NT5C2 Gene Polymorphisms and the Risk of Coronary Heart Disease.

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY
Public Health Genomics Pub Date : 2020-01-01 Epub Date: 2020-06-15 DOI:10.1159/000507714
Xianghong Chen, Zaozhang Zhang, Xingfan Wang, Yuewu Chen, Chao Wang
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引用次数: 6

Abstract

Background: Increasing studies have reported that 5'-nucleotidase cytosolic II (NT5C2) has a strong relationship with coronary heart disease (CHD) development. This study was designed to examine the relationship between NT5C2 polymorphisms and CHD in the Chinese Han population.

Methods: We studied 501 CHD patients and 496 healthy controls from the Second Affiliated Hospital of Hainan Medical University in Hainan Province, China. Four single nucleotide polymorphisms (SNPs) in NT5C2 were selected and genotyped using Agena MassARRAY technology. Odds ratios and 95% confidence intervals were calculated using logistic regression after adjusting for age and gender. Stratification analysis was performed by age and gender in all individuals; we especially investigated the effects of NT5C2 SNPs on hypertension and diabetes among CHD patients.

Results: rs2148198 of NT5C2 was strongly associated with an increased risk of CHD (allele: p = 0.045; codominant: p = 0.007; additive: p = 0.016). Stratified analysis revealed that rs2148198 was associated with increased CHD risk in individuals aged ≤61 years and males. For CHD patients, rs2148198 significantly affected the risk of hypertension and diabetes (p < 0.05). Further, rs79237883 of NT5C2 was associated with decreased susceptibility to hypertension in multiple genetic models for individuals with CHD (allele: p = 0.007; codominant: p = 0.001; dominant: p = 0.001; additive: p = 0.008).

Conclusion: This study reports the association of NT5C2 gene variants and CHD susceptibility in the Chinese Han population. Especially, NT5C2 rs2148198 was significantly associated with CHD risk in the subgroups of males, hypertension, and diabetes.

nt552基因多态性与冠心病的风险
背景:越来越多的研究报道5′-核苷酸酶胞质II (NT5C2)与冠心病(CHD)的发展密切相关。本研究旨在探讨中国汉族人群中nt52c多态性与冠心病之间的关系。方法:选取海南医科大学第二附属医院的501例冠心病患者和496名健康对照者作为研究对象。利用Agena MassARRAY技术对nt52c基因的4个单核苷酸多态性进行了基因分型。在调整年龄和性别后,使用逻辑回归计算优势比和95%置信区间。按年龄和性别对所有个体进行分层分析;我们特别研究了nt52c snp对冠心病患者高血压和糖尿病的影响。结果:NT5C2的rs2148198与冠心病风险增加密切相关(等位基因:p = 0.045;共显性:p = 0.007;加性:p = 0.016)。分层分析显示,rs2148198与≤61岁人群和男性冠心病风险增加相关。对于冠心病患者,rs2148198显著影响高血压和糖尿病的发生风险(p < 0.05)。此外,在多种遗传模型中,NT5C2的rs79237883位点与冠心病患者高血压易感性降低相关(等位基因:p = 0.007;共显性:p = 0.001;显性:p = 0.001;加性:p = 0.008)。结论:本研究报道了中国汉族人群nt52c基因变异与冠心病易感性的相关性。特别是,在男性、高血压和糖尿病亚组中,NT5C2 rs2148198与冠心病风险显著相关。
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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
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