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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Investigating the genetic characteristics of CAD: Is there a role for myocardial perfusion imaging techniques?

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Author
Angelidis G., Valotassiou V., Satra M., Psimadas D., Koutsikos J., Skoularigis J., Kollia P., Georgoulias P.
Date
2022
Language
en
DOI
10.1007/s12350-020-02403-x
Keyword
hydroxymethylglutaryl coenzyme A reductase inhibitor
coronary artery disease
coronary risk
endothelial dysfunction
genetic risk
genetic trait
genome-wide association study
human
myocardial perfusion imaging
positron emission tomography
Review
single nucleotide polymorphism
single photon emission computed tomography
coronary angiography
diagnostic imaging
genetics
procedures
x-ray computed tomography
Coronary Angiography
Coronary Artery Disease
Genome-Wide Association Study
Humans
Myocardial Perfusion Imaging
Tomography, Emission-Computed, Single-Photon
Tomography, X-Ray Computed
Springer
Metadata display
Abstract
Several environmental and genetic factors have been found to influence the development and progression of coronary artery disease (CAD). Although the effects of the environmental hazards on CAD pathophysiology are well documented, the genetic architecture of the disease remains quite unclear. A number of single-nucleotide polymorphisms have been identified based on the results of the genome-wide association studies. However, there is a lack of strong evidence regarding molecular causality. The minority of the reported predisposing variants can be related to the conventional risk factors of CAD, while most of the polymorphisms occur in non-protein-coding regions of the DNA. However, independently of the specific underlying mechanisms, genetic information could lead to the identification of a population at higher genetic risk for the long-term development of CAD. Myocardial single-photon emission computed tomography (SPECT) and positron emission tomography (PET) are functional imaging techniques that can evaluate directly myocardial perfusion, and detect vascular and/or endothelial dysfunction. Therefore, these techniques could have a role in the investigation of the underlying mechanisms associated with the identified predisposing variants, advancing our understanding regarding molecular causality. In the population at higher genetic risk, myocardial SPECT or PET could provide important evidence through the early depiction of sub-clinical dysfunctions, well before any atherosclerosis marker could be identified. Notably, SPECT and PET techniques have been already used for the investigation of the functional consequences of several CAD-related polymorphisms, as well as the response to certain treatments (statins). Furthermore, therefore, in the clinical setting, the combination of genetic evidence with the findings of myocardial SPECT, or PET, functional imaging techniques could lead to more efficient screening methods and may improve decision making with regard to the diagnostic investigation and patients’ management. © 2020, American Society of Nuclear Cardiology.
URI
http://hdl.handle.net/11615/70617
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19674]

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