Assessing different approaches to estimate single-subject metabolic connectivity from dynamic [18F]fluorodeoxyglucose Positron Emission Tomography data.

Abstract

Metabolic connectivity is conventionally calculated in terms of correlation of static positron emission tomography (PET) measurements across subjects. There is increasing interest in deriving metabolic connectivity at the single-subject level from dynamic PET data, in a similar way to functional magnetic resonance imaging. However, the strong multicollinearity among region-wise PET time-activity curves (TACs), their non-Gaussian distribution, and the choice of the best strategy for TAC standardization before metabolic connectivity estimation, are non-trivial methodological issues to be tackled.In this work we test four different approaches to estimate sparse inverse covariance matrices, as well as three similarity-based methods to derive adjacency matrices. These approaches, combined with three different TAC standardization strategies, are employed to quantify metabolic connectivity from dynamic [18F]fluorodeoxyglucose ([18F]FDG) PET data in four healthy subjects.