLong
Park, Jin Ho
Kim, Jong-Il
author_sort Son, Ki Young
collection PubMed
description BACKGROUND: Genome-wide association studies have been used extensively to identify genetic variants linked to metabolic syndrome (MetS), but most of them have been conducted in non-Asian populations. This study aimed to evaluate the association between MetS and previously studied single nucleotide polymorphisms (SNPs), and their interaction with health-related behavior in Korean men. METHODS: Seventeen SNPs were genotyped and their association with MetS and its components was tested in 1193 men who enrolled in the study at Seoul National University Hospital. RESULTS: We found that rs662799 near APOA5 and rs769450 in APOE had significant association with MetS and its components. The SNP rs662799 was associated with increased risk of MetS, elevated triglyceride (TG) and low levels of high-density lipoprotein, while rs769450 was associated with a decreased risk of TG. The SNPs showed interactions between alcohol drinking and physical activity, and TG levels in Korean men. CONCLUSIONS: We have identified the genetic association and environmental interaction for MetS in Korean men. These results suggest that a strategy of prevention and treatment should be tailored to personal genotype and the population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-015-0111-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-45680702015-09-14 Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men Son, Ki Young Son, Ho-Young Chae, Jeesoo Hwang, Jinha Jang, SeSong Yun, Jae Moon Cho, BeLong Park, Jin Ho Kim, Jong-Il Lipids Health Dis Research BACKGROUND: Genome-wide association studies have been used extensively to identify genetic variants linked to metabolic syndrome (MetS), but most of them have been conducted in non-Asian populations. This study aimed to evaluate the association between MetS and previously studied single nucleotide polymorphisms (SNPs), and their interaction with health-related behavior in Korean men. METHODS: Seventeen SNPs were genotyped and their association with MetS and its components was tested in 1193 men who enrolled in the study at Seoul National University Hospital. RESULTS: We found that rs662799 near APOA5 and rs769450 in APOE had significant association with MetS and its components. The SNP rs662799 was associated with increased risk of MetS, elevated triglyceride (TG) and low levels of high-density lipoprotein, while rs769450 was associated with a decreased risk of TG. The SNPs showed interactions between alcohol drinking and physical activity, and TG levels in Korean men. CONCLUSIONS: We have identified the genetic association and environmental interaction for MetS in Korean men. These results suggest that a strategy of prevention and treatment should be tailored to personal genotype and the population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-015-0111-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-13 /pmc/articles/PMC4568070/ /pubmed/26365620 http://dx.doi.org/10.1186/s12944-015-0111-5 Text en © Son et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Son, Ki Young
Son, Ho-Young
Chae, Jeesoo
Hwang, Jinha
Jang, SeSong
Yun, Jae Moon
Cho, BeLong
Park, Jin Ho
Kim, Jong-Il
Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men
title Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men
title_full Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men
title_fullStr Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men
title_full_unstemmed Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men
title_short Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men
title_sort genetic association of apoa5 and apoe with metabolic syndrome and their interaction with health-related behavior in korean men
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568070/
https://www.ncbi.nlm.nih.gov/pubmed/26365620
http://dx.doi.org/10.1186/s12944-015-0111-5
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