Key result
Hybrid PET/MRI combines the complementary strengths of PET and MRI to allow comprehensive assessment of atherosclerotic plaques, advancing our understanding of atherogenesis and drug development.
Why the study?
Evaluating only luminal stenosis overlooks high-risk plaque features and pathophysiology, missing vulnerable non-stenotic plaques, but hybrid PET/MRI offers the potential to combine morphological and physiological assessment.
Hybrid PET/MRI offers a promising multimodal approach for the comprehensive assessment of atherosclerosis, combining morphological and physiological imaging to better identify vulnerable plaques.
May advance atherosclerosis research; leaves open clinical adoption pending prospective trials.
Atherosclerosis is a systemic inflammatory disease typified by the development of lipid-rich atheroma (plaques), the rupture of which are a major cause of myocardial infarction and stroke. Anatomical evaluation of the plaque considering only the degree of luminal stenosis overlooks features associated with vulnerable plaques, such as high-risk morphological features or pathophysiology, and hence risks missing vulnerable or ruptured non-stenotic plaques. Consequently, there has been interest in identifying these markers of vulnerability using either MRI for morphology, or positron emission tomography (PET) for physiological processes involved in atherogenesis. The advent of hybrid PET/MRI scanners offers the potential to combine the strengths of PET and MRI to allow comprehensive assessment of the atherosclerotic plaque. This review will discuss the principles and technical aspects of hybrid PET/MRI assessment of atherosclerosis, and consider how combining the complementary modalities of PET and MRI has already furthered our understanding of atherogenesis, advanced drug development, and how it may hold potential for clinical application.
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Evans et al. (2020) conducted a review in Atherosclerosis. Hybrid PET/MRI was evaluated. Hybrid PET/MRI combines the complementary strengths of PET and MRI to allow comprehensive assessment of atherosclerotic plaques, advancing our understanding of atherogenesis and drug development.
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