Location: Human Nutrition Research Center on Aging
2008 Annual Report
To investigate the interactions between genetics and nutrients in the development of cardiovascular disease (CVD), the major age-related disorder affecting life expectancy and quality of life in the United States (US). Emphasis is placed on elucidating mechanisms by which genetic variation interacts with dietary and behavioral factors to regulate the homeostasis of the cardiovascular system.
To identify genes newly associated with cardiovascular health and overall longevity and determine their expression response to dietary intervention using animal models of aging.
High blood concentrations of low-density lipoprotein (LDL), triglycerides and low levels of high-density lipoprotein (HDL) cholesterol, are known risk factors for cardiovascular disease. Blood lipid concentrations are heritable, but most of their heritability remains unexplained by known genes and gene variants. More complete knowledge will be crucial to develop better disease prevention strategies. Using cutting edge technical and analytical approaches, we have thoroughly analyzed the genomes of about 9000 subjects and replicated promising findings in about 19,000 additional individuals. Our data reveal that common single nucleotide polymorphisms (SNPs) at six new genes are reproducibly associated with LDL cholesterol, HDL cholesterol, and/or triglycerides. These findings represent advancement in our understanding of the genetics of plasma lipids and underscore the benefits of the new genetic technologies and worldwide collaborations. Understanding the molecular, cellular and clinical consequences of the new genes will provide the basis for new preventive measures in the population as well as for new therapies and clinical care. This addresses Component 6 (Prevention of Obesity and Disease: Relationship between Diet, Genetics and Lifestyle) of the NP107 Human Nutrition Action Plan.2. Non-fasting plasma lipid metabolism is related to variation at the perilipin (PLIN) gene.
The relationship between the after-meal response to changes in blood lipids, a risk factor for coronary heart disease, and genetic differences in the perilipin gene family has not been fully investigated. We investigated whether genetic variation in the PLIN gene relates to individual variability in lipid profiles during the after-meal period. Data from subjects of two populations-USA and Spain- consistently showed that carriers of one form of the PLIN gene displayed lower after-meal levels of triglyceride-rich lipoproteins than did subjects carrying the most common form of the gene. The impact of this study is three-fold: PLIN contributes to the regulation of dietary fat metabolism; a segment of the population has been identified that is better able to handle dietary fat with a lower risk of obesity and lower atherogenic risk; hence PLIN is now a target for dietary and drug intervention to reduce cardiovascular disease risk. This addresses Component 6 (Prevention of Obesity and Disease: Relationship between Diet, Genetics, and Lifestyle) of the NP107 Human Nutrition Action Plan.3. Variation at the PPGARC1A gene is associated with DNA damage, diabetes, and cardiovascular diseases in Hispanics.
Diabetes is an age-related disease and a major risk factor for cardiovascular disease (CVD). Over 23% of the US population, 60 years or older have diabetes, and the numbers are even higher in African American, Asian, Native American, and Hispanic populations. The mechanisms underlying the development of diabetes are not well understood and strategies for effective prevention of this disesae are lacking. We examined DNA damage using a reliable technique that measures urinary 8-hydroxydeoxyguanosine (8-OHdG) concentration and related this measurement with nine genetic variants at the peroxisome proliferator-activated receptor-gamma coactivator-1 alpha (PPARGC1A) gene, DNA damage, diabetes, and CVD in Puerto Ricans living in the Boston area. Two PPARGC1A variants associated significantly with diabetes whereas carriers of variants of 2 other PPARGC1A polymorphisms had lower DNA damage and lower prevalence of CVD. Moreover, we found that physical activity correlated negatively with DNA damage. It is plausible that sedentary lifestyle combined with genetic risk contribute to the high prevalence of diabetes in Hispanics. Our finding support that the PPARGC1A gene influences development of diabetes and CVD via DNA damage. Increasing physical activity is a potential strategy to slow DNA damage, thereby decreasing the risk of CVD for individuals with diabetes. This addresses Component 6 (Prevention of Obesity and Disease: Relationship between Diet, Genetics, and Lifestyle) of the NP017 Human Nutrition Action Plan.
5.Significant Activities that Support Special Target Populations
Ordovas, J.M., Trichopoulou, A., Yiannakouris, N., Bamia, C., Benetou, V., Trichopoulos, D. 2008. Genetic predisposition, non-genetic risk factors and coronary infarct. Archives of Internal Medicine. 168(8)891-896.
