Cardiovascular Diseases, Heart Diseases, Hypertension
Conditions
Keywords
Hypertension, Pharmacogenetics, Hydrochlorothiazide, Candesartan
Brief summary
To determine whether measured variation in genes coding for components of vasoconstriction and volume regulating systems predict interindividual differences in blood pressure response to therapy with a thiazide diuretic, hydrochlorothiazide, or an angiotensin II receptor blocker, candesartan, in hypertensive African-Americans (N=300 treated with each drug) and in hypertensive European Americans (N=300 treated with each drug).
Detailed description
BACKGROUND: Essential hypertension is a common disorder that contributes to morbidity, mortality, and cost of health care, especially among African-Americans. Although a single-drug therapy is commonly prescribed for treatment of hypertension, blood pressure levels are controlled in some individuals but not in others. The study has the potential to identify genes contributing to the etiology of interindividual differences in blood pressure response to diuretic therapy in African-Americans and European Americans. DESIGN NARRATIVE: Hypertensive adults were treated with the diuretic hydrochlorothiazide, 25 mg/day, for four weeks; or with the angiotensin II receptor blocker candesartan, 16 mg/day for 2 weeks followed by 32 mg/day for 4 weeks. Interindividual variations in blood pressure responses and in candidate genes coding for components of systems regulating vasoconstriction and volume were measured. In addition, a panel of 500,000 single nucleotide polymorphisms genome-wide was measured in subsets of the most extreme responders and nonresponders to each drug for genome-wide association of analyses.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
Primary (essential) hypertension
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in blood pressure | 4 weeks for hydrochlorothiazide; 6 weeks for candesartan | The blood pressure response to antihypertensive drug therapy was defined by the difference between blood pressure levels prior to and at the end of drug therapy. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Adverse metabolic changes | 4 weeks for hydrochlorothiazide only | Potentially adverse metabolic changes in response to hydrochlorothiazide include changes in fasting serum glucose and insulin; serum potassium; serum lipids (triglycerides, HDL-cholesterol, total cholesterol); and serum uric acid. |
Countries
United States