Nutrigenomics

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What are Nutrigenomics?

Nutrigenomics can be defined as the study of the relationships between dietary factors and individual genes. Nutrigenomics is sometimes referred to as:

  • nutritional genomics
  • nutrigenetics
  • nutritional genetics
  • the DNA die
Definitions of nutrigenomics often include the determination of individual nutritional requirements based on the genetic makeup of the person, as well as the association between diet and chronic disease. Nutrigenomics is part of a broader movement toward personalized medicine, focusing on a personalized diet.

Some scientists distinguish between nutrigenomics and nutrigenetics. They define nutrigenomics as the identification of genes that are involved in physiological responses to diet and the genes in which small changes, called polymorphisms, may have significant nutritional consequences. Nutrigenetics is then defined as the study of these individual genetic variations or polymorphisms, their interaction with nutritional factors, and their association with health and disease. Others define nutrigenetics as the study of the functional interactions between food and the genome at the molecular, cellular, and organismic levels, and the ways in which individuals respond differently to diets depending on their genetic makeup.

Jose M. Ordovas, a pioneer researcher in the field, uses the following definition: ‘Nutritional genomics covers nutrigenomics, which explores the effects of nutrients on the genome, proteome and metabolome, and nutrigenetics, the major goal of which is to elucidate the effect of genetic variation on the interaction between diet and disease.’ The genome is the DNA that makes up an individual’s genes. The proteome consists of all of the proteins—the products of gene expression—that are produced under specific conditions. The metabolome is comprised of all of the metabolites in the body under specific dietary and physiological conditions. However many authors do not distinguish between the terms nutritional genomics, nutrigenomics, and nutrigenetics.

What are the Origins of Nutrigenomics?

The concept that diet influences health is an ancient one. In 400 B.C. Hippocrates advised physicians: ‘Leave your drugs in the chemist’s pot if you can heal your patient with food.’ Likewise it has long been known that individuals can differ in their requirements for a given nutrient.

Nutrigenomics includes known interactions between food and inherited genes, called ‘inborn errors of metabolism,’ that have long been treated by manipulating the diet:

  • Phenylketonuria (PKU) is caused by a change (mutation) in a single gene. Affected individuals must avoid food containing the amino acid phenylalanine.
  • Many Asians have a defective aldehyde dehydrogenase enzyme, which is involved in ethanol metabolism. Alcohol consumption has unpleasant effects on these individuals.
  • Galactosemia—caused by an inherited defect in one of three enzymes involved in the metabolism of the sugar galactose—is controlled with a milk-free diet, since galactose is a metabolite or breakdown product of lactose or milk sugar.
  • The majority of adults in the world are lactose intolerant, meaning that they cannot digest milk products, because the gene encoding lactase, the enzyme that breaks down lactose, is normally ‘turned off after weaning. However some 10,000-12,000 years ago a polymorphism in a single DNA nucleotide appeared among northern Europeans. This single nucleotide polymorphism—a SNP—resulted in the continued expression of the lactase gene into adulthood. This was advantageous because people with this SNP could utilize nutritionally-rich dairy products in regions with short growing seasons.
With the revolution in molecular genetics in the late twentieth century, scientists set out to identify other genes that interact with dietary components. By the 1980s companies were commercializing nutrigenomics. The Human Genome Project of the 1990s, which sequenced all of the DNA in the human genome, jump-started the science of nutrigenomics. By 2007 scientists were discovering numerous interrelationships between genes, nutrition, and disease.

Known interactions between food and inherited genes

Genetic conditionFoods to avoid
Phenylketonuria (PKU)Food containing the amino acid phenylalanine, including high protein food such as fish, chicken, eggs, milk, cheese, dried beans, nuts, and tofu
Defective aldehyde dehydrogenase enzymeAlcohol
Galactosemia (lack of a liver enzyme to digest galactose)Diets which contain no lactose or galactose, including all milk and milk products
Lactose intolerance (shortage of the enzyme lactaseMilk and milk products
nutrigenomics
plural noun   the study of how food affects people according to their genetic make-up
If you're already thinking, like many Australians, what should I do because I'm half Italian and half Scottish, or half Greek and half Irish, relax. The wizards behind nutrigenomics say that about 65 per cent of us should stick with the fruits, vegetables and proteins that form the basis of good nutrition. Those with the most to gain from gene-determined diets are the fortunate few who will discover they really can eat whatever they want (The Courier-mail )

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Nutrigenomics is the study of the effects of foods and food constituents on gene expression. It is about how our DNA is transcribed into mRNA and then to proteins and provides a basis for understanding the biological activity of food components.[1] Nutrigenomics has also been described by the influence of genetic variation on nutrition by correlating gene expression or single-nucleotide polymorphisms with a nutrient's absorption, metabolism, elimination or biological effects. By doing so, nutrigenomics aims to develop rational means to optimise nutrition, with respect to the subject's genotype.

By determining the mechanism of the effects of nutrients or the effects of a nutritional regime, nutrigenomics tries to define the causality|relationship between these specific nutrients and specific nutrient regimes (diets) on human health. Nutrigenomics has been associated with the idea of personalized nutrition based on genotype. While there is hope that nutrigenomics will ultimately enable such personalised dietary advice, it is a science still in its infancy and its contribution to public health over the next decade is thought to be major.[2]

Contents

Definitions

Nutrigenomics has been defined as the application of high-throughput genomic tools in nutrition research. It can also be seen as research to provide people with methods and tools who are looking for disease preventing and health promoting foods that match their lifestyles, cultures and genetics.

