Smoking-Interaction Loci Affect Obesity Traits: A Gene-Smoking Stratified Meta-Analysis of 545,131 Europeans.

IF 2 4区 医学 Q3 GENETICS & HEREDITY
Won-Jun Lee, Ji Eun Lim, Ji-One Kang, Tae-Woong Ha, Hae-Un Jung, Dong Jun Kim, Eun Ju Baek, Han Kyul Kim, Ju Yeon Chung, Bermseok Oh
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引用次数: 0

Abstract

Introduction: Although many studies have investigated the association between smoking and obesity, very few have analyzed how obesity traits are affected by interactions between genetic factors and smoking. Here, we aimed to identify the loci that affect obesity traits via smoking status-related interactions in European samples.

Methods: We performed stratified analysis based on the smoking status using both the UK Biobank (UKB) data (N = 334,808) and the Genetic Investigation of ANthropometric Traits (GIANT) data (N = 210,323) to identify gene-smoking interaction for obesity traits. We divided the UKB subjects into two groups, current smokers and nonsmokers, based on the smoking status, and performed genome-wide association study (GWAS) for body mass index (BMI), waist circumference adjusted for BMI (WCadjBMI), and waist-hip ratio adjusted for BMI (WHRadjBMI) in each group. And then we carried out the meta-analysis using both GWAS summary statistics of UKB and GIANT for BMI, WCadjBMI, and WHRadjBMI and computed the stratified p values (pstratified) based on the differences between meta-analyzed estimated beta coefficients with standard errors in each group.

Results: We identified four genome-wide significant loci in interactions with the smoking status (pstratified < 5 × 10-8): rs336396 (INPP4B) and rs12899135 (near CHRNB4) for BMI, and rs998584 (near VEGFA) and rs6916318 (near RSPO3) for WHRadjBMI. Moreover, we annotated the biological functions of the SNPs using expression quantitative trait loci (eQTL) and GWAS databases, along with publications, which revealed possible mechanisms underlying the association between the smoking status-related genetic variants and obesity.

Conclusions: Our findings suggest that obesity traits can be modified by the smoking status via interactions with genetic variants through various biological pathways.

吸烟-相互作用基因座影响肥胖特征:对545,131名欧洲人的基因-吸烟分层荟萃分析
导语:虽然许多研究调查了吸烟与肥胖之间的关系,但很少有研究分析遗传因素和吸烟之间的相互作用如何影响肥胖特征。在这里,我们旨在通过欧洲样本中吸烟状态相关的相互作用来确定影响肥胖特征的基因座。方法:我们使用UK Biobank (UKB)数据(N = 334,808)和GIANT (N = 210,323)数据(N = 210,323)对吸烟状况进行分层分析,以确定肥胖性状的基因吸烟相互作用。我们根据吸烟状况将UKB受试者分为当前吸烟者和不吸烟者两组,并对每组的体重指数(BMI)、BMI校正腰围(WCadjBMI)和BMI校正腰臀比(WHRadjBMI)进行全基因组关联研究(GWAS)。然后,我们对BMI、WCadjBMI和WHRadjBMI分别使用UKB和GIANT的GWAS汇总统计数据进行meta分析,并根据每组meta分析估计β系数与标准误差之间的差异计算分层p值(pstratified)。结果:我们确定了4个与吸烟状况相互作用的全基因组显著位点(pstratified < 5 × 10-8): rs336396 (INPP4B)和rs12899135(靠近CHRNB4)与BMI有关,rs998584(靠近VEGFA)和rs6916318(靠近RSPO3)与WHRadjBMI有关。此外,我们使用表达数量性状位点(eQTL)和GWAS数据库,以及出版物,注释了snp的生物学功能,揭示了吸烟状态相关遗传变异与肥胖之间关联的可能机制。结论:我们的研究结果表明,吸烟状况可以通过多种生物学途径与遗传变异相互作用来改变肥胖特征。
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来源期刊
Lifestyle Genomics
Lifestyle Genomics Agricultural and Biological Sciences-Food Science
CiteScore
4.00
自引率
7.70%
发文量
11
审稿时长
28 weeks
期刊介绍: Lifestyle Genomics aims to provide a forum for highlighting new advances in the broad area of lifestyle-gene interactions and their influence on health and disease. The journal welcomes novel contributions that investigate how genetics may influence a person’s response to lifestyle factors, such as diet and nutrition, natural health products, physical activity, and sleep, amongst others. Additionally, contributions examining how lifestyle factors influence the expression/abundance of genes, proteins and metabolites in cell and animal models as well as in humans are also of interest. The journal will publish high-quality original research papers, brief research communications, reviews outlining timely advances in the field, and brief research methods pertaining to lifestyle genomics. It will also include a unique section under the heading “Market Place” presenting articles of companies active in the area of lifestyle genomics. Research articles will undergo rigorous scientific as well as statistical/bioinformatic review to ensure excellence.
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