Authors
Hangyu Xie, Xu Han, Nan Nan, Xiaofen Xie, Zihe Yang, Juan Du, Haiyan Qian, Hongzhi Mi, Wei Dong
Published in
Clinical nuclear medicine. Volume 51. Issue 11. Pages 972-979. Nov 01, 2026. Epub Aug 10, 2026.
Abstract
Persistent inflammatory activity may contribute to recurrent in-stent restenosis (ISR) after percutaneous coronary intervention (PCI). This study aimed to evaluate the efficacy of 18F-FAPI PET/CT for detecting inflammation-related activity in recurrent ISR and to compare it with 18F-FDG PET/CT.
Patients with recurrent ISR after PCI and suspected persistent inflammatory mechanisms were prospectively enrolled. All patients underwent 18F-FAPI PET/CT, and 32 also underwent 18F-FDG PET/CT within 1 week. Patients were classified as having inflammation-related ISR or non-inflammation-related ISR by multidisciplinary adjudication. Visual and semiquantitative PET parameters were compared between groups and tracers.
Forty-four patients (mean age, 56.8±10.3 y) were included, including 31 with inflammation-related ISR and 13 with non-inflammation-related ISR. 18F-FAPI PET/CT showed positive findings in all 31 patients with inflammation-related ISR, compared with 3 of 13 patients with non-inflammation-related ISR (100% vs. 23.1%). Visual score, SUVmax, SUVmean, TBRblood, and TBRliver were all significantly higher in inflammation-related ISR than in non-inflammation-related ISR (all P<0.001). In the dual-tracer subgroup (n=32), 18F-FAPI PET/CT detected all inflammation-related ISR cases (20/20, 100%), whereas 18F-FDG PET/CT detected 8 of 20 (40.0%) (P<0.001). Compared with 18F-FDG, 18F-FAPI showed higher visual scores and significantly greater tracer uptake in inflammation-related ISR (all P<0.05).
18F-FAPI PET/CT demonstrated higher detectability of inflammation-related activity in recurrent ISR and provided better lesion-to-background contrast than 18F-FDG PET/CT. These findings support its potential role in the noninvasive assessment of coronary inflammatory activity after PCI.
PMID:
42853989
Bibliographic data and abstract were imported from PubMed on 10 Oct 2026.
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