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首页> 外文期刊>Proceedings of the Nutrition Society >Nutrigenetics and personalised nutrition: how far have we progressed and are we likely to get there?
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Nutrigenetics and personalised nutrition: how far have we progressed and are we likely to get there?

机译:营养遗传学和个性化营养:我们取得了多大的进展,我们有可能到达那里?

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Nutrigenetics and personalised nutrition are components of the concept that in the future genotyping will be used as a means of defining dietary recommendations to suit the individual. Over the last two decades there has been an explosion of research in this area, with often conflicting findings reported in the literature. Reviews of the literature in the area of apoE genotype and cardiovascular health, apoA5 genotype and postprandial lipaemia and perilipin and adiposity are used to demonstrate the complexities of genotype-phenotype associations and the aetiology of apparent between-study inconsistencies in the significance and size of effects. Furthermore, genetic research currently often takes a very reductionist approach, examining the interactions between individual genotypes and individual disease biomarkers and how they are modified by isolated dietary components or foods. Each individual possesses potentially hundreds of 'at-risk' gene variants and consumes a highly-complex diet. In order for nutrigenetics to become a useful public health tool, there is a great need to use mathematical and bioinformatic tools to develop strategies to examine the combined impact of multiple gene variants on a range of health outcomes and establish how these associations can be modified using combined dietary strategies.
机译:营养遗传学和个性化营养是这一概念的组成部分,将来,基因分型将被用作定义适合个人的饮食建议的手段。在过去的二十年中,该领域的研究激增,文献中报道的发现常常相互矛盾。关于apoE基因型和心血管健康,apoA5基因型和餐后脂血以及周脂蛋白和肥胖症领域的文献综述被用来证明基因型-表型关联的复杂性以及在研究之间的不一致和病因学的显着性和影响大小。此外,目前的遗传研究通常采用非常简化的方法,研究个体基因型和个体疾病生物标记之间的相互作用,以及如何通过孤立的饮食成分或食物对它们进行修饰。每个人都可能拥有数百个“高风险”基因变体,并消耗高度复杂的饮食。为了使营养遗传学成为有用的公共卫生工具,迫切需要使用数学和生物信息学工具来开发策略,以检查多种基因变异对一系列健康结果的综合影响,并确定如何使用综合饮食策略。

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