Biomarkers for Cardiovascular Disease
Information source: National Institutes of Health Clinical Center (CC)
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Coronary Artery Disease
Phase: N/A
Status: Active, not recruiting
Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Summary
Biomarkers for Cardiovascular Disease
Summary: This study will examine the function of the lining cells of blood vessels and
measure substances in the blood to see how they relate to various blood tests, including new
tests under development to determine cardiovascular disease risk. Nitric oxide is a molecule
produced by healthy blood vessels that helps keep them relaxed. Nitrate is a substance formed
from nitric oxide in the blood. The release of nitric oxide by blood vessels is reduced in
patients with coronary artery disease, compared with healthy people. Also, blood nitrite
levels rise in some of these patients. Other substances in the blood and urine also change
with risk for heart disease. This study will measure nitrite levels and other inflammatory
substances in the blood and urine.
Healthy volunteers, people with various risk factors for heart disease, and people with
blockage of one or more major heart arteries or a history of heart attack may be eligible for
this study. Candidates must be 21 years of age or older. People who have an irregular heart
rhythm or who cannot take oral nitrates are excluded.
Participants undergo the following tests and procedures:
- Blood tests: Samples are drawn three times for routine tests and to look for certain
proteins that may affect the heart. Samples are collected once before any other tests,
once before starting the exercise stress test (see below) and again after the stress
test.
- Urine test: A sample may be tested for proteins in the urine and for other research
studies.
- Brachial artery reactivity study: This ultrasound study tests how well a person's
arteries widen. The subject rests on a bed. An ultrasound measuring device is placed
over the artery just above the elbow. The size of the artery and blood flow through it
are measured before and after inflating a pressure cuff around the forearm. The pressure
cuff stops the flow of blood to the arm for 5 minutes and then is released while more
ultrasound pictures are taken. After the subject rests, a nitroglycerin tablet (medicine
that causes blood vessels to relax) is placed under the tongue. After the nitroglycerin
is given, the size of the artery and blood flow through it are measured again. After a
rest period, the study will be repeated in the healthy volunteers and first 20 patients
with heart disease.
- Echocardiography (heart ultrasound): This test involves holding a small probe against
the chest to use sound waves for obtaining pictures of the heart. A small catheter
(plastic tube) may be placed in a vein to inject a contrast agent that enhances the
pictures.
- Metabolic stress testing: Subjects will be asked to breathe in and out of a mask while
baseline measurements are taken. Then they exercise on a treadmill while wearing a
breathing mask. This test shows how much oxygen the body uses at rest and with
exercise.
- Genetic testing (optional): A blood sample is collected to examine DNA - genetic
material that determines inherited traits and contains information about body proteins.
Some parts of DNA may be used as markers of the level of damage produced by oxygen
by-products that may reflect the extent of heart disease in patients. Also, gene
variations may make an individual more likely to develop a heart problem. Such markers
may guide doctors in predicting how fast the disease will progress or may help find a
new type of drug to prevent disease.
- Time requirements: This study is expected to take approximately 5-6 hours for
completion within one or two days.
- Follow-up: Patients are contacted by phone every 6 months for information on chest pain,
surgical procedures related to the heart, and hospitalizations.
Clinical Details
Official title: Nitrite as a Marker of Cardiovascular Risk; Development of Novel Biomarkers in Patients With Coronary Artery Disease
Study design: N/A
Detailed description:
Cardiovascular events are a major cause of morbidity and mortality world-wide and traditional
risk factor assessment is limited in its ability to predict which patients will have an
event. The endothelium is known to play a central role in vascular homeostasis and nitric
oxide (NO) is believed to be the main component responsible for normal endothelial function.
Increasing evidence suggests that oxidative stress leading to reduced NO bioavailability and
subsequent endothelial dysfunction is an important factor in the progression of vascular
diseases. Further investigation of NO metabolites in blood may provide insight into the
mechanisms of endothelial dysfunction and disease progression. Preliminary data suggest that
although plasma nitrite levels are decreased in CAD patients and correlate with endothelial
dysfunction, the nitrite within red blood cells and whole blood is compensatorily increased.
Since this new measure is more reproducible and convenient to measure, it may serve as a
biomarker of endothelial dysfunction. A prospective study of nitrite and other novel NO-based
assays, proteomics, and current biomarkers linked to endothelial function phenotype will
allow further investigation into the pathophysiology of endothelial dysfunction and permit
development of future markers of atherothrombosis.
Eligibility
Minimum age: 21 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
- INCLUSION CRITERIA
Adults older than 21, of both sexes:
The initial study group will consist of 120 subjects, which will consist of 100 subjects
with documented CAD (by cardiac catheterization showing greater than or equal to 70%
stenosis in an epicardial vessel), previously documented MI (based on ECG or cardiac
enzymes) or CAD risk equivalents (diabetes, peripheral vascular disease, abdominal aortic
aneurysm, symptomatic carotid disease, or multiple risk factors that confer a 10 year risk
of greater than 20% as defined by the Framingham Risk Score) and 20 healthy age- and
sex-matched controls.
Written informed consent.
EXCLUSION CRITERIA
Atrial fibrillation
Any contraindications to oral nitrates
Hypotension, bradycardia.
Myocardial infarction within the prior 30 days
Symptoms of acute CHF
Pregnant women
Receiving active treatment for cancer
Any other condition that may interfere with the interpretation of the study results or not
be in the best interest of the subject in the opinion of the investigator.
Since oral nitrate therapy is known to affect serum and possibly whole blood nitrite
levels, we will exclude patients on long-acting nitrates for the initial group of 100
cardiac patients. Those patients on chronic nitrate therapy will subsequently be included
in the later portion of the study but will be analyzed separately.
Locations and Contacts
National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland 20892, United States
Additional Information
NIH Clinical Center Detailed Web Page
Related publications: Ridker PM, Rifai N, Rose L, Buring JE, Cook NR. Comparison of C-reactive protein and low-density lipoprotein cholesterol levels in the prediction of first cardiovascular events. N Engl J Med. 2002 Nov 14;347(20):1557-65.
Starting date: April 2005
Last updated: March 7, 2008
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