The complementary roles of dynamic contrast-enhanced MRI and 18F-fluorodeoxyglucose PET/CT for imaging of carotid
Claudia Calcagno1, Sarayu Ramachandran, David Izquierdo-Garcia
1Translational and Molecular Imaging Institute, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1234, New York, NY, 10029, USA.
Purpose:
Inflammation and neovascularization in vulnerable atherosclerotic plaques are key features for severe clinical events. Dynamic contrast-enhanced (DCE) MRI and FDG PET are two noninvasive imaging techniques capable of quantifying plaque neovascularization and inflammatory infiltrate, respectively. However, their mutual role in defining plaque vulnerability and their possible overlap has not been thoroughly investigated. We studied the relationship between DCE-MRI and (18)F-FDG PET data from the carotid arteries of 40 subjects with coronary heart disease (CHD) or CHD risk equivalent, as a substudy of the dal-PLAQUE trial (NCT00655473).
Methods:
The dal-PLAQUE trial was a multicenter study that evaluated dalcetrapib, a cholesteryl ester transfer protein modulator. Subjects underwent anatomical MRI, DCE-MRI and (18)F-FDG PET. Only baseline imaging and biomarker data (before randomization) from dal-PLAQUE were used as part of this substudy. Our primary goal was to evaluate the relationship between DCE-MRI and (18)F-FDG PET data. As secondary endpoints, we evaluated the relationship between (a) PET data and whole-vessel anatomical MRI data, and (b) DCE-MRI and matching anatomical MRI data. All correlations were estimated using a mixed linear model.
Results:
We found a significant inverse relationship between several perfusion indices by DCE-MRI and (18)F-FDG uptake by PET. Regarding our secondary endpoints, there was a significant relationship between plaque burden measured by anatomical MRI with several perfusion indices by DCE-MRI and (18)F-FDG uptake by PET. No relationship was found between plaque composition by anatomical MRI and DCE-MRI or (18)F-FDG PET metrics.
Conclusion:
In this study we observed a significant, weak inverse relationship between inflammation measured as (18)F-FDG uptake by PET and plaque perfusion by DCE-MRI. Our findings suggest that there may be a complex relationship between plaque inflammation and microvascularization during the different stages of plaque development. (18)F-FDG PET and DCE-MRI may have complementary roles in future clinical practice in identifying subjects at high risk of cardiovascular events.
Insights
This study found a weak inverse relationship between inflammation (measured by FDG PET) and plaque perfusion (measured by DCE-MRI) in vulnerable atherosclerotic plaques. These imaging techniques may complement each other in identifying high-risk cardiovascular patients.
Area of Science:
- Cardiovascular Imaging
- Atherosclerosis Research
- Medical Diagnostics
Background:
- Atherosclerotic plaque inflammation and neovascularization are critical indicators of severe cardiovascular events.
- Dynamic contrast-enhanced MRI (DCE-MRI) quantifies plaque neovascularization, while (18)F-FDG PET measures inflammatory infiltrate.
- The combined role of these techniques in assessing plaque vulnerability requires further investigation.
Purpose of the Study:
- To investigate the relationship between DCE-MRI and (18)F-FDG PET data in carotid arteries of patients with coronary heart disease (CHD) or equivalent risk.
- To explore the correlation between plaque neovascularization (DCE-MRI) and inflammation (FDG PET).
- To assess secondary relationships between PET data, anatomical MRI, and DCE-MRI data.
Main Methods:
- Analysis of baseline data from the dal-PLAQUE trial, including anatomical MRI, DCE-MRI, and (18)F-FDG PET.
- Focus on 40 subjects with CHD or CHD risk equivalent.
- Correlation analysis using a mixed linear model to evaluate relationships between imaging metrics.
Main Results:
- A significant, weak inverse relationship was observed between DCE-MRI perfusion indices and (18)F-FDG uptake.
- Significant correlations were found between plaque burden (anatomical MRI) and both DCE-MRI perfusion and (18)F-FDG uptake.
- No significant relationship was identified between plaque composition (anatomical MRI) and DCE-MRI or (18)F-FDG PET metrics.
Conclusions:
- A weak inverse relationship exists between plaque inflammation (FDG PET) and microvascularization (DCE-MRI).
- These findings suggest a complex interplay between inflammation and neovascularization throughout plaque development.
- (18)F-FDG PET and DCE-MRI may offer complementary roles in identifying patients at high risk for cardiovascular events.
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