Cardiovascular Disease Clinical Trial
Official title:
Evaluation of Non-invasive Measurements of Atherosclerosis in Cardiovascular Risk Stratification: a Study in a Population-based Cohort and Familial Combined Hyperlipidemia
Multiple risk factors contribute to atherosclerosis, which ultimately results in clinical
manifestation of cardiovascular disease. Atherosclerosis results in both functional and
morphological changes in the vessel wall, which can be measured by ultrasonography. The
current study has been designed to
1. To evaluate whether non-invasive measurements of atherosclerosis are independent
predictors of cardiovascular disease and
2. to delineate new biochemical parameters and genetic variations, allowing earlier and
more effective preventive therapy
3. The investigators intend to set guidelines for use of NIMA in an outpatient setting to
facilitate early detection of increased cardiovascular risk and monitor life-style and
pharmaceutical interventions.
In both the general population and in Familial Combined Hyperlipidemia.
Cardiovascular disease (CVD) is the major cause of death in all developed countries.
Atherosclerosis is the main cause of CVD. Abundant evidence indicates the 4 major
independent risk factors for atherosclerosis and CVD include cigarette smoking, elevated
blood pressure, elevated total cholesterol and diabetes mellitus. However, a major problem
in clinical medicine is that at every level of risk factor exposure, there is a large
inter-individual variation in the amount of atherosclerosis and the development of CVD.
Therefore, it is difficult to predict the CVD risk in an individual patient based on risk
factor screening alone.
Non-invasive measurements of atherosclerosis (NIMA): An indicator of the overall effect of
all known and unknown potential risk factors for atherosclerosis in vivo can be assessed by
measuring atherosclerosis directly in the vessel wall. This also provides the opportunity to
measure atherosclerosis before developing symptoms of CVD, as changes in the arterial wall
precede clinical symptoms of CVD.
Objectives: (1)The main objective is to evaluate whether NIMA are independent predictors of
CVD and thus add information to traditional risk factor stratification. (2) Furthermore, we
will delineate new biochemical and genetic risk factors, allowing earlier and more effective
preventive therapy. (3) We intend to set guidelines for use of NIMA in an outpatient setting
to facilitate early detection of increased cardiovascular risk and monitor life-style and
pharmaceutical interventions.
We will evaluate 4 different NIMA, based on ultrasound and tonometry techniques, including
intima media thickness (IMT), endothelial function by flow mediated dilation (FMD),
ankle-brachial index (ABI), Pulse Wave Analyses(PWA) and pulse wave velocity (PWV). The
power of NIMA, to predict cardiovascular events will be studied in two available
populations, a low risk population cohort, the Nijmegen Biomedical Study (NBS) and a high
risk population, families with Familial Combined Hyperlipidemia.
The NBS is a prospective population survey aimed at investigating the frequency of genetic
variations in the general population. The study population is recruited as a sex- and
age-stratified random sample of all inhabitants of Nijmegen 20 to 90 years old (n=10.000).
Recruitment has started in October 2001. The present study is a substudy in the NBS. A
follow-up approach will be used to evaluate whether NIMA are related to future
cardiovascular events. In total 1517 participants aged 50-70 years were included.
FCH is the most common inherited hyperlipidemia in man. Affected individuals are
characterized by elevated cholesterol and/or triglyceride levels and other associated traits
including small-dense LDL, insulin resistance, oxidative stress and increased apoB levels,
which have been proposed to contribute to the increased risk of CVD. So, this population
will be most informative to evaluate the relevance of NIMA in CVD risk assessment as
patients exhibit numerous, additive risk factors, which are missed in traditional
cardiovascular risk assessment. Our data base contains a unique population of 40
well-characterized FCH families, including 687 patients, relatives and spouses with 5 years
follow-up data. These families participate in an ongoing long-term follow-up program with
registration of CVD.
All four NIMA's, including IMT, ABI, PWV/PWA, FMD, and both traditional and new biochemical
and genetic parameters will be measured in both populations. The relevance of NIMA in
identifying subjects at increased risk of CVD will be determined. Furthermore, the effect of
risk factors on IMT, ABI, PWV and FMD will be studied, including clinical and traditional
risk factors and new biochemical parameters and genetic variations.
Innovative aspects: We will develop an evidence based protocol for NIMA to show the presence
of atherosclerosis before clinical manifestation of CVD and to improve cardiovascular risk
stratification beyond traditional risk factor screening. Furthermore, we will delineate new
risk factors, including both biochemical parameters and genetic variations, contributing to
design optimal (new) treatment and to develop new strategies for prevention of CVD in the
general population and in a high risk population, FCH.
Clinical relevance: If NIMA turns out to provide powerful information in identifying
subjects at increased risk of CVD we will incorporate NIMA into clinical practice guidelines
for the purpose of cardiovascular risk stratification and evaluation of risk management
strategies. The identification of potential new biochemical and/or genetic risk factors will
be very helpful to design optimal treatment and to develop new strategies for identification
and prevention of CVD in both the general population and families with FCH.
;
Time Perspective: Prospective
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