Essential hypertension is a common disorder that contributes to morbidity, mortality, and cost of health care, especially among African-Americans. although diuretics are commonly prescribed for treatment of hypertension, blood pressure decreases in response to diuretic therapy in some individuals but not in others. The proposed research will determine whether measured variation in genes coding for components of the renin-angiotensin-aldosterone (RAA) system predicts interindividual differences in blood pressure response to diuretic therapy in 300 hypertensive African-Americans and in 300 hypertensive non-Hispanic whites (total 600 individuals). The investigators will conduct a standardized clinical protocol in which hypertensive adults are treated with the diuretic hydrochlorothiazide, 25 mg/day, for four weeks. They will measure interindividual variation in five RAA system genes-- angiotensinogen, renin, angiotensin-1 converting enzyme, angiotensin-II receptor, and aldosterone synthase --to accomplish the following specific aims in each ethnic group.
Aim 1 : To determine whether variation in genes of the RAA system predicts interindividual differences in blood pressure response to diuretic therapy.
Aim 2 : To determine whether variation in genes of the RAA system predicts interindividual differences in baseline measures of the endocrine RAA system or response of these measures to diuretic therapy.
Aim 3 : To determine whether the predictive effects of variations in genes of the RAA system on blood pressure response to diuretic therapy detected in Aim 1 are mediated through their effects on baseline measures of the endocrine RAA system or response of these measures to diuretic therapy, detected in Aim 2. Results of the proposed research have the potential to identify genes contributing to the etiology of interindividual differences in blood pressure response to diuretic therapy in African-Americans and in non-Hispanic whites.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL053330-01A2
Application #
2029242
Study Section
Special Emphasis Panel (ZRG4-SOH (03))
Project Start
1997-02-01
Project End
2002-01-31
Budget Start
1997-02-01
Budget End
1998-01-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
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Le, MyPhuong T; Lobmeyer, Maximilian T; Campbell, Marcus et al. (2013) Impact of genetic polymorphisms of SLC2A2, SLC2A5, and KHK on metabolic phenotypes in hypertensive individuals. PLoS One 8:e52062
Chai, High Seng; Chapman, Arlene B; Boerwinkle, Eric (2013) Response to genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. Hypertension 61:e6
Turner, Stephen T; Bailey, Kent R; Schwartz, Gary L et al. (2012) Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. Hypertension 59:1204-11
Schwartz, Gary L (2011) Screening for adrenal-endocrine hypertension: overview of accuracy and cost-effectiveness. Endocrinol Metab Clin North Am 40:279-94, vii
Duarte, Julio D; Lobmeyer, Maximilian T; Wang, Zhiying et al. (2010) Lack of association between polymorphisms in STK39, a putative thiazide response gene, and blood pressure response to hydrochlorothiazide. Pharmacogenet Genomics 20:516-9
Chai, High-Seng; Sicotte, Hugues; Bailey, Kent R et al. (2009) GLOSSI: a method to assess the association of genetic loci-sets with complex diseases. BMC Bioinformatics 10:102
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Fridley, Brooke L; Turner, Stephen T; Chapman, Arlene et al. (2008) Reproducibility of Genotypes as Measured by the Affymetrix GeneChip(R) 100K Human Mapping Array Set. Comput Stat Data Anal 52:5367-5374

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