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肥胖的遗传风险作为邻里环境与体重指数之间关联的调节因素:对335046名英国生物银行参与者的观察性研究

Genetic risk of obesity as a modifier of associations between neighbourhood environment and body mass index: an observational study of 335 046 UK Biobank participants.

作者信息

Mason Kate E, Palla Luigi, Pearce Neil, Phelan Jody, Cummins Steven

机构信息

Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

Department of Non-communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, UK.

出版信息

BMJ Nutr Prev Health. 2020 Oct 5;3(2):247-255. doi: 10.1136/bmjnph-2020-000107. eCollection 2020 Dec.

Abstract

BACKGROUND

There is growing recognition that recent global increases in obesity are the product of a complex interplay between genetic and environmental factors. However, in gene-environment studies of obesity, 'environment' usually refers to individual behavioural factors that influence energy balance, whereas more upstream environmental factors are overlooked. We examined gene-environment interactions between genetic risk of obesity and two neighbourhood characteristics likely to be associated with obesity (proximity to takeaway/fast-food outlets and availability of physical activity facilities).

METHODS

We used data from 335 046 adults aged 40-70 in the UK Biobank cohort to conduct a population-based cross-sectional study of interactions between neighbourhood characteristics and genetic risk of obesity, in relation to body mass index (BMI). Proximity to a fast-food outlet was defined as distance from home address to nearest takeaway/fast-food outlet, and availability of physical activity facilities as the number of formal physical activity facilities within 1 km of home address. Genetic risk of obesity was operationalised by weighted Genetic Risk Scores of 91 or 69 single nucleotide polymorphisms (SNP), and by six individual SNPs considered separately. Multivariable, mixed-effects models with product terms for the gene-environment interactions were estimated.

RESULTS

After accounting for likely confounding, the association between proximity to takeaway/fast-food outlets and BMI was stronger among those at increased genetic risk of obesity, with evidence of an interaction with polygenic risk scores (p=0.018 and p=0.028 for 69-SNP and 91-SNP scores, respectively) and in particular with a SNP linked to (p=0.009), a gene known to regulate food intake. We found very little evidence of gene-environment interaction for the availability of physical activity facilities.

CONCLUSIONS

Individuals at an increased genetic risk of obesity may be more sensitive to exposure to the local fast-food environment. Ensuring that neighbourhood residential environments are designed to promote a healthy weight may be particularly important for those with greater genetic susceptibility to obesity.

摘要

背景

人们越来越认识到,近期全球肥胖率的上升是遗传和环境因素复杂相互作用的结果。然而,在肥胖的基因-环境研究中,“环境”通常指影响能量平衡的个体行为因素,而更多上游环境因素被忽视。我们研究了肥胖遗传风险与两个可能与肥胖相关的邻里特征(靠近外卖/快餐店以及体育活动设施的可及性)之间的基因-环境相互作用。

方法

我们使用英国生物银行队列中335046名40至70岁成年人的数据,进行了一项基于人群的横断面研究,以探讨邻里特征与肥胖遗传风险之间与体重指数(BMI)相关的相互作用。靠近快餐店的程度定义为从家庭住址到最近的外卖/快餐店的距离,体育活动设施的可及性定义为家庭住址1公里范围内正规体育活动设施的数量。肥胖遗传风险通过91个或69个单核苷酸多态性(SNP)的加权遗传风险评分以及分别考虑的6个个体SNP来衡量。估计了用于基因-环境相互作用的含乘积项的多变量混合效应模型。

结果

在考虑了可能的混杂因素后,肥胖遗传风险增加的人群中,靠近外卖/快餐店与BMI之间的关联更强,有证据表明与多基因风险评分存在相互作用(69-SNP评分和91-SNP评分的p值分别为0.018和0.028),特别是与一个与[具体基因名称缺失]相关的SNP存在相互作用(p = 0.009),该基因已知可调节食物摄入。我们几乎没有发现体育活动设施可及性方面存在基因-环境相互作用的证据。

结论

肥胖遗传风险增加的个体可能对当地快餐环境的暴露更为敏感。确保邻里居住环境的设计有助于促进健康体重,对于那些肥胖遗传易感性较高的人可能尤为重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bda/7841812/d105d075d037/bmjnph-2020-000107f01.jpg

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