Atherosclerosis Clinical Trial
Official title:
Imaging of Vulnerable Plaques in Coronary Artery Disease by Multidetector Computed Tomography
Atherosclerosis is a chronic and multifocal immunoinflammatory, fibroproliferative disease
of medium-sized and large arteries driven by lipid. Atherosclerosis is rarely fatal unless
thrombosis supervene, causing an acute coronary syndrome. Therefore, for event-free
survival, the vital question is not why atherosclerosis develops but rather why
atherosclerosis, after years after indolent growth, suddenly becomes complicated with
luminal thrombosis.
The great majority of coronary plaques will remain quiescent, at least from a clinical point
of view.
Acute coronary syndrome is primarily precipitated by a ruptured plaque. The precipitating
factor or condition may be found outside rather than inside the plaque.
The challenge is to find the plaque(s) destined for the next thrombus-mediated heart
attack(s), treat, and thus avoid the heart attack(s). Identification of vulnerable plaques
has become a key issue. The natural history of individual plaques (risk of thrombosis) is
unknown and needs to be established.
Multidetector computed tomography (MDCT) can provide angiography and imaging of the vessel
wall (detection, quantification and characterization of plaques).
The intention of this project is to evaluate the accuracy of coronary MDCT in identifying
and differentiating the morphology of coronary atherosclerotic plaques.
Atherosclerosis without thrombosis is rarely fatal. It is the acute thrombotic complications
which account for disability and death. Therefore, for event-free survival, the question is
not why atherosclerosis develops but rather why atherosclerosis, after years after indolent
growth, suddenly becomes complicated with luminal thrombosis.
Post-mortem and clinical observations indicate that patients with acute coronary syndromes
often have many ruptured and/or active plaques in their coronary arteries.
The challenge is to find the plaque(s) destined for the next thrombus-mediated heart
attack(s), treat, and thus avoid the heart attack(s). Identification of vulnerable plaques
have become a key issue. The natural history of individual plaques (risk of thrombosis) is
unknown and needs to be established. Multidetector computed tomography (MDCT) can provide
angiography and imaging of the vessel wall.
Hypothesis:
It is by CT-scanning possible to 1a) identify and differentiate the morphology of coronary
atherosclerotic plaques.
1b) identify vulnerable plaques.
Materials and methods:
1. Development of an MDCT scan protocol for accurate assessment of coronary artery plaque
composition by ex vivo examination of human coronary arteries from the Institute of
Forensic Medicine, University of Aarhus. Scan protocols parameters and intravascular
contrast material will be varied to optimize accurate assessment of coronary plaque
composition. MDCT will be compared to histopathology.
2. A cross-sectional study with clinical application of the efficiency parameters defined
in sub-study 1. Forty consecutive patients with non ST-elevation myocardial
infarction/unstable angina, and 80 consecutive patients with stable angina will be
recruited and investigated with MDCT followed by CAG with IVUS/virtual histology.
3. A prospective, longitudinal study. After a period of 12 months all patients from
sub-study 2 will be re-investigated.
4. Before the cross-sectional study a small pilot-study will be performed. Ten patients
with non ST-elevation myocardial infarction/unstable angina will undergo MDCT and CAG
with IVUS/virtual histology. These patients will after one months undergo another MDCT.
This is done to make sure that it is possible to perform the planned longitudinal
study.
Research plan:
1. Development of an MDCT scan protocol for accurate assessment of coronary artery plaque
composition.
2. Clinical application of the MDCT scan protocol for in vivo differentiation of coronary
artery plaque morphology. Morphologic findings will be categorized and compared with
IVUS/virtual histology for confirmation.
3. Re-evaluation of plaque density and morphology one year after inclusion by a second in
vivo contrast-enhanced MDCT-scanning to define which morphological plaque categories
are at risk of progression.
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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