Bjørnland Thea, Langaas Mette, Grill Valdemar, Mostad Ingrid Løvold
Department of Mathematical Sciences, Faculty of Information Technology and Electrical Engineering, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Cancer Research and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
PLoS One. 2017 Apr 6;12(4):e0175071. doi: 10.1371/journal.pone.0175071. eCollection 2017.
Our aim was to assess the influence of age, gender and lifestyle factors on the effect of the obesity-promoting alleles of FTO and MCR4.
The HUNT study comprises health information on the population of Nord-Trøndelag county, Norway. Extreme phenotype participants (gender-wise lower and upper quartiles of waist-hip-ratio and BMI ≥ 35 kg/m2) in the third survey, HUNT3 (2006-08), were genotyped for the single-nucleotide polymorphisms rs9939609 (FTO) and rs17782313 (MC4R); 25686 participants were successfully genotyped. Extreme sampling was chosen to increase power to detect genetic and gene-environment effects on waist-hip-ratio and BMI. Statistical inference was based on linear regression models and a missing-covariate likelihood approach for the extreme phenotype sampling design. Environmental factors were physical activity, diet (artificially sweetened beverages) and smoking. Longitudinal analysis was performed using material from HUNT2 (1995-97).
Cross-sectional and longitudinal genetic effects indicated stronger genetic associations with obesity in young than in old, as well as differences between women and men. We observed larger genetic effects among physically inactive compared to active individuals. This interaction was age-dependent and seen mainly in 20-40 year olds. We observed a greater FTO effect among men with a regular intake of artificially sweetened beverages, compared to non-drinkers. Interaction analysis of smoking was mainly inconclusive.
In a large all-adult and area-based population survey the effects of obesity-promoting minor-alleles of FTO and MCR4, and interactions with life style factors are age- and gender-related. These findings appear relevant when designing individualized treatment for and prophylaxis against obesity.
我们的目的是评估年龄、性别和生活方式因素对FTO和MCR4促肥胖等位基因效应的影响。
HUNT研究包含挪威北特伦德拉格郡人群的健康信息。在第三次调查HUNT3(2006 - 2008年)中,对极端表型参与者(按性别划分的腰臀比上下四分位数且BMI≥35kg/m²)进行单核苷酸多态性rs9939609(FTO)和rs17782313(MC4R)的基因分型;25686名参与者成功进行了基因分型。选择极端抽样以增强检测基因及基因 - 环境对腰臀比和BMI影响的能力。统计推断基于线性回归模型以及针对极端表型抽样设计的缺失协变量似然法。环境因素包括体力活动、饮食(人工甜味饮料)和吸烟。使用HUNT2(1995 - 1997年)的资料进行纵向分析。
横断面和纵向遗传效应表明,与老年人相比,年轻人中与肥胖的遗传关联更强,且男女之间存在差异。我们观察到,与活跃个体相比,身体不活跃的个体中遗传效应更大。这种相互作用与年龄有关,主要见于20 - 40岁的人群。与不饮用者相比,我们观察到经常饮用人工甜味饮料的男性中FTO效应更大。吸烟的相互作用分析主要无定论。
在一项基于地区的全成年人大型人群调查中,FTO和MCR4促肥胖小等位基因的效应以及与生活方式因素的相互作用与年龄和性别相关。这些发现对于设计肥胖的个体化治疗和预防措施似乎具有重要意义。