首页> 外文期刊>European journal of human genetics: EJHG >Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents
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Dietary fat quality impacts genome-wide DNA methylation patterns in a cross-sectional study of Greek preadolescents

机译:饮食脂肪质量影响希腊青少年前期横断面研究的全基因组DNA甲基化模式

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The type and the amount of dietary fat have a significant influence on the metabolic pathways involved in the development of obesity, metabolic syndrome, diabetes type 2 and cardiovascular diseases. However, it is unknown to what extent this modulation is achieved through DNA methylation. We assessed the effects of cholesterol intake, the proportion of energy intake derived from fat, the ratio of polyunsaturated fatty acids (PUFA) to saturated fatty acids (SFA), the ratio of monounsaturated fatty acids (MUFA) to SFA, and the ratio of MUFA+PUFA to SFA on genome-wide DNA methylation patterns in normal-weight and obese children. We determined the genome-wide methylation profile in the blood of 69 Greek preadolescents (similar to 10 years old) as well as their dietary intake for two consecutive weekdays and one weekend day. The methylation levels of one CpG island shore and four sites were significantly correlated with total fat intake. The methylation levels of 2 islands, 11 island shores and 16 sites were significantly correlated with PUFA/SFA; of 9 islands, 26 island shores and 158 sites with MUFA/SFA; and of 10 islands, 40 island shores and 130 sites with (MUFA+PUFA)/SFA. We found significant gene enrichment in 34 pathways for PUFA/SFA, including the leptin pathway, and a significant enrichment in 5 pathways for (MUFA+PUFA)/SFA. Our results suggest that specific changes in DNA methylation may have an important role in the mechanisms involved in the physiological responses to different types of dietary fat.
机译:饮食脂肪的类型和数量对与肥胖,代谢综合征,2型糖尿病和心血管疾病发展有关的代谢途径具有重要影响。然而,尚不清楚这种调节通过DNA甲基化达到何种程度。我们评估了胆固醇摄入,脂肪摄入能量的比例,多不饱和脂肪酸(PUFA)与饱和脂肪酸(SFA)的比例,单不饱和脂肪酸(MUFA)与SFA的比例以及MUFA + PUFA对SFA的正常体重和肥胖儿童的全基因组DNA甲基化模式。我们确定了69个希腊青少年(约10岁)的血液中全基因组甲基化分布,以及两个连续工作日和一个周末的饮食摄入量。一个CpG岛岸和四个地点的甲基化水平与总脂肪摄入量显着相关。 2个岛屿,11个岛屿海岸和16个地点的甲基化水平与PUFA / SFA显着相关。 MUFA / SFA中的9个岛屿,26个岛屿海岸和158个地点; (MUFA + PUFA)/ SFA的10个岛屿,40个岛屿海岸和130个站点。我们发现PUFA / SFA的34条途径(包括瘦素途径)中有大量基因富集,而MUFA + PUFA)/ SFA的5条途径中有大量基因富集。我们的结果表明,DNA甲基化的特定变化可能在涉及对不同类型饮食脂肪的生理反应的机制中具有重要作用。

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