Nutrition and Genomics Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA.
Int J Obes (Lond). 2013 Sep;37(9):1211-20. doi: 10.1038/ijo.2012.215. Epub 2013 Jan 29.
Low-density lipoprotein-related receptor protein 1 (LRP1) is a multi-functional endocytic receptor and signaling molecule that is expressed in adipose and the hypothalamus. Evidence for a role of LRP1 in adiposity is accumulating from animal and in vitro models, but data from human studies are limited. The study objectives were to evaluate (i) relationships between LRP1 genotype and anthropometric traits, and (ii) whether these relationships were modified by dietary fatty acids.
We conducted race/ethnic-specific meta-analyses using data from 14 studies of US and European whites and 4 of African Americans to evaluate associations of dietary fatty acids and LRP1 genotypes with body mass index (BMI), waist circumference and hip circumference, as well as interactions between dietary fatty acids and LRP1 genotypes. Seven single-nucleotide polymorphisms (SNPs) of LRP1 were evaluated in whites (N up to 42 000) and twelve SNPs in African Americans (N up to 5800).
After adjustment for age, sex and population substructure if relevant, for each one unit greater intake of percentage of energy from saturated fat (SFA), BMI was 0.104 kg m(-2) greater, waist was 0.305 cm larger and hip was 0.168 cm larger (all P<0.0001). Other fatty acids were not associated with outcomes. The association of SFA with outcomes varied by genotype at rs2306692 (genotyped in four studies of whites), where the magnitude of the association of SFA intake with each outcome was greater per additional copy of the T allele: 0.107 kg m(-2) greater for BMI (interaction P=0.0001), 0.267 cm for waist (interaction P=0.001) and 0.21 cm for hip (interaction P=0.001). No other significant interactions were observed.
Dietary SFA and LRP1 genotype may interactively influence anthropometric traits. Further exploration of this, and other diet x genotype interactions, may improve understanding of interindividual variability in the relationships of dietary factors with anthropometric traits.
载脂蛋白相关蛋白 1(LRP1)是一种多功能内吞受体和信号分子,在脂肪组织和下丘脑表达。越来越多的动物和体外模型证据表明 LRP1 在肥胖中起作用,但来自人类研究的数据有限。本研究旨在评估(i)LRP1 基因型与人体测量特征的关系,以及(ii)饮食脂肪酸是否改变这些关系。
我们对来自美国和欧洲白人的 14 项研究和 4 项非洲裔美国人的研究数据进行了种族/民族特异性荟萃分析,以评估饮食脂肪酸和 LRP1 基因型与体重指数(BMI)、腰围和臀围的关系,以及饮食脂肪酸和 LRP1 基因型之间的相互作用。在白人中评估了 LRP1 的 7 个单核苷酸多态性(SNP)(N 多达 42000)和非洲裔美国人中的 12 个 SNP(N 多达 5800)。
在调整年龄、性别和相关人群亚结构后,每增加 1 个单位的饱和脂肪酸(SFA)能量百分比,BMI 增加 0.104kg/m2,腰围增加 0.305cm,臀围增加 0.168cm(均 P<0.0001)。其他脂肪酸与结果无关。SFA 与结果的相关性因 rs2306692 基因型而异(在白人的四项研究中进行了基因分型),其中 SFA 摄入量与每个结果的关联程度随 T 等位基因的增加而增大:BMI 增加 0.107kg/m2(交互作用 P=0.0001),腰围增加 0.267cm(交互作用 P=0.001),臀围增加 0.21cm(交互作用 P=0.001)。没有观察到其他显著的相互作用。
饮食 SFA 和 LRP1 基因型可能相互影响人体测量特征。进一步探讨这一点以及其他饮食 x 基因型相互作用可能有助于更好地理解饮食因素与人体测量特征之间个体间差异的关系。