PAT PROTEINS: GENE-DIET INTERACTIONS OBESITY RISK AND HEALTH

PAT 蛋白质：基因-饮食相互作用肥胖风险与健康

• 批准号: 7570113
• 负责人: Jose M. Ordovas
• 金额: $ 32万
• 依托单位: TUFTS UNIVERSITY BOSTON
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-02-01 至 2011-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7570113
• 关键词: Abdomen; Adipocytes; Adipose tissue; Adult; Affect; Age; Aging; Alleles; American; Amino Acid Sequence; Animals; Asians; Binding Proteins; Biochemical; Body Weight; Body Weight Changes; Body Weight decreased; Body fat; Body mass index; Calories; Candidate Disease Gene; Central obesity; Characteristics; Chinese People; Classification; Clinical; Complex; Conjugated Linoleic Acids; Coronary heart disease; Cultural Backgrounds; Data; Development; Diet; Diet Habits; Dietary Component; Dietary Factors; Dietary Fats; Dietary intake; Disease; Dual-Energy X-Ray Absorptiometry; Eating; Energy Intake; Energy Metabolism; Epidemic; Equilibrium; Ethnic group; Exercise; Family; Family member; Fatty acid glycerol esters; Female; Framingham Heart Study; Gender; Gene Family; Gene Proteins; Genes; Genetic; Genetic Markers; Genotype; Haplotypes; Health; Heritability; Hip region structure; Human; IGF Type 2 Receptor; In Vitro; Individual; Insulin Resistance; Intake; Life; Life Style; Light; Lipids; Lipolysis; Measures; Menopausal Status; Metabolic Pathway; Metabolic syndrome; Modeling; Non-Insulin-Dependent Diabetes Mellitus; Nutrient; Obesity; Observational Study; Overweight; PPAR gamma; Participant; Peptide Sequence Determination; Personal Satisfaction; Phenotype; Play; Population; Population Study; Prevention therapy; Proteins; Public Health; Recommendation; Regulation; Research; Research Personnel; Risk; Rodent; Role; Singapore; Single Nucleotide Polymorphism; Societies; Spain; Testosterone; Thinking; Time; Translating; United States; Variant; Visceral; Weight; Woman; Work; X-Ray Computed Tomography; adipophilin; age related; base; clinically relevant; experience; falls; fighting; gain of function; gene interaction; genetic association; genetic variant; interest; lipid biosynthesis; loss of function; member; men; mortality; neglect; obesity prevention; obesity risk; perilipin; programs; receptor binding; sedentary; sterol esterase; success; trait; waist circumference

DESCRIPTION (provided by applicant): Obesity has been identified as "one of today's most blatantly visible - yet most neglected - public health problems." Like most disorders affecting the well-being of the population at-large, obesity is a complex condition in which multiple determinants interact to produce the undesired end-point. More than 1.1 billion people worldwide fall within the classification of overweight or obese. How and why did the world get so fat? The global answer may be simple: Too many calories and too little exercise. However, at the individual level the answer is more complex as shown by the very limited long term success achieved by weight-reducing therapies. We know that at the individual level obesity is determined by a combination of environmental and genetic factors. The heritability of obesity is estimated to range from 0.37 to 0.52. However, much less is known about the precise contribution of specific genes to the current obesity epidemic. Although hundreds of obesity candidate genes have been identified through different metabolic pathways, the fundamental basis of obesity resides with excessive storage of triacylglycerides (TAG) in adipose tissue. The mechanisms that control the storage and release of TAG in lipid droplets are complex and poorly understood; yet, they are likely to be crucial to the understanding of the regulation of energy metabolism and body weight. In this regard, the evolutionarily related family of PAT proteins (Perilipin (PLIN), Adipophilin, TIP47, S3-12) defined by protein sequence similarity and their association with lipid droplets, may play key roles in obesity. We have recently shown that common variants at the PLIN locus were associated with BMI and obesity risk in females from several large population studies, including Whites, Chinese, Indians and Malays. However, nothing is known about the contributions of other PAT genes to obesity. Moreover, information is lacking about the role that PAT genes may play on the longitudinal changes in BMI that take place in modern societies during aging. Finally, the potential interactions between these genes and dietary factors may shed light on the complex relation between dietary intake and body weight changes observed on an individual basis. Therefore, the primary objective of this application is to identify common genetic variants of the PAT family of genes and to relate those variants with anthropometric measures (BMI, waist circumference, visceral and total body fat) and their changes over time in -2600 men and women from the Framingham Heart Study, using the wealth of cross-sectional and longitudinal data available in this study. Moreover, we will evaluate interactions between genetic variants and dietary habits as modulators of obesity and related anthropometric measures. This research has the potential of translating findings of genetic associations and interactions into dietary recommendations for specific groups selected according to their genetic characteristics in order to increase the success of dietary measures aimed to fight the obesity epidemic.

