Hugh Sinclair Unit of Human Nutrition, Department of Food and Nutritional Sciences, University of Reading, Reading RG6 6AP, UK.
Department of Food Science and Nutrition, Faculty of Health Sciences, The Public Authority for Applied Education and Training, PO Box 14281, AlFaiha 72853, Kuwait.
Nutrients. 2020 May 9;12(5):1357. doi: 10.3390/nu12051357.
Studies in Asian Indians have examined the association of metabolic traits with vitamin D status. However, findings have been quite inconsistent. Hence, we aimed to explore the relationship between metabolic traits and 25-hydroxyvitamin D [25(OH)D] concentrations. We investigate whether this relationship was modified by lifestyle factors using a nutrigenetic approach in 545 Asian Indians randomly selected from the Chennai Urban Rural Epidemiology Study (219 normal glucose tolerant individuals, 151 with pre-diabetes and 175 individuals with type 2 diabetes). A metabolic genetic risk score (GRS) was developed using five common metabolic disease-related genetic variants. There was a significant interaction between metabolic GRS and carbohydrate intake (energy%) on 25(OH)D (P = 0.047). Individuals consuming a low carbohydrate diet (≤62%) and those having lesser number of metabolic risk alleles (GRS ≤ 1) had significantly higher levels of 25(OH)D ( = 0.033). Conversely, individuals consuming a high carbohydrate diet despite having lesser number of risk alleles did not show a significant increase in 25(OH)D ( = 0.662). In summary, our findings show that individuals carrying a smaller number of metabolic risk alleles are likely to have higher 25(OH)D levels if they consume a low carbohydrate diet. These data support the current dietary carbohydrate recommendations of 50%-60% energy suggesting that reduced metabolic genetic risk increases 25(OH)D.
在亚洲人群中进行的研究已经考察了代谢特征与维生素 D 状态之间的关联。然而,研究结果却非常不一致。因此,我们旨在通过营养遗传学方法在 545 名随机选择的来自 Chennai Urban Rural Epidemiology Study 的亚洲印第安人(219 名正常糖耐量个体、151 名糖尿病前期患者和 175 名 2 型糖尿病患者)中探讨代谢特征与 25-羟维生素 D [25(OH)D]浓度之间的关系。我们研究了这种关系是否通过生活方式因素(使用营养遗传学方法)发生改变。使用五种常见的代谢疾病相关遗传变异开发了代谢遗传风险评分 (GRS)。代谢 GRS 与碳水化合物摄入量(能量%)之间存在显著的交互作用(P = 0.047)。摄入低碳水化合物饮食(≤62%)且具有较少代谢风险等位基因数(GRS ≤ 1)的个体具有显著较高的 25(OH)D 水平( = 0.033)。相反,尽管具有较少的风险等位基因,但摄入高碳水化合物饮食的个体 25(OH)D 水平没有显著增加( = 0.662)。总之,我们的研究结果表明,如果摄入低碳水化合物饮食,携带较少代谢风险等位基因的个体可能具有较高的 25(OH)D 水平。这些数据支持当前的饮食碳水化合物推荐量为 50%-60%能量,表明降低代谢遗传风险可增加 25(OH)D。