Shen, J., Arnett, D.K., Parnell, L.D., Peacock, J.M., Lai, C., Hixson, J.E., Tsai, M.Y., Province, M., Straka, R.J., Ordovas, J.M. 2008. Association of common C-protein (CRP) gene polymorphism with baseline plasma CRP levels and fenofibrate response: The GOLDN Study. Diabetes Care. 31(5):910-915.
Ordovas, J.M. 2007. Genetic Links between Diabetes Mellitus and Coronary Atherosclerosis. Current Atherosclerosis Reports. 9(3):204-210.
Ordovas, J.M., Smith, J., Arnett, D., Kelly, R., Sun, Y., Hopkins, P., Hixson, J., Straka, R., Peacock, J., Kardia, S. 2008. The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment. European Journal of Human Genetics. 16(5):603-613.
Lai, C., Leips, J., Zou, W., Roberts, J.F., Wollenberg, K.R., Parnell, L.D., Zeng, Z., Ordovas, J.M., Mckay, T.F. 2007. Speed-Mapping Quantitative Trait Loci Using Microarrays. Nature Methods. 4(10):839-841.
Ordovas, J.M. 2007. Gender, a Significant Factor in the Cross Talk Between Genes, Environment, and Health. Principles of Gender-specific Medicine. 4(B): S111-22.
Lai, C., Tucker, K., Parnell, L.D., Adiconis, X., Garcia-Bailo, B., Griffith, J., Meydani, M., Ordovas, J.M. 2008. PPARGC1A Variations Associated with DNA Damage, Diabetes, and Cardiovascular Diseases: The Boston Puerto Rican Study. Diabetes. 57:809-816.
Ordovas, J.M. 2008. Folic acid, homocysteine and cardiovascular disease: Are the dots connecting?. Current Cardiovascular Risk Reports. 2(1):7-8.
Perez-Martinez, P., Yiannakouris, N., Lopez Miranda, J., Arnett, D., Tsai, M., Galan, E., Straka, R., Delgado-Lista, J., Province, M., Ruano, J., Borecki, I., Hixson, J., Garcia-Bailo, B., Perez-Jimenez, F., Ordovas, J.M. 2008. Postprandial Triglyceride Metabolism is Modified by the Presence of Genetic Variation at the Perilipin (PLIN) Locus in Two Caucasian Populations. American Journal of Clinical Nutrition. 87(3):744-752.
Kathiresan, S., Melander, O., Guiducci, C., Surti, A., Burtt, N.P., Rieder, M.J., Cooper, G.M., Roos, C., Voight, B.F., Havulinna, A.S., Wahlstrand, B., Hedner, T., Corella, D., Tai, E.S., Ordovas, J.M., Berglund, G., Vartiainen, E., Jousilahti, P., Hedblad, B., Taskinen, M., Newton-Cheh, C., Salomaa, V., Peltonen, L., Groop, L., Altshuler, D.M., Orho-Melander, M. 2008. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nature Genetics. 40(2):189-197.
Bureau, A., Diallo, M.S., Ordovas, J.M., Cupples, L.A. 2008. Estimating interaction between genetic and environmental risk factors efficiency of sampling designs within a cohort. Epidemiology. 19(1):83-93.
Ordovas, J.M., Kabagambe, E., Tsai, M., Arnett, D., Peacock, J., Hopkins, P., Borecki, I., Hixson, J. 2008. Red blood cell fatty acid composition and the metabolic syndrome: NHLBI GOLDN study. Clinical Chemistry. 54(1):154-162.
Kathiresan, S., Manning, A.K., Demissie, S., D'Agostino, R.B., Surti, A., Guiducci, C., Gianniny, L., Burtt, N., Melander, O., Arnett, D.K., Peloso, G.M., Ordovas, J.M., Cupples, L.A., Orho-Melander, M. 2007. A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study. BMC Medical Genetics. 8:1.
Tai, E., Ordovas, J.M. 2008. Clinical significance of apolipoprotein A5. Current Opinion in Lipidology. 19(4):349-354.
Ordovas, J.M., Tanaka, T. 2007. Are dietary preferences linked to genes? Future of Lipidology. 2(5):485-488. doi:10.2217/17460818.104.22.1685