Lopez-Miranda J, Ordovas J M, Espino A, Marin C, Salas J, Lopez-Segura F, Jimenez-Pereperez J, Perez-Jimenez F
Hospital Universitario Reina Sofia, Cordoba, Spain.
Lancet. 1994 May 21;343(8908):1246-9. doi: 10.1016/s0140-6736(94)92149-0.
The plasma lipid response to changes in dietary fat and cholesterol can vary between individuals. At present, responders cannot be identified in advance. An adenine to guanine (A-->G) mutation in the promoter of the apolipoprotein A1 gene (apoA-1) has been suggested as affecting plasma high-density lipoprotein cholesterol. In 50 young men we examined the effect of the same mutation on the responses of both high and low density lipoprotein cholesterol to low-fat diet. The frequency for the A allele was 0.14. Subjects were fed a low-fat diet for 25 days, followed by a diet rich in monounsaturated fatty acid (MUFA, 22% out of 40% fat) for 28 days and lipoproteins were measured at the end of each diet. There were no differences in initial total cholesterol between subjects with the G/G mutation (170 mg/dL: 100 mg/dL = 2.59 mmol/L) and the G/A mutation (169 mg/dL) genotypes. After consumption of the high monounsaturated fat diet, significant increases were noted in plasma LDL cholesterol (10 mg/dL, p = 0.035) in the G/A subjects but not in the G/G subjects (1 mg/dL, p = 0.996). These differences showed that a significant diet-gene interaction (p = 0.015) existed. No differences were observed on HDL cholesterol between groups. Plasma low-density lipoprotein cholesterol responsiveness to diet may be explained by variation at the apoA-I gene locus.
个体对饮食中脂肪和胆固醇变化的血脂反应可能存在差异。目前,无法提前识别反应者。载脂蛋白A1基因(apoA-1)启动子中的腺嘌呤到鸟嘌呤(A→G)突变被认为会影响血浆高密度脂蛋白胆固醇。在50名年轻男性中,我们研究了相同突变对高密度和低密度脂蛋白胆固醇对低脂饮食反应的影响。A等位基因的频率为0.14。受试者先食用25天低脂饮食,然后食用富含单不饱和脂肪酸(MUFA,占40%脂肪中的22%)的饮食28天,并在每种饮食结束时测量脂蛋白。携带G/G突变(170mg/dL:100mg/dL = 2.59mmol/L)和G/A突变(169mg/dL)基因型的受试者初始总胆固醇无差异。食用高单不饱和脂肪饮食后,G/A受试者的血浆低密度脂蛋白胆固醇显著升高(10mg/dL,p = 0.035),而G/G受试者无显著升高(1mg/dL,p = 0.996)。这些差异表明存在显著的饮食-基因相互作用(p = 0.015)。两组之间的高密度脂蛋白胆固醇无差异。血浆低密度脂蛋白胆固醇对饮食的反应性可能由apoA-I基因位点的变异来解释。