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The combined effects of genetic variation in the SIRT1 gene and dietary intake of n-3 and n-6 polyunsaturated fatty acids on serum LDL-C and HDL-C levels: a population based study

机译:SIRT1基因遗传变异与膳食摄入n-3和n-6多不饱和脂肪酸对血清LDL-C和HDL-C水平的综合影响:一项基于人群的研究

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Background Dyslipidemia due to high total cholesterol, LDL-cholesterol, triglycerides, or low HDL-cholesterol is an important risk factor for coronary heart disease (CHD). Both SIRT1 and PUFAs can influence the expression of genes for nuclear receptors and transcription factors related to lipid metabolism such as LXRα, LXRβ, PPARα, SREBP-1c. Methods A total of 707 Japanese males and 723 females were randomly selected from the participants who visited a medical center for routine medical check-ups. We analyzed the combined effects of the genotype/haplotype of the SIRT1 gene and dietary n-6-3 PUFA intake ratio on the determination of serum lipid levels. Results We found that the SIRT1 gene marked with haplotype 2 was associated with decreased serum LDL-cholesterol and increased HDL-cholesterol levels. In addition, the associations between the SIRT1 haplotype 2 and decreased LDL-C and increased HDL-C levels were only observed in the low n-6-3 PUFA intake ratio group, but not in the high n-6-3 PUFA intake ratio group. Conclusions Our findings indicate that the combination of genetic variation in the SIRT1 gene and dietary n-6 and/or n-3 PUFA intake influence the determination of inter-individual variations of serum levels of LDL-C and HDL-C.
机译:背景高胆固醇,低密度脂蛋白胆固醇,甘油三酸酯或低密度脂蛋白胆固醇引起的血脂异常是冠心病(CHD)的重要危险因素。 SIRT1和PUFA均可影响与脂质代谢有关的核受体基因和转录因子的表达,例如LXRα,LXRβ,PPARα,SREBP-1c。方法从访问医疗中心进行常规体检的参与者中随机抽取707名日本男性和723名女性。我们分析了SIRT1基因的基因型/单倍型与饮食中n-6 / n-3 PUFA摄入比对确定血脂水平的综合影响。结果我们发现标记为单倍型2的SIRT1基因与血清LDL-胆固醇降低和HDL-胆固醇水平升高相关。此外,仅在低n-6 / n-3 PUFA摄入比率组中观察到SIRT1单倍型2与LDL-C降低和HDL-C水平升高之间的关联,而在高n-6 / n-PUFA摄入率组中则未观察到这种关联。 3 PUFA摄入比例组。结论我们的发现表明,SIRT1基因的遗传变异与饮食中n-6和/或n-3 PUFA摄入量的组合会影响血清LDL-C和HDL-C水平个体差异的确定。

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