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Updated: Nov 6, 2025

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Synthesis of Monocyte-targeting Peptide Amphiphile Micelles for Imaging of Atherosclerosis
Published on: November 17, 2017
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Imaging Immunometabolism in Atherosclerosis
Philip Z Mannes1, Sina Tavakoli2,3,4
1Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Summary
This study explores immunometabolism in atherosclerosis, highlighting how in vivo metabolic imaging can reveal plaque immune cell activity. It reviews advances in understanding and imaging techniques for diagnosing and managing atherosclerosis.
Area of Science:
- Immunology
- Metabolic Imaging
- Cardiovascular Disease
Background:
- Growing recognition of links between intracellular metabolism and immune cell activation (immunometabolism) in atherogenesis.
- Limitations of current in vitro studies in replicating complex plaque microenvironments.
- Need for in vivo approaches to understand clinical implications of immunometabolic alterations.
Purpose of the Study:
- Address the gap in understanding immunometabolism in atherosclerosis using in vivo methods.
- Determine clinical implications of immunometabolic alterations for diagnosis and patient management.
- Review advances in metabolic imaging for atherosclerosis.
Main Methods:
- Focus on macrophages as key immune cells in atherosclerosis.
- Utilizing 18F-FDG (fluorodeoxyglucose) for Positron Emission Tomography (PET) imaging.
- Reviewing other promising PET radiotracers for metabolic imaging.
Main Results:
- 18F-FDG PET imaging shows promise for atherosclerosis risk stratification.
- 18F-FDG uptake in plaques is being further elucidated biologically.
- Metabolic imaging aids in monitoring therapeutic intervention response.
Conclusions:
- In vivo metabolic imaging is crucial for understanding atherosclerosis immunometabolism.
- 18F-FDG PET offers valuable insights into plaque activity and patient outcomes.
- Further research into novel radiotracers can enhance diagnostic and therapeutic strategies.
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