Lipids and Atherosclerosis Research Unit, Instituto Maimónides para la Investigación Biomédica de Córdoba (IMIBIC), Department of Medicine, Reina Sofia University Hospital, University of Cordoba, CIBER Fisiopatologia de la Obesidad y Nutricion, Cordoba, Spain.
J Nutr. 2010 Apr;140(4):773-8. doi: 10.3945/jn.109.115964. Epub 2010 Feb 17.
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.
我们研究了 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易感性。共有 97 名健康志愿者每人分别食用 3 种饮食 4 周:一种 SFA 饮食(38%脂肪,20% SFA),然后是低脂肪和高碳水化合物(CHO)饮食(30%脂肪,55%碳水化合物),或单不饱和脂肪酸(MUFA)饮食(38%脂肪,22% MUFA),采用随机交叉设计。对于每种饮食,我们确定了氧化修饰和 LDL 大小的易感性。为了研究 APOA1 G-76A 和 APOA4 Thr347Ser 单核苷酸多态性(SNP)的联合作用,我们定义了 4 种联合基因型组:GG/ThrThr、GG/ThrSer、GA/ThrThr 和 GA/ThrSer。在参与者食用 CHO 饮食后,APOA1 G-76A SNP 的 GG 纯合子与高脂肪饮食相比,LDL 大小显著降低。然而,在食用 3 种饮食的 GA 携带者中,LDL 大小没有差异。携带这种多态性 A 等位基因的个体在 SFA 饮食后 LDL 大小较小,氧化易感性增加,而 GG 纯合子则较小。此外,APOA1 和 APOA4 基因型的相互作用表明,在食用 MUFA 饮食时,GA/ThrSer 基因型的个体 LDL 颗粒大小大于食用 CHO 饮食时。在这项分析中没有发现 LDL 氧化的差异。我们的研究支持这样一种观点,即 APOA1 和 APOA4 基因中的 SNP 影响 LDL 颗粒的动脉粥样硬化特征,以响应饮食。