Jean Mayer US Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts, USA.
Curr Opin Clin Nutr Metab Care. 2010 Mar;13(2):139-44. doi: 10.1097/MCO.0b013e3283357287.
The number of studies investigating interactions between genes and nutrients for cardiovascular disease continues to grow, and holds tremendous potential for reducing disease risk at the level of the individual genotype. However, understanding the limitations and challenges of interaction studies, whether of observational or interventional design, is essential for critical evaluation of these studies.
Nutrient-gene interactions for cardiovascular disease both parallel and extend nutrition studies, encompassing both traditional and novel cardiovascular risk factors. Fatty acid quality, lipid metabolism, inflammation, postprandial metabolism, fatty liver and macronutrient-gene interactions for obesity and metabolic syndrome represent a subset of the major areas of recent focus. With few exceptions, however, studies of gene-nutrient interactions are limited to a single population.
Gene-nutrient research will continue to expand as genome-wide association studies uncover new sources of genetic variability associated with cardiovascular risk. However, in addition to investigation of newly discovered variants, continuing efforts must focus on the confirmation of previously reported genetic associations and interactions in additional populations.
研究基因与营养物质相互作用对心血管疾病影响的研究数量不断增加,这为降低个体基因型水平的疾病风险提供了巨大的潜力。然而,了解观察性或干预性设计的相互作用研究的局限性和挑战,对于这些研究的批判性评估至关重要。
心血管疾病的营养-基因相互作用与营养研究既相似又互补,涵盖了传统和新型心血管危险因素。脂肪酸质量、脂质代谢、炎症、餐后代谢、脂肪肝和肥胖及代谢综合征的宏量营养素-基因相互作用是近期关注的主要领域之一。然而,除了少数例外,基因-营养相互作用的研究仅限于单一人群。
随着全基因组关联研究揭示与心血管风险相关的新的遗传变异来源,基因-营养研究将继续扩展。然而,除了对新发现的变异进行研究外,还必须继续努力在其他人群中证实先前报道的遗传关联和相互作用。