Randomized Trial of Imaging Versus Risk Factor-Based Therapy for Plaque Regression
| Status: | Completed |
|---|---|
| Conditions: | High Cholesterol, Peripheral Vascular Disease, Cardiology |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 50 - 99 |
| Updated: | 12/2/2018 |
| Start Date: | September 30, 2010 |
| End Date: | February 22, 2017 |
The RIGHT Study: Risk Stratification With Image Guidance of HMG Coa Reductase Inhibitor Therapy
Background:
- Atherosclerosis (thickening of the artery walls caused by cholesterol and other deposits)
commonly occurs in the heart vessels and carotid (neck) arteries of adults. This is often
present in individuals with high cholesterol levels in their blood. These patients are
usually treated with cholesterol lowering medication ( statins ) along with modification of
diet and exercise. Researchers are interested in investigating new approaches including
magnetic resonance imaging (MRI) and computed tomography (CT) imaging studies to detect blood
vessel blockages that would not otherwise be detected by cholesterol levels and risk factors
for heart disease.
Objectives:
- To measure atherosclerosis in the heart vessels and carotid arteries using imaging tests
(computed tomography (CT) and magnetic resonance imaging (MRI)) before and after standard
treatment with cholesterol lowering medication ( statins )
Eligibility:
- Healthy individuals at least 55 years of age who are candidates for therapy to lower their
blood cholesterol levels.
Design:
- This study will involve one screening visit and seven study visits over a period of 2
years.
- Participants will be screened with a physical examination and medical history, as well
as blood samples and tests to ensure that it is safe for them to have CT and MRI scans.
Participants will provide information on current medications, dietary habits, smoking
status, alcohol and caffeine intake, and their level of physical activity.
- Participants will be divided into two groups. One group will receive standard doses of
medication to lower cholesterol according to current treatment guidelines, while the
other group will have MRI scans of the carotid arteries and a CT scan of the heart to
determine the best medication dose levels.
- Visits 3 to 5 will be scheduled 3, 6, and 9 months after visit 2. During these visits,
researchers will monitor for possible side effects and may change or adjust medications
and doses.
- At visit 6, participants will have an MRI scan of the carotid arteries, a physical
examination, and blood tests. Medications may be changed or adjusted.
- At visit 7, participants will have blood tests, and medications may be changed or
adjusted.
- At the final visit, participants will have MRI and CT scans of the carotid arteries and
heart, respectively, as well as a final physical examination and blood tests.
- Atherosclerosis (thickening of the artery walls caused by cholesterol and other deposits)
commonly occurs in the heart vessels and carotid (neck) arteries of adults. This is often
present in individuals with high cholesterol levels in their blood. These patients are
usually treated with cholesterol lowering medication ( statins ) along with modification of
diet and exercise. Researchers are interested in investigating new approaches including
magnetic resonance imaging (MRI) and computed tomography (CT) imaging studies to detect blood
vessel blockages that would not otherwise be detected by cholesterol levels and risk factors
for heart disease.
Objectives:
- To measure atherosclerosis in the heart vessels and carotid arteries using imaging tests
(computed tomography (CT) and magnetic resonance imaging (MRI)) before and after standard
treatment with cholesterol lowering medication ( statins )
Eligibility:
- Healthy individuals at least 55 years of age who are candidates for therapy to lower their
blood cholesterol levels.
Design:
- This study will involve one screening visit and seven study visits over a period of 2
years.
- Participants will be screened with a physical examination and medical history, as well
as blood samples and tests to ensure that it is safe for them to have CT and MRI scans.
Participants will provide information on current medications, dietary habits, smoking
status, alcohol and caffeine intake, and their level of physical activity.
- Participants will be divided into two groups. One group will receive standard doses of
medication to lower cholesterol according to current treatment guidelines, while the
other group will have MRI scans of the carotid arteries and a CT scan of the heart to
determine the best medication dose levels.
- Visits 3 to 5 will be scheduled 3, 6, and 9 months after visit 2. During these visits,
researchers will monitor for possible side effects and may change or adjust medications
and doses.
- At visit 6, participants will have an MRI scan of the carotid arteries, a physical
examination, and blood tests. Medications may be changed or adjusted.
- At visit 7, participants will have blood tests, and medications may be changed or
adjusted.
- At the final visit, participants will have MRI and CT scans of the carotid arteries and
heart, respectively, as well as a final physical examination and blood tests.
The overall aim of this proposal is to compare the effectiveness of an image guided approach
to lipid lowering to standard therapy guided by clinical risk factors and blood lipid levels.
Men and women over age 55 who are candidates for statin therapy will be randomized to usual
cholesterol lowering care, or to care guided by MRI images of the carotid arteries.
Participants randomized to the second, imaging guided, group will be assigned to LDL
cholesterol targets according to the degree of atherosclerosis seen by MRI. The study
endpoints will be the total degree of plaque regression seen, the dosage of statin drugs
required to achieve that reduction, and the rate of cardiovascular events.
FDG-PET is hypothesized to enable visualization of anti-inflammatory effects of statins that
most likely occur before anatomic regression of the plaques can be demonstrated on MRI. A
pilot substudy is to be conducted to explore this relationship. A subgroup of patients
participating in the main study will be asked to participate in FDG PET imaging. The purpose
of this pilot study is to determine if FDG avid lesions undergo a greater degree of
morphologic regression with therapy controlling for the reduction in LDL cholesterol and the
dosage of statins required to achieve that target.
