Jansen S, Lopez-Miranda J, Salas J, Ordovas J M, Castro P, Marin C, Ostos M A, Lopez-Segura F, Jimenez-Pereperez J A, Blanco A, Perez-Jimenez F
Lipid Research Unit, University Hospital Reina Sofía, University of Córdoba Medical School, Spain.
Arterioscler Thromb Vasc Biol. 1997 Aug;17(8):1532-8. doi: 10.1161/01.atv.17.8.1532.
Lipid response to dietary fat and cholesterol is, to a large extent, genetically controlled. Apoprotein (apo) A-IV has been related to fat absorption and to the activation of some of the enzymes involved in lipid metabolism. One mutation has been described in the apo A-IV gene that causes substitution of Ser for Thr at position 347. To study the influence of this mutation on the plasma LDL cholesterol (LDL-C) response in diets of various fat content and fatty acid saturation, 41 healthy male subjects were studied, 25 of whom were homozygous for the Thr allele (347Thr) and the rest who were either homozygous (n = 2) or heterozygous carriers of the Ser allele (347Ser). They consumed three consecutive diets, each of 4 weeks' duration: one rich in saturated fat (SFA diet: 38% fat, 20% saturated), a National Cholesterol Education Program (NCEP) type 1 diet (28% fat, 10% saturated), and a third rich in monounsaturated fat (MUFA diet; 38% fat, 22% monounsaturated). Carriers of the 347Ser allele presented a greater decrease in total cholesterol (-0.7 vs -0.44 mmol/L, P < .034), LDL-C (-0.62 vs -0.31 mmol/L, P < .012), and apo B (-14 vs -8 mg/dL, P < .01) levels when they were switched from the SFA to the NCEP type 1 diet than homozygous carriers of the 347Thr allele. The change from the NCEP type 1 to the MUFA diet resulted in a greater increase in total cholesterol (0.18 vs -0.05 mmol/L, P < .028) and apo B (5 vs -1 mg/dL, P < .006) levels in the 347Ser than in the 347Thr individuals. In a previous study, we demonstrated that the G-->A polymorphism at position -76 of the gene promoter of apo A-I affects the LDL-C response to dietary fat. We therefore decided to study the effect of the interaction between these mutations on this response. We found that both mutations have an additive effect on total cholesterol, LDL-C, and apo B dietary-induced changes. Our results suggest that total cholesterol and LDL-C response to dietary fat is influenced by the 347Ser mutation of apo A-IV.
脂质对膳食脂肪和胆固醇的反应在很大程度上受基因控制。载脂蛋白(apo)A-IV与脂肪吸收以及脂质代谢中一些相关酶的激活有关。已在apo A-IV基因中描述了一种突变,该突变导致第347位的苏氨酸被丝氨酸取代。为了研究这种突变对不同脂肪含量和脂肪酸饱和度饮食中血浆低密度脂蛋白胆固醇(LDL-C)反应的影响,对41名健康男性受试者进行了研究,其中25人是苏氨酸等位基因(347Thr)的纯合子,其余受试者要么是丝氨酸等位基因(347Ser)的纯合子(n = 2),要么是杂合携带者。他们连续食用三种饮食,每种饮食持续4周:一种富含饱和脂肪(饱和脂肪饮食:38%脂肪,20%饱和脂肪),一种是美国国家胆固醇教育计划(NCEP)1型饮食(28%脂肪,10%饱和脂肪),第三种富含单不饱和脂肪(单不饱和脂肪饮食;38%脂肪,22%单不饱和脂肪)。当从饱和脂肪饮食转换为NCEP 1型饮食时,347Ser等位基因的携带者在总胆固醇(-0.7 vs -0.44 mmol/L,P <.034)、LDL-C(-0.62 vs -0.31 mmol/L,P <.012)和载脂蛋白B(-14 vs -8 mg/dL,P <.01)水平上的下降幅度比347Thr等位基因的纯合携带者更大。从NCEP 1型饮食转换为单不饱和脂肪饮食后,347Ser个体的总胆固醇(0.18 vs -0.05 mmol/L,P <.028)和载脂蛋白B(5 vs -1 mg/dL,P <.006)水平的升高幅度比347Thr个体更大。在先前的一项研究中,我们证明了apo A-I基因启动子-76位的G→A多态性会影响LDL-C对膳食脂肪的反应。因此,我们决定研究这些突变之间的相互作用对这种反应的影响。我们发现这两种突变对总胆固醇、LDL-C和膳食诱导的载脂蛋白B变化具有累加效应。我们的结果表明,总胆固醇和LDL-C对膳食脂肪的反应受apo A-IV的347Ser突变影响。