Simon Stute

Younès Moussaoui, Diana Mateus, Nasrin Taheri et al.

Implicit neural representations (INRs) have demonstrated strong capabilities in various medical imaging tasks, such as denoising, registration, and segmentation, by representing images as continuous functions, allowing complex details to be captured. For image reconstruction problems, INRs can also reduce artifacts typically introduced by conventional reconstruction algorithms. However, to the best of our knowledge, INRs have not been studied in the context of PET reconstruction. In this paper, we propose an unsupervised PET image reconstruction method based on the implicit SIREN neural network architecture using sinusoidal activation functions. Our method incorporates a forward projection model and a loss function adapted to perform PET image reconstruction directly from sinograms, without the need for large training datasets. The performance of the proposed approach was compared with that of conventional penalized likelihood methods and deep image prior (DIP) based reconstruction using brain phantom data and realistically simulated sinograms. The results show that the INR-based approach can reconstruct high-quality images with a simpler, more efficient model, offering improvements in PET image reconstruction, particularly in terms of contrast, activity recovery, and relative bias.

Yanna Cruz Cavalcanti, Thomas Oberlin, Nicolas Dobigeon et al.

Factor analysis has proven to be a relevant tool for extracting tissue time-activity curves (TACs) in dynamic PET images, since it allows for an unsupervised analysis of the data. Reliable and interpretable results are possible only if considered with respect to suitable noise statistics. However, the noise in reconstructed dynamic PET images is very difficult to characterize, despite the Poissonian nature of the count-rates. Rather than explicitly modeling the noise distribution, this work proposes to study the relevance of several divergence measures to be used within a factor analysis framework. To this end, the $β$-divergence, widely used in other applicative domains, is considered to design the data-fitting term involved in three different factor models. The performances of the resulting algorithms are evaluated for different values of $β$, in a range covering Gaussian, Poissonian and Gamma-distributed noises. The results obtained on two different types of synthetic images and one real image show the interest of applying non-standard values of $β$ to improve factor analysis.

Yanna Cruz Cavalcanti, Thomas Oberlin, Nicolas Dobigeon et al.

To analyze dynamic positron emission tomography (PET) images, various generic multivariate data analysis techniques have been considered in the literature, such as principal component analysis (PCA), independent component analysis (ICA), factor analysis and nonnegative matrix factorization (NMF). Nevertheless, these conventional approaches neglect any possible nonlinear variations in the time activity curves describing the kinetic behavior of tissues with specific binding, which limits their ability to recover a reliable, understandable and interpretable description of the data. This paper proposes an alternative analysis paradigm that accounts for spatial fluctuations in the exchange rate of the tracer between a free compartment and a specifically bound ligand compartment. The method relies on the concept of linear unmixing, usually applied on the hyperspectral domain, which combines NMF with a sum-to-one constraint that ensures an exhaustive description of the mixtures. The spatial variability of the signature corresponding to the specific binding tissue is explicitly modeled through a perturbed component. The performance of the method is assessed on both synthetic and real data and is shown to compete favorably when compared to other conventional analysis methods. The proposed method improved both factor estimation and proportions extraction for specific binding. Modeling the variability of the specific binding factor has a strong potential impact for dynamic PET image analysis.