Although contrast-enhanced coronary CT angiography (CTA) with multidetector computed
tomography (MDCT) has been used extensively to characterize coronary artery plaque
composition, there is little data regarding its reproducibility. A recent study demonstrated
excellent reproducibility for this technique but this study was performed using the older 64
detector row CT scanners2. A pilot substudy will be conducted to study the reproducibility of
coronary CT angiography using the newer generation of 320 detector row CT scanners.
to lipid lowering to standard therapy guided by clinical risk factors and blood lipid levels.
Men and women over age 55 who are candidates for statin therapy will be randomized to usual
cholesterol lowering care, or to care guided by MRI images of the carotid arteries.
Participants randomized to the second, imaging guided, group will be assigned to LDL
cholesterol targets according to the degree of atherosclerosis seen by MRI. The study
endpoints will be the total degree of plaque regression seen, the dosage of statin drugs
required to achieve that reduction, and the rate of cardiovascular events.
FDG-PET is hypothesized to enable visualization of anti-inflammatory effects of statins that
most likely occur before anatomic regression of the plaques can be demonstrated on MRI. A
pilot substudy is to be conducted to explore this relationship. A subgroup of patients
participating in the main study will be asked to participate in FDG PET imaging. The purpose
of this pilot study is to determine if FDG avid lesions undergo a greater degree of
morphologic regression with therapy controlling for the reduction in LDL cholesterol and the
dosage of statins required to achieve that target.
Although contrast-enhanced coronary CT angiography (CTA) with multidetector computed
tomography (MDCT) has been used extensively to characterize coronary artery plaque
composition, there is little data regarding its reproducibility. A recent study demonstrated
excellent reproducibility for this technique but this study was performed using the older 64
detector row CT scanners2. A pilot substudy will be conducted to study the reproducibility of
coronary CT angiography using the newer generation of 320 detector row CT scanners.
- INCLUSION CRITERIA:
A. Men and Women greater than or equal to 55 years of age
B. Candidates for lipid lowering therapy under NCEP ATP III guidelines without
contraindication to statin therapy
C. Willing to modify therapy to enroll in the study
D. Willing to travel to the NIH for follow-up visits.
E. Able to understand and sign informed consent
F. Lab Eligibility parameters:
- eGFR > 45 mL/min/m2
- For age >60 test GFR within 1 week prior to contrast; For age less than or equal to 60
test within 4 weeks
INCLUSION CRITERIA FOR THE PET SUBSTUDY:
Participants who are not participating in the CT Reproducibility study are eligible.
INCLUSION CRITERIA FOR THE REPRODUCIBILITY SUBSTUDY:
Patients will be selected who had a one RR interval initial CT scan with less that 10.5 mSv
estimated radiation dosage and who will not be participating in the PET Substudy.
EXCLUSION CRITERIA:
A. Ineligibility for MR imaging due to:
- Previous pacemaker implantation
- Automatic implantable cardioverter-defibrillator (AICD)
- Metal implants or other ferromagnetic devices, or
- Foreign material
B. Claustrophobia
C. Contra-indication or allergy to statin medications.
D. Current statin therapy at or above the maximum dosage permitted per study protocol.
E. Use of fibrates, ezetimibe, niacin, or bile acid binding agents within 6 months of
screening visit.
F. Pregnancy and nursing.
G. Liver failure defined clinically and by laboratory data.
H. Mental, neurologic or social condition preventing understanding of the rationale,
procedures, risks and potential benefits associated with the trial.
I. Any other conditions that precludes safety for MRI and/or CT imaging per the researcher
s evaluation.
EXCLUSION FOR PARTICIPATION FOR GADOLINUIM CONTRAST. PARTICIPANTS MAY STILL UNDERGO ALL
OTHER STUDY EVALUATIONS.
(Inclusive of the above exclusion criteria):
1. Allergy to gadolinium for scans using contrast; will be eligible for non-contrast
scans.
2. Acute renal failure, renal transplant, dialysis and renal failure (eGFR < 45 mL/min/m2
and/or clinically diagnosed).
3. Individuals with a history of liver transplant or severe liver disease.
4. Individuals with hemoglobinopathies or severe asthma.
EXCLUSION FOR PARTICIPATION FOR IODINATED CONTRAST. PARTICIPANTS MAY STILL UNDERGO ALL
OTHER SUDY EVALUATIONS.
Prior hypersensitivity reaction to iodinated contrast injection, renal dysfunction (defined
as eGFR < 45 mL/min/ m2) or a current clinical diagnosis of renal failure.
EXCLUSION CRITERIA FOR THE PET SUBSTUDY:
Patients who are unable or unwilling to comply with the physical activity restrictions or
fast for 12 hours prior to FDG PET scanning will be excluded. Due to the need for dietary
manipulation and the maintenance of strict glycemic control we will exclude diabetic
patients from our initial study sample. Blood glucose measurements before injection must be
within normal limits, less than 200 mg/dL (11 mmol/L).
EXCLUSION CRITERIA FOR THE REPRODUCIBILITY
Patients who did not have a one RR interval initial CT scan. Patients who will participate
in the PET Substudy.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
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