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Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

机译:饮食干预研究中葡萄糖激酶调节蛋白基因多态性影响餐后脂血症反应

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Postprandial triglyceridemia is an emerging risk factor for cardiovascular disease. However, most of the genes that influence postprandial triglyceridemia are not known. We evaluated whether a common nonsynonymous SNP rs1260326/P446L in the glucokinase regulatory protein (GCKR) gene influenced variation in the postprandial lipid response after a high-fat challenge in seven hundred and seventy participants in the Amish HAPI Heart Study who underwent an oral high-fat challenge and had blood samples taken in the fasting state and during the postprandial phase at 1, 2, 3, 4, and 6 h. We found that the minor T allele at rs1260326 was associated with significantly higher fasting TG levels after adjusting for age, sex, and family structure (P a = 0.06 for additive model, and P r = 0.0003 for recessive model). During the fat challenge, the T allele was associated with significantly higher maximum TG level (P a = 0.006), incremental maximum TG level (P a = 0.006), TG area under the curve (P a = 0.02) and incremental TG area under the curve (P a = 0.03). Our data indicate that the rs1260326 T allele of GCKR is associated with both higher fasting levels of TG as well as the postprandial TG response, which may result in higher atherogenic risk.
机译:餐后甘油三酸酯血症是心血管疾病的新兴危险因素。但是,影响餐后甘油三酯血症的大多数基因尚不清楚。我们评估了接受Amish HAPI心脏研究的700名参与者的高脂挑战后,其葡萄糖激酶调节蛋白(GCKR)基因中常见的非同义SNP rs1260326 / P446L是否影响了餐后脂质反应的变化挑战脂肪,并在禁食状态和餐后1、2、3、4和6小时采集血样。我们发现,在调整了年龄,性别和家庭结构后,rs1260326的次要T等位基因与空腹TG水平显着相关(加性模型P a = 0.06,P r < / sub> = 0.0003(对于隐性模型)。在脂肪激发期间,T等位基因与最高TG水平(P a = 0.006),最高TG增量(P a = 0.006)显着较高,TG面积相关。曲线下(P a = 0.02)和曲线下的TG增量(P a = 0.03)。我们的数据表明,GCKR的rs1260326 T等位基因与较高的TG空腹水平以及餐后TG反应相关,这可能导致更高的动脉粥样硬化风险。

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