The goal of our SCOR (Molecular Genetics of Hypertension in Mexican Americans) is to identify genes which influence blood pressure, and thus, are responsible for the development of hypertension. Substantial evidence for the importance of insulin resistance in hypertension, as well as the high prevalence of insulin resistance in the Mexican American population has led us to place great emphasis on the examination of insulin resistance as an intermediate phenotype for hypertension in this ethnic group. We will determine how insulin resistance interacts with other important physiologic mechanisms, particularly salt sensitivity, in affecting blood pressure by examining the relationships of these phenotypes in individuals at high risk for hypertension (i.e. the young adult offspring of affected individuals) as well as by examining familial clustering of insulin resistance with specific combinations of other intermediate phenotypes. Project 1 will provide the detailed physiologic data which is so necessary for successful identification of genes and gene regions which will be performed in Project 2, using both systematic mapping and candidate gene approaches. The extensive phenotyping of 800-1000 individuals from 200 Mexican American families with hypertension will provide a truly unique resource for the investigation of the genetic basis of hypertension in Mexican Americans. The studies performed up to now have relied upon either large numbers of individuals who have undergone only limited evaluation or upon intensive investigation of relatively small numbers of individuals from a limited number of families. The in-depth investigation conducted in specific intermediate phenotypes and large numbers of families will generate and afford much greater power in finding the individual genes for hypertension in this population. Projects 3, 4, and 5 (the Molecular Physiology Module) will utilize animal models to further investigate the pathophysiology and etiology of hypertension, providing additional insights into candidate genes which should be investigated in humans and also clarifying the physiology behind genetic loci which are linked to human hypertension. The combination of detailed human phenotypic studies, comprehensive genetic mapping, and careful animal model investigations outlined in this SCOR provides a powerful, multidimensional approach to the genetics of blood pressure regulation, hypertension and insulin resistance.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
5P50HL055005-05
Application #
6151323
Study Section
Special Emphasis Panel (ZHL1-CSR-R (S1))
Project Start
1996-02-01
Project End
2001-07-31
Budget Start
2000-04-25
Budget End
2001-07-31
Support Year
5
Fiscal Year
2000
Total Cost
$1,638,286
Indirect Cost
Name
University of Southern California
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Baudrand, Rene; Goodarzi, Mark O; Vaidya, Anand et al. (2015) A prevalent caveolin-1 gene variant is associated with the metabolic syndrome in Caucasians and Hispanics. Metabolism 64:1674-81
Goodarzi, M O; Guo, X; Cui, J et al. (2013) Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearance. Diabetologia 56:1282-90
Guo, X; Cui, J; Jones, M R et al. (2012) Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis. Diabetologia 55:2183-92
Williams, Jonathan S; Chamarthi, Bindu; Goodarzi, Mark O et al. (2012) Lysine-specific demethylase 1: an epigenetic regulator of salt-sensitive hypertension. Am J Hypertens 25:812-7
Pojoga, Luminita H; Underwood, Patricia C; Goodarzi, Mark O et al. (2011) Variants of the caveolin-1 gene: a translational investigation linking insulin resistance and hypertension. J Clin Endocrinol Metab 96:E1288-92
Goodarzi, Mark O; Taylor, Kent D; Jones, Michelle R et al. (2009) Replication of calpain-10 genetic association with carotid intima-media thickness. Atherosclerosis 205:503-5
Kopf, Daniel; Cheng, Li S-C; Blandau, Petra et al. (2008) Association of insulin sensitivity and glucose tolerance with the c.825C>T variant of the G protein beta-3 subunit gene. J Diabetes Complications 22:205-9
Xiang, Anny H; Azen, Stanley P; Buchanan, Thomas A et al. (2002) Heritability of subclinical atherosclerosis in Latino families ascertained through a hypertensive parent. Arterioscler Thromb Vasc Biol 22:843-8
Bosken, C H; Ko, Y C; Shete, S et al. (2001) Adaptations of linkage and association methods for the study of asthma, a complex trait. Genet Epidemiol 21 Suppl 1:S89-96
Cheng, L S; Davis, R C; Raffel, L J et al. (2001) Coincident linkage of fasting plasma insulin and blood pressure to chromosome 7q in hypertensive hispanic families. Circulation 104:1255-60

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