Niforou Aikaterini, Konstantinidou Valentini, Naska Androniki
Department of Hygiene, Epidemiology and Medical Statistics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
DNANUTRICOACH®, MEDOLIALI SL, Barcelona, Spain.
Front Nutr. 2020 Dec 1;7:558598. doi: 10.3389/fnut.2020.558598. eCollection 2020.
Recent advances in the field of nutrigenetics have provided evidence on how genetic variations can impact the individuals' response to dietary intakes. An objective and reliable assessment of dietary exposures should rely on combinations of methodologies including frequency questionnaires, short-term recalls or records, together with biological samples to evaluate markers of intake or status and to identify genetic susceptibilities. In an attempt to present current knowledge on how genetic fingerprints contribute to an individual's nutritional status, we present a review of current literature describing associations between genetic variants and levels of well-established biomarkers of vitamin status in free-living and generally healthy individuals. Based on the outcomes of candidate gene, genome-wide-association studies and meta-analyses thereof, we have identified several single nucleotide polymorphisms (SNPs) involved in the vitamins' metabolic pathways. Polymorphisms in genes encoding proteins involved in vitamin metabolism and transport are reported to have an impact on vitamin D status; while genetic variants of vitamin D receptor were most frequently associated with health outcomes. Genetic variations that can influence vitamin E status include SNPs involved in its uptake and transport, such as in SCAR-B1 gene, and in lipoprotein metabolism. Variants of the genes encoding the sodium-dependent vitamin C transport proteins are greatly associated with the body's status on vitamin C. Regarding the vitamins of the B-complex, special reference is made to the widely studied variant in the MTHFR gene. Methodological attributes of genetic studies that may limit the comparability and interpretability of the findings are also discussed. Our understanding of how genes affect our responses to nutritional triggers will enhance our capacity to evaluate dietary exposure and design personalized nutrition programs to sustain health and prevent disease.
营养遗传学领域的最新进展为基因变异如何影响个体对饮食摄入的反应提供了证据。对饮食暴露进行客观可靠的评估应依赖多种方法的结合,包括频率问卷、短期回忆或记录,以及生物样本,以评估摄入或状态的标志物,并识别遗传易感性。为了介绍关于基因指纹如何影响个体营养状况的现有知识,我们对当前文献进行了综述,这些文献描述了自由生活且总体健康的个体中基因变异与成熟的维生素状态生物标志物水平之间的关联。基于候选基因、全基因组关联研究及其荟萃分析的结果,我们确定了几种参与维生素代谢途径的单核苷酸多态性(SNP)。据报道,参与维生素代谢和运输的蛋白质编码基因中的多态性会影响维生素D状态;而维生素D受体的基因变异最常与健康结果相关。可影响维生素E状态的基因变异包括参与其摄取和运输的SNP,如在SCAR - B1基因以及脂蛋白代谢中的SNP。编码钠依赖性维生素C转运蛋白的基因变异与人体维生素C状态密切相关。关于B族维生素,特别提到了MTHFR基因中广泛研究的变异。还讨论了可能限制研究结果可比性和可解释性的基因研究方法学特征。我们对基因如何影响我们对营养触发因素反应的理解将增强我们评估饮食暴露和设计个性化营养计划以维持健康和预防疾病的能力。