McCabe-Sellers Beverly, Lovera Dalia, Nuss Henry, Wise Carolyn, Ning Baitang, Teitel Candee, Clark Beatrice Shelby, Toennessen Terri, Green Bridgett, Bogle Margaret L, Kaput Jim
USDA-ARS Delta NIRI. 900 South Shackleford Drive, Little Rock, AR 72211, USA.
OMICS. 2008 Dec;12(4):263-72. doi: 10.1089/omi.2008.0041.
Personal and public health information are often obtained from studies of large population groups. Risk factors for nutrients, toxins, genetic variation, and more recently, nutrient-gene interactions are statistical estimates of the percentage reduction in disease in the population if the risk were to be avoided or the gene variant were not present. Because individuals differ in genetic makeup, lifestyle, and dietary patterns than those individuals in the study population, these risk factors are valuable guidelines, but may not apply to individuals. Intervention studies are likewise limited by small sample sizes, short time frames to assess physiological changes, and variable experimental designs that often preclude comparative or consensus analyses. A fundamental challenge for nutrigenomics will be to develop a means to sort individuals into metabolic groups, and eventually, develop risk factors for individuals. To reach the goal of personalizing medicine and nutrition, new experimental strategies are needed for human study designs. A promising approach for more complete analyses of the interaction of genetic makeups and environment relies on community-based participatory research (CBPR) methodologies. CBPR's central focus is developing a partnership among researchers and individuals in a community that allows for more in depth lifestyle analyses but also translational research that simultaneously helps improve the health of individuals and communities. The USDA-ARS Delta Nutrition Intervention Research program exemplifies CBPR providing a foundation for expanded personalized nutrition and medicine research for communities and individuals.
个人和公共卫生信息通常来自对大量人群的研究。营养素、毒素、基因变异以及最近的营养素-基因相互作用的风险因素,是对如果避免该风险或不存在该基因变异,人群中疾病减少百分比的统计估计。由于个体在基因组成、生活方式和饮食模式上与研究人群中的个体不同,这些风险因素是有价值的指导方针,但可能不适用于个体。干预研究同样受到样本量小、评估生理变化的时间框架短以及可变的实验设计的限制,这些设计往往排除了比较或共识分析。营养基因组学的一个基本挑战将是开发一种方法,将个体分类到代谢组中,并最终为个体制定风险因素。为了实现个性化医学和营养的目标,人类研究设计需要新的实验策略。一种对基因组成与环境相互作用进行更全面分析的有前景的方法依赖于基于社区的参与性研究(CBPR)方法。CBPR的核心重点是在研究人员和社区中的个体之间建立一种伙伴关系,这种伙伴关系不仅允许进行更深入的生活方式分析,还允许进行转化研究,同时有助于改善个体和社区的健康。美国农业部农业研究局三角洲营养干预研究项目就是CBPR的一个典范,为扩大针对社区和个体的个性化营养与医学研究奠定了基础。