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首页> 外文期刊>Frontiers in Nutrition >Genetic Variants Shaping Inter-individual Differences in Response to Dietary Intakes—A Narrative Review of the Case of Vitamins
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Genetic Variants Shaping Inter-individual Differences in Response to Dietary Intakes—A Narrative Review of the Case of Vitamins

机译:遗传变异塑造各种间差异,响应饮食摄入量 - 对维生素案例的叙事综述

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摘要

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.
机译:Nutrigenetics领域的最新进展已经为遗传变异如何影响个人对膳食摄入量的反应提供了证据。对饮食暴露的客观可靠的评估应依赖于包括频率问卷,短期召回或记录的方法的组合以及生物样本,以评估摄入或地位的标志物并鉴定遗传敏感性。为了试图展示关于遗传指纹如何促进个人营养状况的贡献,我们介绍了当前文献的审查,描述了遗传变异与维生素状态良好的生物标志物在自由生和一般健康的个体中良好的生物标志物水平的关联。基于候选基因的结果,基因组关联研究及其荟萃分析,我们已经鉴定了参与维生素代谢途径的几种单一核苷酸多态性(SNP)。据报道,编码参与维生素代谢和运输的蛋白质的基因中的多态性对维生素D状态产生影响;虽然维生素D受体的遗传变异最常与健康结果相关。可以影响维生素E状态的遗传变异包括其摄取和运输中涉及的SNP,例如SCAS-B1基因,以及脂蛋白代谢。编码依赖于依赖性维生素C输送蛋白的基因的变体与身体在维生素C上的身体状态大致相关。关于B-复合物的维生素,对MTHFR基因的广泛学习变体进行了特别参考。还讨论了可能限制研究结果可比性和可解释性的遗传研究的方法论。我们对基因对营养触发的反应的理解将提高我们评估膳食风险和设计个性化营养计划的能力,以维持健康和预防疾病。

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