18 F-FAPI Outperforms 18 F-FDG PET/CT in Detecting Focal Inflammation as a Cause of Refractory In-Stent Restenosis :
Hangyu Xie1, Xu Han1, Hongzhi Mi1
1Department of Nuclear Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases.
Clinical Nuclear Medicine
|June 8, 2026
Summary
Dual-tracer PET/CT imaging identified inflammation-associated coronary artery disease (I-CAD) in a patient with recurrent in-stent restenosis (ISR). This approach revealed fibroblast activity, guiding treatment away from revascularization towards anti-inflammatory therapy.
Area of Science:
- Cardiovascular Imaging
- Nuclear Medicine
- Radiochemistry
Background:
- Inflammation-associated coronary artery disease (I-CAD) is an underdiagnosed cause of refractory in-stent restenosis (ISR).
- Conventional imaging lacks sensitivity for detecting focal inflammatory activity in ISR.
- Fibroblast activation plays a role in peri-stent remodeling.
Purpose of the Study:
- To evaluate the utility of dual-tracer PET/CT imaging in a patient with recurrent ISR.
- To assess fibroblast activity and inflammation in the peri-stent region.
- To guide therapeutic management based on imaging findings.
Main Methods:
- A 74-year-old woman with recurrent ISR underwent dual-tracer ¹⁸F-FAPI and ¹⁸F-FDG PET/CT.
- PET/CT focused on the left anterior descending artery (LAD) stent segment.
- Radiotracer uptake patterns were analyzed to assess inflammatory activity and fibroblast remodeling.
Main Results:
- Dual-tracer PET/CT revealed increased radiotracer uptake in the LAD stent segment.
- ¹⁸F-FAPI uptake was more intense than ¹⁸F-FDG uptake, indicating fibroblast-related activity.
- Findings suggested an active inflammation-associated mechanism contributing to ISR.
Conclusions:
- Dual-tracer ¹⁸F-FAPI and ¹⁸F-FDG PET/CT can detect inflammation and fibroblast remodeling in recurrent ISR.
- This imaging approach aids in identifying I-CAD mechanisms.
- Findings supported anti-inflammatory therapy over repeat revascularization.
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