| Literature DB >> 33244675 |
Wunan Zhou1,2, Amit Dey1, Grigory Manyak1, Meron Teklu1, Nidhi Patel1, Heather Teague1, Nehal N Mehta3,4.
Abstract
Over the past several decades, molecular imaging techniques to assess cellular processes in vivo have been integral in advancing our understanding of disease pathogenesis. 18F-fluorodeoxyglucose (18-FDG) positron emission tomography (PET) imaging in particular has shaped the field of atherosclerosis research by highlighting the importance of underlying inflammatory processes that are responsible for driving disease progression. The ability to assess physiology using molecular imaging, combining it with anatomic delineation using cardiac coronary angiography (CCTA) and magnetic resonance imaging (MRI) and lab-based techniques, provides a powerful combination to advance both research and ultimately clinical care. In this review, we demonstrate how molecular imaging studies, specifically using 18-FDG PET, have revealed that early vascular disease is a systemic process with multiple, concurrent biological mechanisms using inflammatory diseases as a basis to understand early atherosclerotic mechanisms in humans.Entities:
Keywords: 18F-fluorodeoxyglucose (18-FDG); Atherosclerosis; immunology; inflammation
Mesh:
Substances:
Year: 2020 PMID: 33244675 PMCID: PMC8149483 DOI: 10.1007/s12350-020-02439-z
Source DB: PubMed Journal: J Nucl Cardiol ISSN: 1071-3581 Impact factor: 3.872