Sedová L, Seda O
Ustav biologie a lékarské genetiky, 1. LF UK, Praha.
Cas Lek Cesk. 2004;143(10):676-8; discussion 679.
The importance of nutrition for human health and its influence on the onset and course of many diseases are nowadays considered as proven. Only the recent development of molecular biology and biochemical methods allows the elucidation of the molecular mechanisms of diet constituent actions and their subsequent effect on homeostatic mechanisms in health and disease states. The availability of the draft human genome sequence as well as the genome sequences of model organisms, combined with the functional and integrative genomics approaches of systems biology, bring about the possibility to identify alleles and haplotypes responsible for specific reaction to the dietary challenge in susceptible individuals. Such complex interactions are studied within the newly conceived field, the nutrition genomics (nutrigenomics). Using the tools of highly parallel analyses of transcriptome, proteome and metabolome, the nutrition genomics pursues its ultimate goal, i.e. the individualized diet, respecting not only quantitative and qualitative nutritional needs and the actual health status, but also the genetic predispositions of an individual. This approach should lead to prevention of the onset of such diseases as obesity, hypertension or type 2 diabetes, or enhance the efficiency of their therapy.
如今,营养对人类健康的重要性及其对许多疾病的发生和发展过程的影响已被视为确凿无疑。只有分子生物学和生化方法的最新发展,才使得阐明饮食成分作用的分子机制及其随后对健康和疾病状态下稳态机制的影响成为可能。人类基因组序列草图以及模式生物的基因组序列的可得性,再加上系统生物学的功能和整合基因组学方法,带来了识别在易感个体中对饮食挑战产生特定反应的等位基因和单倍型的可能性。这种复杂的相互作用在新构想的营养基因组学领域中得到研究。营养基因组学利用转录组、蛋白质组和代谢组的高度平行分析工具,追求其最终目标,即个性化饮食,不仅要考虑定量和定性的营养需求以及实际健康状况,还要考虑个体的遗传易感性。这种方法应该能够预防肥胖、高血压或2型糖尿病等疾病的发生,或提高其治疗效果。