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dc.creatorAngelidis G., Valotassiou V., Satra M., Psimadas D., Koutsikos J., Skoularigis J., Kollia P., Georgoulias P.en
dc.date.accessioned2023-01-31T07:31:49Z
dc.date.available2023-01-31T07:31:49Z
dc.date.issued2022
dc.identifier10.1007/s12350-020-02403-x
dc.identifier.issn10713581
dc.identifier.urihttp://hdl.handle.net/11615/70617
dc.description.abstractSeveral 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.en
dc.language.isoenen
dc.sourceJournal of Nuclear Cardiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85094981661&doi=10.1007%2fs12350-020-02403-x&partnerID=40&md5=5f3e77b7a97bf65afa7a422bdc243fb6
dc.subjecthydroxymethylglutaryl coenzyme A reductase inhibitoren
dc.subjectcoronary artery diseaseen
dc.subjectcoronary risken
dc.subjectendothelial dysfunctionen
dc.subjectgenetic risken
dc.subjectgenetic traiten
dc.subjectgenome-wide association studyen
dc.subjecthumanen
dc.subjectmyocardial perfusion imagingen
dc.subjectpositron emission tomographyen
dc.subjectReviewen
dc.subjectsingle nucleotide polymorphismen
dc.subjectsingle photon emission computed tomographyen
dc.subjectcoronary angiographyen
dc.subjectdiagnostic imagingen
dc.subjectgeneticsen
dc.subjectproceduresen
dc.subjectx-ray computed tomographyen
dc.subjectCoronary Angiographyen
dc.subjectCoronary Artery Diseaseen
dc.subjectGenome-Wide Association Studyen
dc.subjectHumansen
dc.subjectMyocardial Perfusion Imagingen
dc.subjectTomography, Emission-Computed, Single-Photonen
dc.subjectTomography, X-Ray Computeden
dc.subjectSpringeren
dc.titleInvestigating the genetic characteristics of CAD: Is there a role for myocardial perfusion imaging techniques?en
dc.typeotheren


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