描述（由申请人提供）：肥胖已被确定为“当今最明显但最被忽视的公共健康问题之一”。像大多数影响大众健康的疾病一样，肥胖是一种复杂的情况，其中多种决定因素相互作用产生了不希望的终点。全世界有超过11亿人属于超重或肥胖的范畴。世界是如何以及为什么变得如此肥胖的？全球的答案可能很简单：卡路里摄入过多，运动太少。然而，在个人层面上，答案更为复杂，因为减肥疗法取得的长期成功非常有限。我们知道，在个人层面上，肥胖是由环境和遗传因素共同决定的。肥胖的遗传率估计在0.37到0.52之间。然而，对于特定基因对当前肥胖流行的确切影响，人们所知甚少。尽管通过不同的代谢途径已经确定了数百种肥胖候选基因，但肥胖的根本基础在于脂肪组织中甘油三酯（TAG）的过度储存。控制TAG在脂滴中的储存和释放的机制是复杂的，目前尚不清楚；然而，它们可能对理解能量代谢和体重的调节至关重要。因此，PAT蛋白的进化相关家族（Perilipin (PLIN), Adipophilin, TIP47, S3-12）由蛋白序列相似性及其与脂滴的关联定义，可能在肥胖中发挥关键作用。我们最近从包括白人、华人、印度人和马来人在内的几项大型人群研究中发现，PLIN基因座的常见变异与女性的BMI和肥胖风险相关。然而，对于其他PAT基因对肥胖的影响却一无所知。此外，关于PAT基因在现代社会衰老过程中发生的BMI纵向变化中可能发挥的作用的信息缺乏。最后，这些基因和饮食因素之间的潜在相互作用可能会揭示饮食摄入和个体体重变化之间的复杂关系。因此，本应用程序的主要目的是识别PAT基因家族的常见遗传变异，并将这些变异与来自弗雷明汉心脏研究的-2600名男性和女性的人体测量测量（BMI、腰围、内脏和全身脂肪）及其随时间的变化联系起来，利用本研究中丰富的横断面和纵向数据。此外，我们将评估遗传变异和饮食习惯之间的相互作用，作为肥胖的调节因子和相关的人体测量指标。这项研究有可能将遗传关联和相互作用的发现转化为根据遗传特征选择的特定群体的饮食建议，以提高旨在对抗肥胖流行的饮食措施的成功率。

项目成果

CLOCK gene is implicated in weight reduction in obese patients participating in a dietary programme based on the Mediterranean diet.

时钟基因与参加基于地中海饮食的饮食计划的肥胖患者的体重减轻有关。

• DOI: 10.1038/ijo.2009.255
• 发表时间: 2010-03
• 期刊: INTERNATIONAL JOURNAL OF OBESITY
• 影响因子: 4.9
• 作者: Garaulet, M.;Corbalan, M. D.;Madrid, J. A.;Morales, E.;Baraza, J. C.;Lee, Y. C.;Ordovas, J. M.
• 通讯作者: Ordovas, J. M.

PERIOD2 variants are associated with abdominal obesity, psycho-behavioral factors, and attrition in the dietary treatment of obesity.

时期2变异与腹部肥胖，心理行为因素以及肥胖饮食治疗中的流失有关。

• DOI: 10.1016/j.jada.2010.03.017
• 发表时间: 2010-06
• 期刊: Journal of the American Dietetic Association
• 作者: Garaulet M;Corbalán-Tutau MD;Madrid JA;Baraza JC;Parnell LD;Lee YC;Ordovas JM
• 通讯作者: Ordovas JM