Samblas Mirian, Milagro Fermin I, Gómez-Abellán Purificación, Martínez J Alfredo, Garaulet Marta
Department of Nutrition, Food Science and Physiology, University of Navarra, Pamplona, Spain.
Department of Nutrition, Food Science and Physiology, University of Navarra, Pamplona, Spain Centre for Nutrition Research, University of Navarra, Pamplona, Spain CIBERobn, Physiopathology of Obesity, Carlos III Institute, Madrid, Spain.
J Biol Rhythms. 2016 Jun;31(3):308-17. doi: 10.1177/0748730416629247. Epub 2016 Feb 11.
The circadian clock system has been linked to the onset and development of obesity and some accompanying comorbidities. Epigenetic mechanisms, such as DNA methylation, are putatively involved in the regulation of the circadian clock system. The aim of this study was to investigate the influence of a weight loss intervention based on an energy-controlled Mediterranean dietary pattern in the methylation levels of 3 clock genes, BMAL1, CLOCK, and NR1D1, and the association between the methylation levels and changes induced in the serum lipid profile with the weight loss treatment. The study sample enrolled 61 women (body mass index = 28.6 ± 3.4 kg/m(2); age: 42.2 ± 11.4 years), who followed a nutritional program based on a Mediterranean dietary pattern. DNA was isolated from whole blood obtained at the beginning and end point. Methylation levels at different CpG sites of BMAL1, CLOCK, and NR1D1 were analyzed by Sequenom's MassArray. The energy-restricted intervention modified the methylation levels of different CpG sites in BMAL1 (CpGs 5, 6, 7, 9, 11, and 18) and NR1D1 (CpGs 1, 10, 17, 18, 19, and 22). Changes in cytosine methylation in the CpG 5 to 9 region of BMAL1 with the intervention positively correlated with the eveningness profile (p = 0.019). The baseline methylation of the CpG 5 to 9 region in BMAL1 positively correlated with energy (p = 0.047) and carbohydrate (p = 0.017) intake and negatively correlated with the effect of the weight loss intervention on total cholesterol (p = 0.032) and low-density lipoprotein cholesterol (p = 0.005). Similar significant and positive correlations were found between changes in methylation levels in the CpG 5 to 9 region of BMAL1 due to the intervention and changes in serum lipids (p < 0.05). This research describes apparently for the first time an association between changes in the methylation of the BMAL1 gene with the intervention and the effects of a weight loss intervention on blood lipids levels.
昼夜节律时钟系统已被证实与肥胖症及其一些伴随的合并症的发生和发展有关。表观遗传机制,如DNA甲基化,被认为参与了昼夜节律时钟系统的调节。本研究的目的是调查基于能量控制的地中海饮食模式的减肥干预对3个时钟基因BMAL1、CLOCK和NR1D1甲基化水平的影响,以及甲基化水平与减肥治疗引起的血清脂质谱变化之间的关联。研究样本纳入了61名女性(体重指数=28.6±3.4kg/m²;年龄:42.2±11.4岁),她们遵循基于地中海饮食模式的营养计划。在开始和终点时采集全血并分离DNA。通过Sequenom的MassArray分析BMAL1、CLOCK和NR1D1不同CpG位点的甲基化水平。能量限制干预改变了BMAL1(CpGs 5、6、7、9、11和18)和NR1D1(CpGs 1、10、17、18、19和22)不同CpG位点的甲基化水平。干预后BMAL1的CpG 5至9区域胞嘧啶甲基化的变化与晚间型特征呈正相关(p = 0.019)。BMAL1的CpG 5至9区域的基线甲基化与能量(p = 0.047)和碳水化合物(p = 0.017)摄入量呈正相关,与减肥干预对总胆固醇(p = 0.032)和低密度脂蛋白胆固醇(p = 0.005)的影响呈负相关。干预导致的BMAL1的CpG 5至9区域甲基化水平变化与血清脂质变化之间也发现了类似的显著正相关(p < 0.05)。本研究首次描述了BMAL1基因甲基化变化与干预以及减肥干预对血脂水平影响之间的关联。