López-Miranda J, Jansen S, Ordovas J M, Salas J, Marín C, Castro P, Ostos M A, Cruz G, López-Segura F, Blanco A, Jiménez-Perepérez J, Pérez-Jiménez F
Unidad de Lipidos y Arteriosclerosis, Hospital Universitario Reina Sofia, Córdoba, Spain.
Am J Clin Nutr. 1997 Jul;66(1):97-103. doi: 10.1093/ajcn/66.1.97.
The plasma lipid response to changes in dietary fat and cholesterol can vary between individuals. The SstI polymorphism, arising from a cytosine to guanosine substitution in the 3' untranslated region of the APOC3 gene distinguishes between two alleles--S1 and S2. The S2 allele has been associated with elevated plasma triacylglycerol, cholesterol, and apolipoprotein (apo) C-III concentrations. In 90 young men we examined the effect of the same mutation on the response of low-density-lipoprotein (LDL) cholesterol to dietary monounsaturated fat. The frequency for the S2 allele was 0.14. Subjects were fed a low-fat diet for 25 d, followed by a diet rich in monounsaturated fatty acid (22% MUFA, 38% total fat) for 28 d; lipoproteins were measured at the end of each diet. There were no significant differences in initial total cholesterol between subjects with the APOC3S1/APOC3S1 (S1/S1) and APOC3S1/APOC3S2 (S1/S2) genotypes. After consumption of the diet high in MUFA, significant increases in LDL cholesterol (0.13 mmol/L, P < 0.027) were noted in the S1/S1 subjects whereas a significant decrease was observed in the S1/S2 subjects (-0.18 mmol/L, P < 0.046). Significant genotypic effects were seen for diet-induced changes in LDL cholesterol (P < 0.00034), total cholesterol (P < 0.009), and apo B (P < 0.0014). A study of the effect of the interaction between this mutation with that present in position -76 of the APOA1 gene promoter region (G/A) revealed that both mutations had an additive effect on changes in total cholesterol, LDL cholesterol, and apo B induced by diets. Plasma LDL-cholesterol responsiveness to the diet may be explained, at least in part, by variation at the APOC3 gene locus.
血浆脂质对饮食中脂肪和胆固醇变化的反应在个体间可能存在差异。SstI多态性由载脂蛋白C3(APOC3)基因3'非翻译区的胞嘧啶替换为鸟嘌呤产生,可区分两个等位基因——S1和S2。S2等位基因与血浆甘油三酯、胆固醇和载脂蛋白(apo)C-III浓度升高有关。在90名年轻男性中,我们研究了相同突变对低密度脂蛋白(LDL)胆固醇对饮食中单不饱和脂肪反应的影响。S2等位基因的频率为0.14。受试者先食用低脂饮食25天,然后食用富含单不饱和脂肪酸的饮食(22%单不饱和脂肪酸,38%总脂肪)28天;在每种饮食结束时测量脂蛋白。载脂蛋白C3S1/载脂蛋白C3S1(S1/S1)和载脂蛋白C3S1/载脂蛋白C3S2(S1/S2)基因型的受试者初始总胆固醇无显著差异。食用富含单不饱和脂肪酸的饮食后,S1/S1受试者的LDL胆固醇显著升高(0.13 mmol/L,P<0.027),而S1/S2受试者则显著降低(-0.18 mmol/L,P<0.046)。饮食诱导的LDL胆固醇、总胆固醇和载脂蛋白B变化存在显著的基因型效应(P<0.00034、P<0.009和P<0.0014)。一项关于该突变与载脂蛋白A1(APOA1)基因启动子区域-76位突变(G/A)之间相互作用影响的研究表明,两种突变对饮食诱导的总胆固醇、LDL胆固醇和载脂蛋白B变化具有累加效应。血浆LDL胆固醇对饮食的反应性至少部分可由载脂蛋白C3基因位点的变异来解释。