Corella D, Tucker K, Lahoz C, Coltell O, Cupples L A, Wilson P W, Schaefer E J, Ordovas J M
Lipid Metabolism Laboratory and the Epidemiology Program, Jean Mayer-US Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, Boston, MA 02111, USA.
Am J Clin Nutr. 2001 Apr;73(4):736-45. doi: 10.1093/ajcn/73.4.736.
The effect of alcohol drinking on LDL-cholesterol concentrations is unclear. The reported variability may be due to interactions between genetic factors and alcohol intake.
The purpose of the study was to examine whether variation at the apolipoprotein E gene (APOE) locus modulates the association between alcohol drinking and LDL cholesterol.
We used a cross-sectional design in a healthy population-based sample of 1014 men and 1133 women from the Framingham Offspring Study.
In male nondrinkers (n = 197), LDL cholesterol was not significantly different across APOE allele groups [APOEE2 (E2), APOEE3 (E3), and APOE*E4 (E4)]. However, in male drinkers (n = 817), differences were observed (P: < 0.001); those with the E2 allele had the lowest concentrations. LDL cholesterol in men with the E2 allele was significantly lower in drinkers than in nondrinkers but was significantly higher in drinkers than in nondrinkers in men with the E4 allele. This APOE-alcohol interaction remained significant (P < 0.001) after age, body mass index, smoking status, and fat and energy intakes were controlled for. In women, the expected effect of APOE alleles on LDL cholesterol occurred in both drinkers (n = 791; P < 0.001) and nondrinkers (n = 342; P < 0.001). Multiple linear regression models showed a negative association (P < 0.05) between alcohol and LDL cholesterol in men with the E2 allele but a positive association in men with the E4 allele. No significant associations were observed in men or women with the E3 allele.
In men, the effects of alcohol intake on LDL cholesterol are modulated in part by variability at the APOE locus.
饮酒对低密度脂蛋白胆固醇浓度的影响尚不清楚。报告的变异性可能是由于遗传因素与酒精摄入量之间的相互作用。
本研究的目的是检验载脂蛋白E基因(APOE)位点的变异是否调节饮酒与低密度脂蛋白胆固醇之间的关联。
我们在弗雷明汉后代研究中以健康人群为基础的1014名男性和1133名女性样本中采用了横断面设计。
在男性不饮酒者(n = 197)中,APOE等位基因组[APOEE2(E2)、APOEE3(E3)和APOE*E4(E4)]之间的低密度脂蛋白胆固醇没有显著差异。然而,在男性饮酒者(n = 817)中,观察到了差异(P < 0.001);携带E2等位基因的人浓度最低。携带E2等位基因的男性饮酒者的低密度脂蛋白胆固醇显著低于不饮酒者,但携带E4等位基因的男性饮酒者的低密度脂蛋白胆固醇显著高于不饮酒者。在控制了年龄、体重指数、吸烟状况以及脂肪和能量摄入量后,这种APOE-酒精相互作用仍然显著(P < 0.001)。在女性中,APOE等位基因对低密度脂蛋白胆固醇的预期影响在饮酒者(n = 791;P < 0.001)和不饮酒者(n = 342;P < 0.001)中均出现。多元线性回归模型显示,携带E2等位基因的男性中酒精与低密度脂蛋白胆固醇呈负相关(P < 0.05),而携带E4等位基因的男性中呈正相关。在携带E3等位基因的男性或女性中未观察到显著关联。
在男性中,饮酒对低密度脂蛋白胆固醇的影响部分受APOE位点变异性的调节。