In silico imaging study reveals the potential of dSi-PCCT for assessing liver fat in human models, suggesting clinical utility.
Background Accurate liver fat quantification is essential for early diagnosis and effective management of fatty liver disease. Purpose To investigate the potential clinical utility of a deep silicon-based photon-counting CT (dSi-PCCT), currently in development, for liver fat quantification using human models in an in silico imaging study. Materials and Methods dSi-PCCT is a cutting-edge photon-counting CT (GE HealthCare), with several investigational systems installed globally, used under IRB approval for imaging animals and human volunteers to support FDA clearance. We developed a dSi-PCCT simulator and benchmarked its imaging performance with respect to a prototype. We imaged a computational Gammex phantom with fat fractions (FF) ranging from 0% to 100%, along with five XCAT human models with liver FF ranging from 1% to 50%, using an abdominal CT protocol. The resulting spectral sinograms were processed using a material decomposition (MD) technique. We calculated HU-based Proton Density Fat Fraction (PDFF) from single-energy images in XCAT models and compared it against the MD-derived FF. The MD-derived FF of both datasets were assessed against the digitally-defined ground truth values. Results We observed a strong correlation (R2 = 0.98) between MD-derived, HU-based PDFF and ground-truth FF in a Gammex and XCAT models. There was no statistically significant difference (p = 0.52) in FF quantification accuracy between Gammex and the XCAT human models. The root mean square errors were 4.7% for Gammex and 2.7% for XCAT. Bland-Altman analysis further confirmed good agreement between the ground truth and MD-derived FF, with differences in FF ranging from -6.9% to 7% for Gammex and -3.0% to 37.6% for XCAT. Conclusion The results indicate that dSi-PCCT could enable accurate liver fat quantification across a wide range of fat fractions in multiple objects. These findings suggest that the potential utility of dSi-PCCT for accurate liver fat assessment should be explored in vivo.
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