Sotos-Prieto Mercedes, Luben Robert, Khaw Kay-Tee, Wareham Nicholas J, Forouhi Nita G
Genetic and Molecular Epidemiology Unit, Department of Preventive Medicine and Public Health, School of Medicine, University of Valencia, Valencia, Spain. CIBER Fisiopatología de la Obesidad y Nutrición,Valencia,Spain.
Department of Public Health and Primary Care,University of Cambridge,Cambridge,UK.
Br J Nutr. 2014 Jul 14;112(1):122-31. doi: 10.1017/S0007114514000580. Epub 2014 May 7.
Consumption of a Mediterranean diet (MD) and genetic variation in the glucokinase regulatory protein (GCKR) gene have been reported to be associated with TAG and glucose metabolism. It is uncertain whether there is any interaction between these factors. Therefore, the aims of the present study were to test the association of adherence to a MD and rs780094 (G>A) SNP in the GCKR gene with the markers of cardiometabolic risk, and to investigate the interaction between genetic variation and MD adherence. We studied 20 986 individuals from the European Prospective Investigation into Cancer (EPIC)-Norfolk study. The relative Mediterranean Diet Score (rMED: range 0-18) was used to assess MD adherence. Linear regression was used to estimate the association between the rMED, genotype and cardiometabolic continuous traits, adjusting for potential confounders. In adjusted analyses, we observed independent associations of MD adherence and genotype with cardiometabolic risk, with the highest risk group (AA genotype; lowest rMED) having higher concentrations of TAG, total cholesterol and apoB (12·5, 2·3 and 3·1%, respectively) v. those at the lowest risk (GG genotype; highest rMED). However, the associations of MD adherence with metabolic markers did not differ by genotype, with no significant gene-diet interactions for lipids or for glycated Hb. In conclusion, we found independent associations of the rMED and of the GCKR genotype with cardiometabolic profile, but found no evidence of interaction between them.
据报道,地中海饮食(MD)的摄入以及葡萄糖激酶调节蛋白(GCKR)基因的遗传变异与甘油三酯(TAG)和葡萄糖代谢有关。尚不确定这些因素之间是否存在相互作用。因此,本研究的目的是检验坚持MD和GCKR基因中的rs780094(G>A)单核苷酸多态性(SNP)与心脏代谢风险标志物之间的关联,并研究遗传变异与MD依从性之间的相互作用。我们对来自欧洲癌症前瞻性调查(EPIC)-诺福克研究的20986名个体进行了研究。采用相对地中海饮食评分(rMED:范围0-18)来评估MD依从性。使用线性回归来估计rMED、基因型与心脏代谢连续性特征之间的关联,并对潜在混杂因素进行校正。在校正分析中,我们观察到MD依从性和基因型与心脏代谢风险存在独立关联,风险最高的组(AA基因型;最低rMED)的TAG、总胆固醇和载脂蛋白B浓度分别比风险最低的组(GG基因型;最高rMED)高12.5%、2.3%和3.1%。然而,MD依从性与代谢标志物之间的关联在不同基因型之间并无差异,在脂质或糖化血红蛋白方面未发现显著的基因-饮食相互作用。总之,我们发现rMED和GCKR基因型与心脏代谢特征存在独立关联,但未发现它们之间存在相互作用的证据。