The term "high throughput tools" in nutrigenomics refers to genetic tools that enable millions of genetic screening tests to be conducted at a single time. When such high throughput screening is applied in nutrition research, it allows the examination of how nutrients affect the thousands of genes present in the human genome. Nutrigenomics involves the characterization of gene products and the physiological function and interactions of these products. This includes how nutrients impact on the production and action of specific gene products and how these proteins in turn affect the response to nutrients.

Background and preventive health

Throughout the 20th century, nutritional science focused on finding vitamins and minerals, defining their use and preventing the deficiency diseases that they caused. As the nutrition related health problems of the developed world shifted to overnutrition, obesity and type two diabetes, the focus of modern medicine and of nutritional science changed accordingly.

To address the increasing incidence of these diet-related-diseases, the role of diet and nutrition has been and continues to be extensively studied. To prevent the development of disease, nutrition research is investigating how nutrition can optimize and maintain cellular, tissue, organ and whole body homeostasis. This requires understanding how nutrients act at the molecular level. This involves a multitude of nutrient-related interactions at the gene, protein and metabolic levels. As a result, nutrition research has shifted from epidemiology and physiology to molecular biology and genetics[2] and nutrigenomics was born.

The emergence and development of nutrigenomics has been possible due to powerful developments in genetic research. Inter-individual differences in genetics, or genetic variability, which have an effect on metabolism and on phenotypes were recognized early in nutrition research, and such phenotypes were described. With the progress in genetics, biochemical disorders with a high nutritional relevance were linked to a genetic origin. Genetic disorders which cause pathological effects were described. Such genetic disorders include the polymorphism in the gene for the hormone Leptin which results in gross obesity. Other gene polymorphisms were described with consequences for human nutrition. The folate metabolism is a good example, where a common polymorphism exists for the gene that encodes the methylene-tetrahydro-folate reductase (MTHFR).

It was realized however, that there are possibly thousands of other gene polymorphisms which may result in minor deviations in nutritional biochemistry, where only marginal or additive effects would result from these deviations. The tools to study the physiological impact were not available at the time and are only now becoming available enabling the development of nutrigenomics. Such tools include those that measure the transcriptome - DNA microarray, Exon array, Tiling arrays, single nucleotide polymorphism arrays and genotyping. Tools that measure the proteome are less developed. These include methods based on gel electrophoresis, chromatography and mass spectrometry. Finally the tools that measure the metabolome are also less developed and include methods based on nuclear magnetic resonance imaging and mass spectrometry often in combination with gas and liquid chromatography.

Rationale and aims of nutrigenomics

In nutrigenomics, nutrients are seen as signals that tell a specific cell in the body about the diet. The nutrients are detected by a sensor system in the cell. Such a sensory system works like sensory ecology whereby the cell obtains information through the signal, the nutrient, about its environment, which is the diet. The sensory system that interprets information from nutrients about the dietary environment include transcription factors together with many additional proteins. Once the nutrient interacts with such a sensory system, it changes gene, protein expression and metabolite production in accordance with the level of nutrient it senses. As a result, different diets should elicit different patterns of gene and protein expression and metabolite production. Nutrigenomics seeks to describe the patterns of these effects which have been referred to as dietary signatures. Such dietary signatures are examined in specific cells, tissues and organisms and in this way the manner by which nutrition influences homeostasis is investigated. Genes which are affected by differing levels of nutrients need first to be identified and then their regulation is studied. Differences in this regulation as a result of differences in genes between individuals are also studied.[2]

It is hoped that by building up knowledge in this area, nutrigenomics will promote an increased understanding of how nutrition influences metabolic pathways and homeostatic control, which will then be used to prevent the development of chronic diet related diseases such as obesity and type two diabetes. Part of the approach of nutrigenomics involves finding markers of the early phase of diet related diseases; this is the phase at which intervention with nutrition can return the patient to health. As nutrigenomics seeks to understand the effect of different genetic predispositions in the development of such diseases, once a marker has been found and measured in an individual, the extent to which they are susceptible to the development of that disease will be quantified and personalized dietary recommendation can be given for that person.

The aims of nutrigenomics also includes being able to demonstrate the effect of bioactive food compounds on health and the effect of health foods on health, which should lead to the development of functional foods that will keep people healthy according to their individual needs.

Nutrigenomics is a rapidly emerging science still in its beginning stages. It is uncertain whether the tools to study protein expression and metabolite production have been developed to the point as to enable efficient and reliable measurements. Also once such research has been achieved, it will need to be integrated together to produce results and dietary recommendations. All of these technologies are still in the process of development.

See also

References

  1. ^ Rawson, N. (October 24, 2008). Nutrigenomics Boot Camp: Improving Human Performance through Nutrigenomic Discovery. A Supply Side West VendorWorks Presentation. Las Vegas, Nevada 
  2. ^ a b c Müller M, Kersten S. (2003). Nutrigenomics: Goals and Perspectives.. Nature Reviews Genetics 4. 315 -322. 

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