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首页> 外文期刊>The Journal of Nutrition: Official Organ of the American Institute of Nutrition >APOA1 and APOA4 Gene Polymorphisms Influence the Effects of Dietary Fat on LDL Particle Size and Oxidation in Healthy Young Adults
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APOA1 and APOA4 Gene Polymorphisms Influence the Effects of Dietary Fat on LDL Particle Size and Oxidation in Healthy Young Adults

机译:APOA1和APOA4基因多态性影响膳食脂肪对健康年轻人的LDL粒径和氧化的影响

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摘要

We investigated whether APOA1 and APOA4 genotypes interact with diet to determine changes in LDL size and their susceptibility to oxidative modifications. A total of 97 healthy volunteers each consumed 3 diets for 4 wk: a SFA diet (38% fat, 20% SFA) followed by a low-fat and high-carbohydrate (CHO) diet (30% fat, 55% carbohydrate) or a monounsaturated fatty acid (MUFA) diet (38% fat, 22% MUFA) following a randomized crossover design. For each diet, we determined susceptibility to oxidative modifications and LDL size. To investigate the combined effects of the APOA1 G-76A and APOA4 Thr347Ser single nucleotide polymorphisms (SNP), we defined 4 combined genotype groups: GG/ThrThr, GG/ThrSer, GA/ThrThr, and GA/ThrSer. After participants consumed the CHO diet, there was a significant decrease in LDL size with respect to high-fat diets in GG homozygotes for the APOA1 G-76A SNP. However, LDL size did not differ in GA carriers among participants consuming the 3 diets. Carriers of the A allele for this polymorphism had smaller LDL size as well as increased susceptibility to oxidation after the SFA diet than the GG homozygous. Moreover, the interaction between the APO A1 and APOA4 genotypes revealed that individuals with the GA/ThrSer genotype had larger LDL particle size during consumption of the MUFA diet than when they consumed the CHO diet. No differences in LDL oxidation were found in this analysis. Our study supports the concept that SNP in APOA1and APOA4 genes influences atherogenic characteristics of LDL particles in response to diet.
机译:我们调查了APOA1和APOA4基因型是否与饮食相互作用,以确定LDL大小的变化及其对氧化修饰的敏感性。总共97名健康志愿者每人每周4次食用3种饮食:SFA饮食(38%脂肪,20%SFA),然后是低脂和高碳水化合物(CHO)饮食(30%脂肪,55%碳水化合物)或采用随机交叉设计后的单不饱和脂肪酸(MUFA)饮食(38%脂肪,22%MUFA)。对于每种饮食,我们确定了对氧化修饰和LDL大小的敏感性。为了研究APOA1 G-76A和APOA4 Thr347Ser单核苷酸多态性(SNP)的组合作用,我们定义了4个组合基因型组:GG / ThrThr,GG / ThrSer,GA / ThrThr和GA / ThrSer。参与者食用CHO饮食后,APOA1 G-76A SNP的GG纯合子中的高脂饮食的LDL大小显着减少。但是,在食用3种饮食的参与者中,GA携带者的LDL大小没有差异。与GG纯合子相比,这种多态性的A等位基因携带者在SFA饮食后具有较小的LDL大小以及对氧化的敏感性。此外,APO A1和APOA4基因型之间的相互作用表明,与食用CHO饮食相比,具有GA / ThrSer基因型的个体在食用MUFA饮食期间具有更大的LDL粒径。在该分析中未发现LDL氧化的差异。我们的研究支持以下概念:APOA1和APOA4基因中的SNP会影响LDL颗粒对饮食的致动脉粥样硬化特性。

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