Does arterial wall FAPI uptake on [68Ga]Ga-FAPI-04 PET/CT correlate with calcified plaque burden and cardiovascular risk factors in oncologic patients?
69 patients affected with oncological diseases referred for FAPI-directed PET/CT, mean age 63, 37.7% female.
[68Ga]Ga-FAPI-04 PET/CT imaging
Associations of arterial wall FAPI uptake with calcified plaque burden (number of plaques, plaque thickness, calcification circumference), cardiovascular risk factors, FAP-positive total tumor burden, and image noisesurrogate
[68Ga]Ga-FAPI-04 PET/CT identifies arterial wall lesions linked to calcified plaque burden, but its utility as a cardiovascular risk biomarker may be limited by image noise and lack of correlation with traditional risk factors.
PURPOSE: We aimed to assess prevalence, distribution, and intensity of in-vivo arterial wall fibroblast activation protein (FAP) uptake, and its association with calcified plaque burden, cardiovascular risk factors (CVRFs), and FAP-avid tumor burden. METHODS: Ga]Ga-FAPI-04 PET/CT. Arterial wall FAP inhibitor (FAPI) uptake in major vessel segments was evaluated. We then investigated the associations of arterial wall uptake with calcified plaque burden (including number of plaques, plaque thickness, and calcification circumference), CVRFs, FAP-positive total tumor burden, and image noise (coefficient of variation, from normal liver parenchyma). RESULTS: High focal arterial FAPI uptake (FAPI +) was recorded in 64/69 (92.8%) scans in 800 sites, of which 377 (47.1%) exhibited concordant vessel wall calcification. The number of FAPI + sites per patient and (FAPI +)-derived target-to-background ratio (TBR) correlated significantly with the number of calcified plaques (FAPI + number: r = 0.45, P < 0.01; TBR: r = - 0.26, P = 0.04), calcified plaque thickness (FAPI + number: r = 0.33, P < 0.01; TBR: r = - 0.29, P = 0.02), and calcification circumference (FAPI + number: r = 0.34, P < 0.01; TBR: r = - 0.26, P = 0.04). In univariate analysis, only body mass index was significantly associated with the number of FAPI + sites (OR 1.06; 95% CI, 1.02 - 1.12, P < 0.01). The numbers of FAPI + sites and FAPI + TBR, however, were not associated with other investigated CVRFs in univariate and multivariate regression analyses. Image noise, however, showed significant correlations with FAPI + TBR (r = 0.30) and the number of FAPI + sites (r = 0.28; P = 0.02, respectively). In addition, there was no significant interaction between FAP-positive tumor burden and arterial wall FAPI uptake (P ≥ 0.13). CONCLUSION: Ga]Ga-FAPI-04 PET identifies arterial wall lesions and is linked to marked calcification and overall calcified plaque burden, but is not consistently associated with cardiovascular risk. Apparent wall uptake may be partially explained by image noise.
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Aleksander Kosmala
Universitätsklinikum Würzburg
Sebastian E. Serfling
University of Würzburg
Kerstin Michalski
Klinik und Poliklinik für Nuklearmedizin
European Journal of Nuclear Medicine and Molecular Imaging
Johns Hopkins University
Medizinische Hochschule Hannover
Okayama University
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Kosmala et al. (Sat,) studied this question.
synapsesocial.com/papers/6a07b6427ba19a189e06b486 — DOI: https://doi.org/10.1007/s00259-023-06245-w