TY - JOUR
T1 - Physically informed deep neural networks for metabolite-corrected plasma input function estimation in dynamic PET imaging
AU - Ferrante, Matteo
AU - Inglese, Marianna
AU - Brusaferri, Ludovica
AU - Whitehead, Alexander C.
AU - Maccioni, Lucia
AU - Turkheimer, Federico E.
AU - Nettis, Maria A.
AU - Mondelli, Valeria
AU - Howes, Oliver
AU - Loggia, Marco L.
AU - Veronese, Mattia
AU - Toschi, Nicola
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/11
Y1 - 2024/11
N2 - Introduction: We propose a novel approach for the non-invasive quantification of dynamic PET imaging data, focusing on the arterial input function (AIF) without the need for invasive arterial cannulation. Methods: Our method utilizes a combination of three-dimensional depth-wise separable convolutional layers and a physically informed deep neural network to incorporatea priori knowledge about the AIF's functional form and shape, enabling precise predictions of the concentrations of [11C]PBR28 in whole blood and the free tracer in metabolite-corrected plasma. Results: We found a robust linear correlation between our model's predicted AIF curves and those obtained through traditional, invasive measurements. We achieved an average cross-validated Pearson correlation of 0.86 for whole blood and 0.89 for parent plasma curves. Moreover, our method's ability to estimate the volumes of distribution across several key brain regions – without significant differences between the use of predicted versus actual AIFs in a two-tissue compartmental model – successfully captures the intrinsic variability related to sex, the binding affinity of the translocator protein (18 kDa), and age. Conclusions: These results not only validate our method's accuracy and reliability but also establish a foundation for a streamlined, non-invasive approach to dynamic PET data quantification. By offering a precise and less invasive alternative to traditional quantification methods, our technique holds significant promise for expanding the applicability of PET imaging across a wider range of tracers, thereby enhancing its utility in both clinical research and diagnostic settings.
AB - Introduction: We propose a novel approach for the non-invasive quantification of dynamic PET imaging data, focusing on the arterial input function (AIF) without the need for invasive arterial cannulation. Methods: Our method utilizes a combination of three-dimensional depth-wise separable convolutional layers and a physically informed deep neural network to incorporatea priori knowledge about the AIF's functional form and shape, enabling precise predictions of the concentrations of [11C]PBR28 in whole blood and the free tracer in metabolite-corrected plasma. Results: We found a robust linear correlation between our model's predicted AIF curves and those obtained through traditional, invasive measurements. We achieved an average cross-validated Pearson correlation of 0.86 for whole blood and 0.89 for parent plasma curves. Moreover, our method's ability to estimate the volumes of distribution across several key brain regions – without significant differences between the use of predicted versus actual AIFs in a two-tissue compartmental model – successfully captures the intrinsic variability related to sex, the binding affinity of the translocator protein (18 kDa), and age. Conclusions: These results not only validate our method's accuracy and reliability but also establish a foundation for a streamlined, non-invasive approach to dynamic PET data quantification. By offering a precise and less invasive alternative to traditional quantification methods, our technique holds significant promise for expanding the applicability of PET imaging across a wider range of tracers, thereby enhancing its utility in both clinical research and diagnostic settings.
KW - AIF
KW - IDIF
KW - Metabolic imaging
KW - PET
KW - Physics informed neural networks
KW - TSPO
UR - http://www.scopus.com/inward/record.url?scp=85201677751&partnerID=8YFLogxK
U2 - 10.1016/j.cmpb.2024.108375
DO - 10.1016/j.cmpb.2024.108375
M3 - Article
AN - SCOPUS:85201677751
SN - 0169-2607
VL - 256
JO - Computer methods and programs in biomedicine
JF - Computer methods and programs in biomedicine
M1 - 108375
ER -