Hypertension
Conditions
Brief summary
Investigators recently demonstrated that coronary flow reserve (CFR) significantly improved after rosuvastatin therapy in hypertensive patients with average levels of serum cholesterol by measuring the change in CFR after 1 year treatment with rosuvastatin in the RESERVE (Rosuvastatin Effect on Coronary Flow Reserve in Hypertensive Patients) I trial. However, the absence of a placebo group made it difficult to exclude the possibility that lifestyle modification and antihypertensive medication also played a role in improving CFR in our previous study. In a double-blind, randomized trial, investigators try to examine the hypothesis that rosuvastatin added to lifestyle modification will be superior to lifestyle modification alone in improving CFR in hypertensive patients .
Detailed description
Statin therapy improves coronary flow reserve (CFR) and decreases cardiac morbidity and mortality in patients with coronary artery disease (CAD) and hypercholesterolemia via pleiotropic effects of statins, including regression of atheroma, stabilization of atherosclerotic plaques. Lipid lowering with a statin also provided beneficial effects in hypertensive patients with average levels of serum total cholesterol in the Anglo-Scandinavian Cardiac Outcomes Trial-Lipid Lowering Arm (ASCOT-LLA). Improvements in endothelial dysfunction and CFR may be related to the beneficial effects of statins in hypertensive patients without hypercholesterolemia. Previously CFR could be invasively measured using a Doppler guide wire in a cardiac catheterization laboratory, but recent advances in echocardiographic imaging techniques have made it feasible to measure CFR noninvasively in patients without CAD, which highly correlates with the CFR measured by invasive means.Accordingly, investigators recently demonstrated that CFR significantly improved after rosuvastatin therapy in hypertensive patients with average levels of serum cholesterol by measuring the change in CFR after 1 year treatment with rosuvastatin and also found a weak correlation between the change of CFR and the change of LDL cholesterol in the RESERVE (Rosuvastatin Effect on Coronary Flow Reserve in Hypertensive Patients) I trial. However, this trial could not include placebo-control group due to the limited study budget. Although CFR was measured by blinded, batch reading of stored echocardiographic images, bias in measurement might affect the result. In our previous study, study patients continued taking their antihypertensive medications and were educated to follow lifestyle modification during the study period, which may have influenced the change in CFR during follow-up, and the absence of a placebo group made it difficult to exclude the possibility that lifestyle modification and antihypertensive medication also played a role in improving CFR. Investigators hypothesize that rosuvastatin added to lifestyle modification will be superior to lifestyle modification alone in improving CFR in controlled hypertensive patients with cardiovascular risk, and try to examine this hypothesis in a double-blind, randomized comparison study using echocardiography.
Interventions
DRUGRosuvastatin
BEHAVIORALLife style modification
Sponsors
Dong-A ST Co., Ltd.
Asan Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
35 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Controlled Hypertension: treated SBP\<140 mmHg and DBP\<90 mmHg with angiotensin receptor blocker (ACE inhibitor) and/or calcium channel blocker LDL cholesterol ≥ 130mg/dL * Patients with statin-naive state, defined as receiving no statin therapy for more than 6 months during the previous 12 months. * Any 1 of these cardiovascular risk factors required: smoking, age over 55 (men) or 65 (women), history of cerebrovascular event, family history of early coronary heart disease before age 55, HDL cholesterol \< 40 mg/dL * The patient agrees to the study protocol and the schedule of clinical and echocardiographic follow-up, and provides informed, written consent, as approved by the Institutional Review Board
Exclusion criteria
* A previous history of intolerance or hypersensitivity to statins * Uncontrolled hypertension; SBP≥140 mmHg or DBP≥90 mmHg * Previous myocardial infarction or currently treated angina pectoris * Stroke, transient ischemic attack \< 3 months * Secondary hypertension * Diabetes mellitus * Peripheral vascular disease * Fasting serum triglyceride \> 500 mg/dL * Clinical congestive heart failure * Uncontrolled arrhythmia * Left ventricular hypertrophy: LV mass index \>134g/m2 (male) or \>110g/m2 (female) * Concomitant clinically important hematological, gastrointestinal, hepatic, renal or other disease * Pregnant or lactating women and those of child-bearing potential * Unwillingness or inability to comply with the procedures described in this protocol
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Difference of Coronary flow velocity reserve | 1 year follow-up | Averaged value of coronary flow velocity reserve will be obtained at 1 year follow-up |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change of coronary flow velocity reserve | 1 year follow-up | Change of coronary flow velocity reserve from baseline to 1 year follow-up |
| Change of LDL cholesterol | 1 year follow-up | Change of LDL cholesterol from baseline to 1 year follow-up |
| Change of C reactive protein (CRP) | 1 year follow-up | Change of CRP from baseline to 1 year follow-up |
Countries
South Korea
Outcome results
None listed