Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.

Coronary heart disease (CHD) is one of the leading causes of mortality and morbidity in China. Genetic factors that predispose individuals to CHD are unclear. In the present study, we aimed to determine whether the variation of FoxOs, a novel genetic factor associated with longevity, was associated...

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Main Authors: Ying Zhao, Yanbo Yu, Xiaoli Tian, Xi Yang, Xueqi Li, Feng Jiang, Yundai Chen, Maowei Shi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3904908?pdf=render
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spelling doaj-e008812a6600452daa8e1a8c45d112652020-11-25T00:47:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8625210.1371/journal.pone.0086252Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.Ying ZhaoYanbo YuXiaoli TianXi YangXueqi LiFeng JiangYundai ChenMaowei ShiCoronary heart disease (CHD) is one of the leading causes of mortality and morbidity in China. Genetic factors that predispose individuals to CHD are unclear. In the present study, we aimed to determine whether the variation of FoxOs, a novel genetic factor associated with longevity, was associated with CHD in Han Chinese populations.1271 CHD patients and 1287 age-and sex-matched controls from Beijing and Harbin were included. We selected four tagging single nucleotide polymorphisms (SNPs) of FoxO1 (rs2755209, rs2721072, rs4325427 and rs17592371) and two tagging SNPs of FoxO3 (rs768023 and rs1268165). And the genotypes of these SNPs were determined in both CHD patients and non-CHD controls.For population from Beijing, four SNPs of FoxO1 and two SNPs of FoxO3 were found not to be associated with CHD (p>0.05). And this was validated in the other population from Harbin (p>0.05). After combining the two geographically isolated case-control populations, the results showed that the six SNPs did not necessarily predispose to CHD in Han Chinese(p>0.05). In stratified analysis according to gender, the history of smoking, hypertension, diabetes mellitus, hyperlipidemia and the metabolic syndrome, we further explored that neither the variants of FoxO1 nor the variants of FoxO3 might be associated with CHD (p>0.05).The variants of FoxO1 and FoxO3 may not increase the prevalence of CHD in Han Chinese population.http://europepmc.org/articles/PMC3904908?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ying Zhao
Yanbo Yu
Xiaoli Tian
Xi Yang
Xueqi Li
Feng Jiang
Yundai Chen
Maowei Shi
spellingShingle Ying Zhao
Yanbo Yu
Xiaoli Tian
Xi Yang
Xueqi Li
Feng Jiang
Yundai Chen
Maowei Shi
Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.
PLoS ONE
author_facet Ying Zhao
Yanbo Yu
Xiaoli Tian
Xi Yang
Xueqi Li
Feng Jiang
Yundai Chen
Maowei Shi
author_sort Ying Zhao
title Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.
title_short Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.
title_full Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.
title_fullStr Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.
title_full_unstemmed Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.
title_sort association study to evaluate foxo1 and foxo3 gene in chd in han chinese.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Coronary heart disease (CHD) is one of the leading causes of mortality and morbidity in China. Genetic factors that predispose individuals to CHD are unclear. In the present study, we aimed to determine whether the variation of FoxOs, a novel genetic factor associated with longevity, was associated with CHD in Han Chinese populations.1271 CHD patients and 1287 age-and sex-matched controls from Beijing and Harbin were included. We selected four tagging single nucleotide polymorphisms (SNPs) of FoxO1 (rs2755209, rs2721072, rs4325427 and rs17592371) and two tagging SNPs of FoxO3 (rs768023 and rs1268165). And the genotypes of these SNPs were determined in both CHD patients and non-CHD controls.For population from Beijing, four SNPs of FoxO1 and two SNPs of FoxO3 were found not to be associated with CHD (p>0.05). And this was validated in the other population from Harbin (p>0.05). After combining the two geographically isolated case-control populations, the results showed that the six SNPs did not necessarily predispose to CHD in Han Chinese(p>0.05). In stratified analysis according to gender, the history of smoking, hypertension, diabetes mellitus, hyperlipidemia and the metabolic syndrome, we further explored that neither the variants of FoxO1 nor the variants of FoxO3 might be associated with CHD (p>0.05).The variants of FoxO1 and FoxO3 may not increase the prevalence of CHD in Han Chinese population.
url http://europepmc.org/articles/PMC3904908?pdf=render
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