AI Article Synopsis

  • - The study aimed to see if F-fluorodeoxyglucose-positron emission tomography (FDG-PET/CT) could detect changes in vulnerable atherosclerotic plaques in a mouse model following treatment.
  • - Researchers fed ApoE mice a high-fat diet to create plaques and then treated them with various therapies for 9 weeks, finding that FDG-PET/CT successfully identified changes in plaque stability post-treatment.
  • - The findings indicate that FDG-PET/CT can noninvasively identify unstable atherosclerotic plaques and monitor their therapeutic responses, potentially aiding in drug discovery and assessment.

Article Abstract

Objective: This study sought to determine whether F-fluorodeoxyglucose-positron emission tomography/computed tomography could be applied to a murine model of advanced atherosclerotic plaque vulnerability to detect response to therapeutic intervention and changes in lesion stability. Approach and Results: To analyze plaques susceptible to rupture, we fed ApoE mice a high-fat diet and induced vulnerable lesions by cast placement over the carotid artery. After 9 weeks of treatment with orthogonal therapeutic agents (including lipid-lowering and proefferocytic therapies), we assessed vascular inflammation and several features of plaque vulnerability by F-fluorodeoxyglucose-positron emission tomography/computed tomography and histopathology, respectively. We observed that F-fluorodeoxyglucose-positron emission tomography/computed tomography had the capacity to resolve histopathologically proven changes in plaque stability after treatment. Moreover, mean target-to-background ratios correlated with multiple characteristics of lesion instability, including the corrected vulnerability index.

Conclusions: These results suggest that the application of noninvasive F-fluorodeoxyglucose-positron emission tomography/computed tomography to a murine model can allow for the identification of vulnerable atherosclerotic plaques and their response to therapeutic intervention. This approach may prove useful as a drug discovery and prioritization method.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686289PMC
http://dx.doi.org/10.1161/ATVBAHA.120.315239DOI Listing

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