Olsen Nanna J, Ängquist Lars, Larsen Sofus C, Linneberg Allan, Skaaby Tea, Husemoen Lise Lotte N, Toft Ulla, Tjønneland Anne, Halkjær Jytte, Hansen Torben, Pedersen Oluf, Overvad Kim, Ahluwalia Tarunveer S, Sørensen Thorkild Ia, Heitmann Berit L
Research Unit for Dietary Studies at the Parker Institute and Institute of Preventive Medicine, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark;
Institute of Preventive Medicine, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark;
Am J Clin Nutr. 2016 Sep;104(3):816-26. doi: 10.3945/ajcn.115.122820. Epub 2016 Jul 27.
Intake of sugar-sweetened beverages is associated with obesity, and this association may be modified by a genetic predisposition to obesity.
We examined the interactions between a molecular genetic predisposition to various aspects of obesity and the consumption of soft drinks, which are a major part of sugar-sweetened beverages, in relation to changes in adiposity measures.
A total of 4765 individuals were included in the study. On the basis of 50 obesity-associated single nucleotide polymorphisms that are associated with body mass index (BMI), waist circumference (WC), or the waist-to-hip ratio adjusted for BMI (WHRBMI), the following 4 genetic predisposition scores (GRSs) were constructed: a complete genetic predisposition score including all 50 single nucleotide polymorphisms (GRSComplete), a genetic predisposition score including BMI-associated single nucleotide polymorphisms (GRSBMI), a genetic predisposition score including waist circumference-associated single nucleotide polymorphisms (GRSWC), and a genetic predisposition score including the waist-to-hip ratio adjusted for BMI-associated single nucleotide polymorphisms (GRSWHR). Associations between soft drink intake and the annual change (Δ) in body weight (BW), WC, or waist circumference adjusted for BMI (WCBMI) and possible interactions with the GRSs were examined with the use of linear regression analyses and meta-analyses.
For each soft drink serving per day, soft drink consumption was significantly associated with a higher ΔBW of 0.07 kg/y (95% CI: 0.01, 0.13 kg/y; P = 0.020) but not with the ΔWC or ΔWCBMI In analyses of the ΔBW, we showed an interaction only with the GRSWC (per risk allele for each soft drink serving per day: -0.06 kg/y; 95% CI: -0.10, -0.02 kg/y; P = 0.006). In analyses of the ΔWC, we showed interactions only with the GRSBMI and GRSComplete [per risk allele for each soft drink serving per day: 0.05 cm/y (95% CI: 0.02, 0.09 cm/y; P = 0.001) and 0.05 cm/y (95% CI: 0.02, 0.07 cm/y; P = 0.001), respectively]. Nearly identical results were observed in analyses of the ΔWCBMI CONCLUSIONS: A genetic predisposition to a high WC may attenuate the association between soft drink intake and BW gain. A genetic predisposition to high BMI as well as a genetic predisposition to high BMI, WC, and WHRBMI combined may strengthen the association between soft drink intake and WC gain. However, the public health impact may be limited.
摄入含糖饮料与肥胖相关,且这种关联可能会因肥胖的遗传易感性而改变。
我们研究了肥胖各方面的分子遗传易感性与作为含糖饮料主要组成部分的软饮料消费之间的相互作用,以及与肥胖指标变化的关系。
本研究共纳入4765名个体。基于与体重指数(BMI)、腰围(WC)或经BMI调整的腰臀比(WHRBMI)相关的50个肥胖相关单核苷酸多态性,构建了以下4种遗传易感性评分(GRS):包括所有50个单核苷酸多态性的完整遗传易感性评分(GRSComplete)、包括与BMI相关单核苷酸多态性的遗传易感性评分(GRSBMI)、包括与腰围相关单核苷酸多态性的遗传易感性评分(GRSWC)以及包括经BMI相关单核苷酸多态性调整的腰臀比的遗传易感性评分(GRSWHR)。使用线性回归分析和荟萃分析研究了软饮料摄入量与体重(BW)、WC或经BMI调整的腰围(WCBMI)的年变化(Δ)之间的关联以及与GRS的可能相互作用。
每天每多饮用一份软饮料,软饮料消费与更高的年体重增加量显著相关,即每年增加0.07千克(95%置信区间:0.01,0.13千克/年;P = 0.020),但与WC或WCBMI的年变化无关。在对年体重增加量的分析中,我们仅发现与GRSWC存在相互作用(每天每多饮用一份软饮料的每个风险等位基因:-0.06千克/年;95%置信区间:-0.10,-0.02千克/年;P = 0.006)。在对WC年变化的分析中,我们仅发现与GRSBMI和GRSComplete存在相互作用[每天每多饮用一份软饮料的每个风险等位基因:分别为0.05厘米/年(95%置信区间:0.02,0.09厘米/年;P = 0.001)和0.05厘米/年(95%置信区间:0.02,0.07厘米/年;P = 0.001)]。在对WCBMI年变化的分析中观察到了几乎相同的结果。
高WC的遗传易感性可能会减弱软饮料摄入量与体重增加之间的关联。高BMI的遗传易感性以及高BMI、WC和WHRBMI综合的遗传易感性可能会加强软饮料摄入量与WC增加之间的关联。然而,对公共卫生的影响可能有限。